WO2001062763A1 - Method for inhibiting trypsin-type serine proteases - Google Patents

Abstract

Trypsin-type serine protease inhibitors being compounds having groups represented by the general formula (1) or (2) (wherein R?1 and R2¿ are each hydrogen, halogeno, ethynyl, or the like; R?3 and R4¿ are each hydrogen, hydroxyl, or amino; X¿1?, X2, X3 and X4 are each CH or N; Y1 and Y2 are each CH or N; and Y3 is NH, O or S). When such a compound is made to act on a trypsin-type serine protease, the group enters the S1 pocket to thereby exert an inhibitory activity against the protease.

Description

 Description Technique for inhibiting trypsin-type serine protease

 The present invention relates to a method for inhibiting a serine protease having a trypsin-type substrate specificity. From another viewpoint, the present invention relates to a partial structure of an inhibitor that enters a pocket at the S1 site in the active site of a serine protease having trypsin-type substrate specificity and interacts specifically with the pocket. Further, the present invention relates to a serine protease inhibitor having such a partial structure and having a trypsin-type substrate specificity. Background art

 Beptidases that degrade proteins and peptides are classified into several types based on the type of catalytic site in the active center. One type is a group of peptidases called serine proteases. Serine proteases are characterized by their three-dimensional structure, such as chymotrypsin, subtilisin (subti 1 isin), carboxypeptidase C (car boxype pti dase C), and escherichia D—A1a—D. — A1 a-peptidase A (Escherichia D-A1a-D-A1 aetidase A) Among them, the serine proteases of chymotrypsin, subtilisin, and lipoxypeptidase C have a common catalytic site composed of His57, AsplO2 and Ser195 (Me t hod sin Enzymology, 224, 191-161, 1994).

The serine proteases of chymotrypsin form an S1 site adjacent to the catalytic site. It has a clear pocket called SI pocket. The pocket plays a major role in exhibiting substrate specificity. Chymotrypsin serine proteases are based on their substrate specificity, and have a chymotrypsin-type serine protease and arginine, which have a chymotrypsin-type substrate specificity that recognizes hydrophobic amino acid residues such as phenylalanine residues and exerts substrate specificity. It is classified as a trypsin-type serine protease having substrate specificity that recognizes basic amino acid residues such as residues and exhibits substrate specificity. A serine protease with trypsin-type substrate specificity has Asp 189 deep in the S1 bucket and forms an ion bond with a basic amino acid residue such as an arginine residue. Expressing sex. On the other hand, the serine protease having chymotrypsin-type substrate specificity has Ser189 in the deep part of the S1 pocket instead of Asp189, and recognizes a hydrophobic amino acid residue in the entire pocket. Such differences in the amino acid residues in the S1 pocket are the basis for the differences in substrate specificity between the two groups (Eur. J. Biochem., 260, 571-595, 1999). ).

Serine proteases having trypsin-type substrate specificity (hereinafter, trypsin-type serine proteases) are involved in the activation of enzymes having a physiologically important role. For example, activated blood coagulation factor X f (hereinafter FXa) is a trypsin-type serine protease and is involved in the blood coagulation system. FXa produces thrombin by limited hydrolysis of prothrombin. The generated thrombin activates platelets, promotes platelet aggregation, and converts fibrinogen to insoluble fibrin. This fibrin is a sticky fibrous polymer that plays a crucial role in forming a strong thrombus. FXa is an enzyme that thus plays an important role in thrombus formation. Therefore, FXa inhibitors are expected as preventive and / or therapeutic agents for various cardiovascular diseases associated with thrombus. By the way, in recent studies on enzyme inhibitors, it is considered that a three-dimensional model of an enzyme based on X-ray crystallographic analysis is displayed on a screen using a computer and has an inhibitory effect For example, a method of devising a compound to be used or docking a compound that is considered to have an inhibitory effect on the three-dimensional model and performing virtual screening is used. FXa was also analyzed by X-ray crystallography, and the coordinates of each atom were published in Protein Data Bank (PDB code: 1HCG). Using that data, the three-dimensional structure of FXa and the three-dimensional shape of the active center can be displayed, and can be used to create new FXa inhibitors. For example, the S1 pocket of FXa, which recognizes the arginine residue of prothrombin,

 D As p l 89-Al a l 90-Cy s l 91-G l n l 92-G l y l 93 -A s p 194

 2) Va l 213-S e r 214-Tr p 215-G l y216-G l u217 -G l y218-Cy s 220

 3) G 1 y 226-I I e 227-Ty r 228

It can be seen that it is composed of The number of the amino acid residue is based on the number of the amino acid residue of chymotrypsin as described in J. Mo 1. Biol., 232, pp. 947-966 (1993). The same applies to other serine proteases described below.

 In addition, the X-ray crystallography data showed that the catalytic site of FXa was composed of His 57, Asp 102, and Ser 195, and that the space created by these amino acid residues The size and the three-dimensional mutual positional relationship of each amino acid residue can be known. Furthermore, it can be easily understood that the catalytic site is adjacent to the S 1 pocket.

 Figure 1 conceptually shows the FX1 S1 pocket.

Compounds that have a strong interaction with the S1 pocket of FXa prevent FXa from recognizing the arginine residue of prothrompine in the S1 pocket, thereby inhibiting FXa function. Such interaction with the S1 pocket includes a strong ionic bond between As 189 located deep in the S1 pocket and an amidino or guanidino group. The match is known. FX a inhibitors with amidino or guanidino groups

(Bioc hemi stry, 34, 3750, 1995) include DX-9065a and FX-2212a (Proc. Natl. Ac ad. Sci. USA, 95, 6630-6635, 1998). Figure 2 conceptually shows that DX-965a and FX-2212a interact with the SI pocket.

 Amidine derivatives (or guanidine derivatives), such as the compounds shown in FIG. 2, ionically bind to the S1 pocket and exhibit a strong FXa inhibitory action, whereas FXa inhibitors having an amidino or guanidino group are Due to the strong basicity of the group, oral absorption is low and it has difficulties as an oral preparation. Therefore, in order to create FXa inhibitors with excellent oral absorption, it is necessary to discover new partial structures that interact with the S1 pocket in a manner other than ionic binding to Asp189. You.

 These are examples of FXa inhibitors.Trypsin-type serine proteases all have similar S1 pockets, and we will try to find inhibitors with good oral absorption for them In some cases, it has a common problem that it is necessary to find a new partial structure that interacts with the S1 pocket by an action other than ionic binding to Asp189.

 As described above, in order to find a trypsin-type serine protease inhibitor with excellent oral absorbability, the partial structure of a new inhibitor that interacts with the S1 pocket in a manner other than ionic binding to Asp189 It was essential to discover. Disclosure of the invention

In order to solve the above-mentioned problem, that is, the problem of discovering a new partial structure necessary for the development of a trypsin-type serineb-oralase inhibitor excellent in oral absorption, human FXa and ゥTrypsin. Trypsin-type serine protease As a representative example, we sought to discover a new substructure that interacts with the S1 bottle in a manner other than ionic binding to Asp189.

 The present inventors crystallized a complex of a drug having no amidino group or guanidino group and FXa or trypsin and analyzed it by X-ray analysis.As a result, it was found that the S1 pocket was formed in a manner other than the ionic bond with Asp189. A new partial structure of a trypsin-type serine proteinase inhibitor that interacts was found.

 X-ray crystallography of the complex of FXa and the drug was performed using the following indole derivative (5), benzothiophene derivative (6) and naphthalene derivative (7).

FIG. 3 shows a conceptual diagram of the interaction of the 5_clodindole-2-sulfonyl group with the S1 pocket of FXa based on the results of X-ray crystallography. Further, based on the compound (5) and the complex X-ray crystallography of the FX a result, in FIG 5 Kuroroi Ndoru - and 2-sulfonyl group, 9 chlorine atoms in the group X 10- ⁸ cm The atoms in the S 1 pocket within are shown in stereo.

 In addition, X-ray crystallography of a complex of pepsin trypsin and a drug was performed using the following naphthalene derivative (8).

The results are shown in a stereo diagram in FIG.

 As described above, it can be seen that the indole ring (or benzothiophene ring or naphthalene ring) enters the S1 pocket of FXa, and the naphthalene ring enters the S1 pocket of trypsin. These bicyclic aromatic ring groups or bicyclic aromatic heterocyclic groups (hereinafter collectively referred to as a bicyclic aromatic ring group or a bicyclic aromatic ring group) and an S1 pocket The interaction of

 1) Hydrophobic interaction

2) The following interactions a) Stacking of the i3-sheet consisting of the amino acid residues forming the S1 pocket and the indole ring (or benzothiophene ring or naphthylene ring) b) Consisting of the amino acid residues forming the S1 pocket Π-7T interaction between peptide bond and indole ring (or benzothiophene or naphthylene ring) c) Side chain of amino acid residue forming S1 pocket and indole ring (or benzothiophene or naphthalene ring) ) With CH—7T interaction

And so on.

 FX a S1 pocket, as mentioned above

D As p l 89-Al a l 90-Cy s l 91-G l n'192-Gl y l 93 -A s p 194

 2) Va l 213-S e r 214-Tr p 215-G l y216-G l u217 -G l y218-Cy s 220

 3) G l y 226- I I e 227-Ty r 228

It is composed of The X-ray crystallographic data of trypsin from Escherichia coli has been published in the PDB Tin Data Bank (PDB code: 1TTP).

 D As p l 89-S er l 90-Cy s l 91-G l n l 92-Gl y l 93 -A s ρ 194

 2) Va l 213-S e r 214-Tr p 215-G l y216-S e r 217 -G l y219-Cy s 220

 3) G l y 226-Va l 227-Ty r 228

It is composed of A comparison of the amino acid residues that make up the S1 pocket of both enzymes reveals that some of the amino acid residues are different. In particular, FXa's A1a190 replaces Ser190 in trypsin. However, the partial structures of the inhibitors interacting with the S1 pocket of both enzymes are all bicyclic aromatic groups. From this result, the present inventors have found that the amino acid residue in the S1 pocket is It has been found that these bicyclic aromatic ring groups can be utilized as partial structures of inhibitors even for different tribosine-type serine proteases. In this case, the trypsin is used. Comparing the amino acid residues that make up the S1 pocket of human and human trypsin (PDB c 0 de: 1 TRN), human Ser 217 is substituted for human Asp 217. The S1 pocket has a similar structure and function. : '

 As can be seen from the above stereo diagram of the complex of FXa and compound (5) (Fig. 4),? Deep in the & 31 pocket is a hydrophobic space formed by Alal 90, Va1213 and Tyr228, which is occupied by the chloro atom of the 5-chloroindolyl group. Therefore, it can be seen that the chloro atom has a hydrophobic interaction with A1a190, Va1213 and Tyr228. Above all, it is considered that hydrophobic interaction with Ty r 228 is strongly acting. Figure 6 shows a conceptual diagram of the interaction between the S1 pocket and the 5-drill indolyl group.

 Similarly, there is a similar space formed by Ser 190, Va 1 213 and Tyr 228 in the deep part of the S1 pocket of the trypsin, and the chloro atom of the 5-chloronaphthyl group is also in that space. Occupy. Also in this case, it is considered that the chloro atom has a hydrophobic interaction with Tyr228 and the like.

 Thus, the present inventor has proposed that as the interaction site in the S1 pocket, in addition to the entire amino acid residues constituting the S1 pocket, Alal 90, Va 1213 and Tyr 228, or Ser 90, Va A new interaction site composed of 1213 and Tyr228 was found. This interaction site is useful for drug design of an inhibitor of trypsin-type serine protease.

From the above, the present inventors have proposed a trypsin-type serine protease having an amino acid residue of Alal 90, Va 1213 and Tyr 228, or Ser 190, Va 1213 and Tyr 228 in the S1 pocket. The partial structure of the inhibitor The inventors have found that a cyclic aromatic ring group is preferable, and have completed the present invention.

 That is, the present invention provides the following general formula (1) or (2)

(Wherein, R ¹ and R ² represent a hydrogen atom, an alkyl group of CI—C 3, a halogen atom, an alkenyl group or an ethenyl group of C 2 _C 3, and R ³ and R ⁴ represent a hydrogen atom, a hydroxyl group or Represents an amino group, XX ₂ , X ₃ and X ₄ represent CH or N, and Y ₂ represents CH or 、, and Y ₃ represents ΝΗ, 〇 or S.) An object of the present invention is to provide a method for inhibiting a trypsin-type serine protease by causing a compound having a group to act on trypsin-type serine protease and causing the group to enter the S1 pocket of the trypsin-type serine protease. The present invention also provides a compound that inhibits a trypsin serine protease and has a group represented by the above general formula (1) or (2) that enters the S1 pocket of the trypsin serine protease. Is what you do.

 Further, the present invention relates to a compound having a group represented by the above general formula (1) or (2), which exhibits an FXa inhibitory action by entering the S1 pocket of FXa. To provide.

The present invention also provides a medicine comprising a compound that inhibits trypsin serine protease or a compound that inhibits FXa as an active ingredient by the above method. is there.

 The present invention also provides a trypsin-type serine protease inhibitor comprising, as an active ingredient, a compound that inhibits trypsin-type serine protease by the above method.

 The present invention also provides an FXa inhibitor comprising, as an active ingredient, a compound that inhibits FXa by the above method.

 The present invention further provides a trypsin-type serine protease using data obtained by X-ray analysis of crystals of a complex of the above-mentioned compound that inhibits trypsin-type serine protease and trypsin-type serine protease. It is intended to provide a method for using a computer to screen for a drug that is expected to inhibit the drug. BRIEF DESCRIPTION OF THE FIGURES

 FIG. 1 is a conceptual diagram showing the S1 pocket of FXa.

 FIG. 2 is a conceptual diagram showing that DX-9605a or FX-2212a interacts with the S1 pocket.

 FIG. 3 is a conceptual diagram showing the interaction between the 5_cloin indole-2-sulfonyl group and the S1 pocket of FXa based on the results of X-ray crystallography. In addition, in the figure, the indole ring of Trp215 is omitted.

4, compound (5) and FX a complex with X-ray crystallography analysis result based on 5-click Rollo indole of - 2-sulfonyl group with 9 X 1 0- ⁸ cm or less in the chlorine atoms in the group FIG. 3 is a stereo view showing the atoms of the S 1 pocket in FIG.

 Figure 5 shows that the 6-chloronaphthalene-2-sulfonyl group has entered the S1 pocket based on the X-ray crystallography of the complex of pepsin trypsin and the naphthylene derivative (8). FIG.

FIG. 6 is a conceptual diagram showing the interaction between the 31 pocket of & and the 5-drill indolyl group. BEST MODE FOR CARRYING OUT THE INVENTION

 The C1-C3 alkyl group in the above general formula (1) or (2) means a methyl group, an ethyl group, an n-propyl group, an isopropyl group and a cyclopropyl group. The C2-C3 alkenyl group refers to a vinyl group, an aryl group or an isopropyl group. Halogen atoms include fluorine, chlorine, bromine and iodine.

 The trypsin-type serine protease refers to a serine protease having trypsin-type substrate specificity that recognizes a basic amino acid residue such as an arginine residue and exerts substrate specificity as described above. Such trypsin-type serine proteases have Asp189 in the S1 pocket, which is closely related to exhibiting substrate specificity.

 Also, a group represented by the general formula (1) or (2) enters the S1 pocket and inhibits trypsin-type serine protease when the group represented by the general formula (1) or (2) To enter one pocket, prevent the side chain of the basic amino acid residue of the substrate from entering the S1 pocket, inhibit the trypsin-type serine proteinase from recognizing the substrate, and inhibit the peptide cleavage function That means. The fact that the group represented by the general formula (1) or (2) enters the S1 pocket means that the trypsin-type serine protease and the compound having the group represented by the general formula (1) or (2) It can be confirmed by X-ray crystallography of salts or complexes with their solvates. However, not all of these complexes can always be crystallized and X-ray crystallographic analysis is possible. Also, the group represented by the general formula (1) or (2) is thought to interact not only with the S1 pocket but also with the amino acid residue forming the S1 pocket. Can be Interaction with the entire S 1 pocket includes

1) Hydrophobic interaction

2) The following interactions a) iS consisting of the amino acid residues forming the S1 pocket, and interlocking between the indole ring (or benzothiophene ring or naphthalene ring) b) consisting of the amino acid residues forming the S1 pocket Π-π interaction between peptide bond and indole ring (or benzothiophene or naphthalene ring) c) Side chain of amino acid residue forming S1 pocket and indole ring (or benzothiophene or naphthalene ring) C と — 7Τ interaction with)

And the like. In the past, in addition to these, interaction by ionic binding with Asρ189 was known, but the partial structures (1) and (2) of the trypsin-type serine protease inhibitor in the present invention are as follows: In addition to interacting with the entire S1 pocket, it has a hydrophobic interaction with sites consisting of Alal90, Va1213 and Tyr228, or Ser190, Va1213 and Tyr228. It is characteristic.

 Hereinafter, the group represented by formula (1) or (2) will be described in detail.

 The groups represented by the general formulas (1) and (2) are represented by the following general formulas (3) and (4)

(Wherein, R ′, R ² , R ³ , R ⁴ , XX ₂ , X ₃ , X ₄ , YY ₂ and Y ₃ represent the same as described above, and A and B represent a sulfonyl group, a carbonyl group, Represents a methylene group, an oxygen atom, a zeolite atom or a nitrogen atom.) Alternatively, it is preferable that the compound binds to B and further binds to various groups to form a compound that inhibits trypsin-type serine protease.

 Specific examples of the partial structures represented by the general formulas (3) and (4) include:

 1) naphthalene 1-sulfonyl group, indole-2 (or 3) monosulfonyl group, benzofuran 1-2 (or 3) —sulfonyl group, benzothiophene-2 (or 3) —sulfonyl group, benzimidazole-2-sulfonyl group Bicyclic aromatic ring sulfonyl groups such as benzothiazol-2-sulfonyl group, indazo-l-3-sulfonyl group, benzoxazo-l-2-sulfonyl group, and benzisoxazole-3-sulfonyl group;

 2) Naphthylene-1 2-carbonyl group, indole-2 (or 3) low-potency liponyl group, benzofuran 1-2 (or 3) low-potency luponyl group, benzothiophene 1-2 (or 3) —carbonyl group, Benzoimidazole-2-carbonyl group, benzothiazol-2-carbonyl group, indazo-l-un 3-ruponyl group, benzoxazo-ru- 2-carponyl group, benzisoxazo-l-un 3-bicyclic aromatic carbonyl group etc. Group,

 3) naphthalene 1-2-methyl group, indole 1-2 (or 3) —methyl group, benzofuran 1-2 (or 3) —methyl group, benzothiophene 1-2 (or 3) —methyl group, benzimidazole-2-methyl Bicyclic aromatic ring methyl groups such as benzothiazole-2-methyl group, indazol-3-methyl group, benzoxazoluru-2-methyl group, and benzisoxazoluru-3-methyl group;

 4) Naphthylene 1-oxy group, India 1 2 (or 3) — oxy group, benzofuran — 2 (or 3) — oxy group, benzothiophene 1 2 (or 3) — oxy group, benzimidazole — A bicyclic aromatic oxy group such as 2-oxy group, benzothiazole_2-oxy group, and indazol-3-oxy group;

5) Naphthylene-1 2-thio group, India 1-Lu 2 (or 3) —thio group, benzofuran—2 (or 3) —thio group, benzothiophene 1-2 (or 3) —thio group, Bicyclic aromatic ring thio groups such as benzimidazo-l-uthio group, benzothiazo-l-uo 2-thio group, indazo-l-uo 3-thio group,

 6) naphthalene-1-amino, indole-1 (or 3) —amino, benzofuran 1-2 (or 3) —amino, benzothiophene 1-2 (or 3) —amino, benzimidazole_2-amino Group, benzothiazole-2-amino group, indazole-3-amino group, benzoxazole-1-amino group, benzisoxazolu-3-amino group, etc.

And a bicyclic aromatic ring amino group.

As the substituents R ¹ and R ² on the benzene ring part of these groups, a fluoro group, a chloro group, a bromo group, an odo group and a ethynyl group are preferable, and a chloro group, a promo group and an ethynyl group are more preferable. preferable. Among the partial structures represented by general formulas (3) and (4),

 (1) 6-chloronaphthalene-12-sulfonyl group, 6-chloronaphthalene-12-carbonyl group, 61-ethynylnaphthalene-12-sulfonyl group, 6-ethynylnaphthalene-12-caprolponyl group,

 (2) 5-cycloindole-2-sulfonyl group, 5-cycloindole-2-carbonyl group, 5-ethynylindole-2-sulfonyl group, 5-ethynylindole-2-caprolponyl group,

 (3) 6-chloro-benzothiophene-2-sulfonyl group, 6-chloro-benzothiophene-2 monoluponyl group, 6-ethynylbenzothiophene 1-2-sulfonyl group, 6-ethynylbenzothiophene _ 2 _ carbonyl group,

 (4) 5-chloro-benzo-furan-2-sulfonyl group, 5-chloro-benzo-furan-2-fluoropropionyl group, 5-ethynyl benzofuran-12-sulfonyl group, 5-ethynyl benzofuran-12-yl sulfonyl group Are preferred.

As mentioned earlier, deep in the & 31 pocket there is a hydrophobic space formed by Alal 90, V a 12 13 and T yr 2 28, There is a similar space formed of Serl90, Va1213 and Tyr228. These spaces are occupied by black or ethynyl groups. Among the sound 15-minute structures in the present invention, 6-chloro-naphthylene-12-sulfonyl group, 5-chloro-indole-12-sulfonyl group, 6-chloronaphthalene-12-force luponyl group, 5-chloro-indolole 2-Ruponyl group, 6-Ethynylnaphthylene 2-Sulfonyl group, 5-Ethynylindole-2-Sulfonyl group, 6-Ethynylnaphthalene One-one-strength luponyl group, 5-Ethynylindole 2- Particularly preferred is a sulfonyl group and the like, because the chloroethynyl group occupies the above space and interacts with the amino acid residues forming the space. In particular, it is considered that the contribution of hydrophobic interaction with Tyr228 is large.

 Therefore, in the present invention, a compound having the above-mentioned preferred group as a partial structure is a preferred trypsin-type serine protease inhibitor.

 By the way, as described above, not only Fxa but also other trypsin-type serine proteases have similar S1 pockets. Thus, the findings obtained for the inhibition of human Fxa and pepsin trypsin are applicable to other serine proteases. Hereinafter, this point will be described in detail.

3 has a hydrophobic space formed from Alal 90, Va1 2 13 and Tyr2 28 deep in the 3 1 pocket, but that part is Ser1 90, Va1 The same bicyclic aromatic ring group, for example, 6-chloronaphthalene-12-sulfonyl group, also exists in S 1 Interacts with the above hydrophobic spaces in the pocket and the S1 pocket. This means that the hydrophobic space formed from A1a190, Va1213 and Tyr228 in the S1 pocket of FXa is Ser190, Va1 It also shows that common bicyclic aromatic ring groups can be used as partial structures of inhibitors as well as in trypsin of Psi that has been changed to 213 and Tyr228. As described above, the bicyclic aromatic ring group of the present invention comprises a trypsin-type serine protease. Widely applicable to general, especially in S1 pocket

 1) A l a l 90, V a 1 213 and Ty r 228,

 2) S er l 90, Val 213 and Ty r 228,

 3) S er l 90, T h r 213 and T y r 228,

 4) A 1a 190, Va 1 213 and P he 228,

 5) Th r l 90, T h r 213 and T y r 228,

 6) A la 190, I 1 e 213 and T y r 228,

 7) S er l 90, I 1 e 213 and T y r 228,

 8) G l y l 9'0, T h r 213 and T y r 228, or

 9) Th r l 90, T h r 213 and T y r 228

This is useful for a trypsin-type serine protease having a space formed from. A human trypsin-type serine protease having a space formed from these amino acid residues is exemplified below. Examples of Ala90, Va1213 and Tyr228 include FXa, thrombin, activated protein C (PDB code: 1 AUT) and the like. Examples of Serl 90, Va 1 213 and Tyr 228 include human (and human) trypsin (PDB code: 1 TRN), complement factor D (PDB code: 1B IO), activated blood Coagulation factor VEa (PDB code: 1DAN), tryptase (PDB code: 1 AOL) and the like can be mentioned. Examples of Ser 190, Thr 213 and Tyr 228 include enterobeptidase

(PDB code: 1 EKB). Examples of A 1 a 190, I 1 e 213 and Tyr 228 include t-PA (PDB code: 1 A5H). Examples of Serl 90, 1 16213 Pho 228 include blood coagulation factor Ka (PDB code: 1 RFN). Examples of Glyl 90, Thr 213 and Tyr 228 include plasmin (PDB code: 1 BU I). What The examples of these trypsin serine proteases do not limit the trypsin serine protease to which the present invention can be applied.

 In order to facilitate understanding of the present invention, an FXa inhibitor which exhibits an inhibitory action by entering into the S1 pocket will be described below.Examples of the trypsin-type serine protease inhibitor of the present invention will be described. Is not limited at all.

 Specific examples of F Xa inhibitors include the following general formula (9)

(In the formula, A benzene ring, a pyrrole ring, a furan ring, Chiofen ring, an imidazole ring, a thiazole ring, Okisazoru ring, indicates isoxazole ring or a pyrazole Ichiru ring, X is shows a halogeno group or Echiniru group, R ⁵ Represents an unsaturated 5-membered to 6-membered or 6-membered to 6-membered bicyclic fused heterocyclic ring or a tetrahydro form thereof, which may have a substituent; R ⁶ represents an alkyl group having 1 to ⁶ carbon atoms; An alkoxycarbonyl group having an alkoxy group having 1 to 6 carbon atoms, a carboxyalkyl group having 1 to 6 carbon atoms, an alkoxyl group having 2 to 7 carbon atoms having an alkoxyl group having 1 to 6 carbon atoms, a substituent And a functional rubamoyl group which may have a substituent.) An FXa inhibitor represented by the formula:

The substituents in the above compound will be described below. The halogeno group means a fluoro group, a chloro group, a bromo group and a halide group, and a chloro group and a bromo group are preferred. Unsaturated 5- to 6-membered or 6- to 6-membered bicyclic fused heterocyclic ring means isoquinoline, quinoline, indole, benzofuran, benzothiophene, benzui Specific examples include midazole, benzothiazol, indazole, chenopyridine, flopyridin, pyridine, thiazolopyridine, oxazolopyridine or oxazolopyridazine. Preferred condensed forms of chenopyridine, flopyridin, pyropyridine, thiazolopyridine, oxazolopyridine and oxazolopyridazine are thieno [2,3-c] pyridine, flo [2,3-c] pyridine, pyro [2 , 3-c] pyridine, thiazolo [5,4-c] pyridine, oxazolo [5,4-c] pyridine and oxazolo [4,5-d] pyridazine. Examples of the group which may be substituted on these bicyclic fused heterocycles include an alkyl group, a hydroxyl group, an amino group mono- or di-substituted with an alkyl group having 1 to 6 carbon atoms, or a methanesulfonyl group. Can be. Specific examples of the mono- or di-substituted amino group include linear, branched or cyclic alkyl having 1 to 6 carbon atoms such as methylamino, ethylamino, propylamino, butylamino, cyclopentylmethylamino, etc. Amino, dimethylamino, dimethylamino, dipropylamino, dibutylamino, N-methyl-N-ethylamino, N-ethyl-N-propylamino, N-methyl-N-cyclopentyl Amino group, pyrrolidino group, piperidino group, homopiperidino group di-substituted by a linear, branched or cyclic alkyl group having 1 to 6 carbon atoms such as an amino group, N-methyl-N-cyclopentylmethylamino group, etc. 3- to 7-membered aliphatic cyclic amino group, morpholino group, piperazino group, etc. In the ring of the ring-shaped Amino group include a further nitrogen atom, 3-7 membered cyclic Amino group containing an oxygen atom and 1 or allogeneic or more heteroatom heterogeneous selected from Iou atoms.

Examples of the substituent group that may have a substituent include an unsubstituted carpamoyl group (H ₂ NCO _), a methylaminocarbonyl group, an ethylaminocarbonyl group, a propylaminocarbonyl group, and an isopropylaminocarbonyl group. , Butylaminocarbonyl group, isobutylaminocarbonyl group, pentylaminocarbonyl Linear group having 1 to 6 carbon atoms such as group, isopentylaminocarbonyl group, hexylaminocarbonyl group, isohexylaminocarbonyl group, cyclopropylaminocarbonyl group, cyclopentylmethylaminoamino group, etc. Mono-substituted aminocarbonyl group with branched or cyclic alkyl group, dimethylaminocarbonyl group, ethylaminocarbonyl group, dipropylaminocarbonyl group, diisopropylaminocarbonyl group, dibutylaminocarbonyl group, diisobutylamine C1-C6 linear or branched, such as minocarbonyl group, dipentylaminocarbonyl group, methylethylaminocarbonyl group, ethylpropylaminocarbonyl group, methylisopropylaminocarbonyl group, methylbutylaminopropyl group Or a ring of the same kind Or a 3- to 7-membered aliphatic cyclic aminocarbonyl group such as an aminocarbonyl group, a piperidinocarbonyl group, a pyrrolidinocarbonyl group, etc., which are disubstituted by a different alkyl group, a morpholinocarbonyl group, a piperazinocarbonyl group, etc. A cyclic aminocarbo having one or more of the same or different heteroatoms selected from a nitrogen atom, an oxygen atom and an iodine atom in the ring of the aliphatic cyclic amino group of the above-mentioned 3 to 7-membered aliphatic cyclic aminocarbonyl group. And a benzyl group. Examples of the carbamoylalkyl group which may have a substituent include a group in which an alkyl group having 1 to 6 carbon atoms is substituted by the carbamoyl group which may have the substituent.

In the above FXa inhibitor, not only the partial structure interacting with the S1 pocket but also the aryl binding site composed of Tyr99, Phe174 and Trp215 is called. It has an interaction site with the substrate. Therefore, if the FXa inhibitor has a hydrophobic substituent that interacts with the aryl binding site along with a partial structure that interacts with the S1 pocket in the structural formula, Exhibits FXa inhibitory action. Trypsin-type serine proteases do not necessarily have the same aryl binding site as FXa. ^ Each trypsin-type serine protease has a selective and potent inhibitory action. It goes without saying that in order to create a drug that possesses this, it is necessary to devise parts other than the partial structure that interacts with the S1 pocket. Another object of the present invention is to develop an orally absorbable trypsin-type serine protease inhibitor. Therefore, a trypsin-type serine protease inhibitor having a group represented by the general formula (1) or (2) or the general formula (3) or (4) is a compound having a molecular weight in a range capable of oral absorption. The one having a molecular weight of 100 or less is preferable, and the one having a molecular weight of 600 or less is particularly preferable. Needless to say, these compounds may form a salt or a solvate.

 FXa inhibitors also inhibit blood coagulation and are prophylactic and / or Z-clots for thrombosis. Not only Fxa but also the enzymes mentioned above as examples of trypsin-type serine proteases have high substrate specificity and are involved in the activation of proteins that play important physiological roles. Therefore, a compound that inhibits trypsin-type serine protease is likely to have utility as a pharmaceutical.

Furthermore, data obtained by X-ray analysis of a crystal of a complex of the compound having the group represented by the general formula (1) or (2) or the general formula (3) or (4) and the trypsin-type serine protease is obtained. The present invention can be used for creating a novel trypsin-type serine protease inhibitor having a group that enters the S1 pocket of the trypsin-type serine protease. In other words, using the data obtained by X-ray analysis of those crystals, a drug predicted to inhibit trypsin serine protease can be screened using a computer. In this case, for example, software such as Quanta or Insight H may be used on a UNIX computer (Silicon Graphics). Hereinafter, examples of the trypsin-type serine protease inhibitors of the present invention and their activities are shown, and examples of the results of X-ray analysis of complexes of those inhibitors with FXa or trypsin are shown. Example

 [Example 1] 1— [(5-tert—butoxycarpineol 4, 5, 6, 7-tetrahydrothiazolo [5, 4-c] pyridine-2-yl) carbonyl] —4—

(6-Chloronaphthalene-2-ylsulfonyl) 1-ethoxycarbodilpazine

1-[(6-Chloronaphthalene-1-yl) sulfonyl] -3-[[ethoxycalponyl] pidazine hydrochloride (WO 94 21599) (742 mg), 5-tert-butoxycarponyl—4,5,6 7-tetrahydrothiazolo [5,4-1c] pyridine-12-carboxylic acid (W〇96 / 10022) (1.00 g), benzotriazo-l-yloxystris-pyrrolidinophosphonium hex Safluorophosphite (1.50 g) was dissolved in N, N-dimethylformamide (30 ml), triethylamine (0.40 ml) was added, and the mixture was stirred at room temperature at room temperature. The reaction solution was concentrated under reduced pressure, ethyl acetate was added to the residue, and the mixture was washed once with water and saturated saline, and the organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (silica gel 40 g, hexane: ethyl acetate = 4: 1) to give the title compound (505 mg, 30%) as a pale yellow foam. Obtained.

_{Ή- NMR (CDC 1 3) δ} : 1. 24- 1. 37 (3Η, m), 1. 47 (9 H, s), 2. 45 - 2. 60 (lH, m), 2. 62- 2.71 (1H, m), 2.75-2.90 (2H, m), 3.65—3.94 (3H, m), 4.19-4.31 (2H, m), 4 45-4. 72 (4H, m), 5.35 [, Brs), 5.71-5.77 (1 / 2H, m), 6.72 (1H, brs), 7.58 (1H, dd, J = 8.8, 2.0Hz), 7 7 7 (1H, dd, J = 8.8Hz, 2.OHz), 7.88-7.92 (3H, m), 8.33 (1H, s).

MS (FAB) m / z: 649 [(M + H) +, CI ³⁵ ], 651 [(M + H) ⁺ , CI ³⁷ ].

 [Example 2] 1-[(5-tert-butoxycarbonyl-4,5,6,7-tetrahydrothiazolo [5,4-1c] pyridine-2-yl) force luponyl] _2_ force Rubamoyl 4- (6-chloronaphthalene-2-ylsulfonyl) piperazine

The compound (487 mg) obtained in Example 1 was dissolved in tetrahydrofuran (5 ml), methanol (5 ml) and a 1N aqueous sodium hydroxide solution (3 ml) were added, and the mixture was stirred at room temperature for 4 hours. 1N hydrochloric acid was added to the reaction solution to adjust the pH to 1-2, and ethyl acetate was added to separate the layers. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was dissolved in tetrahydrofuran (5 ml), and N-methylmorpholine (0.09 ml) and isobutyl chloroformate (0.11 ml) were successively added dropwise at 120 ° C. After the reaction solution was stirred at 120 ° C for 10 minutes, a saturated ammonia-dichloromethane solution (0.50 ml) was added, and the mixture was stirred at 120 ° C for 10 minutes. A 1N hydrochloric acid-ethanol solution (10 ml) was added to the reaction solution, and the reaction solution was heated to room temperature. After the reaction solution was concentrated under reduced pressure, the residue was dissolved in dichloroethane and washed with 1N hydrochloric acid. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and the resulting residue was subjected to silica gel column chromatography (dichloromethane). Purification by dichloromethane: methanol = 100: 0 to 100: 1) afforded the title compound (317 mg, 68%) as a colorless foam.

_{Ή-NMR (DMSO- d 6)} 6: 1. 41 (9H, s), 2. 39- 2. 86 (4H, m), 3. 60- 3. 80 (4H, m), 4. 25- 4.34 (1H, m), 4.36 -4.34 (1 / 2H, m), 4.62 (2H, brs), 4.97 (1 / 2H, brs), 5.44- 5. 52 (1/2 H, m), 6.19 (1/2 H, brs), 7.30-- 7.39 (1 H, m), 7.63-

7.85 (3H, m) 8.15 (1 H, d, J = 8.8 Hz), 8.20-

8.29 (2H, m), 8.48 (1H, s).

MS (FAB) m / z 620 [(M + H) +, C 1 35], 622 [(M + H) C l 37].

 [Example 3] 2-Fervamoyl 4 _ [(6-chloronaphthalene-1-yl) sulfonyl] -1-[(4,5,6,7-tetrahydrothiazolo [5,4-c] pyridine 1 2 _ yl) Capillonyl] piperazine trifluoroacetate

Trifluoroacetic acid (1 ml) was added to the compound obtained in Example 2 (303 mg), and the mixture was concentrated under reduced pressure, and the deposited precipitate was collected by filtration, washed with getyl ether, and treated to give the title compound (263 mg, 83 mg). %).

lH-NMR (DMSO—d ₆ ) δ: 2.39-2.70 (2H, m), 2.92—3.06 (2H, m), 3.42-3.77 (4H, m), 4.25-4.50 (7 / 2H, m), 4.97 (1,2 H, brs), 5.35-5.44 (1 / 2H, m), 6.14 (1 / 2H , brs), 7.30—7.39 (1 H, m), 7.66—7.73 (2H, m), 7.77-7.82 (1H, m), 8.16 (1H, d, J = 8.8Hz), 8. 21—8.28 (2H, m), 8.49 (1H, s), 9.26 (2H, brs).

MS (FAB) m / z: 520 [(M + H) ⁺ , CI ³⁵ ], 522 [(M + H) +, CI ³⁷ ].

Elemental analysis: as _{C 22 H 22 C 1 N 5} 0 4 S 2 · CF 3 C0 2 H · 0. 6H 2 0, Calcd: C, 44. 29; H, 3. 73; C 1, 5. 40 F, 9.55; N, 10.67; S, 9.77. Analytical values: C, 44.59; H, 3.79; C1, 5.26; F, 9.54; N , 10.28; S, 9.72.

 [Example 4] 2-force rubamoyl-4-1 [(6-chloro-naphthylene_2-yl) sulfonyl] — 1 — [(5-methyl-4,5,6,7-tetrahydrothiazolo

 [5,4-c] Pyridine-2-yl) caprolponyl] pidazine hydrochloride

The compound (400 mg) obtained in Example 3 was suspended in dichloromethane (10 ml), and triethylamine (0.08 ml) and acetic acid (0.03 ml) were added, followed by stirring at room temperature for 5 minutes. A 30% aqueous formaldehyde solution (0.03 ml) and sodium triacetoxyborohydride (96 mg) were added to the reaction solution, and the mixture was stirred at room temperature for 10 minutes. The reaction solution was concentrated under reduced pressure, dichloromethane was added to the residue, and the mixture was washed twice with water and once with a saturated saline solution. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. After the residue was dissolved in a 1 N hydrochloric acid / ethanol solution (10 ml), the reaction solution was concentrated under reduced pressure. The deposited precipitate was collected by filtration and washed with ethyl acetate to give the title compound (94 mg, 57%) as a colorless amorphous powder. Ή-NMR (DMSO-d ₆ ) (5: 2.37-2.70 (2Ή, m), 2.91 (3H, s), 3.00-3.78 (6H, m), 4.28 -4. 77 (7/2 H, m), 4.97 (1/2 H, brs), 5.40-5.50 (1 / 2H, m), 6.14 (1 / 2H, brs) , 7.32-7.40 (1H, m), 7.68-7.75 (2H, m), 7.77-7.83 (1H, m), 8.15 (1H, d, J = 8.8 Hz), 8.2 1 -8.28 (2H, m), 8.49 (1 H, s).

MS (FAB) m / z: 534 [(M + H) +, CI ³⁵ ], 536 [(M + H) +, CI ³⁷ ].

Elemental analysis: as _{C 23 H 24 C 1 N 5} 0 4 S 2 · HC 1 · 2. 5 H 2 0, Calcd: C, 4 4. 88; H , 4. 9 1; C 1, 1 1. 52; N, 1 1.38; S, 10.4 2. Analytical value: C, 44.83; H, 4.89; C1, 1 1.65; N, 11.31; S, 1 0. 46.

 [Example 5] 1-[(5-cycloindole-2-yl) sulfonyl] —4 -— [(5-methyl-4,5,6,7-tetrahydrothiazolo [5,4-1c] pyridinine— 2-yl) carbonyl] pidazine hydrochloride

 1) 5-ethoxycarbonyl-4,5,6,7-tetrahydrothiazolo [5,4—c] pyridine

E

Diphosphorus pentasulfide (500 g) was suspended in formamide (3000 ml) under ice cooling and stirred overnight. Water and getyl ether were added to the reaction solution, and the mixture was separated. The obtained organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off to obtain a yellow oily substance. This was dissolved in n-butanol (350 ml), and the solution (Tetrah edron, 39 Vol., 3767-3776, 1983), and add 150 g of 3-chloro-11-ethoxycarbonyl 4-piperidin-4-one (100 g). Allowed to stir for hours. After the reaction solution was cooled to room temperature, it was filtered using celite, and the filtrate was washed successively with a saturated aqueous solution of sodium hydrogen carbonate and a saturated saline solution. The organic layer was dried over anhydrous sodium sulfate and the solvent was distilled off. The residue obtained was purified by silica gel column chromatography (dichloromethane-ethyl acetate: hexane = 1: 2) to give the title compound (79. Og). Obtained as a brown oil. Ή one _{NMR (CDC 1 3) δ:} 1. 30 (3Η, t, J = 7. 3Hz), 2. 9 6 (2H, brs), 3. 82 (2H, brs), 4. 19 (2H, t, J = 7.3 Hz), 4.73 (2H, brs), 8.68 (1H, s).

MS (FAB) m / z: 2 13 (M + H) +.

2) 5-Methyl-1,4,5,6,7-tetrahydrothiazolo [5,4-c] pyridin

Dissolve the compound (21.0 g) obtained above in anhydrous tetrahydrofuran (500 ml), add a solution of lithium aluminum hydride in tetrahydrofuran (1.0 M, 20 Om 1) under ice cooling, and stir at room temperature for 2 hours. did. After slowly adding water (7 ml) to the reaction solution to terminate the reaction, a 1 N aqueous solution of potassium hydroxide (7 ml) and anhydrous magnesium sulfate were sequentially added. The reaction solution was filtered using celite, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by distillation under reduced pressure (1.5 mmHg, boiling point 82-85 ° C) to give the title compound (6.10 g) as a colorless oil.

_{Ή- NMR (CDC 1 3) δ} : 2. 52 (3Η, s), 2. 83 (. 2H, t, J = 5 9Hz), 2. 98 (2H, t, J - 5. 9Hz), 3 . 70 (2H, s), 8.63 (1H, s).

MS (FAB) m / z: 155 (M + H) ⁺ .

3) Lithium 5-methyl-4,5,6,7-tetrahydrothiazolo [5,4-c] pyridine-2-carboxylate

The compound obtained above (6.43 g) was dissolved in anhydrous tetrahydrofuran (200 ml), and a solution of n-butyllithium in n-hexane (1.47 M, 34.00 ml) was added dropwise at _78 ° C. Then, the mixture was stirred for 40 minutes. Carbon dioxide gas was blown into the reaction solution at 178 ° C for 1 hour, and the temperature was raised to room temperature. Concentrate the reaction mixture under reduced pressure to give the title compound.

(9.42 g) was obtained as a light brown foamy solid.

— NMR (DMSO-d ₆ ) δ: 2.37 (3Η, s), 2. 64-2.77

(4Η, m), 3.54 (2H, s).

4) 5-chloro-1-phenylsulfonylindole

N-Butyllithium (1.61M hexane solution, 12.3 ml) was added to a solution of 5-cycloindole (2.86 g) in tetrahydrofuran (25 ml) at _78 ° C, and the mixture was stirred. The temperature was raised to 140 ° C over time. The reaction solution was cooled again to 178 ° C, benzenesulfonyl chloride (3.5 g) was added, and the temperature was raised to room temperature in 3 hours. Water was added to the reaction mixture, and extracted with dichloromethane. The organic layer is dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by chromatography (hexane: ethyl acetate = 5: 7), and the obtained white solid was recrystallized from ethanol to give the title compound (5.38 g, 93%) as a white solid.

_{Ή-NMR (CDC 1 3)} δ: 6. 61 (1 Η, d, J = 3. 9Hz), 7. 2 6 (1Η, dd, J = 8. 3, 2. 0Hz), 7. 45 ( 2H, t, J = 7.3 Hz), 7.50 (1H, d, 1 = 2.0Hz), 7.56 (1H, m), 7.59 (1H, d, J = 3.9Hz) ), 7.86 (2H, m), 7.92 (1H, d, J = 8.3Hz).

Elemental _{analysis: C U H 1 () C} 1 N_〇 as ₂ S, Calculated: C, 57. 63; H, 3. 4 5; C 1, 12. 15; N, 4. 80; S, 10. 99. Analytical values: C, 57.82; H, 3.58; C1, 11.91; Ν, 4.79; S, 10.92.

5) (5—black mouth— 1 _phenylsulfonylindole—2-yl) sulfonyl

To a solution of the compound obtained above (5.38 g) in ether (100 ml), add tert-butyllithium (1.56 M pentane solution, 10.4 ml) dropwise at -78 to 0 ° C in 30 minutes. The temperature was raised. After stirring for 1 hour, the reaction mixture was cooled again to −78 ° C., sulfur dioxide was introduced, the temperature was raised to room temperature in 1 hour, and the mixture was stirred for 1 hour. After the reaction solution was concentrated under reduced pressure, hexane was added and the mixture was concentrated again under reduced pressure. The obtained residue was dissolved in dichloromethane, N-chlorosuccinimide (2.47 g) was added at 0 ° C, the temperature was raised to room temperature in 1 hour, and the mixture was stirred for 30 minutes. Dichloromethane and water are added to the reaction solution, and the mixture is separated. The organic layer is dried over anhydrous sodium sulfate, and the solvent is distilled off under reduced pressure. The obtained residue was solidified from methanol to give the title compound (4.41 g, 64%) as a white solid.

_{'Η - NMR (CDC 1 3} ) δ: 7. 46- 7. 54 (2H, m), 7. 58 (1 H, dd, J = 9. 3, 2. 0Hz), 7. 6 3 (1H , T, 1 = 7.3Hz, 7.64 (1H, s), 7.67 (1H, d, 1 = 2.0Hz), 8.06 (2H, d, J = 7.3Hz) , 8. 26 (1 H, d , J = 9. 3Hz) MS (EI) m / z:. 29 1 (M +, CI 35), 293 (M +, CI 37).

Elemental analysis: as C ₁₄ H ₉ C 1 ₂ N_〇 ₄ S _2, Calculated: C, 43. 09; H, 2. 3 2; C 1, 18. 27; N, 3. 59; S, 16. 43. Analytical values: C, 42.98; H, 2.51; C1, 18.36; N, 3.59; S, 16.47.6) 1-tert-butoxycarponyl _4_ [(5-chloro Mouth— 1-phenylsulfonylindole—2_yl) sulfonyl] pidazine

(5-chloro- 1-phenylsulfonylindole-21-yl) To a solution of sulfonyl chloride (4.41 g) in dichloromethane (75 ml) under ice-cooling was added tert-butyl-1-pyrazinecarboxylate. (2.21 g) and trieduramine (1.65 ml) were added, and the mixture was stirred at room temperature for 3 hours. After completion of the reaction, water and dichloromethane were added, and the mixture was partitioned. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate: hexane = 1: 20) to give the title compound (3.63 g, 60%) as colorless crystals.

_{[H- NMR (CDC 1 3) δ} : 1. 45 (9Η, s), 3. 35- 3. 42 (4 H, br), 3.50-3.55 (4H, br), 7.40-7.48 (4H, m), 7.53-7.58 (2H, m), 8.00—8 05 (2H, m), 8.23 (1H, d, J = 8.8Hz).

 7) 1-[(5_Cro-indole-2-yl) sulfonyl] pidazine hydrochloride

The compound (3.63 g) obtained above was dissolved in methanol (100 ml), and a 0.2 N sodium hydroxide methanol solution (100 ml) was added thereto under ice cooling, followed by stirring at room temperature for 12 hours. After adding a saturated aqueous ammonium chloride solution under ice-cooling, water and dichloromethane were added, and the mixture was separated. The organic layer was dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure, and the precipitated solid was collected by filtration, dissolved in saturated ethanol with hydrochloric acid, and stirred for 30 minutes. The solvent was distilled off under reduced pressure to obtain the title compound (1.25 g, 54%) as a colorless powder.

Ή— NMR (DMSO-d ₆ ) δ: 3.25-3.43 (8Η, br), 7.46 (1Η, d, J = 8.8 Hz), 7.64 (1 H, d, J = 8.8 Hz), 7.93 (1H, s), 9.33 (1H, br), 12.70 (1H, br). MS (EI) m / z: 298 (M ⁺ , CI ³⁵ ), 300 (M +, CI ³⁷ ).

Elemental analysis: as C ₁₂ H ₁₄ C 1 N ₃ 〇 _{2 S · HC 1 · 0. 5} H 2 0, Calcd: C, 4 1. 75; H , 4. 67; C 1, 20. 54; N , 12.17; S, 9.29. Found: C, 41.78; H, 4.98; C1, 20.40; N, 11.88; S, 9.34.

8) 1 — [(5-cycloindole-2-yl) sulfonyl] —4 — [(5—methyl 4,5,6,7—tetrahydrothiazolo [5,4-c] pyridine—2— ^ f Le) carbonyl] piperazine

1-[(5-Chloroindole_2-yl) sulfonyl] piperazine (400 mg) in N, iV-dimethylformamide (100 ml) was added at room temperature to 1-hydroxybenztriazole (10 5 mg), 1- (3-dimethylaminopropyl) — 3_ethylcarbodiimide hydrochloride (194 mg), lithium (5-methyl-4,5,6,7-tetrahydrothiazolo [5,4- c] Pyridinecarboxylate (175 mg) and N-methylmorpholine (86.8 mg) were added, and the mixture was stirred at room temperature for 10 hours.After the reaction was completed, the reaction solvent was distilled off under reduced pressure, and distilled water and acetic acid were added. The organic layer was washed three times with distilled water, dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. This was subjected to column chromatography (methanol: ethyl acetate = 3: 100). A 1N hydrochloric acid-ethanol solution and distilled water were added to the product, the solvent was distilled off under reduced pressure, and the residue was dried under reduced pressure overnight at 60 ° C to give the title compound (106 mg) as a brown amorphous solid. Obtained.

_{Ή-NMR (CDC 1 3)} δ 2. 49 (3Η, s), 2. 78- 2. 83 (2 H, m), 2. 85 - 2. 94 (2H, m), 3. 1 5- 3.28 (4H, br), 3.67 (2H, s), 3.82-3.95 (2H, br), 4.50—4.65 (2H, br), 6.96 (1H , d, J = 2.0 Hz), 7.32 (1H, dd, J = 8.8, 2.0 Hz), 7.36 (1H, d, J = 8.8 Hz), 7.67 ( 1H, s), 8.71 (1H, br).

MS (FAB) m / z: 480 [(M + H) ⁺ , CI ³⁵ ], 482 [(M + H) ⁺ , CI ³⁷ ].

Elemental analysis: C 2 _Q H ₂₂ C 1 N ₅ 〇 ₃ S ₂ · HC 1 · 0.5 H ₂₀ Calculated: C, 44.64; H, 4.76; CI, 13.18; N, 13.02; S, 11.9 2. Found: C, 44.69; H, 4.72; C1, 13.36; N, 12.76; S, 11.76.

 [Example 6] 1-[(5-chlorobenzo [b] furan-2-yl) sulfonyl] 1-41-[(5-methyl-4,5,6,7-tetrahydrothiazolo [5, 4—c] Pyridine-2-yl) caprolponyl] pidazine hydrochloride

1) (5-benzene benzo [b] furan 2-yl) sulfonyl chloride

To a solution of 5-benzofuran [b] furan (362 mg) in ether (5.0 ml) at _78 ° C was added tert-butyllithium (1.56 M heptane solution) (1.6 ml). After stirring at 78 ° C for 10 minutes, the mixture was stirred at 0 ° C for 2 minutes and again at 1 78 ° C for 3 minutes. Sulfurous acid gas was injected at -78 ° C, and stirred at -78 to 140 ° C for 1.5 hours and at 0 ° C for 10 minutes. The reaction solution was concentrated under reduced pressure, and the remaining pale yellow solid was washed with hexane to form a dichloromethane suspension (5.0 ml). At 0 ° C, N-monomethyl succinimide (355 mg) was added. The mixture was stirred at 0 ° C to room temperature for 12 hours. After dilution with dichloromethane, water was added to make two layers. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (hexane: ethyl acetate = 20: 1), dissolved in ethyl acetate, hexane was added and crystallized, and the title compound (38 1 mg, 64%) was pale green Obtained as needles.

_{Ή-NMR (CDC 1 3)} δ 7. 57 (1 Η, dd, J = 8. 8, 2. OH z), 7.59 (1H, s), 7.61 (1H, d, J = 8.8Hz), 7.76 (1H, d, J = 2.0Hz).

MS (EI) mZ z: 250 (M ⁺ , CI ³⁵ ), 252 (M ⁺ , CI ³⁷ ).

Elemental analysis: as C ₈ H ₄ C 1 ₂ 〇 ₃ S, Calculated: (:, 38. 27; H , 1. 61;

C I, 28.24; S, 12.77. Analytical values: C, 38.33; H, 1.71; C1, 28.16; S, 12.57.

2) 1-[(5-chlorobenzo [b] furan-2-yl) sulfonyl] piperazine hydrochloride

To a solution of 1- (tert-butoxycarbonyl) pidazine (195mg) in methane (3.0ml) in dichloromethane is added (211mg) sulfonyl chloride (211mg), Triethylamine (1.0 ml) was added, and the mixture was stirred at room temperature for 1 hour. After dilution with dichloromethane, 2N hydrochloric acid was added to form two layers. The organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate and a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (hexane: ethyl acetate = 5: 1). To a dichloromethane (1.0 ml) solution of the obtained purified product, ethanol (2.0 ml) and a saturated hydrochloric acid ethanol solution (2.0 ml) were added, and the mixture was stirred at room temperature for 2 days. After concentration, the residue was azeotroped with ethanol, and the precipitated colorless precipitate was collected by filtration and dried with a vacuum pump to give the title compound (264 mg, 93%) as a white powder.

Ή— NMR (DMSO-d ₆ ) δ 3.20 (4Η, br), 3.45 (4Η, br), 7.62 (1Η, d, J = 8.8 Hz), 7.76 (1Η, br) s), 7.85 (1H, d, J = 8.8 Hz), 7.96 (1H, s), 9.41 (1H, br).

MS (FAB) m / z: 301 [(M + H) +, CI ³⁵ ], 303 [(M + H) +, CI ³⁷ ] ·

Elemental analysis: C ₁₂ H ₁₃ C 1 N ₂ 0 ₃ S · HC 1 · 0.1 H ₂ 0, calculated: C, 42.51; H, 4.22; C 1, 20.91; N , 8.26; S, 9.46. Analytical values: C, 42.38; H, 4.33; C1, 20.92; N, 8.18; S, 9.58.

3) 1-[(5-chlorobenzo [b] furan-2-yl) sulfonyl] -4-[(5-methyl-1,4,5,6,7-tetrahydrothiazolo [5,4— c] pyridin-2-yl) pyruponyl] pidazine hydrochloride

1-[(5-chlorobenzo [b] furan-12-yl) sulfonyl] piperazine obtained above and lithium 5-methyl-4,5,6,7 obtained in 3) of Example 5 —Synthesized in the same manner as in Example 1 from tetrahydrothiazolo [5,4-1c] pyridine-12-hydroxyloxylate.

Ή-NMR (DMSO-d ₆ ) <5: 2.91 (3H, s), 3.11 (2H, br), 3.25-3.90 (6H, m), 3.76 (2H, br) ), 4.30—4.80 (4H, br), 7.46 (1H, d, J = 8.8Hz), 7.73 (1H, s), 7.84 (1H, d, J 8.8 Hz), 7.96 (1H, s), 11.48 (1H, br).

MS (FAB) m / z: 481 [(M + H) +, C 1 3S], 483 [(M + H) +, C l 37].

Elemental analysis: C _2. As _{H 21 C 1 N 4 0 4} S 2 · 1. 1HC 1 · 0. 3H 2 0, Calculated: C, 45.63; H, 4.35; C1, 14.14; N, 10.64; S, 1 2.18 Analysis: C, 45.81; H, 4.29; C1, 13.93; N, 10.44; S, 12.26.

 [Example 7] 4 — [(5-chloro-indole-2-yl) sulfonyl] —1 -— [(5-methyl-4,5,6,7-tetrahydrothiazolo [5,4-1c] ] Pyridin-2-yl) carbonyl] -2-[[(morpholine-14-yl) caprolponyl] methyl] pidazine hydrochloride

1) 1-tert-butoxycarbone 3-methoxycarbonylmethylpiperazine

In a 2000 ml eggplant flask, 1,4-dibenzyl-2-methoxycarboxymethylpiperazine (30.4 g) was dissolved in methanol (800 ml) and concentrated hydrochloric acid (15 ml). 1.5 g) was added. The suspension was then vigorously shaken at room temperature under a hydrogen atmosphere for 4.5 hours. After completion of the reaction, triethylamine (31 ml) was added to dissolve insolubles, and the mixture was slightly concentrated. Then, the catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. The obtained residue was dissolved in dichloromethane, dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. Dichloromethane (600 ml) and triethylamine (27.5 ml) were added to the residue to dissolve it. Under ice-cooling, 2- (tert-butoxycarporinylimino) -12-phenylacetonitrile (12.89 g) was added. The mixture was stirred at 0 ° C for 3.5 hours. Further, 2- (tert-butoxycarbonilimino) -12-phenylacetonitrile (3.76 g) was added, and the temperature was gradually raised from 0 ° C. to room temperature, followed by stirring for 22 hours. After completion of the stirring, the solvent is distilled off under reduced pressure, and the residue is subjected to silica gel column chromatography. Purify (1st; dichloromethane and methanol, 2nd; hexane and ethyl acetate, and 10% methanol-dichloromethane) to give the title compound.

(9.77 g, 42%) was obtained as a pale yellow amorphous powder.

_{Ή-NMR (CDC 1 3)} δ:.. 1. 46 (9Η, s), 2. 15-3 10 (8 H, m), 3. 70 (3H, S), 3. 80-4 00 ( 2H, m).

2) 1-[(5-chloro-1-phenylsulfonylindole-2-yl) sulfonyl] -1-3- (methoxycarbonylmethyl) piperazine

To a solution of piperazine (5.03 g) obtained above in ethanol (50 ml) was added a solution of saturated hydrochloric acid in ethanol (20 ml), and the mixture was stirred for 30 minutes. After evaporating the solvent under reduced pressure, the residue was dissolved in dichloromethane (200 ml). To this was added (5-chlorophenyl-1-sulfonylindole-2-yl) sulfonyl chloride (7.64 g) and triethylamine (9.5 ml), and the mixture was stirred at room temperature for 4 hours. Distilled water and dichloromethane were added to the reaction solution, and the organic layer was separated and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (methanol: dichloromethane = 1: 50) to give the title compound (4.97 g) as a colorless oil.

. E one _{NMR (CDC 1 3) δ:} 2. 15-2 30 (1 Η, br), 2. 34 - 2. 49 (2H, m), 2. 72 - 2. 76 (lH, m), 2.90—3.22 (3H, m), 3.17-3.25 (1H, m), 3.67 (3H, s), 3.7 1-3.77 (2H, m), 7 . 39— 7.47 (4H, m), 7.52- 7.58 (2H, m), 8.02 (2H, d, J = 7.8Hz), 8.23 (1H, d, J = 9.3Hz).

MS (FAB) m / z: 512 [(M + H) +, C 1 35], 514 [(M + H) +, CI 37].

 3) 1— (tert-butoxycarbonyl) 1-41-[(5-Chloro-1-phenylsulfonylindole-1-yl) sulfonyl] —2— (methoxycarbonylmethyl)

 Ethanol solution (250 ml) of 1 _ [(5-chloro- 1-phenylsulfonylindole-2-yl) sulfonyl] -3- (methoxycarbonylmethyl) pidazine (2.00 g) obtained above To the mixture was added di-tert-butyl dicarbonate (3.91 g) at room temperature, and the mixture was stirred for 17 hours. After concentrating the reaction solution under reduced pressure, dimethyl ether was added to the residue, and the precipitated crystals were collected by filtration to give the title compound.

(2.01 g) was obtained as colorless crystals.

_{¾- NMR (CDC 1 3) δ} : 1. 45 (9Η, s), 2. 45- 2. 54 (1 H, m), 2. 74- 2. 8 6 (1 H, m), 2. 92—3.03 (1Η, m), 3.07-3.27 (1Η, m), 3.37 (3Η, s), 3.67—3.77 (2Η, m), 3. 94-- 4.06 (2H, m), 4.52-4.67

(1H, m), 7.38-7.49 (4H, m), 7.57—7.60 (2H, m), 8.03 (2H, d, J = 6.8Hz), 8.23 (1H, d, J = 9.3Hz).

MS (FAB) m / z: 6 12 [(M + H) ⁺ , CI ³⁵ ], 6 14 [(M + H) +, CI ³⁷ ].

 4) 1— (t ert—butoxycarbonyl) — 4 _ [(5_cycloindole-2-yl) sulfonyl] 1-2 — [[(morpholine-1-4-yl)] carbonyl] methyl]

1_ (tert_butoxycarbonyl) 1-4 _ [(5-chloro-1-phenylsulfonylindole-1-yl) sulfonyl] -2- (methoxycarbonylmethyl) pidazine (1.0 g obtained above) ) Was dissolved in 1,4-dioxane (100 ml), 1N aqueous sodium hydroxide solution (4.9 ml) was added at room temperature, and the mixture was heated and stirred at 80 ° C for 6 hours. After adding a saturated aqueous ammonium chloride solution under ice-cooling to make the reaction solution neutral, distilled water was added, and the aqueous layer was extracted four times with dichloromethane. After the extract was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The obtained residue was dried under reduced pressure, and then rapidly dissolved in dichloromethane (150 ml). At room temperature, 1-hydroxybenzotriazole monohydrate (0.24 g), 1- (3-dimethylaminopropyl) _3-ethylethyl carposimid hydrochloride (0.41 g), Morpholine (0.16 g) and N-methylmorpholine (0.41 g) were added, and the mixture was stirred at room temperature for 12 hours. Distilled water was added to the reaction solution, and the aqueous layer was extracted three times with dichloromethane. After drying over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (methanol: dichloromethane == 1: 50) to give the title compound (0.71 g). Was obtained as a colorless solid.

Ή one _{NMR (CDC 1 3) (5} : 1. 41 (9H, s), 2. 23 - 2. 30 (3 H, m), 3.34-3.84 (12 H, m), 3.91 -4. 12 (1 H, m), 4.49 -4. 64 (lH, m), 6.98 ( 1H, s), 7.27-7.33 (1H, m), 7.37 (1H, d, J = 8.8Hz), 7.66 (1H, s).

MS (FAB) m / z: 527 [(M + H) ⁺ , CI ³⁵ ], 529 [(M + H) +, CM ³⁷ ].

 5) 4-[[5-cycloindyl-2-yl) sulfonyl] -1-[(5-methyl-4,5,6,7-tetrahydrothiazolo [5,4-c] pyridine-2 — ^ (） 力 ル 力 2 一 2 — — — — — [[[[[(

1- (tert-butoxycarbonyl) -4-1-((5-chloroindole-2-yl) sulfonyl] 1-2-[[(morpholine-1-yl)] potulponyl] methyl] pidazine ( To a solution of 710 mg) in ethanol (50 ml) was added a solution of saturated hydrochloric acid in ethanol (20 ml) at room temperature, and the mixture was stirred for 3 hours. The reaction solution was concentrated under reduced pressure. Getyl ether and ethanol were added to the residue, and the precipitated crystals were collected by filtration. This was converted into an N, N-dimethylformamide solution (50 ml), and 1-hydroxybenzotriazole monohydrate (68.8 mg) and 1- (3-dimethylaminopropyl-3-ethylcarbodiimide hydrochloride (68.8 mg) were added at room temperature. 115.4 mg), lithium 5_methyl-1,4,5,6,7-tetrahydrothiazolo [5,4-c] pyridine-12-carboxylate (189.Omg) and N-methylmorpholine (140 5 mg), and the mixture was stirred at room temperature for 19 hours. Water and ethyl acetate were added to the residue, and the organic layer was separated. After drying with sulfuric anhydride: solvent, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (methanol: ethyl acetate == 1: 50), crystallized by adding getyl ether and dichloromethane, and collected by filtration. The obtained crystals were dissolved in a 1N hydrochloric acid / ethanol solution (0.5 ml) and a small amount of distilled water, and the solvent was distilled off under reduced pressure. 187 mg) as a yellow amorphous solid.

NMR— NMR (DMS〇—d ₆ ) (5: 2.66-2.89 (3 H, m), 2.99 (3H, s), 3.03-3.29 (3H, m), 3 34-3. 46 (1H, m), 3.47-3.72 (4H, m), 3.75—3.92 (8H, m), 4.42-4.53 (1.5H, m) m), 4.73-4.81 (1H, m), 5.10-5.17 (0.5H, m), 5.39--5.47 (0.5H, m), 5. 82- 5.92 (0.5H, m), 7.12 (1H, br), 7.41 (1H, dd, J = 2.0, 8.8Hz), 7.58 (1H, d, J = 8.8Hz), 7.87 (1H, br), 12.57 (1H, s).

MS (FAB +) m / z: 607 [(M + H) ⁺ , CI ³⁵ ], 609 [(M + H) ⁺ , ^C137 ]

 [Example 8] 4-[(6-ethynylbenzo [b] chen-2-yl) sulfonyl] -1-2_ (N-methylcarbamoyl) -1-[(5-methyl-4,5,6,7 —Tetrahydrothiazolo [5,4—c] pyridine_2-yl) carbonyl] piperazine

1) 6-bromobenzo [b] thiophene

6-Bromobenzothiophene-2-carboxylic acid (14 g) and copper powder (874 mg) were added to quinoline (45 ml), and the mixture was heated and stirred at an oil temperature of 220 ° C for 2 hours. After cooling, ether was added to the reaction mixture, and the copper powder was removed by filtration. The filtrate was washed successively with a 1N aqueous hydrochloric acid solution, a 1N aqueous sodium hydroxide solution, and a saturated saline solution, and dried over anhydrous sodium sulfate. The residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane) to give the title compound as a pale-yellow solid

(5.56 g) was obtained.

_{Ή-NMR (CDC 1 3)} δ: 7. 29 (1H, d, J = 5. 4Hz), 7. 4 2 (1H, d, J = 5. 4Hz), 7. 46 (1 H, dd, J = 8.3, 1.5 Hz), 7.67 (1H, d, J = 8.3Hz), 8.01 (1H, d, J ί .5Hz).

MS (EI) m / z: 212 (M ⁺ , ^Br79 ), 214 (M ⁺ , ^Br81 ).

2) 6-trimethylsilylethynyl benzo [b] thiophene

6-Bromobenzo [b] thiophene (2.13 g) is dissolved in tetrahydrofuran (15 ml), and triphenylphosphine (787 mg), triethylamine (40 ml), N, N-dimethylformamide (15 ml), trimethylsilylacetylene (1 47 g) and palladium acetate (225 mg) were added, and the mixture was refluxed for 5 hours. After allowing to cool, the mixture was diluted with dichloromethane (150 ml), and washed sequentially with water and saturated saline. After drying over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (hexane) to obtain the title compound (1.38 g). _{Ή-NM (CDC 1 3)} (5: 0. 27 (9H, s), 7. 30 (1 H, d, J

= 5.7Hz), 7.44 (1H, dd, J = 8.3, 1.0Hz), 7.49

(1H, d, J = 5.7Hz), 7.73 (1H, d, J = 8.3Hz), 8.00 (1H, s).

MS (EI) m / z: 230 (M ⁺ ).

 3) (6-trimethylsilylethynyl benzo [b] chen-2-yl) sulfonyl chloride

6-Trimethylsilylethynyl benzo [b] thiophene (408 mg) was dissolved in dry getyl ether (10 ml), cooled to 178 ° C, and tert-butyllithium (1.54M n-pentane solution, 1. 15 ml) was added dropwise. Thereafter, the temperature was raised to 0 ° C over 30 minutes, and the mixture was stirred at the same temperature for 1 hour. The solution was cooled again to 178 ° C., sulfur dioxide gas was introduced, and the temperature was raised to room temperature over 1 hour, followed by stirring for 1 hour. After the reaction solution was concentrated under reduced pressure, hexane (20 ml) was added, and the insoluble precipitate was collected by filtration. This was dissolved in dichloromethane (10 ml), cooled to 0 ° C, and N-chlorosuccinimide (248 mg) was added. After stirring at the same temperature for 30 minutes, the temperature was raised to room temperature, and the mixture was further stirred for 1 hour. Water was added to the reaction solution, and the organic layer was separated. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain the title compound (498 mg) as a pale yellow solid.

_{Ή- NMR (CDC 1 3) δ} : 0. 28 (9Η, s), 7. 58 (1H, dd, J = 8. 3, 1. 5Hz), 7. 89 (1 H, d, J = 8 3Hz), 8.02 (1H, s), 8.10 (1H, s). MS (EI) mZz: 328 (M ⁺ , CI ³⁵ ), 330 (M ⁺ , CI ³⁷ ).

4) 1,4-dibenzyl-2 _ (N-methylcarbamoyl) piperazine eHNCO

 Bn-N N-Bn

1,4-Dibenzyl-2- (ethoxycarbonyl) pidazine (6 g) was dissolved in ethanol (100 ml), 1N aqueous sodium hydroxide solution (18 ml) was added, and the mixture was heated under reflux. The progress of the reaction was monitored, and a 1N aqueous solution of sodium hydroxide was added (using a total of 28 ml), followed by heating and refluxing for a total of 2 hours and 30 minutes. The reaction solution was neutralized by adding 1N hydrochloric acid, and the solvent was distilled off under reduced pressure. Dichloromethane (100 ml) was added to the residue, and the insoluble material was removed by filtration. Then, 1-eluene 3- (3-dimethylaminopropyl) carbodiimide hydrochloride (4.1 g), 1-hydroxybenzotriazole monohydrate (2.39 g), methylamine hydrochloride (1.79 g) and triethylamine (7.4 ml) were added, and the mixture was stirred at room temperature overnight. The organic layer was washed with water, dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate) to obtain the title compound (3.88 g). _{Ή-NMR (CDC 1 3)} δ: 2. 24- 2. 37 (3Η, m), 2. 59 -

2.62 (1H, m), 2.73- 2.77 (1 H, m), 2.83, 2.84 (total 3 m, each m), 2.89-2.92 (1 H, m ), 3.15-3.18 (1

M, m), 3.39 (1Η, d, J = l 3.4 Hz), 3.48 (2Η, s),

3.75 (1Η, d, J = 13.4Hz), 7.23-7.34 (1 1H, m).

5) 3- (N-methylcarbamoyl)-1-[(6-trimethylsilylethynyl benzo [b] chen-1- 2-yl) sulfonyl] piperazine MeH

1,4-Dibenzyl-2_ (N-methylcarbamoyl) pidazine (437 mg) was dissolved in methanol (15 ml), palladium hydroxide (22 mg) and concentrated hydrochloric acid (0.22 ml) were added, and hydrogen gas was added. After introducing (1 atm), the mixture was stirred at room temperature for 1 hour. After adding triethylamine (0.9 ml), the palladium was removed by filtration, and the solvent was distilled off under reduced pressure. The residue was dissolved in dichloromethane, triethylamine (0.5 ml) was added, (6-trimethylsilylethynylbenzo [b] chen-2-yl) sulfonyl chloride (399 mg) was added under ice cooling, and the mixture was cooled to room temperature. For 20 hours. The reaction solution was washed with a saturated aqueous solution of sodium hydrogen carbonate, dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (methanol: dichloromethane = 1: 19) to give the title compound (462 mg) as a pale yellow solid.

Ή one _{NMR (CDC 1 3) δ:} 0. 28 (9Η, s), 1. 52 (1 H, brs), 2. 5 7 - 2. 66 (2 H, m), 2. 80, 2. 7 9 (3H, each s), 2.97 (1H, dt, J = 3.3, 11.5Hz), 3.09 (1H, dt, J = l 3.2, 3.1Hz) , 3.51 (1H, dd, J = 9.8, 3.4 Hz), 3.59 (1H, dd, J = 1.1.7, 0.98Hz), 3.92 (1H, dd, J = 1 1.7, 2.4 Hz), 6.56-6.57 (1H, m), 7.52 (1H, dd, J = 8.3, 0.98Hz), 7.77 ( 1H, s), 7.82 (1H, d, J = 8.3Hz), 7.97 (1H, s).

MS (FAB) m / z: 436 (M + H)

6) 2- (N-methylcarbamoyl) 1-111 [(5-methyl-4,5,6,7— Tetrahydrothiazolo [5,4-1c] pyridine-2-yl) carbonyl] _4-I-[(6-trimethylsilylethynylbenzo [b] chen-1-2-yl) sulfonyl] pidazine

3- (N-Methylcarbamoyl) 1-111 ((6-trimethylsilylethynylbenzo [b] chen-1-yl) sulfonyl] piperazine (218mg) in N, N-dimethylformamide (5ml) Lithium 5-methyl-4,5,6,7-tetrahydrothiazolo [5,4-c] pyridine-2-carboxylate (188 mg), 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide Hydrochloride (24 Omg) and 1-hydroxybenzotriazole monohydrate (68 mg) were added, and the mixture was stirred at room temperature for 30 hours. The reaction solution was diluted with dichloromethane, washed with water and then with saturated sodium hydrogen carbonate, dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (methanol: dichloromethane) to obtain the title compound (9 Omg).

 MS (FAB) m / z: 616 (M + H) +.

7) 4- [(6-ethylbenzene [b] chen-1 2_yl) sulfonyl] _2— (N-methylcarbamoyl) 1 1 [[(5-methyl-4,5,6,7-tetrahydrothiazolo '[5, 4-c] Pyridine-2-yl) Capillonil] Piperazine

2- (N-methylcarbamoyl) — 1-[(5-Methyl-4,5,6,7-tetrahydrothiazolo [5,4-1c] pyridine-2-yl) dipropionyl] —4-1 [(6-Trimethylsilylethynylbenzo [b] chain-2-yl) sulfonyl] pidazine (270 mg) is dissolved in a mixed solvent of tetrahydrofuran (1.5 ml) and methanol (1.5 ml). A 1N aqueous solution of sodium hydroxide (1.3 ml) was added, and the mixture was stirred at room temperature for 2 hours. The reaction solution was made weakly acidic by adding a saturated aqueous solution of ammonium chloride, and then weakened with a saturated aqueous solution of sodium hydrogen carbonate. Then, dichloromethane was added thereto, and the mixture was separated. After drying the organic layer over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The obtained residue was purified by preparative thin-layer chromatography (methanol: dichloromethane = 1: 9) and Sephadex LH-20 (methanol). The obtained amorphous substance was dissolved in dichloromethane, added dropwise to hexane, and the precipitated solid was collected by filtration to obtain the title compound (82 mg) as a pale gray solid.

_{Ή-NMR (CDC 1 3)} δ:. 2. 49 (3H, s), 2. 80- 2. 90 (1 OH, m), 3. 15-3 18 (1Η, m), 3. 22 ( 1H, s), 3.5 3-3. 62 (1H, m), 3.67 (1H, s), 4.49 (1H, d, J = 12.2Hz), 4.65, 5.74 (total 1H, each d, J = 13.7 Hz), 5.26, 6.18 (total 1H, each s), 6.45, 6.49 (total 1H, each s), 7.54 (1H, d, J = 8.3Hz), 7.80 (1H, s), 7.82 (1H, d, J = 8.3Hz), 7.97 (1H, s).

MS (FAB) m / z: 544 (M + H) ⁺ .

Example 9 (3S) -3- (6-chloronaphthalene-1-yl) sulfonamido DO 1-[(4,5,6,7-Tetrahydrocheno [3,2-c] pyridin-2-yl) methyl] pyrrolidine hydrochloride

 1) (3 S) 1-3-amino-11-tert-butoxycarbonylpyrrolidine

(3R)-1-tert-Butoxycarporinol 3-Methanesulfonyloxypyrrolidine (1.50 g) is dissolved in N, N-dimethylformamide (20 ml), and sodium azide (736 mg) is added and the mixture is added at 100 ° C. For 6 hours. The reaction solution was concentrated under reduced pressure, ethyl acetate was added to the residue, and the mixture was washed once with water and once with a saturated saline solution. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was dissolved in tetrahydrofuran (10 ml), water (1 ml) and triphenylphosphine (2.23 g) were added, and the mixture was stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (dichloromethane: methanol = 100: 2) to give the title compound (892 mg, 85) as a colorless oil.

_{! H- NMR (CDC 1 3)} δ: 1. 46 (9Η, s), 1. 98- 2. 11 (2 H, m), 2. 95- 3. 10 (1 H, m), 3. 26-3.60 (4H, m).

MS (FD) m / z: 187 (M ⁺ ).

2) (3 S) 1-3-[(6-chloronaphthalene 1-2-yl) sulfonamide] lysine trifluoroacetate

(3S) 13-Amino-1-tert-butoxycarbonylpyrrolidine (20 mg) was dissolved in pyridine (20 ml), and triethylamine (0.15 ml) and 6-chloro-2-naphthylsulfonyl chloride (281 mg) were added. The mixture was stirred at room temperature for 20 minutes. The reaction solution was concentrated under reduced pressure, ethyl acetate was added to the residue, and the mixture was washed with 1N hydrochloric acid. The extracted organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue obtained was dissolved in trifluoroacetic acid (20 ml), concentrated under reduced pressure, and the residue was washed with getyl ether to give the title compound.

(38 lmg, 84%) was obtained as a colorless solid.

Ή-NMR (DMSO-d ₆ ) δ: 1.69-1.80 (1Η, m), 1.88-1.99 (1Η, m), 2.95—3.28 (4H, m) , 3.75-3.84 (lH, m), 7.71 (1H, dd, J = 8.8, 2. OHz), 7.57 (1H, dd, J = 8.8, 1. OHz), 7.83—7.96 (4H, m), 8.53 (1H, s), 8.91 (1H, brs), 9.06 (1H, brs).

MS (FD) m / z: 311 [(M + H) +, CI 35], 313 [(M + H) +, C l 37].

3) (3 S)-1-[(5-tert-butoxycarbone-4,5,6,7-tetrahydrocheno [3,2-c] pyridin-2-yl) methyl] -1 3— [( 6-chloronaphthalene_2-yl) sulfonamide] pyrrolidine

(3 S)-3-[(6-chloro-naphthyl-1-yl) sulfonamide] Pyrrolidine trifluoroacetate (25 Omg) was suspended in dichloromethane (10 ml), and triethylamine (0.08 ml) was added. Was added and stirred at room temperature for 5 minutes. 5-tert-butoxycalponyl-2-formyl-1,4,5,6,7-tetrahydrocheno [3,2-c] pyridine (15 Omg) synthesized according to the method of Patent (W094 / 21599) and triacetoxy Sodium borohydride (200 mg) was added, and the mixture was stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure, ethyl acetate was added to the residue, and the mixture was washed twice with water and once with a saturated saline solution. The extracted organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 4: 1 to 2: 1) to give the title compound (255 mg, 77%) as a colorless foam.

_{Ή- NMR (CDC 1 3) δ} : 1. 49 (9Η, s), 1. 52 - 1. 63 (1 H, m), 2. 03- 2. 12 (1Η, m), 2. 1 9 — 2.27 (1H, m), 2.35-2.54 (2H, m), 2.73-2.85 (3H, m), 3.59 (1H, d, J = l 3. 9Hz), 3.66 (1 H, d, J = l 3.9 Hz), 3.70 (2H, brs), 3.88- 3.95 (1 H, m), 4.39 (2H, s), 4.99 (1 / 2H, s), 5.02 (1 / 2H, s),

6.49 (1H, s), 7.55 (1H, dd, J = 8.8, 2.0Hz),

7.82-7.90 (4H, m), 8.40 (1H, s).

MS (FD) mZz: 561 (M ⁺ , CI ³⁵ ), 563 (M +, CI ³⁷ ). 4) (3 S) —3— (6-Chloronaphthalene-1-yl) sulfonamide-111 [(4,5,6,7-tetrahydrocheno [3,2-c] pyridine-1-2-) Le) Methyl] pyrrolidine hydrochloride

(3 S) — 1— [(5-tert-butoxycarbonyl—4,5,6,7—tetrahydrocheno [3,2-c] pyridin-2-yl) methyl] 1 3— [(6— Chloronaphthalene-1-yl) sulfonamide] pyrrolidine (229 mg) was dissolved in a saturated ethanolic hydrochloric acid solution (10 ml), and the reaction solution was concentrated under reduced pressure. The residue was azeotroped with water to give the title compound (203 mg, 90%) as a pale yellow foam.

[] _D =-69. 72 ° (25. C, c = 1.00, CH ₃ OH).

_{Ή-NMR (DMSO- d 6 at} 1 00 ° C) δ: 1. 88- 1. 8 9 (1 H, m), 2. 1 0 - 2. 2 5 (lH, m), 3. 0 2 — 3.07 (2H, m), 3.10-3.50 (6H, m), 4.02 (1H, s), 4.12 (2H, s), 4.45 (2H, s) , 7.12 (1H, s), 7.65 (1H, d, J = 8.3Hz), 7.91 (1H, d, J = 8.3Hz), 8.10 (1H, s) d, J = 8.3Hz), 8.14 (1H, s), 8.16 (1H, d, J = 8.3Hz), 8.18 (1H, brs), 8.48 (1H, s) ), 9.65 (2H, brs).

MS (FD) mZz 462 [(M + H) ⁺ , CI ³⁵ ], 464 [(M + H) +, CI ³⁷ ].

Elemental _{analysis: C 22 H 24 C 1 N} 3 0 2 S 2 · 2. 1HC 1 - 1. 0H 2 as 〇, Calculated: C, 47. 47; H, 5. 0 9; C 1, 1 9. 74, N, 7.55; S, 1 1.52. Analytical values: C, 47.55; H, 5.13; C1, 19.85; Ν, 7.45; S, 1 1.48.

Test Example 1 (Measurement of FX a inhibitory activity (IC _5. Value))

 Sample solution 10 ^ 1, l O OmM Tris200 mM sodium chloride0.2% BSA (pH 7.4) buffer 40 1, 0.05 U / m 1 Human FXa (Cosmobio ERL HFXa — 1 0 1 1 Dissolve and dilute in the measurement buffer) Dispense 10 II 1 into a 96-well microplate and add 75 0 MS 2 2 2 2

(Chromogenix) 4 Oml was added, and the increase in absorbance at 405 nm (mOD / min) was measured at room temperature. The inhibition percentage of each sample was calculated by the following formula, and the final concentration of the sample was plotted on the horizontal axis and the inhibition percentage was plotted on the vertical axis of the log-probability paper to determine the 50% inhibition concentration ( _IC5Q ).

 Inhibition rate (%) = (1 OD of one sample ÷ OD of control) XI 00 The following table shows that compounds having a group that enters the S1 pocket of FXa strongly inhibit FXa.

Test Example 2 (Bok Ribushin inhibitory action (measurement of IC _5. Value)) Dispense 10 OmM Tris · 20 OmM NaC 1 (pH 7.4) 355 1, sample solution 100 1, 4 mM S 2222 (Daiichi Kagaku) 25 ^ 1 into a glass tube and add 1 g / m 1 human trypsin ( Cosmo Bio, 20 mM tris - 0. 2% BSA - dissolution and dilution with _{10 mM C aC 1 2 · 0.} 8% NaC 1 (. pH7 45)) 20 1 , and the mixture was incubated 3 7 ° C 1 5 min .

The reaction was stopped by adding 1M citric acid 1001, and the absorbance at 405 nm was measured. The following formula to obtain the percent inhibition of each sample, the analyte final concentration on the horizontal axis of the logarithmic probability paper, plotting the% inhibition in ordinate, was determined 50% inhibitory concentration (IC ₅ "). Inhibition rate ( %)-(1-(Sample 〇D—Blank 0D) ÷ (Control OD_Blank 0D)) X 100

 The table below shows that compounds having a group that enters the S1 pocket of trypsin inhibit tribcine.

Table 2

Test Example 3 (X-ray crystallographic analysis of complex with FXa)

 The following X-ray crystal analysis example shows that the bicyclic aromatic ring group or aromatic heterocyclic group referred to in the present invention enters the S1 pocket of FXa.

 The abbreviations used in this test example mean the following.

 G 1 a: gamma-carboxyglutamic acid

 PEG: polyethylene glycol

 HEPES: 2- [4- (2-hydroxyethyl) pidazine-1 11

 Yl] ethanesulfonic acid

 DMSO: dimethyl sulfoxide

F o: absolute value of observed structure F c: Absolute value of calculation structure factor

1) Crystallization

 In this test, first, a benzamidine / human Gla domain-deficient FXa complex was used using commercially available benzamidine and a commercially available human G1a domain-deficient BExa FXa (Haematologicotectecnology). Crystals were prepared, and a soaking method was applied to the crystals to replace the benzamidine in the complex with a 5-chloroindole derivative (5) or a 6-chloronaphthalene derivative (7). However, since spontaneous crystal formation of human FXa-deficient FXa was not observed in the presence of benzamidine, spontaneously generated DX-9065 / human FXa-deficient beta FXa was first created. The benzamidine Z-human G1a domain-deficient FXa complex microcrystals were obtained by the streak-seeding method using this as a seed crystal, and then the diffraction data could be measured by the Mcguchi-seeding method. It was grown to a large size and used for the soaking method. For the 6-ethyl benzothiophene derivative (6), the macrocysing method was applied to the benzamidine / human G 1 a domain-deficient FXa complex microcrystals prepared in the same manner, and 6-ethyl benzothiophene was applied. A method of obtaining a complex crystal by growing in a solution in which the derivative and the G1a domain are deleted in the presence of FXa overnight was used.

1 a) Preparation of seed crystal

After dialysis of commercially available human G 1 a domain deleted base Isseki FX a to the buffer i (Murray doo-imidazole 5mM, p H 5. 0Z4mM C a C 1 2/1 OmM of DX 9065 a), It was concentrated to a protein concentration of 1 OmgZm1 with Centricon 30 (Mi 11 ipore). 12.5 PEG6000 / 0.3M sodium acetate 0.1M maleated imidazole, pH 5.0 Using a hanging drop vapor diffusion method, DX-9065Z human G1a domain deleted FXa A composite crystal was obtained. Crystals formed within one week at 20 ° C. lb) benzamidine / human G la domain deleted Beta:. FX a human G 1 Creating commercial complex crystal a-domain deficient beta FX a buffer (5 mM malate I Midazo _{Ichiru, pH5 0 / 4mMC aC 1 2} Z1 OmM After dialysis against benzamidine), it was concentrated to a protein concentration of 1 Omg / m1 with centricon. 12. 5% PEG6000 / 0. 3 M sodium acetate / ⁷ 0. 1 M malate imidazole separately used for supersaturated solution by PH5. 0 solution hanging de port-up vapor diffusion method using the. The supersaturated solution is planted with fine crystal nuclei extracted by piercing the seed crystal with pointed human hair (eyelashes) and allowed to stand at 20 ° C for 10 days or more to obtain a 0.0 lmm square. A small amount of benzamidine Z human G1a domain deficient FXa complex microcrystals were obtained [streak-seeding method]. Next, the microcrystals were washed with 12.5% PEG6000 / 0.3 M sodium acetate ZO. 1 M malate 'imidazole, PH 5.0 several times, transferred to the above supersaturated solution, and allowed to stand at 20 for 2 weeks or more. A benzamidine non-human G1a domain-deficient beta-FXa complex crystal was obtained from which diffraction data could be collected [Macrocyceding method].

 1 c- 1) 6-Chloronaphthalene derivative (7) / Human G 1 a domain deletion FXa Complex crystal formation

 The above external solution of the benzamidine / human G1a domain-deficient FXa complex crystal was subjected to two-stage dialysis to 25% glycerol / 25% PEG6000 / 0.3 M sodium acetate 2.5 mM CaC 12 / 2.5 mM 6-chloroform Naphthalene derivative (7) hydrochloride / 0.1M maleate.imidazole: H5.0 was substituted for the composition. Thereafter, a crystal (0.13 × 0.13 × 0.25 mm) was immersed in the same external solution, and the benzamidine in the crystal was replaced with a 6-chloronaphthalene derivative (7) [soaking method].

 1 c-2) 5-monoclonal indole derivative (5) / Crystal formation of FX a complex lacking human G 1 a domain

By two-stage dialysis, the above-mentioned benzamidine Z human G1a domain deletion The external solution of the FX a complex crystal was replaced with 20% PEG6000Z 0.3 M sodium acetate Z 2.5 mM CaCa 12 / 2.5 mM 5-cloth indole derivative (5) /0.1 M HEPES, pH 7.0 did. Thereafter, the crystal (0.16 × 0.32 × 0.13 mm) was immersed in the same external solution for a while, and the benzamidine in the crystal was replaced with a 5-cycloindole derivative (5) [Soaking method].

1 c-3) Preparation of 6-ethynyl pentazothiophene derivative (6) / human G 1 a domain-deficient beta F Xa complex crystal

 A 6-ethynyl benzothiophene derivative (6) was added to the supersaturated solution prepared in the same manner as in 1b) above, so that it would be equivalent to 10 equivalents to FXa lacking the human G1a domain. It was left still for a day. A 0.01-mm square benzamidine / human G1a domain-deficient beta-FXa complex microcrystal, prepared as in lb, was prepared using 12.5% PEG6000 / 0.3M sodium acetate Z0.1M maleate imidazo. After washing several times with pH 5.0, transfer to the above supersaturated solution and leave it at 20 ° C for more than 2 weeks to collect the solution overnight. 6-ethynyl benzothiophene derivative (6) Z Obtained FXa complex crystal lacking human GIa domain [Macroseeding method] 2) Diffraction experiment

 2 a) Diffraction data of β-FXa complex crystal lacking 6-cloth naphthylene derivative (7) / human G1a domain

The crystals were scooped together with the external solution using a nylon loop (cryo-1oo, Hampton Research) and attached to an X-ray generator (RU-H3C, Rigaku) operated at 10 kW. The crystals were fixed by freezing in a nitrogen gas stream at 170 ° C, and the diffracted images were blown with a nitrogen gas stream at 170 ° C using a diffractometer (R-AxisIIc, Rigaku) using an imaging plate as a detector. I took a picture. Using the software attached to the device; PROCES S, the densitometry of the diffractogram was performed on the Indy Work Station (Silic on Graphics), and the 2.2 X 1 (T ⁸ cm This crystal was obtained on Protein Day. Evening bank DX— 9065 a / human G 1 a domain deleted, identical to FXa complex (PDB code: 1 FAX), space group P 2 ^, 2, lattice constant a = 56. ^{04X 10- 8 cm, b = 71.} 93 X 10 - 8 cm, was ^{c = 78. 76 X 10- 8 cm} .

 2 b) 5 ____________________ Indole derivative (5) Measurement of the diffraction data of F Xa complex crystal deficient in Z-human G 1 a domain

 The crystals were sealed in a diffraction sample capillary and mounted on a rotating anti-cathode X-ray generator (RU_H3C, Rigaku). Diffractometer using imaging plate as detector

(R-AxisIIc, Rigaku) and a diffraction photograph was taken at room temperature. Software included with the device; using PRO CE S S, Indy's work station

(S ilic on Gr aph ics) ascending Les densitometry diffraction photograph, 2. give the diffraction data 2 X 10- ⁸ cm. This crystal has the same type as the DX-9065a / human G1a domain-deficient FXa complex (PDB code: 1 FAX) of the protein data bank, and the space group is P2, 2 ^^ and the lattice constant is a2. ^{56. 72 X 10- 8 cm, b} = 72. 60 X 10- 8 cm, was ^{c = 79. 77 X 10 "8} cm.

 2 c) 6-ethynyl penzothiophene derivative (6) Measurement of diffraction data of F Xa complex crystal with deletion of Z human G 1 a domain

5-Droin indole derivative (5) Diffraction data was measured in the same manner as in the case of the beta FXa complex crystal lacking the Z human G1a domain. This crystal is isomorphic to the protein data bank DX-9065 aZ human G1a domain-deficient beta FXa complex (PDB code: 1 FAX), the space group is P 2,2 ₁ 2 ₁ , and the lattice constant is a = ^{57. 04X 10- 8 cm, b =} 73. 43 X 10 "8 cm, was ^{c = 79. 91 X 10- s cm} .

Structural analysis

REFMAC and PROLSQ used in the following structural analysis are CCP The one in 4.

 Literature on CCP4: "The CCP4 Suite: ProgoramsforProiteinCrysta l logog aphy (ActaCryst., D50, 760-763, 1994)

 Literature on RE F MA C: "R e f in e m e n t o f M a c ro m o l e c u l a r S t r u c t u r e s b y t he e M ax i mum — L i k e l i h o o d Me t ho d (Acta Cry s t., D 53, 240-255, 1997)

 Literature on P ROL SQ: "Ste r e o c he em i c a l 1 y R e s t r a i n e d R e f i in e m e n t o f Ma c r omo l e c u l a r S t r u c t u r e s (Me t ho d s in En z ymo l., 115, 252-250

3 a) 6-Chloronaphthalene derivative (7) Structural analysis of beta FXa complex lacking Z-human G1a domain

The structure of the protein part was modeled using the FX-complex (PDB code: 1 FAX), a model lacking the DX9065 aZ-human G1a domain from the Protein Data Bank, and subjected to rigid body refinement using X-PLOR. Were determined. The phase refinement and the atomic model were improved by standard methods using the phase refinement program RE FMAC and the molecular graphic program Turbo-Frodo. | Fourier maps using Fo—Fc i and I 2 F 0—F c I as coefficients gave continuous electron density peaks near the catalytically active site of FXa. The atomic model of the 6-chloronaphthalene derivative (7) was fitted to this electron density peak and refinement was continued. The cycle of phase refinement and model improvement is repeated several tens of times, and finally the crystallographic reliability factor (2. I Fo—F c IZ∑Fo) at 1 22 X l (T ⁸ cm resolution) is 18.7% All calculations are performed in O 2 ZR 500 0 0 (S i 1 1 icon Graphics) or indigo 2 X-stream (S i 1 1 icon (Graphics).

 3 b) 5-cloth indole derivative (5) / Human G 1 a domain deletion

Structural analysis of FX a complex

Structural analysis was performed in the same manner as for the FX-complex that lacked the 6-chloronaphthalene derivative (7) / human G1a domain. However, the acetyl-morpholine structure bound to the piperazine ring was not observed as a significant peak on the Fourier map using I Fo-Fc I and I 2Fo-Fc I as coefficients, so it should not be included in the refinement calculation. Was. Crystallographic reliability factor in the final 2. 2 X 1 0- ⁸ cm resolution

18. Down to 1%.

 3 c) 6-ethynyl penzothiophene derivative (6) Structural analysis of F Xa complex with deletion of Z human G la domain

Structural analysis was performed in the same manner as described in 3b) above. However, the N-methylcarbamoyl group bonded to the piperazine ring was not observed as a significant peak on the Fourier map using IFo-FcI and I2Fo-FcI as coefficients. Was not included. Crystallographic reliability factor in final 2.4's 10- ⁸ (111 resolution was reduced to 8% 17..

 Among the X-ray crystallographic data obtained here,

(5) Table 3 shows the data of the structural analysis of the beta FXa complex lacking the / human Gla domain. The data is shown in PDB format. From left to right, atom name, residue name, ch ain ID, residue number, X, Y, Ζ, occupancy, and temperature factor are shown. In addition, ChainID in the following data indicates A; heavychain, B; 1 ightchain, C; solvent.

Test Example 4 (X-ray crystallographic analysis of complex with Escherichia coli trypsin)

 The following example of X-ray crystal analysis shows that the bicyclic aromatic ring group or aromatic heterocyclic group referred to in the present invention has entered the S1 pocket of trypsin.

1) Preparation of complex crystal of compound 8 and trypsin from bovine kidney Commercially available trypsin (Sigma) derived from human kidney was added to a 40% saturated ammonium sulfate / 2% (w / v) benzamidine / 0.05% (w / v) CaC12 at a concentration of 1 Omg Zml. Dissolved, 53% saturated ammonium sulfate Z 2% (w / v) benzamidine / 0.05% (w / v) CaC12, pH 6.0 Thus, a benzamidine / trypsin complex crystal derived from citrus offal was obtained. Crystals formed within one week at 20 ° C.

 The dialysis method was used to convert the extracrystalline solution to 70% saturated ammonium sulfate / 0.1M sodium cacodylate buffer, pH 6.0 / 0.01% (w / v) C a C 12/5% (vX v) DMSO. Substitution was performed and benzamidine was removed from the crystal by several solution exchanges. The crystals were converted to 70% saturated ammonium sulfate Z0.1M sodium hydroxide codylate buffer, pH 6.0 / 0.01% (w / v) CaC12 / 25mM D61-8811/5% (v / v) DMSO After immersion, the mixture was allowed to stand for 70 hours to obtain a composite crystal of D61-8811 and trypsin derived from the citrus viscera.

2) Diffraction data measurement of crystal of complex of compound 8 and trypsin derived from human kidney Similar to the crystal of FX-a complex lacking beta-closure indole derivative (5) / human Gla domain in Test Example 3 The diffraction data was measured by the method. © Shi滕臓derived trypsin The crystals Puroti down de Isseki Bank: In (PDB c ode 1 TLD) the same type, space group P 2 2 had a lattice constant ^{a = 63. 92 X 1 0- 8} cm , b = 63. 20 X 10 - was ^{8 cm, c = 69. 29 X} 10- 8 cm.

 3) Structural analysis of complex crystal of compound 8 and trypsin derived from bovine kidney

The structure of the protein portion was determined by rigid-body refinement using X-PLOR, using a model of the trypsin derived from pest of the protein databank (PDB code: 1TLD) as a model. Phase refinement and improvement of the atomic model were performed by standard methods using the phase refinement program PROLSQ and the molecular graphics program Turbo-Frodo. Fourier maps with IF o — F c I and I 2 F 0 — F c I as coefficients gave a planar electron density peak near the S 1 site of FX a. The atomic model of sulfonylchloronaphthalene, a partial structure of D61-8811, was fitted to this electron density peak, and the refinement was continued. The other structural parts were not included in the refinement calculation because they were not observed as significant peaks on the Fourier map using I Fo-Fc I and I 2Fo- Fc I as coefficients. Repeated cycles of phase refinement and model improvement dozens of times, the crystallographic reliability factor in final 1. 8X 10- ⁸ cm resolution (Σ | Fo- Fc | ZΣFo) up to 1% 17. Dropped. All computations were performed on an Indigo 2 stream (Si 11 ic on Graphics).

 Table 4 shows the X-ray crystallographic data obtained here. Data are shown in the PDB format, and the names of atoms, residues, ch ain ID, residue numbers, X, Y, Z, occupancy, and temperature factors are shown in order from the left. In addition, ChainID in the following data indicates A; heavychain, B; 1ightchain, C; solvent.

 Table 3

 ATOM 1 CB ILE A 16 11.741 14.874 33.014 1.00 34.10

ATOM 2 CG2 ILE A 16 12.300 14.052 34.186 1.00 26.75

ATOM 3 CGI ILE A 16 12.784 15.144 31.931 1.00 30.81

ATOM 4 CD1 ILE A 16 13.554 13.948 31.360 1.00 27.85

ATOM 5 C ILE A 16 9.454 13.931 33.505 1.00 32.83

ATOM 6 0 ILE A 16 8.927 14.871 34.087 1.00 33.36

ATOM 7 N ILE A 16 9.882 14.985 31.329 1.00 33.80

ATOM 8 CA ILE A 16 10.493 14.182 32.413 1.00 32.86

ATOM 9 N VAL A 17 9.084 12.678 33.684 1.00 31.58

ATOM 10 CA VAL A 17 8.219 12.287 34.779 1.00 30.56 ATOM 11 CB VAL A 17 7.473 10.961 34.480 1.00 37.04

ATOM 12 CGI VAL A 17 6.524 10.632 35.614 1.00 27.56 19

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00 in '3ΐ 19, V V3 ozt ΙΪΟΧΥ 麵 oar /) d C9.Z9 / 10 OAV 99

 9f 'AC 00' Ί 6 ・ ΐΖ 0 ^ 8 * 92 '9 6S V ίΙΊΒ V3 8 ΐ Dish V

99 '8S 00 9S8'9Z 6t6 "9 6S V ΠΊ3 N ΑΖΐ 舰 V srot 00 Ί 918" 8S V NSV 0 9 隐 V

Of 62 00, 1 300 "8Z 6 Z 8S V NSV 0 9ΑΙ Dish V

08-83 00 m-u 968 "8 88 V NSV so-called thigh V

06 • 00 '• I 8 6Ό2 "6 8S V NSV ιαο S Thigh V

00, ΐ 0 6-81 Ζ0 8 88 V NSV Bandit V

09 00 ■ ΐ IZ8'6I 9687 8S V NSV ao UT Thigh V

If ^ 00 'ΐ Z' 61 m 'i 88 V SV vo 0 "WOIV

\ Vl \ 00, ΐ 692 -8ΐ 189 -8Z 128 "9 82 V NSV N 691 Thigh V

86 'St 00 m-Qi 0Z \ "9 AS V 1113 0 891 WOXV

6Z'8t 00 "ΐ SA9" 9 ε v mo 3 Z91 thigh V

00 'ΐ Ζΐ9 "Αΐ 88' 8 LZ v ma ao Z9I Thigh V

00 • ι ΐΐ · ΙΑ 11 V ΠΊ9 V3 191 Thigh V

00 • I 191 -U 19Z "B 11 v mo N 091 Thigh V

00 6ΐ '9 9S v ma 0 691

00 'ΐ ΟΑΙ' 9ΐ 9ST9 92 v ma 0 891 WOIV

00 'ΐ 8ΗΊΙ 92 V HID 33 Thigh V

00 'ΐ 2S8' 9S v mo 93 SSI thigh V

00 Ί ΙΙΟ Ϊ 8ΐΟ8Ζ 198 "9 9S v rra V3 Ζ3Ϊ Thigh V

0, 00 00 SSffl 98 v mo N 191 Awake V

98 'It 00 Ί Uf9l ZOf 8 92 V NSV 0 09 腿 thigh V

0 U o un u • τ ι T iOjTi o CO

 V iv V l iVUdi V

00 • ΐ 919 -U 9S V NSV 8 皿 Plate V

99 -Zf 00 • I 669 990 "9 98 V NSV ιαο i 隐 V

93 'S 00 Ί 0S8'9I 991 9 5S V NSV 30 9 ^ 1 Thigh V

C9.Z9 / T0 ΟΛ \ Z9

 8Z'92 00I 60Ζ '11 68 8Ι OAC 'SI V ΙΎ V3 80Z Thigh V

Ζ0 · 9Ζ 00 "l 980 '1 8SZ-\ V ΑΊ9 N iOZ Thigh V

8 6Ζ 00, ΐ 928 '8ΐ' 9i l V S13 OS 90Z W0IV

89-ΟΖ 00 'I Α09 • 61 96f Zl m-n-l \ V S ao 90Z Dish V

68 Ζ 00 • ΐ i · \ ι I98'6l 89C81 Z V SA3 0 Thigh V η -ιι 00 • i t6S ■ \ i t9'8l Zf V S13 3 views V

00 • ΐ 9 6 • oz 8l0'8l -n Zf V SA3 vo Thigh V

9 ^ 82 00 • ΐ LU • QZ l \ V SA3 N 102 plate V

U Ί800, ΐ • QZ 80S · ”66S'6 It V V 0 ooz Thigh V

99 Ό8 00 'ΐQZ 20Γ8Ϊ If V aHd 3 661 WOXV

00 '92 00 • ΐ 606 • SI ZOfOZ torn \ f V thigh Ώ 861 plate V

00 'ΐ '91 09 * ΪΖ \ f V ΖΏ Thigh V

96'8Ι 00 • ΐ% n • 91 V ΙΏ 961 thigh V

99'2S 00 'ΐ 68f Ζΐ Ϊ6' 6 V Thigh S6t 隐 V

9 8Ζ 00 • ΐ

Thigh V

00 • ΐ 8,6 'LI 066 * 61-V edition S61 thigh V

AO ^ S 00 ■ ΐ IZO • 61 Ζ · 8 It V Z6I Comfort V

99 'IS 00 • ΐ 09 • 02 28Γ6Ϊ m- It V mi vo 161 plate V

09 · 00 • ΐ IU • 02 9Z1 Ζ It V N 061 Bile V

68 'SS 00 ■ ΐ' 1 629-12 m'i o V 0 681 Dish V ζ ^ ζη 00 • ΐ 0Z9 • \ i m- \ z SS9'8 0 V Π3 3 881 Hidden

69 -22 00 • ΐ zn '9ΐ8'6 o V Π3 vol \ Dish V t υ 00 ■ \ on ■ u 06T -fz V ΑΊ3 M Q «T WOTV

00 Ί miz 6S v mo 0 981 dish V

00 • ϊ • \ z m-L 68 v rra 3 n \ 舰 V

8Z'2 00 'ϊ 06 Ζ 99Z'9 6S v mo go u \ thigh V

C9.Z9 / 10 OAV Fiber /: / O ϊοΙ £ 3AV

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00 '' ΐ 668 '' SI 'OC OS V i 092 舰 V n-Li 00' 'ΐ 918 Ι 068-82 09 V 3Hd \ Ώ 69Z Thigh V

09-9Z 00 'Ί η \ Ί \ Q Q-LZ OLf • oc OS V HHd 89Z Dish V

18-61 00 'ι ιι \' CI m-Li 088 • 8Z OB V i A9Z Thigh V

00 'Ί ■ ετ 881 '62 OS V HHJ 992 Thigh V

Z0'9I 00 '' ΐ m-062 -SZ 9998Ζ09 v i ao Thigh V

00 '' ΐ m ^ z OS V HHd vo Thigh V

Π'ΖΙ 00 '' ΐ '91 99f m'u 09 V N 8SZ Plate V

69 00 '' ΐ m 'LI -aLI 6 V 1113 0 i Thigh V

80 '00' 'ί 809 • L \ m • u 6 v mo 3 m Plate V

00, ΐ STO8ΐ 6 V 1113 zao osz Plate V

81 "2 00 • ΐ 66 • 91 969 • εε 6 v mo ■ 6 Z W0IV

00 6 S 'LI 09ΐ 8Ζ -Z 6 v ira Thigh V

ZC "9S 00 Z 9 -LI • IS 6 V ίΙΈ) 03 in thigh V

00 Ί 60S '81 90SOS 6 v ηΐΰ Plate V

Zt 00 • ΐ 9Α9 · 8ΐ W9Z m • 62 6 v mo vo W0IV

00 • 61 6I '92 001 Ό8 6 v mo N m W0XV

90 · 00ΐ61m61 61 990 8 v 0 m Dish V

00 • ΐ u • 61 QZ \ -U 8 • 6Z 8 ^ v 3 m Thigh V

6i'0C 00 • ΐ 088 OS 8 v ¾as 30 \ u VIEW V

00 • ΐ 059 • 81 'zz 8 v ¾as Ώ on Marauder V

00 • ΐ m • 61 891 • OS 8 v VO 6SZ Thigh V

RQ -07

 Oo o o no • τ ι 810 -QZ ¾P0-T7 860 • 6Z o¾ V Q 006 M JfVOUiLTV V

IS'lZ 00 • I '02 699 'OS L v nai 0 Thigh V

00 'ΐ -QZ οζ 92 ^ L v nai 3 隐 V

IVLl 00 'ΐ 699 -QZ CS9 * 9l UL-ll L v nai Zdd 9CZ Optional

C9.Z9 / 10 OAV Oi,

 Ζ '8Ζ 00 • Ϊ in • 61 969' 9ΐ 869 89 v nai S3 98Z ■ Thigh V

Ζ ΌΖ 00 'ΐ 28' 9ΐ 198 '1 29 v nai V3 picture

00 • ΐ SIf 81 396- I ■ 1 89 v nai M 8Z thigh V

% -u 00 • ΐ • 91 I f 81 1 V ΗΊΙ 0

69 -SZ 00 ■ I nz ■ L \ ΙΖ8 · 8Ι is • u Z9 V ΗΊΙ 3 thigh V

00 • I m • 61 u \ -u Z9 v an I (D m Sat l \ -QZ 00 • iL \ 98C '11 v an 133 08Z Band V

LQ'ZZ 00 ■ ΐ · 8ΐ · \ ι v an 62-Z Thigh V

00 Ί 69 'l 880 ΊΖ 69Z 29 v an ao LZ Plate V

00 • ΐ · οζ S69 • n V ΗΊΙ V3 III Hidden V

99 00 • I • 91 928 * 02 Z9 v an N Plate V

00 Ί ■ 81 • 9Z 19 V Ul 0 thigh V n ^ z 00 "I 160 • L \ 9ΠΊΖ • Z IS V MI 3 VLZ thigh V

00 "l • 01 69 98BQZ IS V Ul HO Zll Thigh V

00 • I m • ΐϊ • 6Z 19 V Ul ZD III

00 • I 686 • π 608 · 0Ζ m-n 19 V MI ΖΏ Ml 隐 V

00 • ΐ in • SI 589 '02 19 v zao 0LZ Thigh V

80 · Ζ 00 • ΐ m • n UfU 666 • 6Z 19 V MI iao N0XV

09ΊΖ 00 • I 890 · ΐ · ΐΖ 629 19 V Ul iao 89Z Thigh V

00 • ΐ 906 ΌΖ • 8Z IS V Ul DO Thigh V

00 • ΐ I6i • 91 208 -a 19 v Ώ m

00 Ί SA6 • SI 985 • u 19 V ¾ AI vo Thigh V

QT "77 no • τ 291 • 91 981 • LI TC

99'ΐΖ 00 • I SSS '921 -U 021 • 92 OS V Thigh 0 Thigh V

IfZZ 00 • ΐ • 91 n \ -n I6 • 9Z 09 V 3Hd 3 dishes V

9fU 00 • I '9ΐ 90Γ6Ζ 8 ΐ • οε OS V HHi ZD m Thigh V

C9.Z9 / 10 OAV 11 • 9Z 00 'Ί 0 9ΐ SOS' Όΐ 908'ΐΐ V SIH 33 V

, 82 00 '' ΐ 62Ζ'3ΐ 801 '' Οΐ V SIH 93 Thigh V

60 ■ Z2 00 '' ΐ n \ '' Ιΐ V SIH V3 οιε V

86OS00 '' ΐ Z80, U 9Ζ6εΐ V SIH 60S Hidden V

00 '60ΓΖΪ 999, 9S V V1V 0 80S Intestine V

If • οε 00 '' ΐ 898 '21 89Z ■ um l 93 V V1V 3 AOS Thigh V

19 * 92 00 • ΐ m'i \ 0Z8 Όΐ 9 9 "9i 99 V V1V ao 90ε V V l \ • 8Z 00 • ΐ 188 • II 291 -91 99 V V1V VD 90S 舰 V n U '9i 99 V V1V N

0L • SZ 00, ΐ Appendix SI 269 ■ 16-91 S3 V V1V O SOS 舰 V

9Z "92 00 • ΐ 629 S9 V V1V 0 zoc Dish V

S6 • 81 00 • ΐ% LL'L \ 809 \ 0.99ΐ S V V1V Ώ 102 hidden V

S2 ■ u 00 • ΐ ^ ΙΟ 'ΐ · ι \ η \ Ί \ S3 V V1V V3 008 Dish V

69 '11 00 • ΐ WL \ 093 • 1 V V1V N 662 Thigh V

OA -u 00 • I 988 * 91 • ei 096ΐ V thigh 0 86Z thigh V

L 'U 00 • ΐ V Thigh 3 6Z Hidden V

LO 'St 00 • ΐ 961 '91 • 91 ιιι · \ V 舰 96Z

89 • 61 00 • ΐ 96ΐ '81 509 • 91 69071 V Thigh 190 96Z

89-\ z 00 Ί 009 • 91 οε '8ΐ V dish ao 6Z thigh V

Z6 00 • ΐ 09S • 91 SIZ * 61 V wish vo C6Z plate V

U • 11 00 Ί '9ΐ V Thigh N Z6Z Plate V

• oz 00 I 3-6T • 91 616 S9 V nan 0 162 隐 V c;

 \ 6 n unu * τ QQC 'QT 08S '91 1 ρ

 6Λο Τ CQ

 V 6 J V V i ΠmΐΠ l Uuo iVUX V

Z • 00 • I S6ZOZ 989 • si 89 V

08 'l \ 00 • I • SI S9 ν nai mo Thigh V

62 • 91 00 * ΐ 0ΪΓ6Ι 581 ^ 1 69 'δΖ 89 ν nai 33 m thigh V -1-fIO / lOdf / X3d 9Z 9/10 O ZL

 OS '00 • Ϊ 969 • 6 Z09-\\ ZZl · Ζΐ 09 V Ul iao 8se V

69 00 • I • 01 9 Z • Ζΐ ZQl ΊΙ 09 V MX ιαο AS8 woxv

62 • St 00 • i • 6 196 • Ζΐ 09 V Ul 9SS WOIV

S • St 00 • i • 01 899 'SI · 6 09 V MX 982 plate V

89 00 • i 189 ΌΙ 6AI9 ΐ 09 V Ul vo Dish V

Π • it 00 ΊΙ 9S-01 09 V MX N Thigh V

9S 00 • \ m • ot 891 -LI 69 v nai 0 plate V

96 • 0, 00 Ί 881 • n 692 • 91 69 · Π 69 v nai 0 thigh V

28 • 92 00 • I 069 ΊΙ 909 'LI 6S v nai Zdd οεε Thigh V

99 • 98 00 • i 298 • 01 • 91 Ζ0 9Ϊ 6S v nai iao 舰 V ει • hi 00 • I 989 • n i90 • 91 6S v nm Thigh V

16 • n 00 • I 8S0 196 • 91 69 v Thigh Ώ S 隐 V

69 * 6e 00I 980 -i \ Z9ΐ m-z \ 69 v nai vo 9ZS 舰 V

2Z • ze 00 • I 681 • SI m • SI 608 • Ζΐ 69 v Thigh N Thigh V

Z9 • 9Z 00 • ΐ fL \ '81 0ΐ8 · ΐ 6Π '8ΐ 89 V SAO 3S m Plate V

9Zn00I9S'91SI088'SI89 V AO93 pan V

TO • 6S 00 • ΐ 90A • 91-\\ 89 V SAO 0 m Dish V

L2 S 00 Ί 99 '3ΐ Z61' Zl 8S V D m HOXV

• 9S 00 • i "91 LZ'Z \ 89 V m V3 0Z9 V

• sc 00 Ί • 91 m ■ 81 U9'ZI 89 V m N 61S Thigh V

66 ε 00 • i 9ΐΐ · ΐ688 • n 928 Όΐ Z9 V SIH 0 818 V

00 • i 'Zl 8Ζ6ΊΪ

V SIH 3 thigh V 'π on • T 889 • 81 05Z • Π QQP -TT) c V siH zm QTP ran TV s 00 • I Ufl 9 • oi V SIH iao 丽 V ΐδ 00 • I SIS • LI 962 • 01 8Α8Ζΐ V SIH ταΝ ti Thigh V

• 62 00 • ΐ ZZf • LI l \\ • u 9 8ΌΪ Z9 V SIH ζαο SIS 舰 V

C9.Z9 / 10 OAV Si

 89 -g 00Im6 98Au US'6 29 ν m N 89S Thigh V

Ζ8 6 00 • ΐ 6S '8 QLZ' 1 29 V SAl 0 i9C V

90 '8 00 • ΐ 86' 8 983 '11 29 V SAl 3 99S 隐 V

6A'89 00, ΐ 998 ■ \ i 29 V SAl ao 192 Thigh V 9'8 00 • ΐιη9IS

v sn V3 092 dish V

80 -6t 00 Ί U6 • 6 • \ i 196 Ζ9 V SAl N 6S8 V

0Γ6 00 • ΐ 'Οΐ 211 -QZ IZl ^ V19 V V1V 0 8SS 隐 V

00 • ΐ si6'0im · οζ I9S'S VT9 V V1V 3 Z98 舰 V

AS * 88 00 • ΐ "21 661 Ζ oo V19 V V1V ao 9SS Thigh V

WLf 00, ΐ 96ΐ ι \ 692 -i V19 V V1V vo 938 舰 V

I0-9 00 • ΐ 6S9 -n L '81 9961 V19 V V1V N view V

9rst 00 Ί 8U'81 19 V ΝΊ3 0 S98 Dish V zr oo Ί S9n 8ΐ -i 19 V ΝΊ3 3 298 PJ0IV

Ζ8 9 00 • ΐ 908 'SI 0Α9.919 V ΝΊ3 zm 138 舰 V

10 * 59 00 • ΐ ηο-ί \ • SI C9'9 19 V ΝΊ3 iao 098 Thigh V

00 9 00 • ΐ Ζ • 91 6Π 'i 19 V N1D ω W0JLV

00 'ΐ 909 • 91 m • SI 9.819 V ΜΊ3 m 隐 V

96 '00 Ί 88 ΐ • 91 • 91 09 8 19 V ΝΊ9 in thigh V

89 00 • ι 8 • ει • 91 19 V ΝΊ3 vo Dish V

8600 Ί 99Α • 21 u \ • 91 OZS'8 19 V ΝΊ3 N Thigh V

10 00 • ι Alt • II 9 • 91 6 • 9 09 V UL 0 m Marauder V

99 -0 00 'ΐ 609 • π m • 91 9T8 09 V Ul 3 舰 V

9i'6 00 • τ 8f9 • L no • Π ΐ6ΐ 'ST u nnu 0 WO TV

89 '8 00 • ΐ LL9 • U U \ Ι 09 v m Z3 \ n Thigh V

SfZ 00 • ΐ 09 • L ■ ίΟΖ Ι 09 V UL on 隐 V

A8 't 00 • ΐ 682 • 8 88Γ0Ϊ 09 V Ul zao 6SS Plate V

C9.Z9 / 10 OAV 00 Ί ■ ■ 'OS 9ZI' SI 99 V SAl ao ^ 68 Thigh V

00 062 '62 n \ -ft .59 v sn S6S dish V ζο9ε 00 ', 1 mSI S9 ao ZQZ thigh V

00 • I • 91 TOO • ii U9 '99 v sn V3 16S Thigh V

00, 1 268 • 9Z 99 V SAl N 062 Thigh V

88 "08 00 Ί UL • n '92 \ U1 \ V HHJ 0 68S Thigh V

6Z-8S 00 • I 093 'SI 09Z • 9Z v mi 3 882 view V if' IS 00 0A9 • n S86 -QZ 120'91 V 3Hd Z3 Z8S Fragile V

00 920 ειο-\ z 808-S1 n V thigh ΖΏ 98S thigh V

00 Ί 9f 'SI 0 ^ 8 v HHJ 133 S8C O V

06 -22 00, ΐ M • Ζΐ 098-\ z S18'Z1 v aHi

29 8 00 • I 08 ΐ 989 '1 Ι Ι v i iaa dish V O' AS 00 ι ι π \ OU '11 ZIO'SI V 3HJ W0IV 6'6S 00

00 'ΐ mEpsilon 820BZ, 086Πn V 3Hd vo 082 V

H'6S 00 • ΐ • π -u 99ΓΠ n V N 6AS Thigh V

9800 'I 886 Z9 -6 S9 v m 0 8A8. 隐 V

00, 1 • u 293 Όΐ 89 V, 3 Αζε

89 '8S 00 • ΐ 9Z6 • 6 991 • 18 m-Qi 89 v m ZHN 9AS

00 • ΐ m • 6 09S 386 1 89 V 3W ΪΗΝ 9AS Hidden V

6A'89 00 Ί • 6 089 • οε S98-U C9 V 3W Ώ H8 i¾0IV

00 • 1 • 8 • 6Z 9S'll 29 V, Thigh V

 9 '00 9 9 8 866 • 9Z S9 v m 33 US 隐 V

Zf S 00 • I o o • 6 LLQ • 9Z 981.01 89 v Ώ OAS 'Thigh V

60 '00 "ΐ Ϊ Α • 6 2 ^ fU 05f0I S9 V 3W VO 692 隐 V

C9.Z9 / 10 OAV 9Z

π '92 00 'Ί' τι Π9 · 9Ζ 89 V 1VA 133 隐 V

AS • 61 00 '• ΐ s'sz Ζΐ9 -11 89 V ΊΥΛ ao 6 隐 V n • 8Z 00 Ί 000 · 89 V 1VA vo m Thigh V

SZ 00, ΐ Ζ66 'τι -n 98 -81 89 V ΊΥΛ N Alt Thigh V

• εζ 00 'Ί ηι-ιι 66971 Z9 v m 0 m request V δΐ • εζ 00 • ΐ 9IS 991' il L9 v m 3 s request V

OA 00 899 ^ 2 8A9 V 3W ring f \ f 舰 V

00 Ί 881 '1 m6ζ l \ V \\ A9 V ΪΗΝ sit dish V

98 · ι 00 Ί 26611 A9 v m Ώ zn Thigh V

96 '38 00 860 'Ζ 86 9Ϊ i9 V 9W m n W0IV

86 'l 00-\ m-n 88Γ Z9 V, αο o Thigh V

00 • I 981 6Ζ A9 V 3HV m Thigh V

89 • 92 00 'ΐ 991 '11 in · ι OZf SI A9 V, Ώ m W0IV

18 00 'ΐ-\ z 92Γ9Ϊ A9 V, vo LO thigh V

90 • SZ 00 • ι 699 '9Ζ 939'9ΐ i9 v Ν 90 Thigh V

82 • οε 00 • ί ZS6-81 -i \ 99 V 1VA 0 Thigh V

18 • a 00 • ΐ \ U "61 99 V 1VA 3 Thigh V n • 61 00 • ΐ 9 Γ91 m-u 0SZ-81 99 V 1VA Thigh V

8S • 9Z 00 • 1 m- \ 888 * Z 0 · 6Ι 99 V 1VA 190 舰 V fL • 6Z 00 'I 6S' 98Γ8Ι 99 V 1VA 93 Thigh V

98 • ii 00 • ΐ '81 968 · 9ΐ 99 V 1VA V3 00, Marauder V

99 • 6Z 00 • ΐ ^ 6 "9l 68Z'9t 99 V 1VA Ν 662 hall V

90 ■ oc nn-τ LVO υ o J l qq u c Oia 丄 υ WflTV il • 12 00 • ΐ 60 '91 99 V S Ί 3

A9 00ZLS-21 099 'Zl 99 V SAl m 962 Thigh V

90-00 Ί 08 ^ -81 0S9.IS 99t'SI 99 V SAl 969 Fragile V 9A

 0'ie 00 'Ί νι 690 -9Z 96 ^' 'δΐ ν 0 Appendix V

S 6Z 00 '' ί 'l 236' 9Ζ 80Γ 'I \ ι 3 Marauder V rit 00' 'ΐ 89Γ Ί \ U ν Ran m V

00 'Ί 960 Z96'8Z IL ν m ΪΗΝ m Plate V

00 'Ί 89Z'98 899 Ζ69' ΐ Ιί V 3W Ώ zn Thigh V

00 'Ί ZSI' LI · 81 \ ιν m m in Awake V sroc 00 '' ΐ m-iz 9A9 · 8ΐ U V 3W αο m V

00 '' ΐ628628808ΑΐΑΐ U V 3W 33 W0IV

Yl'U 00 '' ΐ 98 9δ HVLZ '9ΐ U v 93 Thigh V

00 Ί ^ 6 "18 6SSI U v VD Thigh V

00 '' I 296-08 8S0 • 91 U v m N 丽

00 • ΐ 610 · 9ΐ οζ V JSV 0 plate V

00 • ΐ ΐ69'62 n \ • 91 0i V iSV 3 hall V

00 • I · 8ΐ U V d V Orchid se dish V

00 • ί 86 '8Ζ • 81 U V iSV ιαο z WOIV 6' 00 • ΐ SSI '62 001 · U V iSV 33 is plate V i9'8S 00 Ί 96Γ8Ζ o s' 3ΐ

00 Ί 69S • 91 0L V JSV V3 62 Thigh V

8ΐ · 9Ζ 00 • ΐ m'u 188 · ί \ Οί V iSV N 舰 V

IC'9Z 00 Ί UL-U m 'os 699' 8ΐ 69 V Π30 0 丄 ^ Dish V

00 • ΐ 88Γ8Ζ n \ · 6Ζ 69 V ΑΊ3 0 9 Hidden

66 · 00 Ί 883 mQZ 69 V ΑΊ 9 V3 Dish V

GO V 6 υυ • τ U6 G y 6 UDU 00 8866 ΐ C νQν V Λ 丄 kl

 IV v by ™ ητν os'sz 00 · \ 608 * 62 Z60 • 61 89 V 1VA 0 thigh V 'νι 00 199 199 -8Z 093 * 6ΐ 89 V 1VA 3 m Dish V

90 1 00 • ΐ SAS Ζ 89 V ΊΥΛ Z93 Thigh V ft'ClO / lOdf / lDd £ 9LI9 / T0 OAV 00 'ΖΟΙ OS 909 "SS Ul''01 V ΝΊ30 0 舰 V

00 '05ΓΪ8 Z06'SS 809 ΌΙ Si V ΝΊ3 3 8 Thigh V

U'09 00 'Ί 189 · εδ LU "8S S v mo 93 Thigh V

00 '"S S WSS 199' ■ 6 V ΝΊ3 V3 Hidden V

80Ί9 00 '' ΐ IZ6.IS 896 * 8 SA V ΝΊ9 N thigh V l \ 8 00 '268 268 OC SO' L U V ΠΊ30 thigh V

89-81- 00 '• ΐ ° Μ Π8 Ί n V ΠΊ3 3 thigh V

Z0 00 '• ΐ Α68Ί8 829 · 6Ζ • 9 fL V ί1Ί3 33 dishes V

00 'ΐ 88f OS9 L V ί1Ί3 93 m 隐 V

8 9 00 • ΐ 6,6 'OS • i M v rra V3 Thigh V

S8 '00 • ΐ 189-02 ^ z · 8 n V 1ΊΊ3 N m Dish V ίζ · η 00 • ΐ -u 18f OS Ζ69 "8 £ i V Dish 0 Thigh V

08 • 00 • ΐ IS '6Ζ Si V Thigh 3 09 Thigh V

00, ΐ LLfLZ 689 · 9Ζ in • oi SI v mi 69 thigh V L '00 Ί298 · 9Ζ £ 1 V plate 190 89 Marauding V, 00 • ΐ 909 · Ul • 6 £ 1 V plate 93 iS 舰 V

89 * 62 00I ULSZ III6 SI V Dish V3 隐 V

0 Ά2 00 • Int'os 0Ϊ 8Ζ m '01 SI V dish N s 隐 V

00 'ΐ ufm 8ΪΓ09 109 • Π U V NSV 0 Ran ίί' ^ 00 Ί oio'ie 9S6'8C 832 • nuV NSV 3 thigh V

00 oirss 199 • 01 u V NSV 圆 舰 V ιη 00 • ΐ 81S-e8 809 -6Z m • 6 u V NSV ιαο thigh V νο 1 V π υπυ 1 00

 ooL ； 06 089 · 0ΐ 76m l J J mountain

08Ί8 00 • ϊ Ζ9Γ88 866 • Π li V NSV 93 m Dish V

00 * ΐ ι \ ι · η 69S * 8Z 180 'Ζ \ u V SV VD m Thigh V

8Γ28 00 • ΐ 980 '8Z 6 ^ 8Ϊ u V NSV M m Thigh V

C9.Z9 / 10 O 8

ifZ 00, ΐ m • ii m9Ι 08 v mo 03 609 Thigh V

\ Vl \ 00 • I ZSi'9I 08 v mo ao 809 hidden V S'IS 00 • i '92 S68 "2C III, 81 08 V ΩΊ3 V3 AOS plate V

99 -ZS 00, ΐ9Z U'81 08 V ίΠ3 N 909 Thigh V

U "AS 00 • I in • ii 819 • η 699 -0Z V ΙΎ) 0 SOS plate V

89'92 00 Ί ■ ii 018-61 6A V ΑΊ33 t09 plate V

I8'8S 00 • ΐ 899 • n oot'oz 6i V ΑΊ3 V3 809 Thigh V

00 • I zn • 6Z 9i ss 6A V Π3 N 209 Thigh V

00I-ii 816'9S 888.81 V ΑΊ3 0 109 Marauder V

91 W 00 • ΐ m • 62 6 '9ε 8Z V ΑΊ3 3 OOS Thigh V

00 • i 820 Ό8 8A V Πϋ V3 66 Thigh V

Π '6 00 • i 166 • 08 A08-9S, 8A V Π3 N 86 Thigh V

69 ^ 9 00 • I 88 • is 808 Z68 1 V ΠΈ) 0 6 Thigh V

U 9 00 'I 0Z9 • 18 186-91 11 V ί1Ί3 3 96 ^ Thigh V

00 • ΐ HL ζ · η OZf 91 LI V ίΠΟ 93 Thigh V

66 * 29 00 • i 0S9 088'9ΐ hi ν mo V3 06t 麵

S3 -8S 00 • I 196 • te -n 8U 'I 11 V ΠΊ9 N 68 ^. WOIV

00 • I 160 • IS S9 Hν η ΐΰ 0 thigh V 9'S5 00 Ί m 8A9'SS 0Z6'8I V ί1Ί3 3 thigh V

8 ^ 28 00 • I 982 ■ ii 9 S-H n V ί1Ί3 z Akebono

S9.88 00 • ΐ 886 • sz W9S 665 'Ζΐ ν mo iao

9Ζ · ε8 00 • ΐ n \ ■ ii 208'99 9i ν mo a. Thigh V

IffL 00 • τ ■ i 00 Q) Ί PS WO JTJV

6Γ63 00I SI0-98 690 Ϊ V RID thigh V

18 't 00' ΐ 989 • 08 800 '2 V ί1Ί3 V3 m Dish V oz- 00 • is 06S' 69-Π n V N 08 Thigh V

C9.Z9 / 10 OAV 6Z

 89 8 00 00 961 "91 I9g • 6Z SZ8 '81 S8 V SIH ο 9SS woiv L 'Π 00 • I 99 ^ '61 688 OS 229' 1 88 V SIH zm s WOIV 6 'U 00 • U gg '81 01IS Wi U 28 V SIH C89 WOIV

00 I ZSS 'L \ 9SSOS 100 "SZ S8 V SIH ZSS Hall V

99 ΊΙ 00 ■ I 900 '61 291 OSS8 V SIH 189 Thigh V

2L * 9ΐ 00 • I

88 V SIH 93 029 Thigh V

99 'it 00 Ί 6 9 '91 9 ΐε62 206 88 V SIH 629 Thigh V

Π 'hi 00 • I \ '91 UO • 08 IZ9.6I 88 V SIH vo 8Z9 Thigh V

Lf '92 00 'ϊ m Ί \ '08 U · 8Ι 88 V SIH N ll ^ Thigh V l \ '92 00 • I 989' LI glO "6I 28 V 1VA o 929 Easy V f9 · 9Ζ 00 • ΐ • is 1% V 1VA 0 WOIV

00 • I 190 '02 661 -91 28 V 1VA S WOXV l \ "02 00 • I ZA6 'LI • OS nrsi 28 V 7VA 929 Thigh V ss -is 00 • t 918" 81' IS 0S0'9i z V ΊΥΛ ao ZZ9 Thigh V

02, 'LI 00 • \ 991 '61 mIS 6ffLl V V A vo IZS Thigh V

A9 "82 00 • \ 981 ΌΖ mii Z \\ 8Ι 28 V 1VA N 0Z9 Thigh V '62 00 ■ \ 89 sig-oe 968 '8ΐ 18 V V1V 0 61S Thigh V

28 · 8Ζ 00 ■ \ 808 ΊΖ m • 18 m- \ 18 V V1V 81S Thigh V

^ '6 00 ■ \ ZOO' 1 696 -m 18 V V1V ao Z19 Plate V

88 '92 00 • ΐ 522 ΊΖ mi 08Z.6I 18 V V1V vo 9Ϊ9 W01V

15 ίΖ 00 • I 5S9 '66Z' 6 0-6t 18 V ΥΊΥ 913 KOIV

00 • I 081 'U SA9-8I 08 V ΠΊ30 HS WOIV

09 * 62 00 Ί OS 'U • ss ΙΙΓ8Ι 08 V ΊΟ3 8IS Parent V οε 00 • i 898 * 82 • cs O' I 08 V [ΙΊΟ ZI9 Hidden V

68 '00 • ΐ Ring · 8Ζ ■ n 99Γ9Ϊ 08 v mo \ Π9 WOIV

00 • ΐ9H • ss 20 '5l 08 V ί1Ί3 019 WOXV

C9.Z9 / 10 OAV 08

 Π 'S 00 Ί 089 • 9 UfOZ 98 v mo 0 I9S plate V

\ fn 00 ■ ΐ 06, · Α 98 v mo 3 099 Thigh V

9 ^ Ί9 00 • ΐ 89S • 9 98 v mo zm 6SS Cheom

Ζ9'89 00 ■ I 9C8'9 m ^ i 98 V ΠΊ3 iao §S9 WOXV 9 900, ΐ • 9 ml 98 v mo (19S thigh V

00 'ΐ m-ii 98 v mo 3D 9S9 art

61 9 00 • ΐ 9ΖΓ8 629 * 92 98 v m ao 993 Hidden V ΖΉ 00 88 831 Ζ 98 v mo VD tS Thigh V

00 '9S 00 • ΐ 99'6 896 -9Z-\ z 98 v im N S9S Fragile V

00 • ί 02Γ6 190 '61 S8 V 7VA 0 2SS Marauder V

89 -te 00 Ί '6 991 * 9Z IS6-61 98 V ΊΥΛ 3 IQ9 thigh V SS 00 Ί 899' S2 ΠΓδΐ 98 V ΊΥΛ OSS bile V

ST9S 00 • 899'Ζΐ 69ftZ 38 V IVA 6 ^ 9 Thigh V

80 'AS 00' ΐ 0S9n m-n 680 '6ΐ 98 V ΊΥΛ ao 8 9

00 • ΐ82S • u 638 -9Z Ζ89'6ΐ S8 V IVA V3 S Thigh V

96ζε 00 • ΐ • n 866 '92 99Γ81 98 V IVA N drive V

00 Ί 9ΖΙ Q% Q'LZ 929 ΌΖ 8 v mo 0 plate V

Ι6'ΐ2 00 • ί U Ι U0'8Z HfQl n v ίπΰ 3 images ιι00 • I L • 6 91609 Ϊ n v mo zao Thigh V

00 • ΐ Ζ • oi m- \ z ΐθ 'SI n V ΠΊ3 iao i Ran

A9'99 00 'ΐ m • 01 WIS ZS9 9ΐn v im ao \ n

0Z'6 00 • I m \ S-IS 80 Ϊ n V ΠΊ3 os Thigh V

L ov 11 UJ o D 丄 V

96 * 02 00 • ΐ -n 829 · 8ΐ n v mo vo 8S9 Thigh V

16 '62 00 996SI t9T6T n v rm N AS thigh V

99 'OS 00 Ί zn • 91 89 611 V SIH 0 9SS Dish V

C9.Z9 / 10 OAV 18

 88 * ^ 00 Ί Ζ006 06971 909 1 06 V SAT 3D 8S Hidden V

ASOC 00 • ΐ 90Ζ-8 08Ϊ 'SI 9S9-8I 06 V SAT ao 989 Thigh V

S6- S 00 Ί δ6.8 Α6-6Ϊ 06 V SAT vo 98S 舰 V

2Z 'AS 00 • ΐ 162-8 Π -Π 06 V SAT N ^ 83 Thigh V

Z6-9S 00, ΐ 98 -0I Ζ ^ ίΊΖ 68 V an 0 889 隐 V

00 • ϊ 8tl · 6 8Ζ0- Ϊ 669'ΐΖ 68 V HI I 3 thigh V

LZ ^ f 00, 1 Ζ80 · 6 00Γ8Ϊ 68 V an ιαο 189 Thigh V

00 • ΐ U0 * 8 ζ-ιι 68 V an 193 089 Dish V t6-8S 00 Ί 188 68 V an 6Z9 隐 V

U'9S 00I8 90ΐ '9ΐ 808-82 68 V an ao 8 Thigh V

Of 92 00 • ΐ m ^ i Ζ Ζ 68 V an vo S 舰 V

ZO-92 00 ■ ΐ 286 '8 68 V HI I N 9 舰 V

00 • ΐ 8Ζ6'9 · 8ΐ η \ · \ ζ 88 V 1VA 0 SAO Thigh V

Lf ^ 00 • ΐ 8 8 · 8 66 · 0Ζ 88 V 1VA 3 Thigh V

86'I 00 Ί 0806 nfoz 88 V ΊΥΛ Z W0XV

00 86Ζ6 696 Άΐ nz '\ 88 V 1VA 133 Thigh V

00 • ΐ 99S-8 80Ζ'6ΐ 88 V 1VA 93 U9 隐 V

00 • I \ ιι- S '61 88 V ΊΥΛ VO OAS 瞧

96 -2S 00 • ΐ 88 V ΊΥΛ N 693 Thigh V

00 399 '6 1% V ΊΥΛ 0 893 Thigh V

9 SS 00 • ι 89f 8 1 V 1VA 3 A99 Thigh V

00 • ΐ 6Ϊ9-9 ZQfZZ Z8 V 1VA Z3D 993 W0IV

• τ f] 7C ,, | 7 V 1VA 193

 18 -SS 00 • ΐ 698 ΊΖ L V 1VA 93 Thigh V oi · ζε 00 • ι n \ -ii 1% V ΊΥΛ VO 899 Thigh V

00 'ΐ 066' i A61 '11 1 V 1VA N 舰 V

C9.Z9 / 10 OAV 89 00 ΐ mL 099 g 999 S6 vm 93 819 Thigh V

• ot 00 ΐ Uff 6 9 96ΐ S6 v m V3 2Ϊ9 隐 V n • It 00 · I 691 Z86 s ISS'OZ 26 v m N Π9 Thigh V

00 ΐ 9f 9 6 ^ 9 26 V NSV 0 019 Thigh V

L, 00 1 991 '9 m9 906 6ΐ Z6 V NSV 3 609 ίϊΟΙΥn • 99 00 1 0 \ fl9 oo Z6 V NSV 809 Thigh V

98 • ii 00 I 989 * 9 90ΐ8 199 "SZ Z6 V NSV mo A09 Thigh V

• 8S 00 Π Π mL 96Z • 11 Z6 V NSV 93 909 thigh VS 00 ΐ 669, 9 0 • 8 ■ \ ι 26 V NSV ao 909 thigh V n -Zf 00 I LH ^ OSt8 1% V NSV V3 09 隐 V

L '00 • ι 2QVL 89 · 8 Ml • \ i V NSV N 909 Thigh V

88 00 I 688 -8 m '6 m • 61 16 V SIH 0 Z09 O V 6 00 1 ίί \ "8 m • 6 969" 0Z 16 V SIH 3 Ϊ09 Thigh V

6Z • 9S 00 • i 99B • 9 16 V SIH zm 009 Thigh V

19 00 · 6 196 • B • u 16 V SIH 669 Comfort V

63 • 82 00 eu • 9 m 'U 16 V SIH ■ 869 hidden V

0000 Ί 9 ^ 8-01iL \ l 16 V SIH Thigh V

29 • 0 00 • I 069 'L 8ZS' 16 V SIH 33 969 隐 V

• Ot 00 'I O f Οΐ 89 -8 i09 • \ i 16 V SIH 93 969 舰 V

SS'8S 00 • t 06Γ6 ffL • 6 ■ \ z 16 V SIH V3 Comfort V

16 • n 00 929 '6 000 • n m • oz, 16 V SIH N 869 Comfort V

11 00 • Π ■ \ i 06 V SAT 0 Z69 Thigh V l nn • T

 I q 1

 j q 3 · ο o \ n • Π flL • oz UD V SAT u T RQ πυ V

9, • S 00 'ΐ 9 • 01 m "91 06 V Ski m 069 隐 V

88 00 • I 96Z • 01 80S • 91 06 V SAT ao 689 Thigh V

00 ■ \ ZLQ-682 ■ • 91 06 V SAT ao 883 PJOXV 麵 odf / ェ :) d C9.Z9 / 10 ΟΛ \ S8

 00 • iπ SCI-99Γ6 96 V SA1 3 Z 9 pan V

68 • 09 00 ■ ΐ IC'9 96 V SA1 ao Thigh V

00 • St 00 • I 60ΐ · Π 88Γ0ΐ 96 V SA1 V3 I 9 Thigh V

8 '9 00 t 68Γ0Ϊ 666 Olf ΐΐ 96 V sn N 0t9 I¾0XV

16 '8 00' ΐ i 068 'Ζΐ 96 V MI 0 689 WOIV

I 00 '' ΐ is Ό1 ΖΖ 'Ζ \ 36 V dish D 889 W01V

6A '98 00 'ΐ 085'8 90S '21 S6 v mi 293 A89 Dish V

SI • 800 • I 108 '8 l \' l 96 v mi 190 989 Thigh V

00 • 9 00 ■ ι 069 'I 96 v mi go 9S9

Zf 00 • ΐ S6 · 6 mi 9 'SI S6 v dish vo ^ 89 dish V

19 'S 00 • ΐ S6 v Fox N SS9 Face

Π '9 00 • ΐ 8ST8 066 * 5 86 Ζ'9ΐ Π v edition 0 Z29 thigh V

00 • ΐ 98Γ6 68f 9 699'9ΐ V HHi 3 189 Dish V

0L • 8S 00 • ί 60S'Zt 0 ^ 6 808-21 Π V ZD 089 丽

Z9 • 98 00 • ί • π ΐ86 ·? Ϊ́ Π V ΖΏ 6Z9 W0XV 6 '11 00 • ί III 'SI-Π V 3Hdiao 8Z9 W0XV

• OS 00 • ΐ 189 "01 62Γ8 Π v aHd ζαο AZ9

U • ii 00 'ΐ' zi 911 'L so-called' SI η V HHd ιαο 9Z9 Plate V

99 00 Ί 6ΪΓΠ η v i 93 9Z9 face

91 ■ i 00 • I 009 Ot -L 0 "· 9ΐ 6 v mi Dish V

66-\ 00 • ί 8 '6 020-9 6 ^ 6' 9ΐ 6 v aHi vo 829 W0IV

21 '00 Ί 90'9 0 ΐ 0.8 · ^ 6 V HHi N ZZ9

 n n c 'o

 A '00 L οο τ ο τ bb v m 0 L69

 86 'Οί ^ 00 • ι 0λ8S6 D 0Z9

^ 6 '6S 00 • I' L 6'ΐ 08ΓΖΖ S6 v m αα 919

08-ι 00 ΖΖ ΖΖ6 · 962 -e ζη · \ ζ 86 V 3W 3D 19 dishes V ii ^ cio / iodf / xad C9.Z9 / T0 OAV 8

 66 * εε 00 'Α Α60 \ 98 Ί S99' 3ΐ 001 V dSV N 9

 68 OS 00 Ί 966 '9 ΐ 000' f 639 'SI 66 V ΗΑΙ o 9 9 KOXV

09 'ζε 00 • I 866 * tt 0S9' S 190 "91 66 V MX3 9Z9 e V

9Α "ZS 00 • I 6A '9ΐ S8Z" 8 S9Z§66 V HOHO woxv

U '9S 00 • \ S6Z' 9ΐ W 9886 66 V ¾1Ι ZD Thigh V

16 2 00, 1 OSS Ί \ nz Ί 669 ΌΙ 66 V ΗΑΙ

 81 'S 00I3C2 Ί \ m * 9 6UΠΠ 66 V MX zao U9 Dish V 1 Ή 00 "l U \" 91 9SZ "9 86' 6 66 V MX iao 0Z9 WOIV

8 Ή 00 • I no -si U 'S 200' Π 66 V MX iao 699 Thigh V

00 "t 8i0 '9ΐ Z19' S 016 'Π 66 V l 899 Hidden V

98 'Ζξ 00 • ΐ' si 'f 920' U 66 V ΗλΧ ao i99 Hidden V

Ζ \ * 88 00II \ S80 309 'Π 66 V MX va 999 Hidden V

89 Ή 00 • I · η 0C6 'I 898' ΖΙ 66 V MI N S99 Thigh V

L '98 00I S08'91 96f ΐ 0ΐ0 "8ί 86 v mi 0 腿 Thigh V

99 00 • I 9 9 'ΖΙ 86 v plate 0 S99 thigh V

Of 'Ot 00 • \ S99' ΖΙ 02S 'I-one fZl 86 v mi 299 Thigh V

09 '0, 00Im Ί \ 998 0 820' ^ ΐ 86 v plate 130 199 W0IV

80 If 00I 'SI m0-890' 8Ι 86 v dish ao 099 thigh V

11 -92 00 • \ · ο ^ 96'ΐΐ 86 v mi VO 699 KOIV

SO 'AS 00I 861 Ί S81 ΐΙ 86 V HHl N 8S9 Image S 00 9SS `` SI nfo Α6 v ma 0 Z99 l' Z 00 II m

S "6 00 • ΐ OO * Οΐ UL Ό 996 '8 Ζ6 V ΠΊ3 93 199 Thigh V 8S 00 • ΐ Ζ 1 60Γ6 L6 v fra VO 099 舰 V

U'l 00 Ί ZQ-U 166 i-6 v αΐΰ N 6 9 W0XV

W9 00 'ΐ 961 SS'6 96 V SAl 0 m Thigh V

C9.Z9 / 10 OAV 98

 19 "62 00 • I 6Ζ8 · 9ΐ 68Ζ" 8 Ο ΐ "61 zoi V dSV o oz Thigh V

86'6Z 00 • I 999 "9ΐ 09 · 8 Γ6Γ81 ΖΟΐ V JSV 舰 V

OZ 'Π 00 • ΐ · ί \ Ϊ6Ζ · 8 SSO'SI ΖΟΐ V dSV zao 101 Thigh V

11 -8f 00I I Ζ99 '3ί 909' 6 609 '9Ι 201 V JSV iao 00 VV

99 Ή 00Im '9ΐ ZQl V dSV 33 669 D

68 Ή 00 • ΐ Ζ9ΐ '9ΐ 162' ί 9A9ΐ ZQ \ V dSV 93 869 ROXV

88 "62 00 • I • 91 299 Ί 2 8 Ί \ ZOI V dSV V3 69 Dish V

98 '6Ζ 00 • ΐ m-fi ΐ6 9 699' 8ΐ ZQl V JSV N 969 woxv

60 "CS 00 • ΐ 0S ΊΙ 966 · 8ΐ ΐθΐ v mi 0 969 Fragile V

00 • ΐ 6 9 "81 IU · 9 刚 · 6Ι ΐθΐ v mi 3 views V

90 "LS 00 'ΐ S8" 01 9Ζ8 "ΐ m'u Ϊ0Ι V HHd zo S69 dish V ^ z 00 • I 88Π ι \\ · \ ι ΐθΐ v edition zao Z69 WOIV

00 "ΐ QLZ \ ZLfZ ιη -η ΐθΐ V Tria iaa 169 Thigh V

IL'U 00 • ΐ L • II 66S '988 "0Ζ ΐθΐ V ΆΜ mo 069 UV

00 • I 8ΐ9 ΐ 289 "8 m'zz ΐθΐ V 689

 98 '92 00 • ΐ 69S • Π 095 '9 910 * 12 ίθΐ V HHd 93 889 WOIV

U "62 00 • I 8S6 'Π 08 Ml · 0Ζ ΙΟΐ V 93 Z89 OXV

88 * Z8 00 m • ei 986 ^ 8 '61 ΐΟΙ V HHi V3 989 views V

00 • ΐ 106 '8ΐ 0ΐ8'8 Z90'61 ΙΟΐ V leakage N 989 WOIV

0S'9S 00 Ί ί \ ί 66Z 'm'Li ΟΟΐ V dSV 0 89 丽

Z6 * S8 00 Ί 023 ■ η 99S "9 l8" Zt 001 V dSV 3 S89 WOXV

6 ^ 2 00 ■ \ 6 ^ 0 'SI · 0-980 * 61 001 V dSV zao Z89 WOIV

96 '00 Ί m n ΠΖ "0 IZl" 61 ΟΟΐ V JSV mo 189 MOXV

99'3δ 00 m • 81W0I8 001 V dSV 089 Dish V

00 • I 968 'δΐ ΟΖΙ' ΐ 0Ζ 001 001 V JSV go 6 9 WOIV o ss 00 • ΐ 991 9 · ΟΟΐ V JSV V3 8Z9 Plate V

C9.Z9 / 10 OAV 98

 99 ΊΙ 00 '' ΐ ξ, ΖΖ '81 9ΖΙ6ΐ '6ΐ 90ΐ v nai zao Fragile V

6g "ΟΖ 00 '■ \ ίί' 9ΐ 6SL · 0Ζ 998 '8ΐ 901 v am m KOIV

11 "81 00 '■ \ g66 '61 068 '61 90t v nai III WOIV 0' 9ΐ 00 '■ \ 99' CI 0Z6" 02 901 v ao marauder V 6 Ή 00 '■ \ 066' Ζ \ Z ΌΖ fZ \ '11 901 v nai V3 woxv

Π ΊΙ 00 '■ \' δΐ 820 "61 i99 'l 901 v Thigh N UL Dish V

* 6Ζ 00 ■ \ Ζ09 'Π 806' LI gg 'll 901 V ΊΥΛ 0 V

2,9 'ίΖ 00 · \ 62Ζ' ΖΙ S6 Ί \ 89Z 'll 901 V 1VA D m Thigh V

If 'ΙΖ 00 • I 2 6 "2ΐ fZ '91 Z" 92 901 V 1VA Z O \ u

80 '98 00 Ί '81 'l 9AS' 9Z SOI V 1VA I9D 0ZL Fragile V

'8S 00' ΐ 091 '8ΐ 9S' 9T 99Z Ή 901 V 1VA ao 6U W0IV8Ζ 00 969 969 '91 QLZ 'U 901 V 1VA VD 8 Comfort V

00 \\ 9Α6 'Zl 669 '91 q \' l 901 v N L \ L 丽 V

Of ΊΖ 00 • I ZOO * 9ΐ 刚 \ m ΊΖ n \ V V1V 0 9U ΙΪ0 ェ V

OA '9Ζ 00 ■ \ 96' 9ΐ 刚 'fl CS9 "Ig m V V7V D 9U Thigh V

98 'S2 00 • ΐ 190 "2ΐ S 11 m V V1V ao 腿 Thigh V os' γι 00 • I 60Ζ 'S1 888' SI ^ ZL ΌΖ n \ v vo III Comfort V

00 'ΐ 9ir l 8Si' l \ 139 ΌΖ ni V V1V N III Plate V

98 * S2 00 • ΐ 83 'Ζ \ 09ΐ ΊΙ 863 '02 SOI v an 0 UL thigh V '92 00 Ί iu * ει L f \ l 29 ΌΖ 801 v an D OIL thigh V

6 'l 00 • I 160 "91 860 ΌΙ 210 Ή 20Ϊ v en mo 60A Thigh V

91 · ΐΖ 00 • ΐ 628 * 01 wu soi v an m 80i V

18 00 'ΐ £ 26' 8 U0 'll coi v an m WOIV

1Λπ 00 • ΐ 6S8'6 SOT v aii eo 90i V

06'9Ζ 00 • ΐ 986 9 S'OI m "02 SOI v an V3 SOi, hidden V

98 '82 00 • ΐ 089 'tl 8 S'6 92Γ6Ϊ eoi V 3ΊΙ N V

£ 9 9 / ΐ0 OAV L

 00 'Ί in ΌΙ 9ΑΙ 601 V SAl 0 69A Recommended V

Ϊ9'6Ζ 00 '' ΐ 'π 601 v sn 3 Fragile V ί' ΙΖ 00 ■ i S 'OS m' i 601 V SAl 93 Thigh V

08'8Ζ 00 'Ί ■ οι 601 V SAl VO Plate V

20 "82 00 • I 199 'Π 60f * 82 m'u 601 V SA7 N V

18 '82 00 I III • π ^ lfLZ m ^ z 801 V Thigh 0 dishes V

ΙΖ'ίΖ 00 • i οεο ■ ι \ ssi -u 801 v nai 3 dishes V

Zl'QZ 00 • I 198 • 91 89Z "92 989" S2 801 v nai plate V

00 'ΐ 96Z, 3ΐ 89Z'SZ 896ΊΖ 801 v nai view V

89 'SZ 00 Ί91 91 · 6 6 801 v 90 9U W0IV

6S 00 • I I 263 * 92 801 v Thigh Ώ 9U V

\ ι -η 00 • I 6 Ί \ own m 'Z 801 v thigh V3 m V

00 • I 589 Ί \ 190 662 ^ 2 801 V ΠΗΊ N W0XV

Μ'ΙΙ 00 • Ϊ in • π 998 · Z0I V 3W 0 ZfL Plate V

Ιΐ 'ίϊ 00 • I 09A • π ui'n ~ u A0I ν m 3 \ L Basket V

39 * 89 00 • I • 6 983 OS Α0Ϊ v m zm O i M0IV

96 '00' ΐ m Όΐ iOt v ΪΗ K0IV

89 '6 00 m' 6 6Ζ iOl V D¾V ZD 8S Dish V

00 • I 199 • 6 m 'Z A0I v, 3N L £ L Plate V

86 00 'I ΪΖ0ΌΙ -n 680 * Z ΖΟΐ v m ao 9SZ 丽 V

00 • ΐ 029 • 6 'u A01 v m

68.8S 00 'ΐ 9ΑΓ0Ϊ 0I V 3W Dish V p

 16 86 uu I 2,89 'ΐΐ 00δ 66 i01 V DW VJ

 6f9Z 00 'I εοδ • U Ι0Ϊ v N m Haze V

00 • ΐ Z96 'SI Ζ0 901 901 v nai 0 m thigh V "92 00 • I 096 \ ΙΗΊΖ -u 901 v thigh 3 0SA Dish V mio / iodf / i3d £ 9 £ Z9 / 1 O 9'9C 00 ΐ ΖΖΙ ΊΖ 920 ^ 2 en v mi 130 981 Thigh V

00 1 SOS • 28 επ v mi ao m Thigh V

S9'9Z 00 Ϊ m-zz Z60 018 "Z επ v mi V3 m Fragile V

Zl -9Z 00 Ϊ 'IS 6S6 "92 cn v thigh N woxv

00 ΐ 309 6 2 "0S 669 -8Z V HI I 0 m 隐 V

00 I 6 9'0Z 60S 'OS 88

81 'LI 00 ΐ πζ · οζ LU • 9Z zu v an ταο Thigh V

10 -sz 00 t 938-61 006 ^ 2 zu v an 133 m thigh V

8 Γ 92 00 ΐ 68 868 -3Z l \\ v an ill 舰 V

9A * 0S 00 I -QZ 98Su 0ΖΓ9Ζ l \\ V ΗΊΙ ao 舰 V

00 ί S A ■ 6Z zu vo thigh V 'Lz 00 ΐ 9 ^ 5 * 6Z 8 6'9Z zu v an N Thigh V

89 8 00 00Ζ 99 'IS 6S9 '92 III V ou 0 m Thigh V

Ll-LZ 00 1 • 08 890 in V ou 3 III WOIV

00I isrsi 080 2 960 '62 III V ou 33 ILL 隐 V

899 Ζ 00, ΐ 91 lOi, * 02 eoi6Ζ ΪΠ V ou 93 QLL 隐 V

89 '92 00 • ΐ ZLZ l 661 • OS ΠΙ V ou vo 69A Thigh V

9S'9Z 00 • ι SS6 • IS Πΐ V ou αα 89i Thigh V

9Z-LZ 00 • ΐ 08Γ91 926 • OS 860 2 Πΐ V OM N A9A Thigh V

00 9Z0 'OS on V wish 0 99Z V

IfLZ 00 mix 89 -οε on V thigh 3 S9Z thigh V

00 Ί 999 '28 156 'SZ on vi Z33 WOIV

 zros 00 Ί 80-l 86Zze on V dish ao zu WOIV 9.800ΐ 6SB "ie on V dish vo I9A W0IV

A9'62 00 • ί 029 • oe 96S on v mi N 09A Hidden V no / iodr / iDd £ 9LZ9 / 10 ΟΛ \ 68

 00 'Ί ■ ie C 9 · 9Ζ 9Π v im N Π8 images

00 '' ΐ • 6Z m ^ i sn v m 0 018 Thigh V

2fU 00 '69Ζ '62 89-08 060 2 SIl V 9HV 3 608 woxv

09 Ό9 00 '' ϊ '98 688 -SZ 911 v zm 808

AS '99 00 '' ί 9Ζ9 il sn v m ΪΗΝ L08

06Ί9 00 'ΐ 881' 6Ζ 60 • 2 sn v, ZD 908

9f 29 00 '' ΐ m · 8ζ m-n -n 9Π v m HN 908 Thigh V l \ 'S 00' 'ΐ 96 SS 9Π v αο, face 08

A8'TC 00 'ΊΖ 002ZS S8f 9Z v 00 S08 Thigh V

00 Ί SU Ί2 Z08'9Z sn v ao 208 舰 V

00 ■ \-% i Z8S • IS 911 v, vo 108 隐 V

98 -SZ 00 869'OS 866 9Π v m N 008

69 * 82 00 • ΐ W9Z zso • m v aHd 0 66 V

2VLZ 00 • I 88 210 • \ i til v mi 0 86i Hidden V

ΟΟ'ΪΖ 00 • I \ LfZZ 181 • 9Z -OS u V HHd ZD L <1

00 • ΐ Π \ 'Ζ • 9Z n \ V 3HJ ΖΏ 96i V

00 ■ I Πί 'ΖΙ "92 m-z n \ v aHd m S6Z hidden V

Z9'61 00 • ΐ in 'U -hi n \ v aHd Thigh V

00 '92 00 • ΐ \ n • ii · 6Ζ tn v mi ιαο K0IV

Ο9 ・ 0Ζ 00 'ΐ 990 9H'0S ΠΙ V HHi 3D Marauder V l 00 • ΐ 099 • 6Z V 3Hd 93 m Hidden

009 Ζ 00 • ΐ 866 • u Z08'8Z tn V thigh V3 06A thigh V

06 υ ηη • τ ι 71 Τ 'VI' os O 0C 1 -070 V ll V iHilQ

 00 • I 863 ^ 2 • 18 8 V dish 0 m hidden V

00 • ΐ OlfLZ sn v mi 0 m Marauder V

9T9C 00 80S S6c e Sit v dish zoo m thigh V t't'Cio / iodf / xad C9.19 / T0 OAV 06

 8 · 0Ζ 00 'l' 9Z AS9'S2 0Ζ6 · ^ 6Π V V1V 3 AC8 Hidden V

00 'Ί 101 "SC 6Π V V7V VD SS8 woxv f8'6I 00' 'ΐa 6Π V V1V N ^ 88 Dish V

00 'η ηι · ιι 269 2 8 · ΖΖ 8Π V 1VA 0 2S8 V

86 · 0Ζ 00 '' ΐ m-ιι 6889Ζ 0ΐ9'9Ζ 811 V 1VA 3 ZC8 Thigh V

00 '' ΐ 9 • u 0Ζ9 '82 8It V 1VA ZOO m Basket V

19 9Ζ 00 '' ΐ ΟΖΐ m-u 8Π V 1VA 133 088 Dish V

10 Ό8 00 'ΐ 319 Ή 6098Ζ8Π V 1VA ao Plate V

91 Ή 00 Ί -ii m ^ i 8Π V 1VA vo 8Z8 Thigh V

Α0'9Ζ 00 "ΐ t96'82 m-Li 096 8Π V 1VA N 舰 V

62 * 08 00 All • 62 LU V MSV 0 m Marauder V

Π · Ζ 00 • ΐ 199 • 62 098-82 ill V NSV 3 Marauder V

88 • 00 • ΐ 80S • εε 699 "6Z LU V NSV zm Thigh V

00 • ΐ H 'LI Ι 6 · ΐΖ LU V NSV ιαο Plate V

19 '02 00 • ΐ 918 • S ι · \ ι LU V NSV 33 m Thigh V

ZV Z 00 'ΐ 8 IOS'SZ LU V NSV 93 m 舰 V

8 '00I \ n 8 AA9' LI L \\ V NSV V3 0Z8 Dish V

^ Z-LZ 00I 989 'IS 90S' U LU V NSV N 618 V

08-82 00 • ΐ 089 • OS 88 02 ml 9Π V through 0 818 Thigh V

00 'ΐ m' IS 06Γ6Ζ 9Π.v im 3 l \% W0IV

00 • ι m • 9S S8g "08 08ΐ -S2 9Π v im 33 918 Dish V nn-τ ι • 2 u nsn" Q7 OTT πς CTQ

00 Ί m- 816 'OS 911 V through H8 舰 V

SO OS 00 • ΐ 980 • C8 6 · ιε 9Π V through 218 dishes V

00 Ί 086IS 3'οε ΠΓ9Ζ 9Π V through V3 m dish V £ TO / lOdf / X3d £ 9Ζ.Ζ9 / Ϊ0 OAV 16

 68 00 ■ \ 8SfSZ 99S 'SS ezi v nai 0 S98 V

69 "02 00 '• ΐ 099 -QZ 0' SI 8eo'og v thigh Z98 thigh V

60 'SS 00' ϊ x l8'I8 S21 v nai 198 Thigh V

39 · Ζ 00, ΐ m-Qz v nai 098 Dish V

66'Π 00 69f 12 v nm go 698 V 6.8ΐ 00 η ^ -ζζ v request V3 898 thigh V

90ΌΖ 00 6A9 'Ζ Z \ V ΠΗΊ N 8

Of 02 00 093m -Li 8ΐ8 92 u \ V SAO 9S 9S8 舰 V

386Ι 00 • ΐ 109.92 006'Sl 636 'Ζ8 u \ V SAO 90 9S8 PiOIV

8S 00 'ΐ 688' ft ZZl V SAO 0 S8 Dish V

ZS * 6l 00 • ΐ osrsi ZZl V SAD 3 8S8 Dish V

28'6ΐ 00 • I 888-91 696 "18 ZZl V SAO vo 2S8 Dish V

60 '02 00I 69 · 89 'OS ZZl V SAO N Ϊ98 Hidden V

00 • ΐ8ΐ m V V1V 0 098 Thigh V

00 • ΐ OIO'OS m V V1V 3 68 Thigh V

0Z 'Z 00 • ΐ' Lz u \ V V1V 93 m Dish V

96'8ΐ 00I 668 * 92 199 '8ΐ m V V1V VO V

Sf9l 00 • ΐ 809 'SZ 9Ζ9'6ΐ Z9f m V V1V N Dish V

00 9A6-9Z 880 999 -6Z oz \ V ou 0 Thigh V

S9-8I 00 026 '2 689 * 02 BZ0 "6Z QZ \ V ou 3 V

ΑΓ8ΐ 00 • I ml 061-Ζ 99ΑΌ8 OZl V ou 33 m hidden V

8Ζ'8Ϊ 00 • ΐ 068 -6Z oz \ V ou ao zn 隐 V 丄 'I on • τ ηζϊ WOTV

08'8ΐ 00 • I m-u OZl V OM ao 08 Awake V

00 • ΐ 92Γ2Ζ 9 6 · 8Ζ QZ \ V ou N 6S8 O V

00 • ΐ 9Ϊ6-9Ζ 6Π V V1V 0 8S8

C9.Z9 / 10 OAV Z6

 88 "St 00 Ϊ 26 8 ΐ 09f 0 Z80 'AS 921 ν m 688 Thigh V

26-09 00 • ΐ 906 • 91 · 0 III • ss 3Ζΐ ν m IHN 888 Thigh V

81 Ό9 00 ΐ 030 • 81 S98'0 8 SZl v m ZD WOIV

LfLf 00 ΐ 68 '81 099 'ΐ 681 v m 3N 988 Thigh V

08 00 I 908 • 81 nz'z 098 εε v ma. 988 thigh V

00 • ΐ 880 809 21 v m 33 88 WOIV

6 0S 00I on v m 90 888 PJOXV

61 -Π 00 • i 699 Ζ v VD Z88 舰 V

00 • ΐ 889 Ζ z ^ 960 • 98 v N 188 Thigh V

6nz 00 'ΐ SI8 ■ u 693'9 ν v ma 0 088 Plate V

90 9Ζ 00 • ΐ 969 • ii S98 * 9 • 98 Rinse v ma 3 m

69 * 99 00 • ΐ 989 '11 695 * 8 • Ot rinse v mo zm V

06'U 00 • I SI6 ■ \ i '01 196 • 69 v mo iao plate V

09-89 00 Ί S 0 '11 998 '68 ji v mo (D 9A8 thigh V

0 8t 00 • ΐ 895 ΊΖ 6 8 m • 8S amount v mo 33 9Z8 Thigh V

96 ε 00 • I UL 'Z90'8 8 V ΠΊ3 93 Thigh V

8f 9Z 00 • ΐ 'LZl * 8 • 9S v v mo VD m V

90'9Z 00 • ΐ ΊΙ 06 • 52 mi v ma N ZL

00 • ΐ • \ i 688 '6 m-n π \ v ou O U8 Fragile V

00 'ΐ 09ΐ · η' 6 m 'Ul V O D 0Z8 Thigh V

00 • I 99 '6 • is πι V 0¾d 698 Thigh V

00 • ί 899 '6 u \ V OM ao 898 MOIV

00-τ HOP

L end 66 ί, 7 Τ

 v U d VJ Lao

 Z8-6I 00 'ΐ 996 · 0ΐ 889IS HI V ou ao 998 I¾0IV

00 • ΐ m 910 V ou N 998 Thigh V

6C I 00 Ί Z9 '1 961' SI ZLfK v nai 0 98 隐 V

£ 9LZ9 / 10 ΟΛ \ S6

 0Γ6Ι 00 't 8ΐ9 -9Ζ 6 S' '9 0ΪΓ29 8ZI V V1V V3 9Ϊ6 pan V

69'6ΐ 00 '' ΐ 190 '' S Z \ V V1V N 16 KOXV

8S'1Z 00 '' I m'f LZl V 0 816 Thigh V

9Γ6ΐ 00 '' ΐ 860 Ζ 9 '098 "SS LZl V 3 ZU Thigh V

66 -S2 00 '0S6'6Z Z90 • 6 S69 "9S in V m Π6 Marauder V -LZ 00' 'ΐ S89'8Z ZS8'8" 92 III V 016 V

LO-LZ 00 Ί 989 * 028 LU V ΖΏ 606 Thigh V

00 'ΐ 188 • 9 860 * 88 LZl V \ m 806 plate V

96 Ί 800 Ί S6SS60f 82 LZl V A06 V

99'8Z 00 Ί m-LZ m-L 988 "BS LZl V eao 906 Thigh V

19 'OS 00 9986Ζ' L LZl V ΖΏ 906 Thigh V

86 00 · \ 805 · 8Ζ 850 • L LZl V 06 Easy V

9Γ08 00 • ΐ 080 · 8Ζ, 86 ■ S LU V 93 S06 Thigh V

88 • 00 • I 21Γ9Ζ * 9 889 9 ll \ V in ao Thigh V ίζ Ζ 00 • ϊ 189 9 '' 89Γ92 ll \ V V3 106

99ΐΖΐΖ 00 • I 90A • 8 U8'9S LU V iU N 006 Hall V

00I8 9'9Z228228ΐ 1 ^ 9ZI V JSV 0 668 V

S9.0Z 00Im-n '08S * 92 V iSV 0 868 Thigh V

6 '89 00 • ΐ m • 0 U8 "88 n \ V dSV zao i68 Thigh V

06 Ot 00 Ί 69ΐ ΊΖ Z09 • 0 V d V iao 968 Thigh V

00 • ΐ O • 0 918 "AS V iSV 90 368 舰 V

U'U 00 'ΐ 898 · ΖΖ AS8 • ΐ 868 "AS V dSV 93 68 Akebono uu • τ 007 7 Q7 T TATHTV

6U 66 L 000 GO 002 'TDK 9o V dSV V J GOO

 00 9l • e 620 "92 V asv N Z68 Dish V

00 869 "SZ 088 • s 6i6" 2S v 0 168 Thigh V

00 \ U8'S ZI v m 0 068 Thigh V

C9.Z9 / 10 O 66 * 92 00 • I SS9OS m S νιετ v nai Ν 6 舰 V

00 'I oti ^ • 11 ISI v thigh Ο 0 6 plate V

99'9Z 00 ■ I 899'ΐε 6.S S08 ■ ZS iei v mi 36S6 dish V

91 'ίΖ 00 • ΐ 6ΐ8 * Ζδ A3 • 98 V MX 886 Bile V

86-12 00 ■ I 809 -g I • 98 m v mi Ο A86 thigh V

ZfU 00 'ΐ ει ^ 18 -f 961 9S mv mi 93 926 Thigh V

6800, ΐ o's 190 v thigh VO 9S6 thigh V

00 • I Ϊ6Γ08 nvn m v Dish 腿 Thigh V

00 • ί 61Π8 098 Ό 99S'98 ost v Has Ο S96 Marauder V

66 00 ■ ΐ 166 '88 021 v Ha 3 296 隐 V

06 · ΑΖ 00 • ι 698 Ό 86S '98 OSI v ¾as 00 186 隐 V

89 'ΐ 00' ΐ 6Ζ9'8Ζ SIS'O-9S9 • 98 οει v 93 096 V V π -u 00 • I 826 · 8Ζ 2L \ 0m l 081 v ¾a V3 6Z6 Thigh V

M'H 00 UL'Ll ΑΐΟ 9Z8sc 08 ΐ v ¾a 皿 Plate V

00 • ΐ 99ΐ · 8Ζ WO OZi, • IS mv rm 0 LZ6 Thigh V rsz 00 'ΐ' LZ 6.0 • ζε V 1113 3 9Z6 Thigh V 9'0t 00 • ΐ ^ fZZ 'o- A06 • IS V IS ) zm 9Z6 Thigh V

98 · 9 00 Ί Ι98ΐΖΐΖ 8Ζ0Ί III • OS m V ί1Ί3 iao 隐 V 8'6S 00 • ΐ 9 9'0 SZ0 • IS V ί1Ί3 αο ίϊΟΙΥ

00 • ΐ 6SS'l 901 • is m V ί1Ί3 m Plate V

00 6S6'tZ 88Zzs v rra Thigh V

Z8 "Z 00 Ί 'ni'i 9 0 ■ n m V ί1Ί3 νο V V nn • ΐ ZS9 -n m V ί1Ί3 iv fiTfi Noriyama TV

81'02 00 \\ S88'8 6S9IS V V1V 0 816 Thigh V

Ζ6 · 00 00 6 SS m V V1V 3 L Thigh V

00 • ΐ 8Ι9V V1V 93 916 隐 V

C9.Z9 / 10 OAV 36

n l 00 • I log-^ e m • 5 'os eci V ΝΊ3 DO Z96 V n • 61 00 • I 90 Γ98 106 -8Z V ΝΊ3 ao 996 plate V

60 • sz 00 • ΐ 9 S "9S m • 8 86Γ8Ζ 8δΐ V ΝΊ9 V3 396 V

99 • 22 00 • I 160 'I 180-62 V ΝΊ3 N m Dish V

98 • OS 00 • ΐ ΐ80'98 • 0 z V mi 0 696 Thigh V

QZ 'LZ 00 • ΐ ίη · κ m • I Z 1 v mi 3 Z dish V u • οε 00 • I 868-12 380 • ΐ-Z 1 v mi 196 NOXV

L • LZ 00 • I 96-ZS 69 • 0 ZSI v Wish 130 096 Thigh V

08S 00 • I \ Ζί 998 '0- 989 -oe V Ml 93 636 舰 V

89 'LI 00 Ί 61S "0 · 6Ζ V thigh VO 8S6 Dish V

01 • LI 00 Ί 983 'ΐ8 m • ΐ V wish N i96 plate V

00 • I 966 * 02 960 • I \ u-ii aiei v im 0 9S6 plate V n 'LZ 00 Ί 098 * 02 m • I aiei v flat 3 996 plate V

S6 • 91 00 0 9Ζ 'aisi v im ao 96 V

OS '08 00s 099 2 eisi v flat as S96 dish V

11 δ 00 -LZ m 'aiei v through 33 Z96 plate V

88-\ ι 00 088 • \ \ v flat 196 dishes V oe 00 99Γ6Ζ III 'I 9181 v im VO 096 dishes V zoLZ 00 m-Qz Z99

99 • u 00 • I 019 ^ VIST v thigh 0 8 6 thigh V

00 • i Ζ9Γ08 ll ^ VIS! V request 36 6 丽 V u • 61 00 • Ϊ 69, · 8 VI2I V nai zao 9H Dish V to • 61 nn • I Ζ9Γ8 VI81 v nm WOTV

60 • oc 00 'I ZS8 "VIS! V 33 Marauder V

St 00 Ί 999 -6C m • 9 826 OS VICI ν nai 93 W0IV

6ε • 9Z 00 Ί in VI81 v nm VO Z 6 dish V

C9.Z9 / 10 OAV si -sc 00 • I 6S8 "ge L 1 'SI v an Ώ 566 thigh V 81 00 • ΐ 992" 22 619 Ζ v an V3 ^ 66 V

Ϊ3-81 00 • ί 9 ι · εε 908 ΌΙ V 311 N 266 ν

9f 81 00 Ί 082 'S' 6

921 V Π3 0 Z66 Thigh V

Π'ίΙ 00 Ί 8896 V ΑΊ3 3 166 Hidden V

86-6Ϊ 00 909 '8 981 V ΑΊ3 VD 066 ΐϊοχν

98 '^ 00 · \ Qhvn T8S'Z 692 '22 921 V no N 686 V

00 896-^ e Πΐ 'L 581 V thigh 0 886 plate V 9 -U 00 • ί sio'se Ζ06 * 9 Ζ0ΖΉ SSI V plate 0 IS6 隐 V

98 -22 00 • ί 0.99SI V plate 986 Thigh V

61, 00 Ί 908 'AS UfL 981 V Dish 130 S86 Thigh V

38 -61 00I 991 'AS 38Γ9 981 V thigh ao 86 plate V

ΪΓ9Ζ 00 • I ZZ0 "9S 868 'S SSI V dish V3 286 Marauder V

88 00 Ί 169-98 686 ·, 6 9 Ή V request N 286 丽 V

99 * 9Z 00 • I 090-99 86f εζ V SA1 0 186 Dish V

00 • ΐ S99'98 8f9-S V sn 3 086 Dish V

66 'At 00 • ΐ wz- \ Ϊ06.Ζ S66'92 V sn ao 116 Thigh V

00 • ΐ 099 61S'9Z ^ ει V SAl 33 916 隐 V

00 • I TO'8 ^ δΐ V sn 33 916 舰 V

00 • ΐ \ 'Z 9I9'9Z n \ V SAl VD fl6 舰 V

06 00 • I ZO'L ?, 891 -C 9I6'9Z n \ V sn N S16 Dish V

SI 00 ΐ 089 Ζ 893 '92 221 V ΝΊ30 m Dish V

QT-^ Z on • τKen'QP (J PPT wnTV srz 00 • I 08Γ38 898SSI v o 0Z6 隐 V

2Γ6δ 00 • ΐ 0 '9S U6 "9 I60-IS 881 V ΝΊ3 130 696 V ΐΐ -9S 00 • ΐ 90f 9' IS 881 V ΝΊ3 ao 896 ΙΪΟΐν

C9.Z9 / 10 OAV A6

 00 '' ϊ ΙΟΖ '• 8Z OS' 1 m, Ζΐ V HHd 33 IZ01 plate V9Ζ 00 '' ΐ 868 ■ LI • \ i \ L \ • Π \ n v mi 93 0ZO1 舰 V

00 '' ΐ 2,98 '■ iz • 02 SI2' ΐΐ in V thigh V3 6101 Thigh V nil 00 '' ί m ■ 61 00 -ζι m V HHd N 8Ϊ0Ϊ WOXV

%-\ ι 00 'Ί 289' OS SI8 • 81 Z80 • si 0 I V ΑΊ3 0 Z10I Thigh V ίΖΊΖ 00 '' ΐ f9t ■ 6Z 0 Γ8Ϊ • ei o ^ t V ΑΊ3 3 9101 隐 V

6ΐ Άΐ 00 U8'8Z 0 8ΐ OH V ΑΊ9 VO 9101 Thigh V

I8'il 00 '' ΐ L68, 6Z 009 'ί \ m '91 O l V AID N Thigh V ί \ Ζ 00 • ΐ 829 · 8Ζ SAO • 91 W91 681 V H3S 0 ειοΐ Thigh V

90-6Ϊ 00 • I Ζ89 289 "91 '9ΐ 681 V 3 Awake V

89 * 9Ζ 00 6Ζ8 • 6Z 12S -L \ A80 '6ΐ 6SI V 30 not thigh V ί ^ Ζ 00 • ΐ 196 '08 A6' LI v Ha ao Οΐθΐ thigh V

ΪΓ6Ι 00 Ί m • 08 '91 m -LI 681 V V3 600Ϊ Thigh V

6 1 00 • ί m • SI ■ i \ 681 v ¾as N glue 腿 thigh V

Ζΐ '81 00 • ΐ 139 ■ n x% L • L \ 821 V IVA 0 A001 舰 V

69 · ϋ 00 • ΐ 89S ■ un · ΐm V IVA 3 9001 W0IV

Οί Ζ 00 • ί 6 ^-z 980 Ί \ l \ l '9ΐ 821 V IVA Z d SOOl Plate V

00 · 00 • ΐ m • 18 ^ Lf • Π 269 '9ΐ 821 V IVA 133 ^ OOI dish V

Η Ι 00 • ΐ • OS 8 Z • U ΖΪ9 -LI 821 V IVA ao SOOl Thigh V

Si '8ΐ 00 • ϊ 996 • OS 988 • ZI 1,9 • 81 881 V IVA V3 m \ thigh V-\ ι 00 • ΐ 921 ■ n 8 ^ • i \ 09 • 61 881 V IVA N ΐθθΐ 隐 V

89 'Z 00 • ΐ 886 • oe H Ί \ 892 • \ z L 1 V ΗΊΙ 0 0001 WOIV

0 y-τ L 76 υυ ι S90 • n 'Ζΐ m • OZ 1 OT y

 V α aαiτl J Τ iΛVΙΠUdΤν V

60 • 00 • ϊ LI • 92 m \ ML '1 v an 866 thigh V

00 • I ΐΟΟ 0S6 m • imv an 193 WOIV

99 • 00 • ΐ sorts 89S Ζ L l v an m 966 Thigh V

C9.Z9 / T0 OAV 86

 -LZ 00 • ΐ 006 · 6ZI 'LI U6 • s n v mi 130 V

00 • I • 91 SM n \ v thigh ao 9 OI brittle V

00 • ΐ 6Sf se • SI 8C9 • s n \ v Thigh V3 Thigh V

99'6Ζ 00 • ϊ 080 -ZS • 91 • s n \ v Plate N 腿 Thigh V

00 • ΐ Ζ0ΓΪ8 19 -fl zeo • i Π v 0 S OI dish V

00, 1 6S0-18 09SI 80Z '9 v m 3 z oi Thigh V

00 Ί 6 'SI oos • 0 n v m orchid I Ol 隐 V

00 • ΐ -um • 1 S9I • I Π v IHN otoi 舰 V

^ '8t 00 • ΐ inn 69S • \ S l v Ώ 6801 Thigh V

00 • I Z66.9Z, 86'ST OSZ • I Π v m 8901 plate V

LI 'I 00 661' LZ 86Z 11 A09 'ε S l v m Z801

91 00 • I -LZ 689 • SI 60 8 ^ 1 v, 9S01 Thigh V

6ΐ8Ζ 00 Ί 121 • 91 90A 2 l V 9W ao 9901 Thigh V

00 • ΐ 200 • 91 • S 2f \ V 3W V3 no \

S9 -11 00 • ΐ Ϊ08.8Ζ UO '91 996 • 9 e i v N 8S0T Thigh V

Ζί Ζ 00 • ΐ 0Π 'OS 989 -LI m V ΑΊ3 0 Ζ80Ϊ Hidden V

Ζ0 · 6Ζ 00 Ί 890-6Z S 0 ■ i \ Z88 'im V no 3 Ϊ80Ι Thigh V ι ^^ ιι 00 • ΐ 99 612 08ZL • 8'8 zn V ΑΊ3 V3 OSOI 舰 V

00 • 61S-82 910'81 666 • 6 Z l V 9 N 6 0 thigh V

00 • ΐ 9 '8Z L% 6ΐ 8.8 \ fl V 0 8Ζ0Ϊ Plate V

00 'ϊ 903-82 sss • 61 S06 • 6 I l V HHd 3 Ζ20Ϊ dish V

16'ΐΖ 00 * ΐ 092 ΊΖ U8SI in V HHd ZD 9Ζ0Ϊ Thigh V

• τ TC¾ -0.7 .ic ΊΖ 189 -z \ Qnu Q _J7nTran TV

01 -L 00 • ΐ 6 ^ • u m-n in v i UOl 隐 V

08 'IS 00 • ΐ 909 • II \ n V 3HJ zad Z01 Thigh V

01 '00 • ΐ f -ίζ 6 '11 V Thigh IQ3 ZZOI 隐 V

C9.Z9 / 10 OAV 66

 6ε -z 00 'Ζ Ζ90Ό8 S99' CI OSS '■ \-8tl V 3 LLQl Thigh V

00 'ΐ AO, U Ί- 8tl V SAT 90 ZL0 \ Thigh V

01-£ f 00 'Ί S 9 "62 ιιζ Ι • I- V SAl V3 UOl Plate V

00 '' ΐ 881 OS • II S01 · ο- V SAl N 0Ζ0Ϊ Awake V

00 '' ΐ QZZ 'Z 869 Ίΐ in V ΠΊ3 0 6901 Dish V

8ε '6S 00' 60 ^ 62 m 'Π 626'0 in v mo 3 8901 V

6Γ99 00 '' ΐ Z ^ -LZ9,0 in V 1113 zao Α90Ϊ V

U-Qf 00 '• 9 ZIO' I in V 1119 \ 9901 Thigh V

S6 '^ 00' 'ΐ m-% z 098 • 9 06 • I in v ma ao S90I Thigh V

6A'6S 00 '' ΐ lSg-8 989I in v HOI thigh V

00 'ΐ ΐθΓοε 900 • 6 998 • ΐ in V ί1Ί3 S901 Thigh V

90-98 00 • ΐ 086 · 6Ζ IS · 0ΐ 891 'I V ΠΊ3 vo 2901 Dish V

00 'ΐ 66 Ϊ9 9Ϊ6-0Ϊ 189% in V ί1Ί3 N Ϊ901 PiOXV

09 * 92 00I9 OS 091 'SI' I V SIH O 0901 PJOXV

00, ΐ 9ZS ξ 691 • ζι Z98 • I V SIH 0 6901 Plate V

00 • ΐ 986 ZA6'0-l V SIH im 890Ϊ 舰 V

00 • ΐ -n ^ fn m • o- V SIH Z901 Thigh V

60 '00 Ί -n 812 -fl • 0 s i V SIH ■ 9S0I plate V

60 '00 • ΐ ss 098' Zl n \ ο- V SIH 9S01 Hidden V

U'9 00 • ΐ 686 -SS ΖΠ • 21 Ί ^ 1 V SIH 33 隠 Hidden V

00 Ί OO 'S • Ζΐ' I V SIH 93 8901 Dragon V

01 2 00 • ι 586 S 'Ζΐ • V SIH V3 z Plate V U 0' τ

uu 7 o0UfiO '7600 90A8ΐ oso j 1V SIH TQOT MOTV s os 00 Z ^ f SI101 • si V MX 0 OSOl Thigh V iris 00 Ί 908 -SS ll \ 0l Marauder V fl '8S 00 mn 629' ΐ m • 9 m V thigh 293 mi thigh V no / iodr / iDd £ 9LZ9 / 10 ΟΛ \ ΟΟΐ

 8Γ9Ζ 00 '' ΐ 8sne 869 S9I V dish N 60Π thigh V

Ζ9.8 · 00 '' ΐ '0 6'i Z91 v ¾as 0 80Π thigh V

98'8Ζ 00 '' ΐ m '' 1 on Ζ5Ϊ 0 LOII KOIV

69'82 00 '' ΐ 990 • \ z Z91 V HH 90 90Π Plate V

00 '' ΐ 081 Ί2 ZSI v ¾as eo son

8f 02 00 '' ΐ ΟΐΖ ■ \ z Ζ9Ϊ v ¾as vo ton WOIV os-εε 00 '' ΐ i9f oe 80 Z99 * 9 ZSl V HHS N son Thigh V

00 'Ί 098 Ό8 Πΐ • \ z Ϊ3Ι V ΝΊ3 O Ζ0Π Thigh V

Of 9S 00 '• ΐ 99ΐ Ό8 Ζΐ3 69S'S V ΜΊ3 3 ion H0IV η'ζ ^ 00, ΐ 890 Ή 036 • 61 191 V ΝΊ9 zm 0011 Thigh V

Z 8t 00 '' ΐ 96A61 H9 '191 V ΝΊ3 130 6601 Thigh V

Ζ9 · 00 'Ί O * 6l 08S "9 IS! V Ί3 ao 8601 V

00, ΐ L0f9Z 9Z961 ZSf 9 191 V ΝΊ9 A60I 隐 V

9 ^ Ό2 00 Ί 'iz mOZ ISI V ΝΊ3 ao 960Ϊ Plate V

98'92 00 Ί 2ΐ6Ζ8ΐ6ΐm V ΝΊ3 vo 960Ϊ KOXV

98 00 • ΐ 988 · 8Ζ 969 "61 191 V ΝΊ3 N Π0 \

90 '82 00 Ί Z '81 98f 8 091 V 3W 0 2601 pan V

00 • ΐ 989 '6Ζ 928 '81 606 * 2 091 V 0 Ζ60ΐ thigh V 9ε 00 ΐ m-QZ ΐ • 02 9 0 OSI v ao 9801 plate V

92 * 82 00 • ΐ 16 '6Ζ8ΐ S6S'T 031 V V3 Pan V

00 • ΐ \\ l i68'0 OSI v m N S80I W0IV

00 • ϊ89 · 8Ζ on • 91 S6S · 0 m V 0 zm Thigh V

92 * 62 00 • τ ι]

 LL 06 199 • 91 l D V U V Λ liJ τοητ

 00 S06-0S 983 • 91 880 "0- V Π3 vo 0801 KOXV

00 Ί 9θ ^ · οε Ι6Ϊ '0— 6tl V Π3 N 6Α0Ϊ 舰 V

90 · 00 • ΐ Α9Γ02 • 'z-8W V sn 0 8 0Ϊ Thigh V

C9.Z9 / 10 OAV ΙΟΐ

QZ 'OZ 00 "ΐ A6Z'S8 966" 6ΐ 8S6 "2I 93 ΐ V SA1 9δΐΐ WOXV

ΟΟ'Ϊ t -n τοδ'ΐζ s 'ν ν nai ο ππ κοιν ΐΓ8ΐ 668 668' εε εοδΊζ rw 991 ν nai ο εεπ woxv ΐ6'Ζΐ 00Ί 9Ζ0'Ϊ2 Πΰ Ζ 61f Αΐ SSI V ΠΞΊ 200 ZSU NOIV

69 'SI 001 982 OS 590 "9ΐ 59 ΐ V 1131 103 Ϊ2ΙΙ PiOIV

96 "9Ι ΟΟ'ΐ 68f 18 〖0Γ IS" 9ΐ 99 ΐ V 1131 33 OSU V

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16-6Ϊ ΟΟ ^ i V 88Γδ2 816'ΖΙ 991 V ΠΗΊ Ν ΖΖΠ WOIV

Ζ0 * 9Ζ 00 "ΐ 9Z6" ZS 6S8 "1Z SOZ'U 51 V 0 9ΖΠ KOIV OO'I AZO'SS 966 2 WW SI V 3W 3 9ΖΠ ROXV

U "9S 00 * 1 0'8S SB! * 6Z 906" 6 t9l V 3W ZHN ZH WOIV

90 OO'I Ll "8S 900" 8Z i88 * U Sl V ΪΗΜ S2U PiOXV

69OO'I 9il '82 969 "01 i V ZD ΖΖΠ WOXV Γ ΟΟ'ΐ 9Z9-9S ΑΟ ^ ΆΖ 88Γ0Ϊ Sl V 9W ΗΝ ΪΖΠ KOXV

3800 996 '38 68Ζ '9Ζ tS6'0T 91 V OW (D 0ΖΠ KOIV

91 2 00'ΐ Z ^ Z'SS 8 T9Z 866 '6 tSI V 3W 33 6ΙΠ WOIV

60-98 00 Ί 9H'gS 9S6 Ζ69ΌΪ SI V 3 V 93 8ΪΠ WOXV

89 oo'i 9 * ss εει ・ η s6rot t3i v vo zin woiv

89-ZZ 00 t80'S8 8ZZ "Z 0Zf6 I V 3HV N 91Π KOXV

00 Ί 999'ie 0Z6'92 〖28 66 Sl V ¾HX 0 9ΙΠ WOIV

TTSZ OO'I 880 'ZS ΐΖΐ6 29 ΐ V mi 3 fill KOXV

02-s oo'i ns S9i -u 9 9's ssi v mim sin XLV s * 32 oo'i AS 'ss ssrgz ou'9 85 Ϊ v mi 130 zni rouv

90- 81 00'ΐ O'ZS 660 '9Z i98' 9 CSI V HHX 93 ΠΠ WOXV tl'AZ OO'I IS 06 -U IOA 'SSI V ¾HI VO ΟΠΙNOIV 麵 Odf / ェ d C9.Z9 / 10 O / A 18 "SZ 00Ί S68" 9S ZSO'OI SS "6I 691 V ni3 VO Ϊ9ΙΙ I¾OIV

9A "9Z ΟΟ'ΐ 1S6 * 9S ΙΟΖ'Ιΐ 8 f 8ΐ 691 V illf) N 09Π WOXV

8f8Z 00 Uf i "U OZI '81 891 V nai O 69It K01V

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90 -ZS 00 'I 0T9' S ΐΑΙ'ΟΙ Α60 ^ ΐ 8 ΐ V l ΐαθ 9SII WOIV rAS 00 'ΐ 099 '92 9Α0ΊΙ' 891 V 1131 33 99Π WOXV

^ 8 '92 00 "ΐ A60" 98 ZIO'Zl C89 '91 831 V Π3Ί 93 i WOIV

6Z'9Z 00Ί 698 'SS U9' Ζΐ ZSA'9I 89ΐ V 1131 VO SSU NOIV

91 'LI 00Ί 66Γ98 SS6'SI l 6'9t 89ΐ V Π3Ί N Ζ9Π KOXV

90-92 00 'ΐ 639' 9S LLl ^ l SO 'SI 1,9 ΐ V I3W 0 ISlt WOIV

89 00 S9'SS 060 'SI 02f 91 Α Ϊ V I 3 09 ΪΙ WO

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69'SZ OO'I Z80 '8 690 "81 90S' SI 991 V SA1 3 PiOIV

82 '82 00'ΐ Zfg'9S 60 '91 9 ^ 6 991 V SA1 ZN l 〖M V 'SS OO'I 69f Αΐ 686' 6 9SI V SA1 30 ΟΗΐ WOXV

8 ^ '2 00 Ί Ul -92 0A ^' 8I SS8 0ί 99 ΐ V SA1 00 6SI 〖I¾0 ェ V

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98-12 00'ΐ m-Π AZ'8l 6Ζΐ 99ΐ V SAl 90 ΖδΠ WOIV

WU 00 88 '8 S80'6I 99 ΐ V Sll VO 9SU KOXV

£ 9Z.Z9 / 10 OAV SOI

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U'02 00 • i z-\ 'Ζ9Ϊ V MI S8II 舰 V

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60 * Z 00 Ί uz-n 9 0'8 191 V OM 3 Ϊ8Π Thigh V

U'ZZ 00 Ί 9ΐ ε 191 V 33 08Π Plate V

00 • I in 969 908 "61 191 V OU 93 6 thigh V

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69 "8Z 00 • I 189-98 191 V OU ao 蘭 Orchid

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69'9Ζ 00i i 906'S's 862-61 091 V 1VA 3 fill thigh V

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00 Ί S6Z'91 09ΐ V 1VA 13D ZLU W01V

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95 00 Ί 696 ^ 8 Η6.9 ZIS-8I 09ΐ V 1VA VO 0ΖΠ Cheom

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00 • ΐ 9.6 tS6-6I 631 v n¾ 93 Ζ9Π 隐 V

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10 '6S 00 • I 2,90 99S99f 9I V dSV iao 9021 Marauder V

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80-62 00 Ί 890 zs 996'S- m V d V 93 ΐ Marauder V

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00 • ΐ • 12 2S0 * 0 S9I V ΊΥΛ N S6II N0IV

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00-\ '9z ΙΖ-9- 990 "9ΐ 891 V SAO 3 LUX Thigh V

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96 * oe 00I 0'8Z ZfVQZ 991 V NSV N \ m K0XV

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06-Ϊ800 ・ I m-Lz 09'9- 126-61 591 v m 3 Drive V

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C9.Z9 / 10 OAV 90ί

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98 'Zf 00' Ί S811 W6'9-096 ΊΙ UI v N 89 ΖΪ V

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90 00 Ί Kasumi StO'6- Oil v nai VO \ Concealed V

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00 "ΐ WS'9I 68Γ9- 610 * 91 9Αΐ V 3ΊΙ Z33 06ΖΪ WOXV

06 '92 00 "ΐ 098 '9ΐ S6H_ 029' SI 9Αΐ V 3ΊΙ 93 68ΖΪ KOXV

6Γ82 00 Ί 6 '-819'81 9il V 3ΊΙ V3 8821 WOXV

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Π '00'ΐ 61S ^-ΟΙΟ'ΖΙ ΐ V 0 98ΖΪ WOXV

60 00 'ΐ 0ΙΓ6Ϊ 86-228'11 V 3Hd 0 98Zt WOXV

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Ζ6 00 • I 190 Ί8 Ζ69-0Ϊ 68ΐ V dSV 81,1 views V

00 • ΐ ζη-η Ζ6Γ01 68ΐ V d V Itl Thigh V

60 00 • ΐ m-n 68f8 Π \ ί 681 V JSV vo 91tl Thigh V

8 8 Ζ 00 Ί ihi- S9Z-8 ΓΟΐ 681 V JSV N 91tl

00 'ΐ m-π 69Γΐΐ 881 V 1113 0 nn Dish V

69 '82 00 zorss m'Ql 881 v mo 3 mi raxv

00 "ΐ 626 '68 ^ 6.0 · v mo Z30 thigh V

6Γ99 00ΐΐ 69S-8t 881 V 1113 130 m \ Dish V

SI 8 00 00 ΐ S19'6S Ϊ 0 Γ 6 ΐ 88 ΐ V ί 1 Ί 3 aa 0 I Thigh V oro 00 ΐ 86 Π 88 ΐ V ΠΊ 9 93 60 dishes V

00 Ί m-ii Ζ ΐΐ 88 ΐ V ί1 ί 3 93 80 ^ 1 Dish V

89'6Ζ 00 • ι 019'99 19ΐ8 881 v mo VO zoti 隐 V

89'ιε 00 Ί 100 'AS Ζ \' L 88ΐ V ί1Ί3 N 90 l

89'28 00 Ί 96ΐ '88 8 17-8 V ΝΊ3 0 i Dish V

89'SS 00 • ΐ 012 V Ί3 3 i Hidden V

21 00 'ΐ 6 6-92 683' 9 V ΝΊ3 ao 皿 Plate V

00 • I OSZ-88 9Ζ0'9 0 8 · V ΝΊ3 OO l Easy V

08 'Zg 00 · \ 899 "82 ^ Ο' 9 AST V ΝΊ3 u u wn TV S 00 ■ \ 9ΐΐ '82 εΐΐ9 V Ύ V3 8621 舰 V

00 \\ 6ΑΓ62 C9T8 V ΝΊ3 N L Thigh V

69 00 988 988 8 Sift 2ΖΓ6 981 V 0 9621 Dish V

C9.Z9 / 10 OAV en

 ΟΟ'ΐ-Z 80Γ 6Ζ6'0ΐ t61 V dSV ΐαθ IGtl WOIV

I9 "91 ΟΟ SCI 'U 908" l 909'Π 61 V dSV 33 OS l KOIV

06ΊΖ 00Ί 9Z8'9Z 092 ^ 1 6ΐ V dSV 93 6 I WOIV 6'AZ 00 389 * 9Z LU ^ l HZ'Zl n \ V dSV VO 8ftl WOIV

06-9Z oo'i m ^ z ow's 〖swoi v asv N z ti woiv

68'8z oo "i iz m ΆΙ Ζ9ΓΠ 26ΐ v no o i won

00 Ί 'U S8f9t 63 ^ Όΐ 86ΐ V 3 mi WOXV

0 ΖΖ 00 'I t2Z "Z Ζ ^ Ι Z96' 8 S6I V λΊ3 VO mi WOXV

0Γ9Ζ 00Ί 691 'U 961 "SI 16S" 8 26ΐ V ΑΊ9 N KOIV oo Ί 02t '92 06s-si m'i m v iD o zni wuv

II 'LI 00Ί 860 -S2 〖fl 19S 261 V ΝΊ3 3 1 ^ 1 WOIV

10 -9 00 Ί 929 t Z'SI Z98 "2 261 V ΝΊ3 03 88 l WOIV

Z8 "6S 00 Ί ϊ '^ 68'8I' S 261 V N1D 93 iS l PJOXV

0 "0S 00" l 9ΪΖ 1 8 9 "9 Z6I V ΝΊ3 H3 98 l K0IV

0Z-8Z 00 Ί -fZ ΖΠ'2 \ 600 "A Z61 V ΝΊ3 VO SSfl KOIV

83'8Z 00 S9'ZI Lil 'L Z61 V ΝΊ3 N S l WOIV

Wll 00 68 50f Π 89 "S ΐ6ΐ V SAO 3S SSf 〖M V

6 00 Ί 0 0'6Z 8 8 "H HS 'Ζ ΐ6ΐ V SAO 93 Ζ Π WOXV

Z9'8Z 00 'ΐ S9Z'9Z Z88 188' 6 161 V SAD O TS l WOIV

00Ί 9Z I 09 8 16Ϊ V SA3 3 OS l PJOXV

ΖΓ Ζ 00Ί 800 '82 9t9! T Ι6ΐ V SAO VO 6ΖΠ) JLV

Η Ζ 00 Ί "8Z 9'U Ui" 6 Ι6ΐ V S13 N 8Z l W0IV

66 '82 00 'ΐ ZSZ'6Z SA9' 6 2I9 "6 06ΐ V V1V 0 ΙΙΠ WOIV

S9'9Z 00Ί m '^ l m "OI 06ΐ V VIV 0 92tl WOIV

96 "0Z 00Ί S99'8Z 169" 01 86f Zl 061 V V1V 93 WOXV

01 "tZ 00 * 1 988" 62 δ ^ ΓΟΙ Ι99ΊΙ 06 ϊ V V1V VO H l PiOXV

M'CTO / lOdf / X3d £ 9Z.Z9 / T0 OAV 09 '8ΐ oo Ί m'hz βδδ'π os ΊΖ mv SIH VD n woiv 8 I 00' ΐ 896 '9Ζ ΙΐΓΖΙ m'U 661 V SIH N 9 tl PJOIV

00 Ί 9 S8S'SI S08'6I 861 V OM 0 S l WOIV ΓΙΖ ΟΟ'Ϊ zoo'zz 9if si m "oz 86i v OM o in won

8 -8 Ϊ 00 Ί 89S-92 SZ6'9l 68Z 861 V Q DO UH WOIV

9f61 00'ΐ 899 'U WL'il 299 ΊΖ 861 V 0M 90 \ W V

OS '61 00 'i 996-32 I' I ZLfOZ 861 V OU V3 Ufl 'WOIV

ΖΓ6ΐ 00Ί 990-92 Z ^ "6l 861 V 0¾i 03 OA l i¾0IV

60 '61 00ΐΐ 9Z9'9Z 8IZ'SI 699 "61 861 V OM N 69 KOIV

001 ^ ZO'H 88 '8ΐ 6Z0'6I Z6I V ΠΟ O 89 l WOIV

9Γ61 00'ΐ i 'U m l-\ Α6Ϊ V AID O λ9 I¾0IV S-61 00Ί ΐ' 06f SI L6 \ V V3 99 l K0IV

IS -81 00 'ΐ 92ΐ ・ 8Ζ fn 006'9I l \ V Π3 N 99 t KOXV

I6 "SZ 00'ΐ Z9 'IZ OSO'SI ZSS'8I 96ΐ V ΑΊ3 0 ^ 9 l i¾01V

ZO'U OO'I 398 ΊΖ 689 192 1 96 ΐ V λΎ) 3 89ti K0XV g OZ 00 'ΐ AZO'tl 68Ζ-9Ϊ 96ΐ V V3 Z9W PiOIV

86'ΐΖ 00Ί SI9'SI 6 l'SI 96ΐ V ΑΊ3 N I9 l WOIV l-Ll 00 Ί 919'ΐΖ tZZ'SI S98 "SI 361 V O 09 I WOIV

68 Z 00 Ί 698 ΊΖ 8S0 'ΐ 96 ΐ V 3 6S l WOIV

OO'I Ζ 808 ΊΙ I 'Π S6I V ¾3S 90 89 ^ 1 W0XV 6000' ΐ SU'Zl 0 ^ 0 'ΖΙ 96 ΐ V HHS 90 A9 l W0XV

9Z'9Z 00 'ϊ 609 Ζ UVU S90'SI 961 V H3 VD 99 ^ 1 WOIV

LfLZ 001 6U'SZ S 8 "SI f Ζΐ 961 V ¾ 3S N 99 ^ 1 K0IV

0Z'6Z 00'I m'H L9L11 m \ HI V JSV O ^ S l WOIV

00 Ί 085 ^ 2 9Z9'tl 60'Sl MI V JSV 3 C9tl WOIV

06 "SI 00 Z66" 9l 008 * U 6T V JSV ZQO 29l WOIV

C9.Z9 / 10 OAV 3Π

 8T6S 00 '' I 926 '2ΐ 696 "6Z ZQZ v m 33 εο ΐ woxv

08 00 • ΐ 62Α'99 089 'ΖΙ 866' 8Ζ m V 3W ao Ζ09ΐ Watch V6Ι 00 '' I 99'6Z ZOZ v m VD ΐ03ΐ Thigh V

00'ΪΖ 00 ■ ϊ 9 'ozs'n m v m N 0091 hidden V

U 'U 00 ■ \ 0Ϊ9-Ϊ8 969ΠΠ m v Thigh 0 66 i Marauder V

Of ΟΖ 00 ■ \ 26ΓΠ v thigh 3 86,1 woxv

98 00 η -ι m v wish Z d A6 l 隐 V

09 00 ■ \ 6 9 · οε 09Γ8 \ oz v dish 0 96 l basket V

00 'ΐ 286'8 S181Z 10Z v thigh ao 96tl thigh V

8f 81 00 • ϊ 80SOI \ QZ v mi V3 6 l 隐 V

69ΆΙ 00, ΐ 008 OS 80ΓΠ 0Z8 "9Z mv mi N 隐 V

6 '8I 00 Ί isf τε 8Ζ6 · 0ΐ-ooz V ΊΥΛ 0 zm Thigh V ΐ9.8 · 00 Ί 999 Ό8 S6S "n ooz V 1VA 3 \ Thigh V

00 ■ ΐ ix 989 "fZ 00Z V 1VA Z33 06 Thigh V

^ 6 'ΐ 00 • ΐ 999' ^ ΐ ooz V 1VA 133 68 l Dish V I 00 • ΐ 86Γ6Ζ UL 'l I 002 V 1VA ao W01V

10'8Ι 00 ■ ΐ A9Z 1 ooz V 1VA V3 tm thigh V 'ΐζ 00 • I 28ΐ 6Ζ 002 V 1VA N 98tl thigh V

00 'ΐ 66S'n 661 V SIH 0 隐 V ι · \ ι 00 • ι 6 O'8Z' z 661 V SIH 3 thigh V

00 • ΐ oso'os m'L 661 V SIH zm S8 V

00 ■ ΐ 960 * 92 661 V SIH Hidden V

C Ο¾ V -7670 πηττ U 03 06 Lo V o 661 V SIH IQN T LQ 0¾T 1 WOTV

00 • ΐ 198 '6Z ΑΟΐ8 966 '02 661 V SIH ZQD Hidden V

00I 203 '82 HL 'U 661 V SIH 33 6A l W0IV

Ϊ6ΆΪ 00I 686 661 V SIH 93 thigh V 麵 oar // :) d C9.Z9 / 10 OAV 911

 ze-82 00 'Ί 699' AS 08 · ΐ 992 'SS v dsv N Thigh V

9C-SS 00 '9S0' 3ΐ 90Ζ "9S z v sn 0 08SI Thigh V

18-6Z 00 '92Ϊ -fl -n oz v sn 3 6Z91 Dish V

89 '00' 'I m '82 8Z0 • 01 m v sn ZN hidden V

89'8ΐ 00 '' ΐ Ά8 98S • 01 1036ε v sn ao i 舰 V

Z6'6l 00 '' ΐ Ml • π v sn 9Z9I Plate V

61 'LI 00 • ΐ · ε m • π m v s 麵

69 * 61 00 '■ ΐ ZWLZ 099 • ζι St9 "92 oz v sn go ^ I Thigh V8Ζ 00' 'ΐ -ι \ m v SAi vo Thigh V

99 · Ζ 00 Ί l6 "98 189 • π v sn zu \ lounge V

00 • ι 196 '8 ■ ι \ 0Z v 0 m \

9Γ82 00 9Z9'BS 8Z8 \\ 686 "29 εοζ V HHJ 3 \ Thigh V

00 'ΐL 90Z V 3Hd ZD 6191 Thigh V

00 m-n '8 m'iz goz v 8Ϊ9Ϊ thigh V

00 Ί • L SOZ V thigh 130 ΐ3ΐ thigh V

99 · 8Ζ 00 589 • 6 soz v Thigh ζαο 9191 Marauder V

00 \% · η S19-t2 V HHi mo 9ΐ3ΐ Thigh V

11 'LI 00 m • 6 202 V HHJ \ Thigh V

90 00 · \ • Οΐ 80Z V 3Hd go gist 瞧

Ιί Ζ 00 S m-oi m v aHj vo z Thigh V

00 8,9 • π 80Z V HHi N \ m thigh V οηι 00 280 -9S 9S0 • Οΐ HS '02 mv, 0 0191 thigh V n wn ran IV 19 00 • ι 689 '6S 960 · Ι 606 * AZ mv, ZD 9091

38 -SS 00 • ΐ \ n • SI 9811 mv 3N S09I

9t'0 00 • ι 098 'AS 996 2''6Z zoz v ao Thigh V mio / iodf / i3d £ 9 £ Z9 / 1 O LU

 00 • I su • 91 ZOZ V MI 0 AS91 Thigh V

LZ-Ll 00 • ΐ no'os inn 801 'OS LOZ V MI 3 9991 Dish V

00 • ί6.9ε Z0 • 9Ι m-u V MX HO SSSl WOXV

Οΐ '9Z 00 • I 089 '32 99ε' 9ΐ V Ul ZD S9I dish V π -n 00 'ΐ • 91 V Ul zao 8991 WOXV

90 00 • ΐ • 31 UVll V HAX zm Thigh V

9ΐ 1Z 00 • ΐ 9I8-S9 • L \ V Ul 13D mi

00 • ι o'ss m • 91 MVU V MI 33 6 9I Thigh V

00 Ί 191 • 91 LQZ V Ul 93

91 '6Ι 00 • ΐ m- \ ηι • SI SZ6'62 LQZ V ¾I V3 ini

88ΊΖ 00 00ΐ · Ζ • si S60'18 v m N 9 SI Marauder V

6f 8ΐ 00 • ι 616 S 0Α8'9ΐ 90Z V thigh 0 m \ dish V I'll 00 Ί S90 • SI m V dish D m marauder V

88 '82 00 • ΐ 'is II • 91 902 V Dish ZD0 m \ Thigh V

00 Ί Ι6Γ88 '91 90Z v mi 130 zn \ 10XV

IVll 00 OIL • si 90Z v wish 93 mi thigh V

01 '2 00 Ί S '88 096 • 91 291 -se 90Z v wish V3 on \ thigh V

98 9 00 00 69 990-28 90Z V plate N 6S3I V

6Ζ9Ζ 00 Ί 609 806 -ζε 90Z V i V 0 8891 Thigh V

91 -η 00 • 91 902 V JSV 0 A8S1 Awake V

S0'S9 00 • ΐ • 91 90 V iSV 9291 Sat ηη • τ '91 90Z V JSV τππ CCGT

 11 Ή 00 • I • 91 863 'ΐ8 SOZ V dSV 隐 V

PI 00 • ΐ 0ZL • 91 VZ 902 V dSV 2291 Thigh V

698 Ζ 00 Ί 839 • 91 V dSV vo V

C9.Z9 / 10 OAV 8Π

 S6'9 〖ΟΟ'Ι L'U iOS "6 ZLQ'U IU V ΑΊ3 M 8891 WOIV

99 '81 00't ^ -fZ Ι9ΓΖ 066 ^ 2 OU V HHI 0 Z89I V

60 '8Ι 00Ί 866 ^ 2 S' 8 ISO'92 012 V ¾HI 0 1891 .WOIV

9f8Z 00 "ΐ m-ll 998 Ά 018" LZ 0ΪΖ V HHI ZOO 083Ϊ HOIV

18 * 92 00 'ΐ i-Z 696' 8 m ^ l Q \ Z V MI 130 6 SI WOXV

29 "8Z 00 860" Z 9ΖΪ '8 Z9S "9Z 012 V l 93 WOXV

99'Zl 00 A68 * 8 962 '92 ΟΐΖ V Ml V3 ZA9I WOIV

9 * 6t 00'ΐ 126 * 92 SZS'OI 8t8 '92 Q \ Z V MX N KOIV

91 -SZ 00Ί 699 189 "01 99Ϊ * 82 60Z V 1VA 0 SASI) e V

S8'6I ΟΟ'ΐ 6Ζ0ΊΪ S0S'Z2 60Z V 1VA 3 SI

86 'os oo' i zn-u -n -u mz v m ¾o ε ^ ι κοχν

91 Ζ 00Ί 898 '92 20ΐ 'U SI9 "92 60Ζ V 1VA 133 2 9ΐ W0XV

00 'ΐ 69111 060' SI Ζ01 ΊΖ 602 V 1VA 90 U91 V

98'8ΐ 00Ί 889 "9Ζ 96S" ZI 00S 60Ζ V ΊΥΛ VO OAS! W0XV

6ε'81 00Ί 86Ζ'9Ζ 190 '81 60Β '8Z 602 V 1VA Ν 69SI ΙΪΟΐν

19 * 02 00 Ί 208 '82 UVl \ S10'82 802 V HHJ 0 8931 R0XV

1Γ6Ι 00 6Ζ8 Ϊ i, 8Z * 8C 80Ζ V 3Hd 3 Ζ9ΒΪ W01V

8 '00'ΐ 83ε6Ζ 60671 986 "tS 80Ζ V HHi ZD 99SI l¾OIV

10 * 02 00 Ί I 'OS 9ifZI 660 80Z V 3Hd 233 99SI UV

OO'I ^ WU I9S 802 V 3HJ 133 ^ 9 1 ίϊΟΧΥ

W ΐ 00Ί 086 '62 ΟΑΟ'Ζΐ IWl 80Z V HHi ZOO S991 PiOIV

62 "9ΐ 00Ί L89 ΊΙ 019" 21 99r8 80Z V SHd ΐαθ Ζ95Ϊ WOIV

00 9982 9fl 'ΖΙ 06Γ28 80Z V 3Η <ί 90 1991 W1V

88-8I 00 Ί 982 '82 888'Π 896 * 08 802 V HHJ 93 099ΐ W0XV

9f6l 00'ΐ ΖΜ- 1 SrSI 0ΖΓ02 80Ζ V SHd VO 6S91 WOIV

08'9ΐ 00 "ΐ '62 ΖΖ9" SI 906 "6Ζ 80Ζ V HHJ Ν 8S91 V t'Cio / iodf / xad C9.Z9 / T0 O 6Π

ιΐ ΐ οο · ΐ ιη'ΐι soz "9 s ν νο 609ΐ HOIV ΐ9 · ΟΟ 'Ϊ rn'ii m · 9 -i \ v in N 809i WOIV

60'ΐΖ 00'ΐ LSI * ΐΖ 5ZS '8 08Ζ'Ζΐ U V ¾3S 0 Α09Ϊ WOIV

00Ί 9ΙΖ Ζ6 i '91 Z V 3 9091 WOIV

S8- S 00 ZSS'61 ΐΖ6'9 SOZ'Sl m V ¾HS 90 S09I WOIV

QfLZ 00 Ί IS8O2 SIS 'Si I2 V HHS 93 091 WOIV

ΟΟ'ΐ 908 '8 Z9S! 2 V ¾3S V3 S091 WOIV

ΪΓ82 001 m ΊΖ 0gr8 9l * 9l l? V N 209Ϊ NOXV

00'ΐ 196 '0 8 ΌΙ I' SI ΠΖ V IVA 0 1091 KOXV

OO'I i8r? 2 186 "6 229 'SI UZ V IVA 3 0091 KOXV O'SZ OO'I S00'9Z 9 8 ΊΙ ^ 8" 9ΐ V ΊΥΛ 6691 WOXV

9Α ^ ΐ 00 "ΐ 609 -SZ m'U 929 '^ ΐ V IVA 133 8631 TOXV

OO'I 8Z8- 2 96f Π 288 'SI 9tZ V IVA 93 Ζ69Ϊ UV B'ZZ OO'I ί ^ Ζ 608 -01 OSf 9Ϊ. 8ΐΖ V ΊΥΛ VO 9631 WOIV ί2 Ζ OO'I SSS'CZ 60ΑΌΪ 2U V IVA N S691 WOIV n'ZZ 00 'I 996' ΖΖ 09L'8 l \ l V 3ΊΙ 0 69l MOIV

^ Ο'ΐΖ OO'I 686 996 '6 Zl9 * 8l 212 V ΗΊΙ 3 S6Si WOIV

Z9'6 00'ΐ IC0-6I A88-0I III V ΗΊΙ 100 WOIV 6'Ϊ 200 '00 m ^ l ΟΟ Π ΖΗ Ζ l \ l V 311 133 1691 WOIV s * 9i oo'i woz usii εζδ'δΐ v an 2DD 069i woiv

CS'Ol ΟΟ'Ϊ 610 Ζ UZ ΌΙ 196-61 III V ΗΊΙ 93 6891 I

86 '81 00-1 ^ Ζ SZ9 "0I 826'61 Ζΐ2 V 3ΊΙ V3 8891 WOXV

OO'I m-ZZ 089 "6 SI6'0Z V 3ΊΙ M I¾0XV

Z iZ OO'I ZOO ^ 2 960 Ϊ lil'll \\ l V kid 0 9891 WOIV

6 6ΐ 00'ΐ ΖΙ% ζΖ 696 '6 ΙΖ6ΙΖ V ΑΊ3 3 S8S 〖M V

00 "AI OO'I l 098 * 8 018 · ^ UZ V ΑΊ3 VD 89I WOIV

C9.Z9 / 10 OAV 6 'Ze 00' ϊ S98'92 996 UZ V ΑΊ9 N 989Ϊ V

86 'SS OO'I Z8 "Z L6' S LIZ V (1Ί3 0 fS9I WOIV

O OO'I fLl Ζ SOZ'S Ϊ 9 'S ΑΐΖ V 1113 0 829 Ϊ WOIV ε8' oo'i 8s- 2 ΐ06-9Z8 '8 i v mo Z30 zm WOIV

OO'I 669 Ή 910-9667 L \ l V Q13 130 1291 WOIV

90'9C OO'I \ LfU SSS'I- 596 '9 ZIZ V H13 00 0S91 WOIV

19'6Z OO'I 9Zft ^ 82Γ0 U6 '9 III V mO 30 6Z91 WOIV

^ LSZ 00 "ΐ 661 -SZ 0f6'0 8 ^ 2 '9 LU V ΠΊ3 33 8291 WOXV

99'ie OO'I 980 * SZ 09f Z '9 LIZ V 1110 V3 WOIV

S OO'I ΐΓ92 9 ^ 8 * 2 92A '£ ΖΐΖ V (113 N 929Ϊ WOXV

6Γ2δ OO'I Ϊ8 '9091 912 V ΑΊ3 0 WOXV

6Π2 00 * 1 9Zr 2 0S6 "S 9Ϊ 8 91Z V Π0 3 tZ9l WOIV

88OO'I ΠΓ92 99 ^^ ΪΖ9 '6 912 V ΑΊ3 V3 9291 WOXV

001 L66 "CZ ^ Ο'Οΐ 9tZ V ΑΊ9 N m \ WOXV

OO'I ZI0 "9 SIC V 0 ΙΖ9Ϊ WOIV

OO'I 08S "S2 ^ S" 9 Ϊ6 Π 9ΐΖ V 5ΆΙ 3 0Z91 WOIV

88 'IS 00 Ί AOS -12 SOTO 06 Π V iU ZH3 6Ϊ9Ϊ WOIV n ^ Z 00' ΐ 828-ΙΖ 988 -0 9 C'0I SIZ V 9Z3 8191 WOXV

S0 * 8Z OO'I SL9 "0 ^ Ι V d¾l CZO Ι19Ϊ WOXV

Α8Ι9 '00'ΐ 96 '61 S06' 2 O ^ S'Sl 5ΐΖ V dM ΪΗΝ 9ΐ9ΐ WOIV

00 860 '02 QQZ '826'21 12 V iU 103 9191 WOXV

9S'92 00 Ί ηί Ζ 6 S "0l SIZ V S33 9I WOXV

96 ΌΖ OO'I 9A0 "2 6 ^" Π 912 V JM 233 8191 WOIV

08 00 -ΐ Ι60ΊΖ S88 flt V dTOl «D ΖΪ91 WOIV

IS -62 OO'I 98 '02 βξΖΊ 29ΓΠ SIZ V 33 Π91 KOXV 8 '92 OO'I 601-\ l t8f 9 ^ 86 ΌΙ 9IZ V 93 019Ϊ WOXV

C9.Z9 / 10 OAV οε'εε oo'i LLVK -Q fLZ ^ v SAI N i99i won

S 'SS 00 Ί SZS'gg 6iS * t 902 "Z III V 0 0991 PJOIV

Wn 00 8 'SS 0Z6 "S V D 699Ϊ WOIV

9600 'I 8S9'9Z lift, S S "ΐ ZZZ V ZW 8991 WOXV

9S '9 00' ΐ 099-82 St8 'S Z S "0 ZZZ V m 1HN i99T KOXV

09 '8 00 Ί m'LZ 6f' ΐ III V 3W Ώ 9991 W0IV

09 '8 00' I 'Z 882 ZZZ V HN S991 PiOXV

96-AS 00 9186Ζ SA9 'Z ZZZ V 9W (D 1 ^ 991 KOIV

8Α 800 Z S'OS 398 "2 928" 8 V 3W 33 WOIV

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Ι9 ε 00 Ί 0S9'ZS 0 ^ 8 "Z 291 ZZZ V VO 1591 PiOXV

00Ί Hf 22 SZ9 * S U6 "S ^ 2 V 9W N 0S9T KOIV oi is oo" i-soo ^ esi '9 m v vivo \ KOIV

6ε ε οο'ΐ ΐ9ε · εε 6ss' se-9 izz v viv a m \ PIOIV

6Γ92 00Ί 686 * SS 2 Z * 9 ZZ8 "9 UZ Ή 90 i 9I KOIV

99 00 'ΐ 080 "S8 f 69" 9 SSTi V VIV VO i V fZ2 00 Ί S99'IS 9S0' 9 160 'Ζ I V VIV N SP91 NOIV

98 Ή 00 6 OZZ V SAO OS 9t WOIV

88-8Z 00 Z99 "8 80-9 OZZ V SAO 33 mi WOIV

98 "SS 00 'ΐ ΪΖΓΪ2 016 * 9 OZO'S OZZ V SAO 0 \ WOIV

89 00'ΐ A60 "IS S99" 9 380 * 9 QZZ V SAO 3 91 ROIV

08'IS 00'ΐ 6S9'6Z 801 Ί 9 Z "9 QZZ V SAO V3 0 9T WOXV

AO'ZS 00't L1 'Z 99' 9 9Z'S V SAO N 6S91 KOIV

00 · ΐ ZSO'ZZ IS! '9 V ΑΊ9 0 8891 WOXV

6Z'SS 00 Ί 0Z6 "9 109 '9 8IZ V AID 3 WOIV

2,0 'SS 00Ί ^ 6 "9Z SAl' 9 8AS ^ 8IZ V ΑΊ3 VO 9S9I WOIV

£ 9Z.Z9 / T0 OAV 9Z'iS 00 'ΐ 888 -ZC 669-Ll' U m V Ul Ώ Ϊ69Ϊ XLV

00 "ΐ i65 -12 Si6 'Ζ- Sf' SI 5 ^ V Ul ΖΏ 0691 HOIV

19'SS 00Ί 8 9-0S U SOi '`` CI V Ul Zad 6891 WOXV 8'SS 00'i 9 Z '99 IS l-66Γ ΐ 9ZZ V MX 133 8891 NOIV

8 '82 00 * t 6S 0-9ZZ V HAX TOO 891 KOXV T 8 001 BIO'I 99 '0- 6S8 1 9 ^ V Ml 93 989Ϊ WOIV

8 οε oo'i e o'os o 'n m v MI ao S89i κοχν

88 "8Z 00 'ΐ 891 '02 66Z Ί ZZS'ZI ll V Ml V3 891 KOXV

A6 "6Z 00 Ί 26 '6Z SS8" 0 S' Π V MIN 9891 PJOIV

LL-QZ ΟΟΊ 98Γΐ2 996 Ό 80fOI 2Z V SAI 0 Ζ89Ϊ ROXV

6S * 0S 00 "I 89Γ02 008 Ό SiS" 01 t2Z V SAI 3 1891 KOXV

86 * 22 00 * 1 9S8 'S-6ZA'9 V Sll ZN 0891 WOIV

00 Ί m-LZ U Z- 8SZ'9 Ul V SAI 33 6Z91 XLV

TO'SS 00Ί W9'I- US * Z ZZ V SAI 03 8Α9Ϊ WOIV

8fS2 00 'I 9SZ'6Z 2ΐ6 Ό- 6207 ZZ V SAI 33 91 WOIV

00'ΐ m-U 800-0- 991 '8 ZZ V SAI 93 9Α9Ϊ M V

OS 'IS 00' I 8 f08 LZL'Q- 6Γ6 HZ V SAI V3 PiOXV

U'SS OO'I 099 'IS SS'I-8Z8 "8 ^ V S N PiOXV n' 6C oo'i Γΐε 8w's- isr6 ve ^ v O εζ9ΐ WOXV

91 "9S 00 'ΐ 9I0'2S 0Z9 Ί- S98' 8 VSZZ V AID 3 m \ DJLV

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99 9 00 • I 9Ζ8ΌΖ m • ΐ 19 SOI a mo O in Thigh V η Ί9 00 'i m • 0 800 • IS 80 ΐa ΠΊ3 3 0 ϊ Bandage V

89 • Z9 00 'I 68, • s 690 * 8 SOI a ma 621 Thigh V

6 'Z9 uu I VLV 66 8S2 1SZ "09 on T o αr 1 n1i 1oJ IdU OCT

 ΟΖ • S9 00 • ΐ U \ • 6 801 a ΆΊ CD L \ Comfort V

91 • 63 00 • i 8ΐδ • s 620 S01 a ΠΊ3 90 9δϊ Thigh V

01 • 99 00 • ΐ 6SZ 't80 • 09 SOI a mo 93 9SI Thigh V

M'CTO / lOdf / X3d £ 9Ζ.Ζ9 / Ϊ0 OAV SSI

9Γ02 00I 90Ζ 'U 08ΓΠ on a Has 0 061 Thigh V

889Ζ 00 • Ϊ 8SZ 'ίΖ t90'St on a m 3 681 plate V Vοε 00 • I 96Z-8 on a ms 30 881 plate V

9871 00 • ΐ-\\ Oil a 匪 Marauder V

LfU 00 • i 0Ζ9ΊΙ on a HHS V3 981 view V fLZ 00 • ΐ 0S -0I on a S N 381 V I '11 00 • ΐ 920'6 08'9t 601 a SA3 3S 81 dishes V

\\ -H 00 • ΐ 688 Ό8 958 '6 IZI' 9 601 a SAD ao 281 Thigh V

6f OS 00 • ΐ 009 · 0ΐ 601 a SAO 0 m Dish V

IfLZ 00 • ί 881 ΌΙ 86A'9f 601 a SAO 3 Ι8Ϊ 丽 V

L type LI 00 Ί 62-0 '6Ζ S016 601 a SAD V3 081 Dish V

Wll 00 • I 699 · 8Ζ 8 8 601 a SAO N 6ΖΪ Dish V

6 ^ 00 • I Z6f 9 801a IVA 0 8 AI Thigh V

00 • ΐ sz Ofl 'i 9S0' Xie a IVA 3 I view V ii- a 00 • ΐ Z99'9 801 9 IVA 233 9Π 丽 V

00 • ΐ 8 80ΐ a 皿 Plate V

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9 ・ ^ 00 • ι -Lz 088 '8 801 a IVA V3 Zl \ Plate V' L 00 • ΐ 289 -8Z A61 '9 80ΐ a IVA N U \ Thigh V

08-IS 00 • ΐ 6ΖΓ09 ΑΟΐ a ΊΥΛ 0 \ l \ 隐 V

98 'OS 00 • ΐ Ζ08 · Π0 L01 a IVA 3 OZl V

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0 on ι Dob L V LV} f) a IVA L JJ

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00 S6S.0S 8Z9-8 101 9 IVA vo 991 舰 V

00 A0f OS ZS8'6 L01 a IVA N 591 Dish V

C9.Z9 / 10 OAV 9CI

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0Γ62 00 I 6Ζ0 · 8Ζ 6Ι 88 9Π a ui ιαο Ml Thigh V

ZI '82 00 I 6ΐΖ '82 9S2'6I 199 62 sn a ui 022 woxv

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IS'IC 00 ι ιι \ ιι 690 0S9 If 9Π a ui V3 Marauder V

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00 I 191 Of Π a ΑΊ3 0 Thigh V

00 ΐ U a person ¾ 0 m 丽 V

ZO'IS 00 009 ^ 2 m '68 I a 入 3 vo nz 隐 V

99-εε 00 Ϊ99 · 0Ζ 8S9 • 68 n \ N Thigh V

8t 'ε 00 • ΐ 966 696' 6Ι a m 0 zu Thigh V

00 'ΐ 88Γ6Ι '82 2Π a m 3 nz Thigh V

19'8S 00 • ΐ 9ΐε · ιζ 69'8I 86Z • 82 2Π a m 93 nz Thigh V

89 '28 00 • ΐ IS9'8I 986 • 82 επ a 3W VO soz W0XV

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00 * ΐ m-π 69i'9I 60 • 68 l \\ a viv 0 ooz 舰 V

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8ros 00 'ΐ 000 -QZ 0198S zu a viv VD 861 thigh V

00 • ΐ 986 · Ι • 62 zu a viv N

99.81 00I 89f 91 'S in a SAD 9S 961 K0XV 8.8ΐ 00

00 Ί 899I '0 in a SAD 3 舰 V

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69 'ΐΖ 00' ΐ 0 9-88 8Π a viv 93 m 舰 V

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ZO 00 'ΐ Α88'6Ζ 161 · 8ΐ LU a nai 0 plate V

91 'ΐε 00 • ΐ Z68'6Z 90Z * 8 Ll \ a nm 3 m Marauder V

Π • 9Z 00 • ΐ 390 '8Ζ Z 8 LU a nai m Thigh V

86 '6Ζ 00-\ U -6Z 610 ^ 1 069 "9 LU a nai ιαα m M0IV

69 00 • ΐ QLfH LU a nai Thigh V

■ u 00 • ι So-called 'SI 988 "^ LU a nai ao Thigh V

9S • IS 00 • ΐ 0 0-6Z 686.91 t6I 'Lf LU a nai V3

19 • IS 00 000 000 '8 Ζ 018 · ”909 · 9 LU a nai N

60'εε 00 -u SSI'61 925 9Π a dish 0 W0IV

11zz 00 'ΐ ζ% ι 188' 8ΐ 9Π a mi 3 z thigh V

■ n 00 'ΐ ^ z 868 688 9Π a

96 00 Ϊ60 · 8Ζ \\ 2ΊΖ 0 ^ 8 '9 9Π a thigh 130 m hidden V m • 92 00 • I 9 • a thigh 3D m thigh V

11 Ί2 00 • ΐ 9ΐΐ 'LI 8996ΐ 9Π a V3 082 Thigh V

51 • ZS 00 • ι ι ^ -ιι 9Π a Thigh N Dish V

00 • ι 013 32 92Γ6ΐ 691 'S SU a UL 0 m W0IV ozZS 00' ΐ 929 "9Ζ 069-61 9Π a ui 3 in Oki

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98 • 92 00 9.6ί 993 '6S 911 a ui z o 2ZZ f¾01V

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86 'Z 00 • i 018' C 19Γ8 80 • 6 U \ a AI ZN 丽

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00 • ΐ too • 9S m • 6 809 "8 U \ a sn CD III WOIV

88 -oe 00 • t 9tS • 98 006 · 0ΐ 988 U \ a Ai 03 III 丽

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00 • ΐ 999 • εε • ζι LlfLf U \ e SAi V3 OLZ ΐϊοιν

99 'Z 00 • t • 82 Ι 909 "8 u \ a SAi N 69Z Thigh V

Ζ 6Ζ 00 • ΐ L • Π 5i9 \ l \ a no 0 892 Thigh V

00 • i OZO -u Ι U • 6 \ l \ 3 LU thigh V

9L'H 00 • i U9 8i6 * ΖΙ ^ 69 "09 \ l \ a no V3 Thigh V

LfU 00 'ΐ 389 896 "91 8S0 Ί9 \ l \ a λΐϋ N m Thigh V

Z9 ^ Z 00 • t 080 S \ UL • 19 OZl a Nsv 0 m

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08 '9Z 00 Ί' 9ΐ 06Z6t OZl a NSV Ran m Thigh V

9Ζ-Π 00 • ΐ 0.6 ΐ • 6, oz \ a NSV ιαο m

U'll 00 • ΐ 9Z0 • 98 L "91 168 • 6 OZl 9 NSV 09Z Thigh V

OfU 00 'ΐ 028 ^ 1 092 Ί5 oz \ a NSV ao Marauder V

99 -Π 00 • ΐ ■ n ZLfH Sit * Ζ9 OZl a NSV VD Thigh V

00 • ι 6Π-890 • 91 8A0

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99 "62 00 'Ί 0Ϊ8 • 08 6Ϊ6 • \ z 989 a an 3 96Z Thigh V ft 00 Ί m ■ η 9 ^ 2 • oz a an ιαο 丽 V

LO • εε 00 • I -η 680 U8 9Z1 a an 133 Thigh V O 00, 1 891 -SS Ζ60 -u 189 * ^ 9 an Bandage V

'Ll 00 ■ ΐ 861 -η 826-\ z a an thigh V

6S 00 • ΐ Z86 • \ z a an vo 06Z Thigh V οε 00 ■ \ i • IS Ζ08 • 61 • S a an N m Thigh V

28 '81 00, 1 803 OS πι • 1 zn • z HI a SAD 3S 88Z 隐 V

99 • oz 00 • ΐ 691 ■ η S • 91 u \ a sio 93 thigh V ΐ • YL 00 • ΐ 968 fS6-8l 060 HI a SA3 0 plate V

81 '11 00 • ί 101 • ιζ 56Γ8Ϊ Z86 n \ 3 SAD 3 Thigh V

06 • i 00 • I OIL ■ \ ζ 189 • L \ mu \ a SAD V3 m Marauder V

00 • ΐ Z86 • η S9 • 91 m • S Ul 9 SAO N m 隐 V

00 • oz 00 • ϊ 90Z 61 • 91 '5 u \ a vav 0 m hidden V

19 ■ n 00 • ι ooi 'εε 9Π • 91 856 a viv 3 m Thigh V

98 '11 n unu • τ ι 199 '99 III • 91 69S • S 07] u V on V Uo 6 win TV

06 ^ 2 00 • ΐ 69S 'S 06Z '91 III' u \ a viv vo Ul Dish V

9 00 • I 981 'Π in · ΐ in a viv% ll 隐 V 0 • 61 00 • I 9Αΐ • gg 8U Ι 291 U \ e ski 0 III Thigh V

C9.Z9 / 10 OAV 00, ΐ 909-82 910'ZS OCI a MI zao 8ZS W0JLV

00, ΐ 968 -oe 163 OS OCI a MI iao 舰 V

09 'ZS 00' Ί 01Γ02 9'8Z 0SI a ui ιαα 9ZS WOIV

88 * 62 00 Ί 9 ^ 6 '8Ζ Z6.8Z 99i'IS οετ a 33 views V

Ϊ0 · 6Ζ 00, ΐ 5ΙΓ8Ζ 98812 οει a ui 93 plate V

80 OS 00 Ί 001 -hi 021 a I V3 隐 V

8flS 00 • ί S86.8Z oei a MI N I Plate V

86 'OS 00, ΐ ΐ £ ΐ -18 6Ζΐ a OM 0 m Thigh V

00 • ΐ 089 -U S ^ l '32 a O a ozs Thigh V

U 'ZZ 00' ΐ -u ειο-ιε 6Ζΐ a ou 3D 618 Thigh V

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80 00, ΐ 6Ζΐ a ou ao 912 Thigh V

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96 'S 00I6 6Ζ 2Ζ \ a ΑΊ9 0 I8 隐 V

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98 '9S 00I 80 a ou 0 SOS thigh V 90 · Ζ 00 I 009 • ζε 026 U 8'SS am 33 S 舰 V

90 'SZ 00 ΐ 990 cc U a sAi ao 292 舰 V

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96 · ”00 ΐ U • 82 ΠΙ • 61 WIS 821a ΑΊ9 N in Thigh V

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90 Z 00 t εζο9Ζ 96i '6ΐ ZSlao V

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2fU 00I -η '11 m a ou 0 o s Dish V

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09 ΊΙ 00 Ί 082 • OS m a ou 93 822 Thigh V ι · \ ι 00 • ΐ 0Ζ6.88 Ζ a ou 93 L Thigh V

LV Z 00 • ΐ 0 0 • 8 • 82 901 -98 m a OHi VD 99S Thigh V

91 'SZ 00 • ΐ 660 • OS m Ζ Z9I -92 a ou (D 92S hidden V

66 '00 • ΐ 089 · 8Ζ LOO • 9Z m a OM Drive V

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80 ε 00 • I 9ZS '62 662 • 18 Ζ93 δ OSi a ui zao 6ZS Plate V

£ 9Ζ.Ζ9 / Ϊ0 OAV in

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00 00 • 8Z 19ΖΌ2 a nm 8AS V

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16'8S 00 092-98 m-Li 98ΐ a mi 0 9Z8 O V

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08 'tZ 00 • ΐ 288 '92 921 a thigh εζ8 thigh V niz 00 889 '88 m-ιι 9i9 * 92 98ΐ a dish 190 m V

00 'ΐ Z fLZ 981 a Thigh 93 Marauder V

00, 1 8Z9 Ζ 09 8Ζ 98ΐ a thigh V3 dish V

98'OS 00 • ΐ 68Γ8Ζ a dish N 699 thigh V

98 00 • ΐ 182 Ζ 9SI a ΝΊ0 0 898 Thigh V

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00 98 018 • 61 SSI 9 ΝΊ3 1H0 S9S Thigh V

99'9Z 00 • ΐ -L • OZ 908 · 9Ζ 99ΐ a ΝΊ3 ao 9S Plate V

00 • ΐ 096 'SS • QZ \' ΐι SS1 a ΝΊ3 so S9S 舰 V ι · ι 00 • I 6Z0'98 SOS '1 8

00 • I 999 'tS' 981 a vo 192 舰 V ΐ '11 00 ΐ m ~ n zm Ζ SZ9 6Ζ SS1 N 09S Thigh V

Wll 00 m • ii m '1 a sn 0 698 Thigh V nn • τ fif) TP 960 • u υ pi ran TV

88 t 00 • ι 069 • 81 Z60-5S η \ a sn ZN Plate V

6S-SC 00 • ΐm • 61 6f 9S π \ 99S Thigh V

S8- S 00 Ί 990 'SS 8UQZ η \ a sn ao S9S WOIV

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8A'S 00 'I ZU ^ l 118 a through SI comfort V

I0'9Z 00I LU6 820 -9Z 09Aoz 018a ivA 丛 0 Zl 隐 V

Wll 00 Ί Z69'5C S2I -U 80Ϊ • 91 608 a through 丛 0 U Thigh V

96 • 00 • I LLQ-fl 80S a XVM AO 01 Thigh V

09 '9t 00 ■ ΐ 629 * 88 \ ι · ιι • 6 A08 a hired 丛 0 6 thigh V

OS '93 00 • ΐ UfZZ- • 0- 908 a Plate 丛 0 8 Thigh V

9 ^ 63 00 • ι ΐ98'6ΐ 908 '92 'l 908a through L 0 L Thigh V

96 00 • Ϊ m'u a through 9 Thigh V

8S t 00 • ΐ Z98OS ιι · \ ι • 61 80S a fan 9 隐 V

80.9Z 00 • ΐ l • \ i ae v 丛 丛 0 views V

89.6Z 00 • ΐ A98-6I 000 • 61 108 a 丛 0 8 Thigh V

96 OS 00 • ι Ϊ08 Ι 919 • 01 008a XVM AO I Thigh V

SI 'i9 00 • I 999'ΐ • 6 666 a 顺 m m \ Thigh V

8 9 00 • ΐ 09Γΐδ 961 • SI ma through ivo \ Thigh V 9t 00 • ΐ 3ΐδ · ιε • 6Z 881 a mo xo 268 Thigh V

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81 00 Ί L6Z-Z6Z 821 a im 3 162 W0XV

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00 • ΐ 93Z '88 61Z • 88 L 1 a nai 2Q3 182

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18 'fS 00 ■ ΐ' um ■ H 988a through AO 82 thigh V

19-82 00 ■ ι ΖΐΖ-51 ΠΪ Ζ A88'S 999 a through AO L Plate V

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S6-0 00 • ΐ 6t0 • 61 no'i a through AO Thigh V

62 Z 00 • ΐ ο ι · ιι Ll σ AO 2S Marauder V

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9f 98 00 • ΐ 6Ϊ -6Ϊ 60Z • 91 9.9 LIZ a through 丛 0 6Z NOIV

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98-13 00 'ί m-n 109 • 08 10' 8ΐ Ml a Haruka AO U Thigh V

98 'Zt 00 Ί Tsuyoshi' 189SS 6S6 1 ozs a through AO 11 W01V

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92 O 00 • τ ι 10 & 0δ · Τ! ■ ί, • 61 812 a ring Mf) U6

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61 't 00 * 1 Z8 • 6 8 Sa IVM 丛 009 ■ V 6t 00 · ΐ 929 * 81 090 • 6 lU' i LH a through 丛 0 6 Thigh V

89 -9S 00 ΐ 89Γ 9Z0I-SIS I a 丛 0 8 舰 V

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9f 9Z 00ί6 08Zi Z 1 c 'a

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98 '02 00 ■ ΐ '91 019 0 68Α'6 OOZ a ΐ6α Lid L

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8Γ 00 • I \ η '9ΐ ISZ'6 OOA a ΐ6α 69

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08 -ZS 00 Ί woz 86 ΐ 86f 9 OOi a ΐ6α \ Ώ 99 dishes V

Π S 00 • ΐ n \ '6ΐ m-i OOi a ΐ6α ΙΏ 39 V

If S 00 • ΐ m 'U OOA a ΐ6α 130 dishes V

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 u ΐ6α UN JVUiL V

93 '8S 00 • ί εζο '11 LS9OI 818 "9 OOi a ΐβα ZO 99 woxv

SKIS 00 • ϊ ΐΐΐ • 92 8Ζ9 · 6 198'9 OOi a ΐβα 10 9S Thigh V

\ LSZ 00 • ΐ Z66 • ii 9 · 6 Πίΐ OOA a IS 9 隐 V

£ 9Z.Z9 / 10 OAV in

 U "61 00 'ΐ 6S9" 6 9ΪΓ0Ι- L \ 1VA VO \ MUV

Z9'6l 00 921 'LI 992' 6 0ΪΓ6- il ΊΥΛ N 21) JLV

AO '61 00ΐΐ3 6ΐ 90 δ Z80 '8- 9ΐ 311 VO II NOIV

U "81 00 Ί m'OZ 9Z9'6 00 '8- 91 311 N 6 WOXV

Ζ2-6Ϊ 00 'I 8 6'8l A00' 6 6ΪΓ0Ι- 9ΐ 311 0 9 WOIV gg-6l 00Ί Ilf 81 OtO'6 60S '6-91 ΗΊΙ3 9 WOIV

S3 '8t 00' ΐ S66'61 9S6 "9 6ZS 'S- 9ΐ 311 TOO HOIV

IS '81 00 'ΐ ZS9 "0Z 998' 9 S 6 '9- 9ΐ 311 133 g K01V

2Γ8ΐ 00Ί 99f 81 6A2 "9 O I '8-91 3ΊΙ 290 I KOIV

Z8'8l 00 Ί f99 -61 \ Vl III '8- 9ΐ 311 93 I WOXV

【Halla】

00 '0 00' 0 9 '1 A61 9 509' t OOZ a 16a to 86 Thigh V

00 '0 00' 0 90Γ9Ϊ Ζ6Γ9 00A a ΐ6α 913 V

00 '0 00 "0 Ζ-9Ϊ W8 00 a 16a io 16 Marauder V

00 '0 00' 0 m-L \ 186 "9 289 * 9 OOZ a I6a ειο 06 Thigh V

00 '0 00 "0 OOZ a ΐβα 68

00 '0 00' 0 92Γ9 U8'8 00A a ΐ6α εο 88 Thigh V

00 '0 00' 0 · 9 109 ·, OOZ a ΐβα L Thigh V

00 '0 00 Ό Z99'61 689' 9 66Z '00A a 16α 98 Hidden V

9 o oo 'i Ζ6Γ0Ζ 920 * 8 OOi a ΐβα πο S8 plate V

90 2 00 Ί 86 9Ζ m'i 608-81 OOZ a ΐ6α Π3 ^ 8 贿

6Z'6I 00 'I 80-2Γ OOZ a ΐ6α 63 S8 隐 V os -u 00' I m Ί ίίΖ Ι OOi, a ΐβα 83 Ζ Marauder V

81 \ ΟΟ'Ϊ 858 898 '6 00A a 16α Ld 18

LQ-Ll 00'ΐ 86f § 08ΠΪ ooz a ΐ6α 93 08 Optional nO / IOdf / IDd {: 9 frost 0 ΟΛ 8tl

 ΐ 00 'Ί ZL0 Ί • s tol \ l mi N n thigh V

S6 00, ΐ οεζ • ΐ eei Ίto oz MX 0 thigh V

U 00 • i 899 * 02 09 ^ · ι \-oz Ul 0 Thigh V

U • 00 Ί 099 '8Ι 9 •-3U -L- QZ Ul HO O WOIV

9i • OZ 00 'I 9Ι9.8ΐ L10' I- 116 '8- oz m ZD 69 Marauder V

99 • 02 00, ΐ 601 • ΐ-8SI • 6- oz m ΖΏ 88 Marauder V

9 • OZ 00 9Z3-Z1 • 0-082 • 01-oz Ul Zdd A8 Thigh V

• oi 00 Ί 009 * 61 Ί ~ 8S8 • 6- oz Ul I ED 92 舰 V

8 • OZ 00 • ΐ 099'6ΐ • ΐ- • n- oz Ul ιαο 38 Thigh V

8 02 00 • ΐ εο9 · ο-60S 'Π- oz Ul 3D n WOXV

1% • oz 00 eos * 8i 6Ζΐ · ο \-oz Ul 82

• \ z 00 · \ 'I • z to oz Ul vo Z2, plate V

'11 00 • ΐ 99 ^ * 81 80, 'I' n- oz Ul N OS WOXV

00 m'i \ 260-81- 61 ΑΊ3 0 6Z Thigh V

19 '00 • ΐ is • ε ei6 • u-61 Π9 3 U Thigh V

08 • \ i 00 • ΐ 2ΐ6'91 811 ^ 88Γ01-61 ΑΊ3 VD 11 Thigh V

93 Ζ 00 Ί 16 Ζ'9 ΐ 6ee ■ sm 61 ΑΊ3 N 9Z Thigh V

90 '1 00 • ΐ iwnπ_ 81 0 腿 Thigh V

19 • \ z 00 • ΐ m • Π-81 0 2Z 丽 6 ■ oz 00 Ί 90fH • 9 686 • u-81 VO U Plate V

A9 ■ oz 00 • ΐ 06 • ι 929 • ΐΐ-81 N QZ Hall V

68 · 6ΐ 00 • ί 188 • L 8S • 6_ L \ 0 61 Thigh V

08 • 61 uu ι 862 60Γ01- L I ΙνΛ J 0 T

 3Z '91 00 • ΐ Α9Γ9Ϊ 8S1 ■ n m • 6_ l \ 1VA LI 丽 hi ■ L \ 00 • ι '96S'H ■ \\ 991 • u-LI 1VA 130 9t Marauder V

80 • 81 00 • I 6SS-9I · 0ΐ m • 6-LI ΊΥΛ 93 91 Reading odf / iDd C9.Z9 / T0 OAV 6 I

 00 'OS 00 Ί' l-ΐδΓ9- NSV ιαο 9i WOIV

IfLZ 00 'Ic-909 Ί-92 NSV 3D Si V

00 • I 80878 S6S 'G L \ lί-92 NSV 93 fL Dish V

68'ZZ 00 • ί 9A6-0S Π9 '8-0907- 9Z NSV VD L MOIV

00 Ί ooros 966 'l-81S-8- NSV M IL V

HI 00 • ί 06SOe ΐ88 'to 88f 6- U V1V 0 OL 丽 V

61 '1 00 • ΐ I9f OC 999 • ε-6-Π V1V 3 69 Dish V

Wll 00 Ί ozf ιε 910 • ε-H V1V 93 89 Marauder V

W \ l 00 'ΐ 282 '09 Πί • ι- 389 · 0ΐ- H V1V V3 Z9 舰 V

Wll 00 Ί no • s-· Π- U V1V N 39 隐 V

6 00 ■ ΐ QZL'LZ 'ι-963 "6- U no 0 WOIV ll 00 • ΐ m-iz% • ι- 908'Οΐ- 2Z a W0IV

00, ΐ Π9-9Ζ 8i9'U- 21 no vo V

\ i- \ z 00 Ί n \ 'ι- 961 ΊΙ- ΑΊ9 N 09 thigh V 81 00 • I 96S.0 688-U SIO 3S 69 舰 V

28 '81 00 in 'o-0 8-U S13 93 Thigh V

00 Ί m ΊΙ • 2-61 'Οΐ-U SAO 0

Thigh V

9000Im it m 'l-6SS * 0l- U SAO 3 99 face

00 • I • ΐ-666 "6-U S VO 99 KOIV

00 • ΐ n \ • ο- 'oi- 11 SAD N 83 WOXV

10 Ζ 00 • ΐ 929 '11 9S 'G U plate 0 Thigh V

88-02 00 'ΐ 8 S • ο-Zll Ί \-\ l i 3 15 Marauder V

 • τ

 υυ ι C T T · P 99 ^ • 0 L 11 V [-an 丄 6JJ n T U

00 Ί 988 Ί U plate 0 8t hidden V

28-02 00 • ϊ 089 -11 689 Ό u mi 93 if 舰 V

00 • ΐ 998 "0 u X VD 9 Thigh V 麵 odf / ェ :) d C9.Z9 / 10 OAV 05Ϊ

if 9ΐ 00 'Ί 289' 6Ζ 6Α6Ό- ・ ΐ 62 Ul V3 801 WO ェ V

A9'9I 00 '398-9610 QZ UL N 901 Thigh V

66'5I 00 'Ί 918'IS 0ΪΓ0- U OU 0 501 Dish V

20-91 00 'Ί Z99OC -z- 309 Ό- U QU 3 m Thigh V

SZ'9I 00 Ί 80 '6 Ζ 191' G OM 00 201 舰 V

9S'9l 00 Ί 863, -91δ-l OU ao ZOl Thigh V

9Γ91 00 'Ί 08'OS 09Γδ-69ΐ-Z OU Ϊ0Ι Thigh V

00 Ί-6Ζ0-Z OU ao 001 WOIV

S6'9I 00 Ί 09 ΐ 6 Ζ 6e s- 582 '1-U OU N 66 hidden V

Of il 00 Ί \% · 90 S90'l- 0 ·-hi 1VA 0 86 隐 V

00 Ί 961 'l- LI 1VA 3 1% thigh V zrw 00 Ί m ^ z 9f l- 98 11 11 1VA 96 隐 V

00 Ί 9 9Ό- 'i- hi 1VA 133 56 隐 V ΐ9ΐ 00 Ί 999 * 9Ζ m-\-LI 1VA 93 ^ 6 Thigh V

LL'Ll 00 Ί L \ 'LI 68f e-11 1VA V3 86 Thigh V Γ6Ϊ 00 Ί 61912% U "8- hi N 16 隐 V

90 * 02 00 Ί 99 ΐ9 886 ト S 'G Thigh 0 06 Thigh V

00 Ί ΐΟΟΆΖ Π \-Wish 0 68 WOIV

00 Ί 969 '92 6S8-3-m8-thigh 88 隐 V

00 Ί 刚 9Ζ 669'8-88n-mi 130 98 Thigh V

00 Ί 920 '9- m

00 Ί Discussion 'S-UC "9-9Z Wish vo 8 Thigh V 7 · 77 uu p

 I Of) 07 p 700 ran T W

 6δδny-96N0

 60

 00 • i III 'OS 609 "S-NSV 0 18 Thigh V

06 00 Ί Γ9Γ9- NSV 3 08 Fragile V

99'9Z 00 • ΐ 8S9-8- 6ors- NSV ring 11 thigh V

C9.Z9 / 10 OAV 19ΐ

 9ΓΠ 00 ■ I hl \ OS ΙΖί · 9 flVl- 18 7VA 0 681 Thigh V

8ΐ · η 00 • ΐ 69Z.IS ε 9 Α80Ί- 18 1VA 3 8CI Thigh V

00 • i 9C6-1S 908 Ί 1C ΊΥΛ Z33 AS! 舰 V

LQ-LI 00I 69 6Z6 'S 399 · ιε 1VA 133 9ST WOIV

00 • I -5 698 Ό IS 1VA 90 9SI Dish V

Μ \ 00 • i 6 90f 0-18 1VA VO ci Thigh V

99 00I 991 '99 0- IS 7VA N woxv

69'9ΐ 00 • I isg-ie 09 ΝΊ3 0 121 舰 V

00 Ί -ι 0Ζ8Ό- OS ΝΊΟ 3 οει Thigh V

00 • I 88 'SZ ^ Ζ'Ζ- OS ΝΊΟ WOIV9Ι 00 • I 099 -ZZ 999' 9 ΖΠ-08 N1D O V

OZ'SI 00 • I LQ \ 'LI 689 OC ΝΊ3 9ZI Thigh V

69-21 00 'I

00 • I 0 01 OS ΜΊ3 images

00 • I S90'6Z 'i-OS ΝΊ9 vo m dish V

00 • I 98 '0 OS ΝΊ3 N 0ΖΪ Dish V εε-9ϊ 00 • ΐ 898 Ί 6Z JL 06 6 Thigh V

00 • i ItS'6Z 06 · 0 8Ζ6Ό U Ml 0 8Π Thigh V

98-91 00I 998-ϊ- ΟΖΟ'Ο- 62 HAX HO 911 Thigh V

WW 00 • I m-\-l Ul ZD 9Π Thigh V

96 'l 00 • I οη · ζ- U l I Thigh V fH 00 • i 62 Ul zao sn Plate V

 • T ΛΤΤ T 7 T T

0 o IUU ί Vo i □ 6 1 ο V U 6UU 1 06 αΛ L a J 6 I Ϊ yvujjV

00 • ΐ 298-0- 9ΐ9 · ΐ 6Z MI ιαο IU Satsu

00 • ΐ S08'l 6Z on plate V

80'SI 00 • I 3ζεΊ- 62 go 601 麵

C9.Z9 / 10 OAV 66ΌΖ 00 • I • ss m '8i Ί-30 woxv

SP6I 00 'I 02971 Ί- 1 ao Thigh V

88ΆΙ 00 • ΐ 8 999 "91 361 'l- L vo on V

18'9Ι 00 • I • 99 98 'Si 06Γ2- ZC HHS N 891 woxv

00 • ΐ zo • L in -n Π0 • I-n NSV 0 A91 O V

6Γ91 00 • I • 92 WW 988 Ί-n NSV 3 991 woxv

S6 "9I 00 ■ \ 119 • 99 099 18S9 • 9- n NSV so-called 291 thigh V f \ -L \ 00 εετ -88 OSS '81 9 g n NSV ιαο Ζ9Ϊ thigh V

8 9Ι 00 • \ 60Ϊ -L 6 8ΖΐΖΐ i- n NSV 191 Thigh V

08 · Ι 00 S6 98 n NSV ao 091 V

00 Ί LL9 • ss 161-£ l 689 'l- n NSV vo 6SI Thigh V

89 00 Ί Z90 ・ ΐ- n NSV N A91 Thigh V

9ε · ΐ 00 in esoI-nai 0 931 Thigh V

00 • \ m-06Z Ί-ss 3 dishes V

00 mz% i66'6 m 'MO n \ thigh V

Ζ9 · ει 00 Ί zu • IS ZLO • 8 ss Wish ιαο 291 Marauder V

IS ^ t 00 • \ m • IS 396 ΌΪ 896 • I nai 00 Plate V

80 '00 Ί L9fZ £ Ι98ΊΙ 168 * 0 191 Thigh V

00 ■ \ • ee m-\\ \ U • 0-ss ilHT vo OSI thigh V so'w 00 • \ -n 6ΖΖ · 0ΐ 186 • 0-22, nai N 舰 V

ΪΓδΐ 00 -n Ζΐ8 · 8 0LI • ΐ- zs 0 Thigh V

00 • \ • gg 68Γ6 09 • ί-3 V o onU 'CT L n unu • T

 L Z08 '1 one' fi 99Z f-700 T

 0 JO WU V

00 • I '1 98Γ8 0SA • 2- n m woxv

00 • I 8ZI • 8 662 • l-Z2, aas V3 zn Thigh V

6Z'tI 00 • ΐ 86Z • n U8'9 2i9 • ΐ1 N m Plate V

C9.Z9 / 10 OAV S9I

 6Γει 00 • ΐ Ι6Γto O SIH 2HN nz o V 9Ζΐ00 'I ΐοε6ζ SlS'Ol L2Z'-Of SIH ΙΏ wz WOIV

9fZl 00 Ί Ζ0 Ό8 · 0Ι 869 · T Of SIH ■ Thigh V

99 I 00, ΐ 080 · 6Ζ 69ΓΖΪ 899S-Ot SIH zao ooz O V

28-81 00 • ι 6g-08 m-\\ 019 '9- Of SIH 661 Marauder V

If fl 00 'ϊ 962 • 9- 0 SIH 33 861 Thigh V

00-91 00 • ΐ t89-Sl • S-O SIH VD V

98 "91 00 Ί isi · εε • 9_ Ot SIH N 961 Thigh V

8 '91 00 • ΐ Z9I '91 OfL 'to 68 Ul 0 ΠΙ 舰 V

Si · ΖΙ 00 • I -π OSO'SI • S- 68 Ul 3 861 舰 V

^ Ζ 00 • ι 126 'ZS 809 · 0Ζ * 2- 69 Ul HO Ϊ6Ϊ Thigh V

00 • ι Ζ9Ζ'6ΐ 68 Ul ZD 061 Thigh V

S8-0Z 00 • ι 9 8ίS A '-6S Ul 68ΐ Thigh V

9S-02 00 • ΐ Ϊ99-Ζ9 000 '8ΐ 68A • S-6S m zao 88ΐ Thigh V

60'ΐΖ 00 • ι 8 · 6 998 6S Ul 133 Bile V

00 • ΐ m-696 '8ΐ S16 • s-6S Ul iao 981 Marauder V 8 '61 00 • I o6-se 220-81 • 9-6C Ul 381 W0IV

68-81 00 • ΐ m n 'ί- 6S Ul aa n \ Thigh V

18 1 00 ooo -ss 918 * 91 196 • 9_ 6S Ul vo plate V

69 * Ζΐ 00 • ΐ 08Z-92 ΐ9Ι • 9-62 l N m Thigh V

09-81 00 • ΐ 0AO 1 86 • ί-8S ΑΊ3 0 081 Marauder V

90 '81 00 • ΐ L • 9-8δ ΑΊ9 3 6it view V πη • τ ι u (τ τη ·; τ 918 '9- op Π3 V3 Qm; T! ■ WDTV

Sg'8I 00 ^ 90 '88 6Lff-8δ no N 9 thigh V

98-6Ϊ 00 0 9-81 9A9 8-0 9il thigh V 9-81 00 SI 'SI 00 • I 909 • 9 208 n ΑΊ3 3 SS2 舰 V -zi 00 • i 820 • i nfz n Π3 V3 舰 V

IVI \ 00 • I 96 ■ i n N I 舰 V

00 • ΐ 8 l · 8Ζ 699 • 6 66'I S ΑΊ3 0 Ml Dish V

69 '21 00 • ΐ-OSl · ΐ Π9 3 osz view V

00 'ΐ' LZ 901 • 6 9 S'0_ s ΑΊ3 V3 6 pan V

06εε 00 • ϊ 6 0l UK0- 8t Π9 N Thigh V

00 • I L ■ 66 · 0 Zf SAO DS 隐 V u- 00 • ϊ 088 • 21 809 Ό SAO ao Bile V

S9'tl 00 Ί 618 * 62 6S6'0i IS! ト Zf SAD 0 隐 V

9 'ΐ 00 • ΐ 292 • n ZS8'0- l \ SAO D m Thigh V

00 • ι 9,8 -i \ 8'0- Zf SAO vo III 贿

86 00 • ΐ • si 99Ί-z SAO Nozzi V

A0'9l 00 * ΐ III • si 1 0-Hen 0 Thigh V

ZA'9I 00 • ι 99rtl Ϊ6ΓΖ- HHd 3 thigh V

89'8ΐ 00 • ΐ m m • 91 m- \ If edition ZD 隐 V

00 • ι m • SI 0 · 0 If zao Thigh V -z \ 00 • ΐ H 'lg 99' SI If Thigh iao 91Z Plate V

8071 00 • ί 868 • 91 If HHd mo m Marauder V

00 • ΐ 8 'OS 6SI '91 fU · 0 It Thigh ιαο m Thigh V

96'Ζΐ 00 • ΐ 6Ϊ9Ί8 881 • 91 6ΐΟ'Ι-I HHd 03 III 隐 V

66'2ΐ 00 ■ \ 29Γ0δ 989 '91 It edition \\ l Marauder V

69 'gi 00, 90 "OR 98 • SI fipn'?,-I edition ntz

 Ϊ9'9Ι 00 • ΐ 6 9 ^ 1 029-C- If N m Plate V

00 Ί 3Z9OS ogSI 1ΖΓ9- SIH 0 L0Z 贿

68'SI 00 Ί 9 6-SIH 3 90Z Thigh V

C9.Z9 / 10 OAV 991

 29 '1 00 • i ζοτ-^ e-160'Π 8 NSV 皿 Plate V

96'6 ΐ 00 Ί 8A8'Sg 9S9-9096 8 NSV V3 m V

86'8t 00 'Ί ζο8ζε 09L • 0-89 6 S NSV Otori V

80-61 00Izsris BS6ΐ-80

6Γ8ΐ 00 • I 9ZS "19 UQ • I-89 6 Lf an 3 m Thigh V fl '61 00 • i 86 V

U'9I 00 • ΐ L f Z III Ί 9ΐΙ · 6 L an 89Z Plate V

28 1 00 • ϊ 8Ζ9 ”62 ^ 99 Ό 38Γ6 Lf an ao A92 Plate V

U'Ll 00 • ι ΐ8 · οε ΠΙ • 0- Lf V3 9 Thigh V

Of 91 00 • ΐ 680-lS 'o Lf aii N Z V 91 00 • ΐ 99ΐ Ό8 6 0-9 nai 0 S Z Plate V

0Γ9Ι 00 • 0 8 9 9t am 3 Awake V

36 'SI 00 • ΐ ίί · η 616 • 0--9t nai KOIV

0Γ9Ϊ 00 ■ ΐ LZ9-H in • ΐ 9 nai 09Z V dffl 00 • I 969 -SS 8Z0 • 0 O O'S 9 V

^ ΖΊΙ 00 • ι 688 • 0 0 9 nai ao Thigh V

00 • ΐ Ί 9 'nm vo in Marauder V

QfH 00 • 99 SOS 826 • 089 * t 9 nai N WOIV

00 Ί -606-6 803 • g SI'9 9 ^ as 0 m PiOIV

Lffl 00 6896Ζ 86 Ί Has 3 m Thigh V

Z9'8I 00 • ϊ ΐ9ΐ · 9Ζ • S 980 ·, 9 30 in dish V aa 'T

 DO V Ϊ n unu • r y ο m 6 9Z0 • S T iO yO

 o V V αα aJ U76

 00 • ΐ m • ε 69T ¾as vo 6 thigh V

8S'SI 00t t 66'δ St Ha N Marauder V

\%-z \ 00 ίί 8Η πΰ 0 9SZ V

C9.Z9 / 10 OAV / no99 /:

 NSVV 3 strokes 囊

Picture V

Picture ¾3

 Concealed V

Picture V

o-oo oo oo oo oo o o o oo c oo σ¾

Picture V

 Concealed V

 Surface V

 V

Picture 围 V picture Α9ΐ

srsi 00 Ί 9 l · 8 Ζ ZOO • u 30 OSS thigh V

90-Ζΐ 00, ΐ 909 · 8Ζ 9Αΐ • 01 U'9 Thigh V

ΖΓδΐ 00 • I • ιι IS9 • 6 Ϊ9Γ9 vo Thigh V

86'S1 00, 1 9Ζ9.8 06f i N Thigh V

Wfl 00 • ι 086 • ιι 998 • 9 8A0-9 ΊΥΛ 0 9ZS Thigh V

83 00, 1 99ΐ · 8Ζ ■ i ss ΊΥΛ 3 Request V

9f 00 • ΐ Ζ66 • ιι ΐδΟΌΐ SB ΊΥΛ z 隐 V

08 9Ι 00 • I 038 9Ζ • 9 '6 S9 1VA m III Fragile V

89 'Si 00 • ι Ζ19 • 188' 8 es 7VA ao m Thigh V

90'9Ι 00 • I 6998Ζ6 • 9 89 1VA V3 Dish V

00 • ϊ m-9U * 9 868 'A S9 ΊΥΛ N 812 隐 V

6 9ΐ 00 • ΐ ηζ in • 9 Ϊ9Γ6 1VA O ΑΪ8 O V 6'Sl 00 • ΐ 190 Ί8 686 * 9 m- 1VA 3 912 Thigh V

93 ^ ΐ 00 • I Ϊ9Ζ • SS m • 9 A69-B 1VA 912 Thigh V

96'8Ι 00 Ί • ιε • 9 66f S ZB 1VA 133 ie Thigh V

10 "3ΐ 00 • ΐ 608 • 28 8A6 • S 69 9 1VA Ώ SIS view V

Ϊ9'9Ι 00 • ΐ 88ΐ '1 881' 9 -i 1VA VO ZIS Marauder V

99 "9ΐ 00 • ΐ 0U '88 168 829 * 8 ΊΥΛ N 018 Thigh V

80'9ΐ 00 'ΐ 99ΐ -S8I 99f8 19 O 602 Thigh V

9 9 ΐ 00 • ΐ 929 • 2S 189 · ε 9A6 * 8 19 3 80S Thigh V

00 • ΐ 58S • 32 • i 9ΖΪ 'SI 19 2H3 AOS Thigh V

9Ζ9ΐ 00I19 SZ3 90S Thigh V bo J

 L ϊ υυ • τ ι ΠΖ • 98 S26 '9 T e * \ TT

 l 77 bub J 丄 V

89 9ΐ 00 • ΐ 99S • 98 Π9 'δ 19 i SOS Thigh V

89-91 00 • ι ηιS8 086 • I 15 ταο zos Plate V

3Γ9Ι 00 9AS • ^ 2 9ZS • 9 98Γ2Ϊ 19 10S Thigh V

C9.Z9 / 10 OAV 891

 00 '■ i · οε 06A '91 901-8S SAD 0 plate V

6, '81 00 'Ί 262 86Z, '91' f 89 SAO 3 zn V

Ζ8'9ΐ 00 Ί 8Z0 -u OiS '91 '89 SAO V3 view V

U'SI 00 Ί 166 • 92 609-91 96Z'S 89 SAO N 6SS Hidden V

SIH 0 89S plate V

8S'Sl 00 '' ΐ 0S8 1Z -L \ S SIH 3 丽 V

Ζ0 · 9Ι 00 Ί IfL '11 SIH zm 99S hidden

69'9ΐ 00 892 • 11 816'SI SIH IHD image

00 • I Ϊ9 '1 8Α8-9Ϊ 806 ·, SIH ιαΝ Plate V

Ϊ2'9Ι 00Ims s SIH ZQd W0IV trsi 00 'I 3ζε% i AS SIH 33 OSS 舰 V

00 ■ \ m'u 96Ζ * 8ΐ Z68'9 SIH S3 m

68 'l 00 • I nz ΟΠ'ίϊ SIH V3 m view V

6T l 00 Ί Ϊ8Α-9Ϊ -L SIH N Thigh V ΐ 00 • ΐ 89Z 'LI' Ll 99 V1V 0 舰 V

90I 00 • ΐ m 09 '91 8 93 V1V 3 m

06 ΐ 00 • I 0 8'9t 6 Οΐ 95 V1V 93 m Hidden

00 • ΐ m OZf 9ΐ 63Γ6 99 V1V VO in 舰 V i6'8l 00 • I 089 il 8S9'8 99 V1V N ots Plate V

82'81 00 • ΐ m -n 8S8'9 S3 V1V 0 6SS Read

62 '21 00I 186-^ z ssrsi 90 S9 V1V 3 882 舰 V

61 · ΐΐ 00 • i ηζ-π 8 rs 99 V1V Ώ LU 舰 V · 7 Τ

 I L no I ZLl q7τ

 to oq □ 00 Ό qe t 00

 89 "ZI 00 • \ 890 999'Π 95 V1V N

00 Ί 990 • u IQS'OI was 0 舰 V

OS'S! 00 • 9Z 9 ^ 9 Όΐ 3 thigh V t no / iodr / iDd 6SI

 00 Ί 60 · 0Ζ m • 9 19 ¾ias 90 968 隐 V

09 '92 00 • I ■ L 3ΐε · 6ΐ m • 9 19 Has VO 968 views V

00, ΐ ΟΟΐ • 98 08Γ6Ι 899 • 19 N 868 woxv ΐΓδ2 00 Ί 69Ζ OS ZZfLl Z96 "9 09 SAT O Z69 Drive V

89 '22 00 'ΐ εοι • ss 006 '81 829' 9 09 SAT O 168 Plate V

6 -SZ 03 • 0 Α06'6ΐ 89ΖΌ- 09 SAT ZN Thigh V

00 • ΐ Simple · 0Ζ 8 · 0 09 sn ao m 舰 V

00, ΐ m '28 896 "8ΐ • I 09 SAT σο 982 Thigh V

S9'9Z 00 • ΐ 0Ζ6 · 8Ι 'I 09 SAT 33 O V

00, ΐ 219 8S8 • ε 09 SAT 93 Thigh V

00 Ί oores' 6i * 9 09 sn VO thigh V

00 • ί W8I '9 09 n N 088 Plate V ΐΖ 00 • ΐ 606 ■ OS 089' 6ΐ • 9 69 Ul 0 Thigh V

SS'IZ 00 • ΐ n Ζ99 · 8ΐ “9 6S Ul 3 thigh V zvn 00 • ΐ 999 • ss S9Z'6l • Οΐ 63 Ul HO 9ze thigh V

00 • I SO 61 189 • 6 69 UL ZD Thigh V

00 • ι • 6 6S UL 隐 V

00 • ΐ 098 • n 980 • 6 69 Ul mo m WOIV

29 'SZ 00 • ΐ oee '89 UZ-QZ 89S • 6 6S Ul ZL Thigh V

00 660gg fLL'Ql SZ6'8 6S Ul tao US Thigh V

0Γ82 00 ΊIS I8ΐ 6ΐ8'8 69 Ul 30 OAS WOIV

9S.IZ 00 Ί • OS m • 8 69 UL 33 699 Thigh V i? * T 7 uu L ou • 08 G 'i T • 9 u M a person I 丄 TVJ one win TW 'LI on • 9 69 MI N 99S thigh V

ΖΓ9Ι 00 • I OZL ■ u 388 'I 8S SAO OS 99S Thigh V

S9'tl 00 • ΐ 82 • 82 S88 'l fU • S 83 SAO ao ^ 92 W0XV

C9.Z9 / 10 ΟΛ 091

 9'9I 00 • I 86 8 LU 99 IVA vo f Thigh V

19 '91 00, 1 9ST8S LLf & 6S8I 99 1VA N LZf 舰 V

9071 00I 866 -9S Ζ68ΌΪ SOO'O ^ 9 ΝΊ30 Thigh V

Ϊ8.99 Ί 929 * 01 60i • 0 ^ 9 ΝΊ33 3 隐 V 61 00 Ί9U 88SO1 996 • ΐ- 9 N1D zm m

00 'I 9 80ΖΌΪ o • ε- 9 ΝΊ9 I H0 m Thigh V

U '\ 00 • I m- \ 98SOI 000 • l- ΝΊ9 ao 舰 V

LL-Ll 00 • I 990 Z8f0l '0_ ΝΊ9 93 m 舰 V

Ζί Ι 00 Ί 986-68 'u gss' o- ΝΊ9 93 隐 V

98 1 00 • I 9ΊΙ 916 • 0 n ΝΊ3 V3 Dish V

96'8I 00 • I 00 8S 806 'ΖΙ 0Z8 • I ΝΊ3 N s Dish V

68'6I 00 • I 8S • e 89 ΗΊΙ 0 Thigh V

ZfOZ 00 Ί 288'81 Z99 'l 89 an 3 sit W01V

Η Ζ 00 608 8 0s 89 311 tao Zl Thigh V

00I IZf 99 ll \ '51 9S0 '29 an m llf Hidden V

00 Ί ill • ε S9 HI I 01 HOIV

00 ■ \ ISf 92 mi \ 908 • g 89 an 33 m 隐 V

00 • I 90919 893 ^ 1 006 'l 29 an V3 m hall V

89 -SZ 00 Ί 699 'SI Αΐ9'9 89 an N f 隐 V

Af 92 00 Ί 880 '68 LLf 0S9 ■ \. Z9 0 so W0IV

80 -S2 00 Ί 650 '68 603-91 98A 'l Z9 □ ΑΊ30 Thigh V

69-92 00I I 8'6S 989 0Z9 '8 Z9 vo sot W0XV nnT 7QT -RQ v 70 M ΪΠ MDTV

00 • I 66S-ZS 6S1 6Ι • 8 19 aas 0 00 舰 V

88 -SZ 00 • Ϊ 90Γ82 8 ^ 8 * 81 8 9 • 19 3 662 Thigh V

09 • 0 A 2'8S i Ζ "9 19 30 Z68 Thigh V

C9.Z9 / 10 ΟΛ 191

 '9ΐ 00' Ί IS "9C 100" 0- fLl ·-69 ΑΊ3 vo S9 plate V

8g9Ι 00 'Ί 16S "9δ 888 Ό 6Z0'C-69 N 19 ^ WO ェ V

89 '91 00 '' ΐ ΙΖΖ S90 'I 609 "8-1,9 nm 0 0917 Thigh V

29 -9ί οο 'Ί 66Ζ' 9S HI 818 'l- L9 o 69 Comfort V

10 '1 00' ■ \ 209 '92 9 丄 · ΐ επ 'I L9 nan 89 Thigh V

00 '' ΐ 6 'ίί ggg "g L, ΐ 丄 9 丄 ^ 舰 V

0 '61 00 'Ί ^ 89 "98 ISS Ί 9Z0' ΐ 丄 9 Thigh 99 W01V

02 'Ζ, ΐ 00, ι 868 "ΐ S • o- Ζ9 nai eo 99 thigh V

98 9 Ι 00 'ΐ 091 "9S 9 9 Ί 6 ^ • ΐ-9 nai V3 Thigh V

19 '91 00 Ί U9 • ΐ- 9 iiai N view V

S9 '91 00 • ΐ 68 'Π 9ZI' 9 9S0 'I-99 9HV 0 W01V

99 '91 00I 60 'S 606-99 3W 3 OS W0XV

61 '9Ι 00, ί 9S0' ΐί 016 • s- 99 9¾V ring in thigh V l \-\ 00 • ΐ III '82 19ΐ Όί 'ί-99 9¾V Request V

9ΐ "91 00 • ΐ 6 S Ot 99 ZD m W0XV

92 -9Ι 00 • ΐ 698 '6 08 08 99 m in W0IV

09 ξ \ 00 * ΐ 180 * 6 'T 99 Otori V

68 'Ζ \ 00 • ι 8L9' Li UZ '8 • ε-99 V

69 'ΖΙ 00 ■ \ 161 * 92 6Ζΐ' L m • e- 99 o¾v go Thigh V

20 * 9ΐ 00 ■ \, 96 '98 99S · 9 U6 'to 99 vo WOIV

Lffl 00 ■ \ 0S9 "9S 932 'L m Ό- 99 N

8S '91 00 Ί 8Z9 '88 9869 AOl059 1VA 0 m W0IV

80 '9ΐ 00 Ί' AS Ί 901 • 0 59 1VA 3 W0XV

00 ΖΪ9-92 86S'8 Z89 • ε S9 1VA 233 舰 V

00 • ΐ 0Z0.9S Z6f 9 10S 'ι 99 Ήλ 103 Ran

00 • ι 0 ^ 9 A9S Ί 99 1VA 93 os WOIV

C9.Z9 / 10 ΟΛ \ 69 'LI 00 · \ C98-8C A09g 9' ΐΐ-11 NSV 3 6 Hidden V

IZ '61 00 \\ 8SCSl 6 '91 -11 NSV Lord I6 KOIV

8 '81 00 ■ \ • 9 'l- u N V ι ο 06 Marauder V

Ζξ Ί \ 00 • I 219 -SS 809 • Z99 1- NSV 68 belly V

£ 0 ΊΙ 00 · \ m Sift I i '21-u NSV ao 88 隐 V

11 · ι0000 \ mi 88S21-NSV A8 MOXV

61 1 00 \\ 688 '2 209 Ίΐ- 11 NSV N Thigh V

0 'LI 00 · \ sn • is 8' 0ΐ— u JSV o 8 WOIV

QZ 'L \ 00 · \ nz • ε 0 9 Όΐ- \ L dSV 3 S8 Thigh V

20 'U 00 · \ 099 * οε 819 ΊΙ- IL JSV ZQO 28 WOJLV

69 'ΟΖ 00 • I m • 6Z Π6 • 0 6 丄 9' Οΐ-M JSV IQO Thigh V

2,6 '61 00 • ΐ 899 • OS • 0 m · \\-\ l dSV m Thigh V

I "81 00 · \ ί \ 0 • 0 929 · 0ί- u dSV go Thigh V 6 · 9ΐ 00 '\ 980 • n 090 Ί 08Γ6- \ l JSV VD L Will f'S '91 00 • ΐ 061 '88 9SZ' l 106 '8-\ L dSV N 9 thigh V

AO 'ί \ 00 · \ 690 2 929-\ S80 · ί-oz .1110 o 9Z WOIV l' 9ΐ 00 • ΐ 990 • 88 501 Ζ Ζ89 'i-01 ma thigh V

9Z · 8Ι 00 • I • 98 • 9 f80 "i- Oi Thigh V

61 '81 00IHQS8 92S8- OZ mo lao Thigh V

86 Ί \ 00 ■ \ 020 · 9ε m '9 LU Ί- OA (D \ l WOXV 6 '91 00 ■ \ • 92 610' 9- OZ Thigh V

89 '9ΐ 00 • I 986 • 82 9l0 "* 9- OZ mo go 69 WOXV

9 '9ΐ 00 Ί m-n i • I ZSZ' 9- OZ vo KOXV ε · 9ΐ 00 • ΐ 80S n OZ N thigh V

00 • ι 69 • 92 • 0 999 '9- 69 kid 0 贿

08 * 91 00 Ί • SS • 0 813-9- 69 ΑΊ3 3 m

£ 9Z.Z9 / 10 OAV S9I

Ζ9ΌΖ 00 'Ί 09'0 CS1 1- 9 1VA V3 9Z9 Hidden V

60 · 0Ζ 00 '' ΐ 06Z'S 880 "CI-9Α 1VA N ^ Thigh V

Ϊ6ΌΖ 00 '' ΐ 60 ZI_ 9L ΊΥΛ O 8ZS WOIV

IS02 00 'ΐ 990'Sl- 9Α 1VA 3 thigh V η · \ ζ 00' '\ 860' AS 2I9'9 80 * 91- 9i 1VA Z33 m Otori V

00 • ΐ 9 ^ 9 '88 9Z9 ^ 688 "91- 9Ζ 1VA 130 V

00 • ΐ 289 '9 90S'9I- 1VA 93 613 Marauder V

00 • ΐ Γ8Γ89 60,9 60i -n- 9i Ήλ V3 819 Thigh V

99'0Ζ 00, ΐ SSO'ZS ιινι ι ^ ・ η- 1VA N 919 隐 V

00Im '-fi NSV O 515 Thigh V

00 • ΐ nrei- NSV 3 fI9 Dish V

08 • 0 Ιδβ'Οΐ NSV Ran Π9 Thigh V

08 • 0 915η 806 8S6 1- NSV mo 019 Thigh V

00 Ί m Ή SZO'II 69 · ε Π NSV 3D 603 隐 V

ΙΖ Ζ 00 • I Z96 * 6 η NSV ao 809 Thigh V

99 ΌΖ 00 • ΐ 9 ^ 8 '38 86 6 in inε π NSV V3 A09 Plate V ΐ9.6 · 00 • I "8 ι NSV N SOS Bottle V 81 00 • ΐ [6 ^ rot- ζι ΗΊΙ 0 Rat V

ΙΓ6Ι 00 • ΐ -n 885 * 8 Ζ66-0Ϊ- ΗΊΙ D 809 舰 V

00 • ΐ 82 01 998 ”6- η 3ΊΙ ιαο 20S Intestine V

9Ζ'6ΐ 00I 290 -ZS Α9Γ6 ΪΖΓ0Ι- η 311 133 103 V

8Γ6ΐ 00 • I 389 902 "8- ζι 3Ή 009 舰 V ηη • τ ι κηρ Q) 1 fH

 00 • ΐ Wl ΐ ^ ΓΟΐ- 1 an vo WOIV

Α0 · 8ΐ 00 • I 9ΙΓ9 6Α0ΐΐΐΐ- L HI I N 96t Thigh V

6ΑΐΑΐ 00 • ι I O'SS 01Γ9 61S'U- U NSV 0 96t WOIV

C9.Z9 / 10 OAV ηι

 99'6ΐ 00 'I 228 "88 S6I ■' ΐ- 916 ト U NSV 0 plate V

9Γ6ΐ 00 'ΐ 0A8 * 6S 9Z0' 'ΐ-0Ζ0.9-9-6A NSV 3 999 舰 V nsz 00' 'ΐ 6Z NSV S99 Dish V

00 'Ί 280 "68 19Γ Lin-6Z MSV ιαο CSS Plate V

L 'Ll 00' Ί OZf 88 09Z Ζ 8Ά-6A NSV 33 199 Thigh V

IffZ 00 'Ί 09Ζ '88 316' '1-59ΐ' ί-NSV 93 099 PiOIV

99 -OZ 00 'Ζΐ Ζΐ9' 6S-2689-QL NSV V3 6 S gall V f0l 00 Ί SO '0 8 6 Ί-gi0 * 8-6Z NSV N S

00 'ΐ 08Z Ί-2If 6-8A Πϋ 0 9 S Thigh V

S '02 00I Sf6 6ε SCfi Ί- ZZZ'6- 8Z ΑΊ3 3 faceoζ 00, ΐ 996 'Of Ll Ί-928-01- L Π9 VD

00 • ΐ n \ 'o— 65ΓΠ- L ΑΊ3 N i thigh V

00 • I 980 * 0t 003 • I 9,6 to 11 mo 0 m Thigh V

26 00I8Z6.6S 90 0-11 mo 3 Drive V

8f 9Z 00 • ΐ 906 'S OSS Ί n ^ z \-11 mo zm 6S9 O V l ^ -ll 00 • t 686-^ ε οεο Ί Ζΐ9-11 mo 1HO 8S9 Thigh V

00 • ΐ “ΐ Α93-8ΐ- 11 1113 ao ASS Plate V

00 • ΐ 910 8 'ΐ 109' SI-LL mo 9S9 K0XV

00 • ΐ wo 89Γ2ΐ- 11 mo ao 9SS Marauder V Ζ Ζ 00 • ΐ US'6S wo 860-Sl- LL mo vo face

00 • ΐ HO 'I OZfZl- LL mo N Hidden V

LfU 00 'ΐ 8 981' 986'SI-9Z 1VA 0 1S3 Akebono T uu ι 196 'I no cn 9Z, 丄 VA J nop T V

Z6'6l 00 • ι Lfl 'f S98g 96ΌΙ-n 1VA ZOO 629 images

02 61 00 'ΐ 899 nS6Ι6ΌΪ-9i ΊΥΛ133 8Z Plate V

0Ζ 00 Ί 990 'Z 833 9Z 1VA ao image

C9.Z9 / 10 OAV 991

 00 • ΐ 936 '62 66Ϊ • 9 889 'thigh V

0Ζ'9ΐ 00 • ΐ S8A • If Ί ζεζ'9- Z ed m m Thigh V

02 "9ΐ 00 ι 0 981 ■ 9 'G Z8 98S Thigh V

86-91 00 'ΐ o z 88S' L ZS6't- Z8 mi ιαο 98S Thigh V

3Γ9ΐ 00 ΐ m '088 • 9 S96'S- Z8 i 93 Thigh V

099 ΐ 00 • ι S60 Z06 • 9 999'Ζ-28 mi Ώ 889 Thigh V

89'9Ι 00 • ΐ 689 'It 6 "9 9SS'l- Z8 thigh vo Z8S thigh V

Α9-9Ι 00 ll ll • \ f 0Z9Z8 N 089 Plate V

8ΓΑΙ 00 699 • 68 6ΪΓΙ- 18 ΝΊ3 O 6ZS 隐 V

86-91 00 969S-\-18 ΝΊ3 3 8Z9 Comfort V

ZL11 00 892 UfQ- 6.0 18 ΝΊ3 9A9 Fragile V

08-02 00 Ί 0Z \ 600 ll-96 Γ0-18 ΝΊ3 ΪΗΟ ^ AB Thigh V ΐ8ΐ 00 \ 0 0 ΐ-60 -18 ΝΊ3 ao 8A9 Dish V

Ζ8 · 9ΐ 00 ■ ι III · ΐ • 0-I9g'I- 18 ΝΊ3 Thigh V

19 * 91 00 Ί 808 O 'ΐ 18- 18 ΝΊ3 U9 Marauder V

9 9 ΐ 00 Ί m 'on' τ 18 ΝΊ3 vo 0 W0IV

9011 00 • ΐ n \, SA6 "I 18 ΝΊ3 N 899 V

86 1 00 • ΐ O '00 • ΐ 069 • t 08 mo O A99 Thigh V

00 • I 009, Ί ト 08 3 99S 舰 V -Li 00 • I 606 '1 926 * 6- 08 ί1 Ί3 zao 399 Thigh V

00 • ί m • 0 829 6 06-08 ιο 130 m MOIV

60'Αΐ 00 • ΐ 90Z • 6S 99 '626 * 8- 08 ao m free c τ 1

 Ό L L τ ϊ π υπ-τ

 ι ι Z6Z * 8S 6 • OLJ rum no 11 丄 J 7QG

 JJ 6i7 JfVUXv

80 * 81 00 Ί • 6S 699 '1 I9f9- 08 ao 19S Thigh V

ΪΓ8Ι 00 Ί S • 6S 6SS • ΐ 569 '9- 08 mo vo 099 Thigh V

8Γ81 00 'ΐ 69A '62 99Ϊ • 0 06f9- 08 N 899 舰 V

C9.Z9 / 10 OAV 991

 09 • 0 SSI6 98 ¾ias 30 619 WOXV

00 Ί O T -if 038 '6 968 · 0ΐ 98 ^ a 93 819 Thigh V fO'ZZ 00 • I 896 "Οΐ ΖΖΟΌΐ 98 ¾as V3 I9 Watch V

00IIII0 W (H 0S6-8 98 N SI9 WOIV

18ΌΖ 00 6 LOZ'Zl 38 V1V 0 I9 Awake V

00 Ί Z09'0 QZZ-Π m'i 98 V1V D ei9 V

A0'6I 00 • \ 59 ^ 88 80Α-Π 699 '9 38 V1V ao Thigh V

9S'6I 00 • ΐ 899 '69 18Γ0Ϊ 98 V1V V3 Π9 Thigh V

Sf 81 00Inot Α08ΌΪ 99f 9 S8 V1V N 609 Thigh V

U'Ll 00 t 98f It '8 f8 HHS 0 809 Thigh V

86'il 00 • ΐ 90S In 3 A09 Thigh V

08 • 0 sot * ΐΐ n 30 909 views V

00.61 00 • I n \ Ί n ao

16 1 00 • ΐ 090 '968 nvo S09 舰 V ei 1 00 • i 8lf 908 * 8 n N 109 隐 V

IVI \ 00 Ί S '8 28 0 009 隐 V

80ΆΪ 00 • I 8 190 · 8 \ L-l S8 an 3 669 plate V

9f -9Ϊ 00 • I Ϊ6Γ Ζ862 920 '2 S8 an ταο 869 PJ0IV

98'9 ΐ 00 'I ΙΜ 862 28 an 193 A69 Thigh V

86 -tl 00 • ΐ ΐ6ΐ 'f 989 "S 28 HI I zo 969 Dish V

88 'SI 00t SSS'S 6f0'g 88 an S6S V

OA * 9I 00 • I \ ηι S8 an vo t69 V n uo y Ti

 00 ■ \ Z98'S IZO'O-8 thighs 0 169 plates V

69'9I 00 8S 8Π9 8ΑΓ0- 1% 3 069 舰 V mi 00 Ί S 9 826 99 169-9-ZS Ώ 683 hidden V

C9.Z9 / 10 OAV Z9I

 Z9 "91 00 • ΐ 2,85 Όδ 69Γ Ι m • SI 06 N C39 Thigh V

89'9l 00 Α6Γ02 ZL ^ -u 9trsi 68 an 0 Z99 Thigh V

88 9ΐ 00 • ΐ 6 'OS 06t • SI 998 • SI 68 ΗΊΙ 3 199 thigh V tO'9I 00 • I 989 • oi' 9ΐ 68 an ταο 0S9 thigh V

SI9ί 00 • i no -n 638 68 an 133 69 WOIV

ΟΟ 'Ι 00 • ΐ m • z \ • 91 68 zoo 89 Thigh V

00 • I 093 'Ζ8 mm 68 an 93 Thigh V

00 • ΐ 9 S zu • 81 vn 68 an V3 m 舰 V

9f 81 00 • ΐ 99ΐ '28 • z \ SA6 -ι \ 68 N m Thigh V

00 691 88 0 m 舰 V 8-61 00 'ΐSI 9 S Ι 88 Has 3 zn Thigh V

86'9Z 00 • I 800 OS m-1 88 "8 88 30 on thigh V to -'ιι 00 • ΐ 86S m-n 001 • 01 88 ao 699 thigh V

66 ΌΖ 00 'ΐ m-n on • si A9Z' Π 88 vo Thigh V

00 • ΐ 06, • u 88 N 929 舰 V

00 • ΐ Z99-9S • n o o • u L SAT 0 Thigh V

00 • ι Α90 · ζε 098 • n • ΐΐ A8 sn 3 thigh V

92 Ί8 00 'ΐ 669 • \\ 999 • L \ Ζ8 SAT ZN 0S9 Thigh V

89 'SS 00 • ΐ 8ΖΓ88 m ■ \\' 9ΐ 1% SAT H3 Thigh V

61 'tS 00 • ΐ 66.8S m · 0ΐ • 91 1% SAT a. 8Z9 舰 V

00 Ί o • ΐΐ 96Γ2Ι 1% sn Thigh V

68 9Ζ 00 ■ ΐ ll ■ n 'SI 1% sn 93 m ■ V

 • τ Q

 AO 06 L V i O 06 A9n)

 'ΐΐ OA 丄 G7Q

 V J 6y nU V u'sz 00 • ΐ 8Zf 68 989 • n 696 • 01 L sn N S29 Thigh V

80 "f 200 • I 69 098 ■ z \ .m • Π 98 0 Drive V

61 'SZ 00 • ΐ S16-\\ 0ΐ 98 ¾a 3 dishes V

C9.Z9 / 10 OAV 891

 90'8I 00 '' ΐ 0ΖΓ9Ι 5Ϊ2-6Ϊ 86 Has ao m thigh V 0.8Ι 00 '' ΐ 929-I 86f 81 S6 vo 889 thigh V

86 9ΐ 00 '' ΐ 8 '91 819-81 S6 N 189 Thigh V

6 -SI 00 'Γ8ί '61 26 O 0 089 WOIV

Ζ9 "9ΐ 00 'z ^ z Z6 OU 3 6A9 picture

6Γ91 00 'Ί -hi 866-61 26 OU 03 8A9 WOIV

00 'Ί ε0ε'9Ι Z6 OU ao 9 Thigh V r9i 00' 'ΐ i, 99 "9Z 88 9Ϊ 9Z8'8I Z6 OU 92,9

Οΐ 9ΐ 00 ', ΐ o'Lz 662 06A'8t OU ao 9Z9 Thigh V

98'SI 00 '8Z0.8I Z6 OU N thigh V gO'91 00 910 A6S'9t l \\ 9ί 16 SIH 0 screen ΐΓ9ΐ 00, ΐ 995 * 9ΐ 0SA'9l 16 SIH 3 W0IV

96 · 08 00 08S'8Z \ Π Ι 16 SIH zm 0A9 PJOIV ΐ9'91 00 16 SIH 699 Thigh V

00, ΐ SU'Zl 16 SIH A99 Thigh V

99 -9ΐ 00 "I 0VU S68'n 16 SIH zao 999

10'St 00 'ΐ ΟίΖ Ζ' 9i 16 SIH S99 Thigh V

00 -fi 00 • I miz ΙΖί-ξΙ 6S 'Si 16 SIH 99 thigh V SI 00 • I 988 "9Z 986" Sl 16 SIH vo 899

T8'St 00 061 Z Ι16 SIH N 199 Thigh V

Z6'9l 00 • ΐ 896 -8Z 8Αΐ '9ΐ 06 1VA 0 099 Thigh V

^ • 91 00 • ΐ 6ΐ6 • I 198 'l 06 1VA D 6S9 Thigh V 7 Ί1 ηη • τ QGQ -R7 Τ Q -Q Til J QCQ

 6Ϊ '9ΐ 00' ΐ IQL'LZ -Li S60 * S1 06 1VA Ϊ30 9 舰 V

St 'Ζΐ 00 901 '62 263 -91 OZO'Sl 06 1VA 3D 939 W0IV

9C * 9l 00I S61 'QZ 89' SI 06 1VA VO 999 images zio / iodr / iDd C9.19 / T0 OAV 69Ϊ

 99 1 00 • ΐ 9SA • SZ 892 Όΐ 96 Has ao III Thigh V

HI 00 • ΐ 189 '1 ZOSOT 96 vo 9U Thigh V

LI '1 00, ΐ -u \\ l' 1 ΐΟδ'ΙΙ 96 N ni free ΐ6'ΐΖ 00 Ί ΙΖ6-6Ι m • oz LWU 96 NSV 0 thigh V

68ΊΖ 00 Ί 09'0Ζ 991 • \% S6 NSV 3 ZIL Ran

Z 'U 00 • ΐ 999 · 8Ι 681 ■ u S6 NSV Orchid 60Z Thigh V 8 · οε 00 • ΐ 96 '11 56 NSV ιαο 80Z

00 Ί 89-81 S6 NSV LQL like f 'U 00 • I Z T6l z ■ \ z m l 36 NSV ao L

6f ΐΖ 00 • ΐ 698 • QZ 08Γ2Ϊ 96 NSV vo 30A

L -0Z 00 Ί 860 Ζ '6 ΐ Si6 "SI 96 MSV N Thigh V

69 * 0Ζ 00 ■ ΐ m • OZ 08Γ9Ϊ Π I 0 m Thigh V

66'6Ϊ 00I m-u ASS '61 SI9 'I Π m 3 m Thigh V

90 · 0 00 • ΐ 998 • 61 Π m HO 669 Thigh V

9Γ6Ι 00 * Ι 9Z8 '61 06Γ6 n MX ZD 869 贿

8 ^ 81 00 'ΐ 982 * 81 n l m

0S'8I 00 'ΐ ILL' 1 ΖΙ8 Ϊ oos'n n MX m 969 Hidden V ΐ6'8ΐ 00 'ΐ m-n 008 • 61 909-01 n Ul 969 Thigh V

09 · 8Ι 00 'Inz' 6ΐ Ζ88'ΐΐ n Ul ιαο Thigh V

Of 21 00 • ι I6Z'g2 09Γ8Ι n MX 33 S69 Thigh V

08 · 00 Ί Z96'8Z UL -LI n I 3D Z69 Optional ΐΖ'61 00 'ΐ IS6 L \ 60Γ ΐ n Ul V3 169 舰 V υυ ί yU6 939' Ζΐ MIT MIT

 People 丄 N

 6Γ6Ι 00 • I on • 81 S88-9l S6 Fox 0 889 plate V

69-81 00 Ί 'zz' LI 980 1 S6 3 89 Thigh V

ZfOZ 00 L9L9t 189 -QZ S6 Has 30 S89 W0IV

C9.Z9 / 10 OAV ΐ6ΐ 00 I 282 · 81 6A0 "9I 18S * 01 66 Thigh 0 0SA

9f 61 00 ΐ 60 ΐ8 ΐ 09 ΓΑΪ 01 66 3 6 K0IV

80 00 ΐ SOt'OZ 8 O'6I 66S 66 Thigh WOXV α ζ 00 I Ϊ99'8Ι 9Z8'9 66 Thigh ιαο in Marauder V

00 ΐ Ζ688Ι 986 '8ΐ lU'L 66 33 9H 隐 V

Οΐ Ζ 00 ΐ 96 Γ 8 Ϊ 690 "81 66 Thigh 93 Thigh V

00 ΐ 8 Ι 66 Thigh V3 Thigh V

00 I 689 'ΖΙ Αΐ9 * 6ΐ 891 '01 66 Thigh N Thigh V

00 ΐ 696 "81 86 mi 0 thigh V

ZflZ 00 I 8i, S'9I 9 '6I 86 dishes 0 OH 隐 V π' ι 00 I 090 ZS9 ΐ 86 wish 233 68Z thigh V

00 'ΐ ΐ9ΐ 86 mi IDO LU V

W \ l 00 • ΐ 6IZ'SI 86 dishes aom view V u-% i 00 • ΐ ZLQ'U 9.0 · 86 dishes V3 舰 V

00 • ΐ 198 '91 nvzz 86 mi N Drive V

00 Ί 08 ΐ '9 Ι Oil Z68'8 1% NSV 0 in 隐 V

89 * 82 00ΐΐ 6Ζ6-91 180 · ε U8'6 1 NSV 3 m PiOIV

90'9Z 09 • 0 8.8ΐ LQ NSV Ran u bile V η Ζ 05 • 0 6 8.8 · 686 -9Z S9Z-01 6 NSV mo in bile V

L ^ -H 05 • 0 '8I ιη ^ ι A6 NSV V

OS '00 • ΐ Z fLl 6Ϊ0ΊΪ A6 NSV 93 隐 V

98'8Z 00 • ΐ 900-81 \ w 360-01 Z6 NSV V3 UL Thigh V

 • τ

 uu 7 ΤΑΤΠ T V

L ¾7 * C completed POP '0

 676 0 I o 66 πτ, η * n end 1 c

 LO N v N

 00 · z 00ΐ 66'ZZ 96 0 UL Thigh V

\ vu 00 • ϊ U \ · 0Ζ 690 · εζ 96 3 07,1 plate V

^ -n OS • 0 96 30 8U dish V

Meng odf / iDd C9.Z9 / T0 OAV 16 'l 00 • ΐ m • Yl Z99 • ΐΐ 2S0 Ι δθΐ an vo m Thigh V

69 00 • I ■ i · ζ \ ISO ■ \\ S01 ΗΊΙ N m Plate V

Iftl 00 'I 06Ζ • uu \ Ί \ I0S • 6 ΖΟΐ JSV 0 m Thigh V ΐ 00 • ΐ' 1 896 • Ζΐ 991 • 01

dSV 3 08A Thigh V

0 SI 00 '1 \ l91 fSt8 ZQI dSV zao Ul woxv

00 ΙΗ ■ \ i Ul '9ΐ 818 • 9 ΖΟΐ JSV mo Thigh V

19 'l 00 Ζ 880 • 91 S96-1 201 d V III Thigh V

00 • ΐ 168 • QZ tI9 'l ΪΖΪ • 6 ΖΟΐ dSV ao Thigh V

99 00 • I ZQL Ζ m-n 9S • 01 ΖΟΐ dSV vo Thigh V

00 • ΐ m • OZ 9ZS • ΐΐ ζοι dSV N Ul 舰 V

00 • I 06 • u Ζ99 · I U6 Ι ΙΟΐ NSV 0 III W0IV

09 'SI 00, ΐ 6oe' \ l £ 91 • Ζΐ ΐθΐ NSV 3 ILL Thigh V

ZO'Sl 00 • ΐ • 61 · 8ΐ 9Ζ9 • 91 101 NSV Ran U Parent V

19 * 61 00 • 61 919 '9ΐ 016 • 91 ΐθΐ NSV mo m 舰 V

Ζ6'9ΐ 00 • ΐ \ n • 61 98 ^ 1 sts9ΐ ΐθΐ MSV m Thigh V

9Ζ9ΐ 00 • ΐ 0Z8 • OZ 6U ”l m • 91 101 NSV ao 99A Thigh V

0Γ9ΐ 00 'ΐ • OZ 66ΐ · ετ ΙΟΐ NSV vo thigh V 91 00 • ΐ 900 • 61 8 · SI' SI ΐθΐ NSV N in thigh V

Π 'LI 00 • ι • 61 Ζΐ6 · 9ΐ' SI ΟΟΐ NSV 0 Thigh V

WLl 00 • ι Αΐΐ · 9ΐ 001 NSV 0 09A 舰 V

WU 00 • ΐ εοι • 91 ι · 9ΐ SOS · 9ΐ ΟΟΐ NSV 舰 V

90 ΌΖ 00 • ΐ 988 • 91 • 91 001 NSV ταο m WOIV

C T * C T • τ

01 0 I υυ L • 91 • 91 · 9ΐ ππ τ N v JJ TATHJ 丄 Ty V

L \ '8ΐ 00 Ί • 91 ιιζ Ί \ 980 001 NSV 腿 thigh V

00 Ί 69 • i \ 9Ζ9 · 9ΐ -ζι 001 NSV VO WOIV 8'8l 00 • ί S89 -LI 989 11 • II ΟΟΐ NSV N KOXV

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 Painting SI Garden V

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ϊν SS '1 08' Ό 90g'9 S09 '6 I' L 601 sn CD 9t8 Dish V

SO '02 00 'ΐ 0 8 990-8 601 SAT 8 dishes V

9A'61 00 '' I -n Ι9Γ8 1697 601 sn ao ε 8 Thigh V

61 00 '' ΐ 99fS 6ZS8 601 SAT vo V

68.81 00 'Ί 8Z0 "Z mί 690' 8 60ΐ SAT N 0,8 Thigh V 81 00 'Ί-\ f 168" 9 08-6 80ΐ nai 0 628

11 '81 00 "ΐ 9L \ '69f 9 06Γ8 80ΐ nai 3 898 Thigh V

96 '81 00S90'9 6tA'9 80ΐ nm zao Z98 Thigh V

00 • ΐ Ζ9Γ88 909 * 2 S16-S 80ΐ am mo 928 plate V η · ι 00 00ΐ6 8S Ζ89'9 80ΐ nai 33 SS8 丽 V

00 Ί 909-68 09Γ5 m't 801 nai 93 88 bile V

9Γ8ΐ 00 • ΐ Ζ9Γ68 Slf 9 0Ϊ 8 Xie nai VO SS8 Thigh V

08 ΐ 00 Ί ZS `` 88 99 6 801 N 188 W0IV

Α9 · 9Ι 00 Ί969 * 8 L01 SAT 0 0S8 Thigh V

ΟΟΆΐ 00 • ΐ SO '8S 9097 9ΐ8.6 LQ \ SAT 3 628

6ΐ 'ίΐ 00 nz- \ 289' SI Z0I SAT ZN 8 thigh V π · η 00 Ί 6Z9 "S 9Η Z0I SAT ao 8 thigh V

00 • ΐ S89-6S Z68'9 966 -9ΐ L0 \ SAT αο

 7, '81 00 'ΐ 918 -8e 109' 9 OZfZl LQ \ sn m Plate V

6 · 9Ι 00 • ι 866 · ζε LOl SAT m W0XV

9Α'91 00 'ΐ 9' L ΙΖ6Ό1 L01 SAT vo 0Z8 Thigh V

01 · 9Ι 00 ■ ΐ πε · 98 619'Οΐ LOl SAT N 818 Thigh V

 68'gi 00 'ΐ 961' SS ΐ9ΐ8 666-6 90Ϊ 3 918 W0XV

05 -Ql 00 • ΐ 999 "01 612'9 901 an ιαο 918 Thigh V

S0-8I 00 uroi 1 LL 901 an too l8 ίϊθΐν mio / iodf / i3d £ 9LZ9 / 1 O Ι8 · Ζ 00 I C6S'68 9Π 'g ml sn as 0 088 Dish V

00 I 90 '' l Sll ¾as 3 6A8 Dish V

09 Ό 6 'C-8εll 30 thigh V

00 ΐ 68 096 Ί επ ao 舰 V

08 "SZ 00 ΐ zn- \ 896 -g- 886 'l sn ¾as VD Thigh V

00 'ΐ m- \ m m plate V

8f ΪΖ 00 ΐ 9εΓ62 S8Z'0- 890 "zu V1V ao m Thigh V

Wll 00 Ί S9S'0 8A9-0- l \\ V1V V3 698 O V

IVM 00 ■ I 6ΖΓ0- • s zu V1V N Thigh V

OfZZ 00 • ΐ 886 SSO'O-999 • s in V1V 0 998 Thigh V

60 ^ 00 • ΐ • 9 in V1V 3 398 won

91 0Ζ 00 • ΐ -zf 9iro- • 8 Πΐ V1V ao m V

09 Ί 00 00 ΐ 90 'S9K0 Πΐ V1V V3 S98 Plate V

00 • I Uf \ Πΐ V1V N 198 KOXV

ΖΖ Ζ 00 • ί • 9 on HHS 0 098 Thigh V

OfU 00 • ΐ nrz 6SS • L on 3 6S8 Plate V

AS'8I OS • 0 OS! 'St 809 · £ 109 • on 30 Z98 V

LI -0Z 00 • ΐ m • 9 on Has ao 998 WOXV

9ΖΌΖ 00 • I 069 -g • L on vo 398 KOXV

00 • ί 98 '^ • L on N 298 Thigh V

Li, U6 uu • τ

 ι one I p np m6 bU I C T T u 7 p 0 Τ yΑVΤΠUl τ yv

90 ΌΖ 00 'ΐ 88'9 • 8 601 sn 3 198 KOIV 9 Z 00 • 0' 8 8Z9-0I • 9 601 s m m κοχν

09 • 0 09Γ6 • i 601 n Ώ m

C9.Z9 / 10 O Fiber 7 Ϊ0Κ concealed V os side V.

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 S • 61 00 • ΐ 0 0.9m an N 86 舰 V u • ΟΖ 00 • ΐ • 62 I0 * 9- OZl 0 Zf6 Thigh V

11 • QZ 00 • ΐ • 6Z 6ΐ9'3 QZl Has 3 9 6 舰 V L '11 00 • ΐ im 'IS 6U' to 89f Z 0Z \ 30 ^ 6 Thigh V

08 • 61 00 • ι 169 Ί8 lo 'ε- 086 "9 ΟΖΐ H3 9 6 WOIV

90 • ΟΖ 00 • ΐ 80 2 6iS'9 0Z \ V3 6 Thigh V

06 • 61 00 'ΐ 188 • \ i 9or 0ΖΪ Has N 0t6 隐 V

SI • ΟΖ 00 * ΐ 8 ^ • is 6θο'ε_ 868 'Z 6Π V1V 0 626 隐 V oe -QZ 00 • ΐ ZZQ' 1 86'S- 's 6Π V1V 3 826 Thigh V

11 • 61 00 • ΐ SSO oer9- 6A1 'I 6Π V1V Ώ S6 KOIV n -QZ 00 • I 398 -gg 916 · 99S 611 V1V V3 9S6 O V

98 Ζ 00 • I ■ m ト 998-ΐ 6Π V1V M 86 hall V

89 '00' ί 6ZSSS 'S-LLfl 811 0 286 隐 V

09 '1 00 899 * S 6-668 Ό 8 Π 1VA 3 6 Thigh V

80 • 61 00 • ΐ '98 owz- ^ 9 · ΐ-8Π 1VA 186 Thigh V

90 · 0Ζ 00 • ΐ • 98 1S8 "0 8Π 1VA 133 0S6 views V

86 · 0Ζ 00 • ι 69Z • 9S 696 ”Z-8lt ΊΥΛ 93 6Z6 Plate V

Π '100' ί 616 '2 89' S-s6ro- 811 1VA V3 8Z6 Thigh V

0 00 'ΐ 106 * 8 999 ト ・ ΐ-8ΐ 1VA N 9Z6 Thigh V

10 • η 00 • ΐ 8Ϊ6-LU 9W 0 926 Thigh V

16 00 • I

8Cf t- LU m 3 Z6 隐 V

18 • 6 00 • 0 102 890-6- ^ 19 "6- ill ΪΖ ΪΖ6 thigh V

, 9 • 6 υυ 909 909 · p 07 · I

 & 6 mm JL V b-L 1 Y I nvru I UN 0 δ T l cb ΤΑ1Π TU

Ζ9 · Ζ 09 • 0 161-8Z -8-9S1 · 8- LU m Z3 Zt6 隐 V ίθ · 9Ζ 09 • 0 III '98 6861 flfi- LU 916 Thigh V

11 Ζ 09 • 0 809 • 92 ZZ6'9- SSf9- LU m ao Thigh V 麵 odf / ェ :) d C9.Z9 / 10 ΟΛ \ LL \

 LI ΊΙ 00 9S8 • 61 m U \ 33 8 6 PiOXV

^ ll 00 • I EST • 61 99 -Ϊ- 9A0 • n Ul ou ao OXV

86 ^ 2 00 • I 191 ■ oz 69 ^ ■ i \ Ul V3 9 6 Thigh V

60 ^ 2 00 • ΐ 66Z Ζ zoro- 100 -i \ Ul ed ao 96 V o V VH 00 • ΐ 61 ΊΖ 981 1-160 ■ n Ul ou N 6 Band V

Ζ0 Ζ 00 • I 999 '1 66'ε- 0Z9 • n Ul iiai 0 plate V

00 • is' 1887-0ΪΖ • ZI nai a V

00 • ΐ t90 • 92 6S8.0 868 • \\ ZI nm zao U6 Thigh V

00 • i S2S • 92 t O'O St6 • SI nai iao 0Z6 View V

00 • I 619 692 * 0- m Ι nai 696 thigh V

U ^ Z 00 • i OS Ή-\-096 · Π m nai ao 896 Marauder V

00 Ί ΖίΟ'Ζ- m • U nai V3 96 dishes V

00 • ΐ • u nm N 996 plate V

0 0Ζ 00 • i III • i on • 6 m 0 96 舰 V

98 '02 00I 0986 m3 S96 Bile V

OS0 99A SS8'9- Ul • 6 m Has 30 196 Marauder V f 6ΐ 00 • I 996 'Z • 6 m 90 096 Dish V

00 • I 829 "9Z G • 6 m V3 696 V

IS '61 00 Ί LZQ ιιν-886 Ί u \ N 6 plate V

85'6I 00 • I -LZ AS9'Z- '8 Ml an 0 9S6 Marauder V

8Κ6Ϊ 00 • I 6 6 • 9Z Π9- Ul an 3 396 Thigh V

00 • I 999 'Z 9 Ul mi iao

Q yQ * QT TAIATU o o i 00 Ί εοο • 9Z 6GC * 76- 102 '9 T7 T

 L 6 I U L JJ yvujj V

00 • I Ζ C06 • S m anz Plate V

Z8'8l 00 • ΐ • 9Z UZ'Z- 2SS • 9 u \ HI I 196 贿

6Γ6Ϊ 00 • I gig • ii SSI • 9 an vo 0S6 HOXV

C9.Z9 / 10 OAV L \

 00 '' I 0690ΐ29ΐ0 SOf 01 V1V 0 Οΐθΐ Thigh V

99-9Z 00 '' ΐ 3ΐ6Όΐ U6O- • 6 V1V 3 6001 WOIV

00 '' ΐ 900 '8ΐ η-\-• 8 m V1V ao 8001 Thigh V

00 'Ί 029ΐ-Z96 • 6 V1V vo 腿 Thigh V

9 9Z 00, ΐ ssrsi 'o- 266 • 01 V1V N 5001 Thigh V

00 '996'εΐ 869' ΐ S9I • 91 m SAO OS Rinse I Thigh V ι \ -u 00 6S0-8I Ι 'Ο 816 • ει SAO ao SOOI WOXV or z 00 η \ · ι- on SAO 0 2001 隐 V

00 刚 · • 21 SAO 3 皿 Plate V

00 098'21 66 ^ 0- zSI SAO vo ΟΟΟΐ

00 • I 60f ΐ- SAON 866 V V onz 00 • ΐ 6'SI 2-2-990 • ει LZl ¾as 0 A66 舰 V

09 2 00 Z6Z'9I in ¾as 0 966 Thigh V

8S.S 00 • ΐ 991 ΊΙ LZl s 30 66 Thigh V

Π 00 \ nSI LZl ¾ias ao 866 舰 V

98 · 8Ζ 00 • I Ζ \ "2- nz • 91 LZl vo 266 hidden V

0Γ6Ζ 00I 9 6 '91 88Γ2-9809 · L N 066 Bile V

LfU 00 • ΐ O 9'Zl 8,8-Plate 0 686 Thigh V

LZ-Q 00I U'l \ Ζ80Ζ-090 · 9 Thigh 3 886 Thigh V

ZS'tS 00 • ΐ m · 9- Π8 • SI plate Α86 plate V

80 '9S 00ΐΐ9 · 8Ι8 · 9-919 ^ 1 plate 0 S86 隐 V

OS'SS 00 'ΐ \ 9-' SI 921 mi WOXV nn • ΐ RQQ¾-669 -9-9 C, Tran TV l \ 8Ζ00 I 992 * 61 zsrt-own MI N 186 WOXV

00 Ί 299 · 0Ζ SOS'Z- U \ OM 0 086 Dish V

00 'ΐ 90Ό2 £ 6 • εΐ n \ OU 0 6 6 Thigh V

C9.Z9 / 10 OAV 6AI

 81 'SZ OA' Ό 601 • 01 998 • s-160 Ί- 981 ΝΊ3 03 S 舰 V u · εζ 00 '' ΐ 66t Ίΐ LU 109 • 0- SSI ΝΊ3 9D Thigh V

00 Ί Ζ89 ΐ ISI 'l-• 0 SSI ΝΊ3 vo \ n \ 舰 V

00 '800 • ίΐ 191 • s-m • ΐ 981 ΝΊ3 N 6201 Thigh V η ΊΖ 00, ΐ 869 · 0ΐ 090 • I-' I n \ Thigh 0 8801 View V

Ιί Ζ 00 • I 889 • Οΐ 69Ζ '-' I m dish 3 thigh V ^ · η 00, ΐ SSI Ί \ 96t • ε-910 • S m thigh 9S0I

9Ζ'9Ζ 00 ΟΟΖ "01 Ζ9Ι • ε-66S • 9 wish 130 no \ thigh V

86'8Ζ 00 'ί 998 • Οί 989' ι-OU • 9 m mi 93 Job V

Οΐ '11 00 06'6 l £ 8 'ι- ειο m mi V3 隐 V

\\ '11 00 • ΐ 9'8 in ·%-ni thigh N οεοι comfort V wn 00 • I WL 186 • z-• I 881 no 0 6Z0I thigh V

00 • I m 'l-m • g 3 8Ζ0Ϊ Thigh V

\ fZZ 00 • ί • 9 ■ ΐ-69S "S eei VO LZ01 Thigh V

00 Ί • 0- εει πϋ N Thigh V

06εζ 00 Ί 606 '9 ■ ΐ-m • 9 z V1V 0 UQ \ N0XV

89 * 22 00 Ί m • 9 • ο-"9 V1V 3 8Ζ0Ϊ Marauder V

SI ΊΙ 00 • ι '9 III • ΐ z V1V ao ΖΖ0Ϊ Thigh V

U ^ l 00 Ί • 9 919 • 0 m • 9 V1V V3 1201 Pan V

^ ΊΖ 00 • ΐ ΠΟ 'ειο • ο-A90 "8 Z \ V1V N 6Ι0Ϊ Thigh V

SI · 9Ζ 00 • ι m • 8 Z86 • ο-lot • i OSI ms 0 8101 Plate V

6Γ9Ζ 00 • ι 2ΖΓ8 n • 0-Ul • 8 OS! Has 3 ZI0I Thigh V

 0 618 • 6 no T λτ ο 0

 05 -0 ■ L bob JU

 86 'fZ 00' ΐ m '1-900 ΌΙ OSI 93 thigh V

99 '9Z 00 • I • 8 m-G 6Z • 6 οει VO ειοΐ 舰 V

6 9Ζ 00 • ΐ 886 • 6 m • I-6 • 6 N UOI Thigh V

C9.19 / T0 ΟΛ \ OS!

 S9'9I 00 • ι 8 ΐ · 0Ζ 82 2 Ζ3Ζ • s- 8δϊ 3Ή 3 oi Thigh V ΐθ'61 00 Ί Ζ08 "9ΐ Γ IS! Ί- 8SI an ιαο SiOl Thigh Ver i 00 • I 290 SZO · ΐ_ 8SI an ZLQl

9Γ9Ι 00 • ΐ 9Ζ8 "8Ι 199 · 5 ^ 18 • I-8S1 UOl 舰 V

ΖΟ ΐ 00 • ΐ Γ8Ι ΖΖΖ 6A0 • l- ΗΊΙ OZOl Marauder V

29'9I 00 • ϊ L \ 6Ι 880-8 S80i-88Ϊ an vo 6901

699ΐ 00, ΐ AS9'8I m- \ 'l- 8S1 an N 901 舰 V C-SI 00 • ι 9 '61 0Ζ6Ό • 0_ LU Π3Ί 0 9901 Dish V 9ΐ 00 Π800 ΐ- Ζ9ΐ Thigh 3 9901 隐 V

8S-6I 00 Ί 89 ^ 61 S08O--L 1 ίΙΗΊ mi Dish V

88 Ό2 00 Ί 6Αΐ-\ 1 821 • g- ίξ \ nai ταο 8901 Thigh V

86'6ΐ 00 • ΐ 8Ζ9'6ΐ ίξ \ nai 33 2901 Thigh V

00 Ί Η0'61 6 • Ϊ- L 1 nai 93 Ϊ90Ϊ W01V

6ΓΑΪ 00 'ΐ ΖΐΟ'δΐ oiro- 629 • ΐ-nm V3 0901 Thigh V

90 · 8ΐ 00 Ί η \ · ι \ 06, • 0- L M 8301 Plate V

8 6Ι 00 Ί 9SI SAD 3S £ 901 Thigh V

99'8ΐ 00 80 9Ϊ 680 Ό ΪΟΑ 'I 9SI SAO ao 990Ϊ 隐 V 9'8l 00 • I 95 • ΐ- 9S1 SA3 0 990Ϊ View V

09'8Ι 00 Ί 998 * 9ΐ m · ο- 099 • 0- 981 SAO 3 \ Plate V

Π -61 00 Ί ΟΖΐ 'SI ISI Ί-9SA • 0 921 SAO V3 SSOI WOIV

11 -οζ 00 6U'Sl 86f 0 981 SAD M tsoi Thigh V

08 '02 00I 26Γ8Ϊ 6 S-909ΐΐ 98ΐ 03 0 0501 隐 V

7 υ00-(U] 70 00 • ΐ G L 6Z6 • 0 GOT

 .1 ο ι 1 \ 丄 iJ Tsu WO TV

OA • 0-826 • ΐ- 98ΐ zm \ plate V οζ • 0 C9f 801 801-2QL · ι_ ΝΊ3 130 plate V ζε · 92 Ο Ό 9Ζ9'6 ίΙί'Ζ- U6 ■ \-Ί3 ί plate V

C9.Z9 / 10 OAV I8t

 82 00 • ΐ ΑΊ3 N 90Π Marauder V

ZO 00 • ΐ ΙΖ \ · 9Ζ-\\ 983 "8- mm 0 ton thigh V

88 '9ΐ 00 • I 669' 9Ζ OS'Ol -i- \ n 3 son 舰 V

99 • 91 00 390'9 \ n ZHO ZOU thigh V L • 91 00 • im ^ z 99Γ9 \ n SZ3 I0II thigh V

18 • 91 00 • ΐ 816 619-9- \ n ΖΏ 00Π Plate V

81 • 91 00 • I 8Ζ9 * 6Ζ ni--in \ m 8601 thigh V

10 • 91 00 -u 961 'I 600-6- \ n in iao A60I Thigh V

86 • n 00 • ΐ -L 833 9601 Thigh V

LQ • 91 00 Ί m ^ z Z06-9 m-i- m 9601 Satsu

96 • 91 00 ■ ΐ UO'L zao ^ 601 隐 V

98 'l 00 Ί m'L \ n 2601 Driving V ZSI00 • ΐ fLZ LlfL- \ v \ ao 2601

66 • 91 00 • I ηι · η 896 '8 \ n mi vo Ϊ60Ϊ thigh V

16 • 91 00 • ΐ · 8 in N 6801 ■ V

OS91 00 Ί 0t8'9 m-i-Of l Π9 0 8801 Dish V

U "91 00 • ΐ l -h Ϊ8 9- 0 ΑΊ ΑΊ3 3 i Thigh V

86 • 91 00-6A0-9- o i kid vo 9801 Thigh V

90 · 9ΐ 00 • I A69'S Otl AID N noi Marauder V

A9 '91 00 • ΐ 902 -sz 998'Z- m ¾as 0 S80I ro v

U • si 00 • ΐ LLV Z Α9Γ9 Z 6'8- 3 Ζ80Ϊ

38 • 91 00 • I 8 Z 621 DO 0801 Thigh V

LI • 1 n unu • τ L Π07 '07 oLv v J

 36 • 91 00 Ί 968 -S 90 · 681 Request V3 8Z0I

88 • 91 00 ^ Κ Ζ 6S1 N 9Α0Ϊ W0XV

Z6 • 91 00 Ζ6Γ6Ϊ i- 82Ϊ 3Ή 0 9A0I

C9.Z9 / 10 OAV Z 1

 8'ie 00 • ΐ 862 • 91 080 '91 6SZ '-9 ^ ΐ SAT 3 Itll Thigh V

Z9'8 00 • 0 168 '81 91 3Ζ6 * 8ΐ- 9 l SAT ZM i Thigh V

00 0 ZLZ- 1 92S'8l- S l SAT ao 98Π MOIV

98 · 9Ζ 09 • 0 Ζ 6 · 8Ι m • 91 99 Γ 9 Ι- 9 ^ 1 sn ao 92 匪 Marauder V n -ii 09 • 0 091 • 81 8S9 "91-9 l sn 33 nu plate V

8f 82 00 • I ι · ι \ • SI 9 ^ 1 SAT 93 mi Thigh V

80 'OS 00I -ι \ -f \ gzz'si- 9 ^ 1 SAT V3 Thigh V

06'Z 00 • ΐ8Ι 219-81 899 "Z1- SAT Nosu Thigh V

I0'92 00 • ΐ 9Ζ9 · ι \ 819 • n 08Γ21- n \ Thigh 0 m \ Thigh V

L \ '92 00 • I OZf 8ΐ ηζ Z fZl- n \ Wish 3 thigh V

6Z'SZ 00 • ΐ 612 ΊΖ • 6 609'Ζΐ- i Thigh V

Zf9Z 00 • ΐ 0S8OZ 00 • um thigh TOO thigh V

69 'Z 00I 919-01 i8iεε-n \ Wish 93 HU W0IV

00 • ΐ 19 • 61 ΊΙ OI \-n \ Plate V3 Thigh V

00 • I • ΟΖ • 21 S8S'U- n \ Clothes N uu Thigh V

00 Ί 866 '6ΐ • 6S' 6- NSV 0 0ΖΠ Thigh V

00 '11 00 'ΐ \\ l • ΟΖ • i \ 6, Z "01- NSV 3 6ΠΙ Thigh V

62 '00 Ί ΟΟΑ ■ 61 • 91 19 '01-NSV 麵 9ΠΙ Comfort V

00 • ΐ Z6S Ό2 • SI NSV tao SHI Thigh V

A3 · 3Ζ 00 'ΐ η ΌΖ 69A • 91 9ΑΓ01- m NSV nu Thigh V 8 00 • I 181 Ζ OS! • 91 09'6- NSV 93 8ΙΠ

 00 • ί 88Ζ Ζ 9A'Sl 868 6-m NSV VD Thigh V

Ζ8'6ΐ 00 ι 9ZS '1 828 "SI Ml 8- NSV N 0ΠΙ Thigh V

00 • ΐ 9Ζ0 • it S9S'6- no 0 60Π Awake V

Ϊ́8ΐ 00 • ΐ 060 • ιι ■ z \ 6S9.8- in 3 80Π Thigh V

Ι6ΆΙ 00 • ΐ 68rsz 198 02εin AID vo LOU 舰 V £ lO / lOdf / X3d C9.Z9 / 10 OAV 11 00 • I 99Ζ '1 m "9i S6 · 091 vo nu dish V

S9'8C 00I fLO 'U 061 9ΐ 061

8 Ot 00 • ΐ SL9 ΊΙ LI9 • 51-6 t MX 0 ZLU thigh V

88 -6S 00 • I 680 'f Zl 109 \-6 l Dish 3 Mil

09 · 0 刚 ■ u 06Z • Z to 6 I mi 0LU Marauder V

OS • 0 699 ΊΖ 'oz 0S8 G 6 l mi 130 89Π Intestine V

00 • i '11 l 9-6l 232 • ε to 6 ^ 1 plate ao Z91I concealed wot 00 • t in ΊΖ · 8ΐ '9ΐ- 6 l thigh V3 99Π 舰 V

6 00 • I ηι • 02 Z6 "8I 6 l Thigh N nu Thigh V

00 • I OZf 81 ■ ζ \-no O S9U 麵

96'l 00 • ΐ · 8ΐ 298 '81 098 • ei-3 29Π Fragile V

8ί 00 • ΐ 86Ζ • L \ 00f 61 Llffl- 8fl ΑΊ3 VO 19Π W0XV

Ζ6 00 'I Lf • 91 8 N 69Π 舰 V

09 • 0 108 'SI 883 * 02 • s in in 0 89Π thigh V

09 '00 • ΐ 693 • 91 98 '61 • 81- in Fox 0 Π Marauder V

Of 81 00 '0 m • z \ • s in 30 9SU PJ0IV

93 "I 00 • ΐ 9Z0-6l in 93 9U W0IV

S8'0 00 * ΐ -n 8.8ΐ 683 • ει-m VO SSU

00 • ΐ oir i 2LfLl Ul • 81- in N ISU 贿

0A.8S 00 • ί 901 ■ \ 066 1 • ο to m Has 0 09Π PJ0XV

86 2 00 Ί SSI -L \ π_ m 3 6 II Hidden

90-98 09 • 0 80S 'Z \ 9' SI 069 • π-m ¾ias 30 hidden

66 bo 00 Ί 189 • ZI n 1 T ■ e T 86Z ΊΙ- i T vr ΙΑΤΠ Τ 17

 do QJ J 丄 V

10'9S 00 Ί 9ir t 039'9ΐ 6i9 • ΐΐ- m V3 Drive V

A9-S8 00 Ί fLO • 91 696 ^ 1 G N W0XV

10 2 00 • ΐ Π • 91 9U'9I 9SS

C9.Z9 / 10 OAV 8 -62 00 "I 969 Ό8 6 9'A SOS • 91- S9I dSV ao Plate V

00 'ΐ • 62 OSO'8 9Ϊ0 ■ i-S91 JSV vo 皿 Plate V

00 • i 9Sf 8 SZ '-891 iSV N ΖΟΖΐ W0IV-LZ 00 • ΐ 59S • 8Z 68' 6 CZ9 G Ζ9Ι u 0 腿 Thigh V

00 • ΐ ISA • ii 808-6 ISt'SI-ZSI ou 3 ΟΟΖΙ Healing V

00 ■ I 9ΐ ΟΖΐ · 6 99 • I 291 ou 90 66Π Thigh V

00 • Ϊ • SZ ε 8 ISO 'S G 291 ou 93 86Π thigh V 8Z 00 • ΐ m • 92 069' 6 80A • 81- Ζ9ΐ ou V3 Ζ6ΐΐ thigh V

8Γ8Ζ 00 • ΐ Ζ 1 • 9Z Π9'0ΐ 6Z8 • Π-ZSl ou ao 96Π Bandit V

09'6Ζ 00 • ΐ 0ΐ8 • 92 188 ΌΙ ΐδΐ2ΐ- ZSI ou N 96Π Thigh V

86 'IS 00 m' ΖΙ 'fl- ISt MX 0 f6tt Thigh V

8s · ιε 00 • I 0S6 • 3Z 900 'ΖΙ SSZ • S G 191 m 3 96ΐΐ Thigh V

69 '6S 00 • ΐ 169' ΖΙ Ζΐ9'8- 191 Ul HO Ϊ6Π 隐 V

00 • ΐ 80 • SZ ZZf • 6-191 MX ZD 06Π WOIV

68 00 • ι I6f • 9Z ΖΟΖ'ίΙ 999 • οι- 191 MX ΖΏ 68Π

98'9S 00 • ΐ 386 • SZ 98Γ9Ι 999 · Π_ 191 Ul zao 88Π 隐 V

99 'AS 00 • ΐ 860 • 92 ASf 9ΐ 180 • 6_ UL 130 8Π Marauder V

A6 * 9S 00 Ί 66S • 9Z Z66 • 6- IS! Ul iao 98Π Thigh V

8ΐ · 9ε 00 • ι 6 0 • 9Z 9S6 'l' Π-191 Ul S8U Bile V wn 00 'ΐ 99 • 9Z • Ζΐ_ IS! Ul ao ηιι Thigh V

00 Ί • Z 6 Ϊ 21 286 Ι-131 m V3 88 腿 thigh V S 00 ϊ 8 'S to Ϊ8 Π dish V

(j mu o n unu • τ ι 8Z9 'ιτρ · ρτ 082-81- no T ααο n u υο 11 yvu

00 Ί 16S ΊΙ ozrti mS 0 091 ¾as 3 6ΑΠ Thigh V

00 9Sf '1 Z9f SI 699' 9Ι-091 30 U rouv

28 'AS 00 Ί LQL • \ i 9f l 9069ΐ-091 ¾as aa 9LU Thigh V

C9.Z9 / 10 OAV S8T

80 'SZ 00 Ί 68A ST 991 SAT 33

Plate V

ZZ'U 00 ■ \ m'li ι% · zi- 99ΐ SAT ao \ Thigh V

U'6l 00 Ί -zz n ■ n- 931 SAT \ hall V

C6 -LI 00 • I 682 "ZZ • oi- 93ΐ SAT ao m \ Plate V

00 • I A66'9 • 6- 991 SAT vo hidden V

96'ZI 00 ■ \ m • 6-99ΐ SAT N% m

69'8ΐ 00 • \ • oi- 991 nm 0 LIU W0IV

AO-81 00 • I 09f8 • 6- S9T nai 0 m \ Oki

Z6'SI 00 • I • 9-93ΐ nm zao m \ Thigh V

69 '81 00 • ΐ 699 "9Z i • 9- 93ΐ iaa n o V

96 'l 00 • i miz -i 86 • 9- 991 thigh zu \

80'S1 00Im 'hi m-z 6Z8'8- S9I ao Thigh V

C9'A1 00 m-n i ^ m6_ 991 nai V3 \ u \

00If -Lz ZLf '0 to 9ΒΙ ai N Thigh V

00 'ΐ' u 999 -S 019 • Port si 1VA 0 Anonymous V 61 00 • ΐ 68 • Port η \ 1VA D LU \ W0XV

00 • I 69ΐ ΊΙ 299 '8 ιιΐ'η- η \ 1VA 9121 Thigh V

09 'U 00 • I 899 * 6Z ε .ε 8l2 "l- η \ 1VA 133 9121 Thigh V

91 'ΐΖ 00 • I m-u ZO • ει- ηι 1VA 93 nn Thigh V

00 • ΐ 6A ΉΚ VO plate V

00 'ΐ 8Z6'9 99Z'Sl- η \ 1VA N \ u \ V

U 00 • I • OS 69 · 9 0I ■ ζι- 891 JSV 0 01ZI Marauder V

Αΐ · ΖΙ n unu * T

 L GQQ * Q

 L V L 06 OZOsi- OC T do V J C OfUl6 T I

 96 -SS 00 • I Ζ9Ϊ 'IS 6 A'6 A08 • SI- S5l JSV zao m \ Thigh V

C9 -S8 00 is6'oe I8 • Αΐ- 231 JSV ιαο L0ZI dish V 6 "Z2 00 • ΐ 138 'OS 9Z9'8 09Z • 91- dSV 33 90Z1 Thigh V

C9Z.J9 / 10 OAV 981

 S9.6I 00 • ΐ -zi l \ l • ΐ in -9- 691 SAT 0 69ΖΪ 舰 V

A8-81 00 • I 692 "SI 8SZ • 0 m 'G 691 SAT 3 8921 Thigh V

8 · 8ΐ 03 • 0 Α89'9ΐ i08 'ト Π6ΖΖ_ 691 SAT ZN mi lounge V

Ϊ8'6Ι 09 • 0 SOS'91 m-LQZ '-691 SAT m \ Plate V

00'8ΐ 09 ■ 0 Z9S 'SI 190 • 8- S 2' G 691 SAT αο zm Thigh V

Οΐ · ΖΙ 09 • 0 861 '91 in%-I69'S- 691 sn 3D m \ 舰 V

0S.8I 00 • \ Ί-S8S-9- 69Ϊ SAT 09ΖΪ Thigh V

93'8Ι 00 • I • 0- '691 SAT vo thigh V

86 1 00 • I • 0 631 AT N W0IV

00 • I Ζ8Γ9Ϊ m • I m-f- 831 nai 0 9S21 Thigh V

6Α ΐ 00 • I il 8 • \ ilt * 9- 891 nai 3 Marauder V

20-81 00 • i 'I • s 891 nai mo mi thigh V ι \ · ι \ 00 • i l 916 • g 8Z9'-831 ilHl ιαο 89ΖΪ thigh V

Ζί'ίΙ 00 • I 986 '^ ΐ \ l \ 0 9_ 891 nai thigh V

6ΓΖΐ 00 • i 88A • s 9 S'9_ 891 ao K0IV

98 'ΐ 00 Ί in' I SS9-9- 891 nai VD 0921 Thigh V

93 1 00I 2Ϊ8-8Ϊ in '8 9'9- 8SI N Marauder V

00 Ί m • 0-998'9- ZSI SAO 3S Request thigh V ΐ 1 00 ■ im • 0 A9I SAO ao V

ZfL \ 00 • I 89 '6 r8- "I SAD 0 Healing V

98 'ΐ 00 • I 681 • i A9I SAO 3 Rinsing dish V

00 • i LU • I m-i- ΐ SAO V3 i Thigh V

1? G Τ uu τι, 7

 L (Π7 * T 7 669 'I Lob * 0_

o ^_ ! 5 people on JNJTW V

LZ'Ll 00 • ΐ 0Z9 'l 169' 8 991 SAT 0 o Thigh V

09 'I 00' I lVll 9Itg 9SI SAT 3 6C I Dish V

19 09 • 0 098 SI9 966 ^ 1-9SI sn ZN f¾OIV

C9.Z9 / 10 OAV L \

 9f8Ι00 ΐ C90 99 000 ss6 8'0 S9I 8621 thigh V 9'8ΐ00 ΐm • 9 69 iim ΐ 291 LQZl thigh V

Π '6ΐ 00 ΐ • 9 880 • 9 291% Zl Thigh V

00 ΐ Ι9ΐ • 9 Rinse ■ 9 m go Z \ Thigh V

Zf8I 00 1 • 9 S9I nai V3 ΠΖΙ Plate V

8Γ8ΐ 00 I m'i-868Epsilon S91 nai N m \ Marauder V 81 00 1 m-i 660 '06Z'8 291 ΗΊΙ 0 \ Basket V

9Ζ "81 00 ΐ n \ 8 'S 8'S an 3 06ZI PiOIV 9ΐ 00 ΐ 69Z" ΐ • 0 90'9 z ΐαα m \ Thigh V

Η'ίΙ 00 Ί • ΐΐ 89Z • \ Ζ96 · Z9I an 193 Thigh V

00 • ι L • 6 968 'T6Z "9 291 an \ V ζβ ・ ιι 00 Ί 9Π · 0ΐ 010' I 060-9 Z9I an Ώ \ W0XV

0 8 ΐ 00 Ί A6S6'I 08 Γ 8 Z9I HI I V3 \ V

31 '81 00 Ί 9SA • 6 • \ 999 · Ζ Z91 an N m \ Plate V

00 089 • 6 m • 8 no '\ Ϊ9Ι ou 0 m \ thigh V

00 • ΐ 699 • 6 860 'I ΟΙΓΐ 191 ou 3 m \ V

9ΓΖ1 00 • ι Ί • I 961 'G 191 ou 33 m \ Thigh V

00 • ι '8 • 0 Ζ60Ό- 191 ou 93 \ thigh V

00 Ί 169 • 6 910 • I ΐ9ΐ ou V3 m \ ΐϊοχν

09 Ι 00 Ί 082 '6 Ϊ8 • I 191 ou (D thigh V

8871 00 Ί 862 • οι zn • I 06'0- 191 ou N m \ V

9ΐ · 8Ι 00 'ί • 0 81SO- 09ΐ V1V 0 \ V ο τ' τ

οθ 1 66S • ίί 80S 'ΐ no T' T— no τ V V J ^ 17 T

 JfvU V

9ΓΑΐ 00 • I S89 · ι \ • 8 8 Z-09ΐ V1V m \ V

ΪΓ8Ι 00 • I 601 · ι \ • ΐ--09ΐ V1V V3 m \ V

5Ζ8ΐ 00 • ϊ n \ 'SI 826 • 0 9 6 ー 09ΐ V1V N m \ Thigh V

C9.19 / T0 ΟΛ \ 8δΐ

 Οΐ • Z 00 • I Z68.0 -L 698 -g 9 Ϊ 30 0221 Thigh V

16 '1 00 • I LZVZ Ϊ9 8 000 91 Has 6Ζ2Ϊ WOIV ίζ ΊΖ 00 • I 6S6.I Z9C6 S 0 "9 Α9Ϊ vo 8ζει V

89 Ζ 00 • ΐ m- \ L 'A9I N 9Z8I Thigh V

Π '1 00 • I Ϊ6Γ0Ϊ 891' I 991 ¾as 0 9Ζ8Ϊ Thigh V

Α6 • \ i 00 ■ \ 6Ϊ8Ί m-L 991 3 πη

8ΐ 03 • 0 Sf 0- QU'L 6 0 · 8 991 Has 30 m \ thigh V

0L • \ i 00 • ΐ o o- 6 8 ZI6 * 8 991 ao \ WOIV

9 Ζ 00 • i Ί 800-6 9 88 991 V3 OZSl 舰 V

0 ΊΖ 00 Ί 6 ΪΓ 8 8 Ζ 0.6991 N 8 ISI V

Π-QZ 00i S9 '8 Of 8' 6 86'8 S9I dSV 0 i Thigh V

8ΐ ΊΖ 00 86f S6 991 dSV 3 9Ϊ8Ϊ thigh V i '11 OS • 0 -i 081 '8 309 0Ι m JSV mo 9ΐ2 thigh V

80 • i 09 • 0 9S8'9 96S.9 εδπι m dSV mo ici WOXV

L \ '11 09 Ό 6 9 6S8'Z 980'Π 991 d V DO SIS! Plate V

89 • \% 00 • I 286 1097 606 Όϊ 991 dSV 2181 Thigh V

08/02 00 • I 099 * t 8891 S91 JSV vo Π8Ι KOIV l \ • oz 00 • t 882 'iSV N 6081 WOIV

92 • 61 00 • I 109 · ^ 96ΓΖ n \ 0 8081 WOXV

St • 61 00 • I QH SSZ'9 i 3 im WOXV n • \ i 00 • ΐ 806 Ί 36 9 Request 30 9021 Thigh V

Si, • 61 00 • i 686 9 n \ ao m \ V u • 61 00 pn? T ι¾ητν

96 '81 00I 'm N WOXV

• 61 00 • i 60i'9 669, 0 9 S9l nai 0 οοδΐ Thigh V

S8 • 81 00 • i t6S-9 991 nai 3 66ΖΪ WOIV

C9.Z9 / 10 OAV 681

 0 6Ι 00 • ί Ι3 · ISO 'ί Ul V7V ao S9CI Thigh V

00 • ι 199 -ε 8Π · 9Ι 0ΙΓ8 u \ V1V V3 9SI Dish V

00 • ί 1687 Ul V1V N zm Hidden V

00 • I ΑΟΠ 9ΪΓ9Ϊ QLl 0 m \ ΐϊοχν

00 • ί Ζ2ί 90-SI m -f Oil as 3 o Thigh V

09 • 0 028 "0- 998'Ζΐ Oil 30 89C1 Thigh V

01 '11 00 OSO'O ε'ει s ε3 OLl 93 im V ι ^ ί2 Ζ 00 • ί Α98 691 SAT 0 8921 Bile V

00 • ΐ 9Ζ6.Ζ mix 691 SAT 3 zm Thigh V

09 • 0 'S' n 691 SAT ZN

Bile V ί \ Ζ 09 • 0 SS t60-ZI 03Α * 2Ϊ 691 SAT ao Dish V ι · ιι 00 Ί

00 • ΐ Ϊ8Γ 0 6 · Ζΐ LL ^ -Ql 691 sn 30 thigh V

00 • ΐ 699 · 8 2U "6 691 SAl 90 隠 Hidden V

0L-QZ 00 • I 066 -g ii si 09Ζ · 8 69Ϊ SAT vo Dish V

00 • I m- 99ΓΖΙ 89 '69Ϊ SAT N m \ Dish V

69'Αΐ 00 • I 080 '8 8Α8ΌΪ 929 · 9 891 SA3 3S mi Thigh V

W '81 00I 8Zf 9 in -oi C89'9 89Ϊ SAD 93 68SI W0XV

99 · 8ΐ 00 • I 96S'S 09 81 891 SAD 0 \ thigh V

9S'6I 00 • ΐ ISO'S 891 SAO D Z8SI Thigh V? Τ

 0ί7 'β 0 Τ •

 i GQO 'Λ T Ω

 υυ L no · o 0 Ω T person J w V T J noc T end V

 U on V

Z8'6i 00 ■ I 691-ZWOl 891 SAO N mi thigh V

69 00 • ϊ89S'II-Α9Ϊ 0 SSSl Thigh V

69ΌΖ 00Im '8 9SSOI oso's A9I 3

C9.Z9 / 10 OAV 06ΐ

 os -u 00 'Ί S8-8l' 6 3ZI ΝΊΟ N ^ 6 1 thigh V

LI9Ζ 00 '' ΐ ZOO'8 Ul '02 Input Ί3 0 86ST V -u 00 '' ΐ S89-6I 9A8 "0I ΑΊ3 0 2681 Thigh V

00 '' I 's 9 9 "61 I · Π Ί3 vo Ϊ62Ϊ

16 00 '166-81 90Γ0Ι i ΑΊ9 N 68SI Thigh V

62 00 '' ΐ 8 0Z 68f8 OU 0 \ picture

Π 'Zl 00' ■ \ 569 '6ke' 6Ϊ 8S6.8 0M 3.

00, 1 S8I 6Ι 832 "9 8ΖΪ OHd 93 \ thigh V -zz 00 Ί 003 '2 368" 61 OU'A ζί \ OU ao 9881 Bandage V

00-\ 6Π * 8 2LI OM V3 i W0XV V 11 00-\ 699 'S 969 L \ OU ao i Plate V

Wll 00 Ί i Ϊ9Ι · 8ΐ 698 '9 L \ O N zm Thigh V

W \ l 00 90S 'ZLl MX 0 mi Dish V VM 00 SIS' 9 m-L 088 * 9 III Ul 3 0821 瞧

S9'0Z 00 Ί 9if 91 '0 ZLl Ul HO L2l Thigh V

00 9ΖΓ6 ΐΟΓΐ ZLl Ul ZD Plate V

96-61 00I 9A011 ZLQ'Z ZLl UL ΖΏ nn Plate V

61 00 • I π · 938 1 908 "2 ZLl Ul zao Marauder V

S9.6I 00 • ΐ 'w m'z III Ul Thigh V

8f6t 00 • I 610-91 99Z'8 III UL iaa Optional 61 00 • I 6S0'8 ZLl Ul m \ Thigh V

U'6l 00 Ί ZLl Ul go m \

9b U6 uu I o9 l n I ϋ 人 ϋ) 1V

80 ΌΖ 00 • ΐ 680-5 39Γ9Ϊ 8ZLl MI N 89SI Thigh V

00 • ΐ m-h \ 8967 U \ V1V 0 皿 Plate V

00 • ΐ 189 "S ILl V1V 3 99ST N0IV 麵 odf / ェ :) d C9.Z9 / 10 ΟΛ \ Ι6Ϊ

 99ΙΖ ΙΖ 00 '' I m 'οι 996'9ΐ 8Αΐ thigh ao i thigh V

00 'ΐ 69ΠΪ 8 '01 Otf 91 8Ζΐ V3 V

80Ή 00 '' I-\\ 18ΓΖΪ '9ΐ 8ΑΪ Has N m \ 隐 V

00 'Ί SZO'U Ζ86Π Ζΐ mi 0 zzn WOn V

89 Ζ 00 '' ΐ 651ΠΠ 92Γ2Ϊ 606 · ει ΑΖΐ Thigh 3 un View V

6S'ZZ 00 '■ ι Q fZ \ 2Α8 "9ΐ εοδ'ει MX un gall V

89 "^ 00 'Ί 095 · 8ΐ OZS'SI 皿 plate 130 6t t thigh V γιτ 00' 'ΐ 688 ^ 1 l LLI plate 93 8 ΐ brittle V

00 ■ I οετπ LLI mi V3 Thigh V

00, ί 3Ζ8Ό1 LL \ mi N 舰 V

00 Ί 9Αΐ an 0 l l 隐 V

00, ΐ ^ 89 '6 6 Π 9Ζΐ an 3 ei i 舰 V

00, ΐ 8 f 6 868 Ί 9Ζΐ an ια. Thigh V εε6ΐ 00 66Ζ8 9ΑΙ an UH PJ0IV

98 6ΐ 00 • ΐ 288 "8 9ΟΖΟΌΐ an W0XV

6 0Ζ 00 • I 9 8 S6i'6 9Αΐ an 93 i 隐 V ινιι 00 Ί 889 '6 I80 * Sl SSf 01 9Ζΐ an V3 l Bandage V

Wll 00 'ΐ 906-8 8Sf 91 68Γ0Ϊ 9Αΐ an N 90 腿 Thigh V

61 Ι 00 • I 396'Οΐ 86Γ6 9ΑΙ ΝΊ9 0 1 Thigh V

U'U 00 'ί m'L \ 698'6 3Αΐ ΝΊ3 3 ΐ W0XV

03 • 0 00'Οΐ 186 "0Z 099 -S 5Ζΐ ΝΊ9 zm I 隐 V

Wll 09 • 0 88fOZ Α09'9 ΝΊ ΝΊ3 130 OO l Thigh V

91 92 00 ι 1 iy bob I

 00 Ί 398 '8 205 "0Z 999 Ά 9ΖΙ ΝΊ3 86SI V

U'H 00 ΖΖ ΖΖ2 "6 · 6ΐ 260 '8 5Αΐ ΝΊ3 ao L Thigh V

SO 00 • ΐ 0ΪΓ6 ΐ8Α "8ΐ Α99 * 6 9ΑΙ ΝΊ3 vo 96SI Thigh V £ TO / lOdf / X3d £ 9Ζ.Ζ9 / Ϊ0 OAV 9S • 91 00 I l8'CI ooo -g 689 's 18ΐ HHd 65 l V

26 • 91 00 I Π0 · ΐ Ϊ 8-3 91C "8 Ϊ8Ι 8S I Thigh V

Z9 • 91 00 I 09 '21 9'S 20S • 9 Ϊ8ί ιισα I Plate V

08 '91 00 I S 8Ζΐ80Ϊ9 809L181 3Hd 33 m \ Thigh V

29 '91 00 Ί C69'U 908-9 • 8 181 HHJ ao ss t Thigh V

91 • LI 00 Ί Q9f Π 68Z * 8 0 0.8 ΐ8ΐ V3 i Thigh V

89 'LI 00 ΐ 66f Zl 9 ΐ'6 0Ζ9'8 ΐ8ΐ N zm O V n -L \ 00 wn 8Ζΐ6 U9 • 01 081 O IStl 舰 V

11 • ΙΛ 00 • i 6 9'6 088 • 6 081 Ring 3 09 ^ 1 thigh V u • SI 00 • I 8ZS · Η 68Γ5ί W0I 081 ao 6HI Awake V

81 00 • I 88S 'SI 018 • 6 081 through as m \ Vn • 91 00 • I 080 • I 0S0-81 • 01 081 舰 V

Z9 • 91 00 Ί 86811 08 Α • 6 081 im

Plate V

69 'LI 00 • I 0Ϊ9ΌΙ • 01 08ΐ im vo \ thigh V

90 • 81 00 • I LlfU 809 Όΐ ηι • ΐΐ 081 Through N i Thigh V

10 -LI 00 • \ ZS6'9I • π 6Ζΐ NSV 0 zn \ Thigh V

00 • I g68'H 0 '01 Ί \ 6Ζΐ NSV 3 mi Thigh V

• OZ 00 • I 900.91 m · 9ΐ 6ΑΙ NSV orchid mi thigh V

Π 00 • ΐ Η0 \ 98Γ01 sis • 91 6Αΐ NSV ιαο io V

ZO 00 Ί 9ΐ0'9ΐ Ζ Ι Ι SS6 '9ΐ 6ΑΙ NSV 03 \ Thigh V

Π • 61 00 • ΐ 8 6'SI 86ΓΠ 6Αΐ NSV 93 Thigh V

IS • 81 00 • I 998 • 21 6 ΐ NSV V3 KU Thigh V

61 • 61 00 • I US J o 1.ο y D ι ι 898 '^ ΐ C I τ MSV N V i

9Z • 02 00 Ί 99 Ϊ 096-8 966 • Η 8Ζΐ s O mi Thigh V

91 -QZ 00 • I Ζ8ΐ '01 3 os i Plate V

SS'8I OS Ό 8Ϊ Π ■ L \ LI 30 mi Thigh V 麵 odf / ェ :) d C9.Z9 / 10 ΟΛ \ e6i

 II '11 00 Ί 9AS-Z 0 6e 98A'9- ^ 81 MI Zdd

C9 \ ι 00 ΙδΓΟΐ U8-C 0Ϊ9 -9- 81 UL mi Thigh V

Z9 • \ i 00 • ΐ 98Γ6 Z 0 • S 9I9'9- n \ Ul ιαο mi Plate V

9 • \ i 00 Ζ Ζ0Γ8 6Π • 0U "S-, 81 Ul mi thigh V

9A Ζ 00 • I 9881 • 9 199 '5- ni m aa Thigh V

91 '11 00 Ί ZZO '• 9 861' G Ul V3 m \ V

81 • \ i 00 Ί 8tZ'8 806 • 9 9If8-m MX N Hidden V

IS 00 ■ \ 158 090 090 • Q Π30 mi Thigh V n 00 Ί 88S.8 6A6 • 9 m 'I- 丽 ΑΊ33 3 o W0IV

91 • oz 00 • I 181 • 9 0Ζ6'ΐ- Enter Ί3 va un picture

80 "61 00 • I 52Γ0Ϊ 908 • 9 82 · 0_ 丽 ΑΊ3 N an thigh V

8Z • 81 00 20Ζ Ι οεζ • L OSO'O-S8l V1V 0 n Thigh V

00 Ί 28Γ01 • 9 86Γ0 281 V1V 3 thigh V n '9ΐ 00 • I' i \ • 996 'ΐ 881 V1V 93 i 舰 V

18 'LI 00 • I Ζ96ΌΙ 291 • 9 09Ζ * ΐ 881 V1V VO zin Thigh V

00 Ί Ζ8 ΌΪ 'L 0097 S8I V1V N un thigh V

'LI 00 • ΐ 010 • n 9S9' Z8i S13 3S \ 舰 V oz 'LI 00 • I 99Γ8 002 • 6 281 SAO 90 69H Plate V

99 • 91 00 • I 108 '6 m • 9 Z \ SAD 0 89tl Thigh V

10 'LI 00 • I 90ΖΌΙ • i S8Z'8 Z81 SAO 3 A9 W0IV

9A • 91 00 Ί 880.01 281 SAO VD 99 ^ 1 Thigh V

88 • 91 00 O Z'Ol A6S • 8

Thigh V

-LI uu I Π U 1 o '7 T

 6 I 931 • 6 Lo I drld U ΪΑΤΠ by? V 丄 T V

 V

U -LI 00 • I 888'Π • 8 09S-9 Ϊ81 HHd 3

Thigh V

Lf • 91 00 • I 96C9 Ι8Ϊ 3HJ Z3 mi Thigh V

89 'LI 00 • I 990 * 91 881 • S Z \ L-L 18ΐ 3Hd \ Plate V

C9.Z9 / 10 OAV πι

 00, ΐ 00S S16-8 6CS6-0 6131 Thigh V

LL-9Z 00 'ΐ 6SA ΖΐΟΌΐ 681' 6-m πϋ 3 8ΐ3ΐ NOXV

90 'iZ 00 • ΐ 6101 m-o \ ζζι • 8- V3 LIS! 丽 V

Whl 00, ΐ 898 '9 Ul' Οΐ L \ N 9191 V

26 · 00 • ΐ 0ΐ9 • 6-98ΐ mo 0 fl9I Watch V

00 • ΐ 296-6 99 8-981 mo 3 S191 舰 V

LfO 00I 998E1S6'99- 981 η zao 2191 W01V

ZO'Ot 00 • ι m ΐΖ08-981 1113 iao Π9Ϊ thigh V gr8S 00 68Γ9 0Ϊ9Ί- 981 ίΠ3 ao 0131 舰 V

80-92 00 mi 8.9 Ζ19 * 8- 98ΐ αιο 33 60SI ■ V

9 'ΐε 00 9 6Ί 9 · 8_ 98ΐ mo 8091 Thigh V

IfLZ 00 809 '2 00Γ6 909 · ί_ 98ΐ mo vo A091 PJ0IV

89'9Z 00 • ΐ ZS6'2 Ml '9- 98ΐ mo N 9091 Plate V

00 • ΐ HS'S 6 '01 m • S-S8I ΙΙΗΊ 0 \ 隐 V

00 • I 888 08Γ6 • 9- 98ΐ iiai 3 80S! Thigh V

69 '92 00 • 1 198 * 2 0ΐ SS8 '0-98ΐ Thigh zao Plate V

6Z'9Z 00 UQ'Z '8 • 0-aai iao 10SI 隐 V

Ϊ9Μ Μ 00 Ζ Ζ'Ζ 816-8 'g nai 0091 隐 V

68-Z 00 Ί 6 6ΖΖ in6 · 1-urn eo 66 ^ 1 舰 V

08 00 • ΐ 198 * 6 S98 • S-98ΐ thigh V3 86 ΐ thigh V

16 * 82 00 • ΐ Ul · 8 658 • 8-981 nai N 96ΐ Thigh V

8000 Ί 8Ζ8'9 00Γ6 IS9-ηι MI 0 96 l V

00-τ ΐ

L 2,86 9 S918 nz-78 I a person J 707 I

08'ZZ 00 • I 000 Όΐ 9 ^ -1 2QL • S-η \ Ul HO W0IV

92 'ZZ 00, ΐ 98S6 9Ζ60AS-η \ Ul ZD m \ W0XV

8 00 • ΐ Α00 "8 Πί'Ζ 86A '5- ηι MI 06 l Shop V -1-fIO / lOdf / X3d 9Z 9/10 O S61

 Lf \ 00 • ΐ 90ΓΠ O -f- 061 ^ as 3 2991 V

^ Ζ 00 • ΐ 061 ¾as 30 TS9I 丽 V

62 81 00 • ΐ S9 'LI ll \ 0Ι 061 ¾as ao 09SI V

898 Ι 00 Ί o roi ·,-061 vo 6t9I Plate V

06 · 8Ι 00 Ί 688 '3ΐ S8'6 ΐΟ

98'8ΐ 00 660 • 91 '6 S3S-9- 681 JSV 0 9 9I 丽 V

8 Γ 61 00 892 • 91 Zf 6 681 d V 3 9 9 I V

9fAI 00 • ΐ • 81 ΖΙΓΟΐ 98Γ2- 681 dSV zao ^ 91 Thigh V

SI Ζ 00 • ΐ ■ 885-21 2SI 'G 681 JSV ιαο 8 3l

98'8I 00 Ί ozrsi own 80 g 681 dSV 3D zm dish V

83-81 00 Ί 281 'SI 8S9'0t 6 S "S- 681 dSV 93 mi WOXV

6B'6l 00 198 198 • 81 6 699'9-681 dSV VD om Thigh V t 'ΟΖ 00 • ΐ 92f' δΐ 969 '8 896-9- 681 dSV N 8291

980 00 00ι ASSn (8 30 9-881 SAT 0 ZS91 Plate V

8ΐ 00 Ί ZQln m- 1607-881 SAT 3 9SSI HOIV

98 '6 00' 0 9i 01 9S6'l ^ 88 -8- 881 ZN zest 舰 V

^ 11 OS • 0 in-\\ 180 '8 190 "6-881 SAT 33 Ϊ89Ϊ dish V

^ Ζ 00 • ί • Οΐ hUl 889 "6- 881 sn aa oesi KOIV

00 • ΐ in • Π ISA'6- 881 S person Ί 6Z91 Basket V π 'ιτ 00 "ΐ • ΐϊ ΐΖΖ'9 68C-8- 881 SAT Thigh V

00 9S8 • π W8_ 881 SAT vo m \ Thigh V

00 • ΐ • 01 0 8 OZO'6-881 sn N 9Ζ9Ϊ Marauder V

00 Ί • π π UηU ni Ό on n * T T— uoo T '

 A 1J U †? 7 P T

 6 00 • ϊ • Οΐ S8Z-01- 丽 3 m \ 丽 V i-00 • ΐ m • 6 9,8 · 6 91Γ0Ϊ- V881 VO m \ thigh V 0 · 9Ζ 00 'ΐ 088-8 Οΐ' Οΐ 699 '6- V88I ΑΊ3 N m \ W0XV

C9.Z9 / 10 OAV 96ΐ

 00 • ΐ 9 '11 13 6 092 n \ iSV zao S89I V

99-91 00 • ΐ • oz 89fS- JSV ■ 891 Hidden V

W8i 00 • I 389 • \% 6Π · 0Ϊ 8 to m JSV 8891 WOXV

689ΐ 00 • I 908 • \ i lOS'Ol Ζ98'2- n \ dSV 90 Z89I Plate V

SZ'91 00 • ΐ m ■ u 966 ΌΙ 'ι- n \ dSV V3 Ϊ89Ϊ Plate V 9.9 · 00 • I 66, \ ιι · ι \ 86S-2- 61 dSV N lounge V

U'L \ 00 096'Π 26ΐ ΑΊ3 0 plate V

00 6S8'S- S61 ΑΊ3 3 \ Plate V

00 • I 190 Ή 0 g 96 ΐ Π3 VD 9 9 Ϊ thigh V

Ζ6ΖΙ ΖΙ 00 • Im • u 800 ト 861 ΑΊ3 N ^ 腿 Thigh V

00 • ϊ 026 'u 899' l ιη ^-m ΝΊ9 0 plate V ΐ8ΐ 00 • ΐ 918 '11 ΖΪΓ9Ϊ Ϊ9 3 舰 V

09'8Ζ 00 • 0 im • \ i ΐ3ΐ · 0Ζ 990 '9- m ΝΊ3 ring 6991

00 • 0 m S8 9- Ζ6Ϊ ΝΊ9 130 \ Plate V

00 • 0 989 • ii 0 · 9- ΝΊΟ aa i W0XV ΐθ 00 • 0 68Z '8 ΖΓ8Ι zw ^-m ΝΊ3 9991 lounge V Ο'61 00

SZ'8I 00 Ί 609 • \ z 266 * 91 ΝΊ3 V3 ^ 99ΐ Hidden V

9Γ8Ι 00 • ΐ 292 "0Z 1 2-91 ΝΊ9 N 2991 Thigh V

99ΖΖΖΖ 00 • I 890'8ΐ lo A- SAO DS 1991 Dish V

9Ζ0Ζ 00Im m81 0ΐ9 · εΐ ΖΖ8 9-161 SAO 33 0991 K0IV

LfLl 00 Ί 9ΐΐ-ΐ6ΐ SAO 0 Marauder V

G V 0 ϊ υυ • τ

 L 920 ■ QZ 1 τ Τ '^ Τ End L o V τ τ people J J 0 GC T

9Ζ'8Ι 00IZ69 "81 895 * 8ΐ SOS'S- 161 SAD VD SSI Thigh V

00 Ί '8ΐ 6 Ι Ι Ι6ΐ SAO N 391 W0XV

9Γ8Ι 00 Ί m91 91εε6SA 'G 06ΐ 0 ^ 9 1 Thigh V

C9.Z9 / 10 OAV 00 ■ \ 'sm • 8 661 ΊΥΛ ao 9191 plate V

09 -3ΐ 00 '■ \ 862-61 08ΑΑ'l 661 ΊΥΛ VD 9191 V

If 9Ϊ 00 m 'l 661 ΊΥΛ N 8191 Thigh V

9S "S1 00 'Ί Ζ • 0 861 0U 0 zm V

00'SI 00, 1 U8 • ΐ 861 0U 3 Π91 plate V Ζ'Π 00 ■ ΐ m • 0 86ΐ 0U 03 0191 隐 V

00 • I 'i A01' l 86ΐ 0U eo 6091 Dish V

89 'l 00 ■ I 9S6 L O ^ ASS' l 86ΐ 0U vo 8091 舰 V

00 • ΐ 'u 60S' 6A9 • 0 86ΐ 0U ao Α09Ϊ Thigh V Ζ Ι 00 "ΐ 8U'S2 861 0U N 9091 W0XV

99 'l 00 Ml'U 908' 9 'Α6ΐ ΑΊ3 0 9091

00 ■ I -u 9 9 ΖΠ • I ΑΊ93 3 刚 ΐ Plate V

00 • ΐ mil 61S'Z 8ZI • i ΑΊ3 V3 S091 Thigh V

91 'SI 00 • ΐ 369' 8 "9 • i 6ΐ people Ί3 N Ϊ091 PJ0IV

82 '21 00 Ί 069 * 92 89S • 8 96ΐ ΑΊ9 0 0091 Plate V oo -ei 00 • ΐ 090 '6 008' I 96ΐ ΑΊ3 3 6691 Thigh V

86 -ZI 00 • ΐ 686 ^ 2 9ZSOI 90Z • ε 961 VO 8691 Thigh V

00 • ΐ οζο 'ζ S9Z-1I' l 96ΐ N 96SI Thigh V

89 'l 00 • I ^ z Ιΰί Ι ISZ • 0 961 0 96SI N0IV

00 • ΐ mil 06ΓΠ S6T ¾a 3 t69l ■ V

00 • I 0ΐ • 0 96Ϊ 30 2691

8Ϊ · 9Ι 00 • ί 8εο · ΐ m • 0 96ΐ go ΐ69ΐ Hidden V no 'τ, τ • τ

y ο F L UU L ΟΠ '07) G '7 O 7o G U λ αΤαΠί> V J τ y

00 • ΐ 80871 • 0-96ΐ Nas N mi Thigh V

19'91 00 • ΐ 0 · 0ΐ • 0- 6ΐ iSV 0 Α89Ϊ 舰 V

96 * 91 00 • I 60 Ι Ί- Π \ dSV 0 98SI Thigh V

C9.Z9 / 10 OAV 86ΐ

 89 ^ Ζ 00 '■ \-\ ι L66'9 m ΑΊ3 3 m \ Thigh V

99 -SZ 00 '696' ΟΖ S6S9-618 'ΑΊ3 VD mi belly V n'u 00' ■ 6ΐ ΖΙ3 9-m ΑΊ3 N hidden V

Ζί Ζ 00 ■ \ m '8Ι 99 9 0 mi V

00 '■ \ 1,6,8ΐ m "S m 3 zm Plate V

00 ■ \ Kasumi 'm 30 o W0IV 8Z 00 · 9ΐ m ¾as 6891 Dish V

00 Ί 6Z1 'ΐ, 06 · 9-m ¾as V3 8891 V

00-\ 986 • 91 89S'B- zw m ¾HS N 9S9I Watch V

8Γ6Ϊ 00 • \ Ζ99 8 90- 619 m AD 3S 3291 Marauder V

9i'6l 00, ΐ 9λ9si 9 S- m SAO 93 m \ K0IV

SI 00 • ΐ 899 666 "S m SID 0 m bile V

00 09ΐ ■ ι \ m'f m SAD 0 zm Marauder V

00 • ΐ 0 ^ 8 • 91 SAO vo im 隐 V n-QZ 00 • I 6S0 · 8ΐ 0Π Ί m SAD N 6Z9I Dish V tS'8l 00 'ΐ 6 · ί \ 988' t- Thigh V

9S-8I 00 Ί 923-8Ϊ-066 * Z ooz 1VA 3 im Cafe V

8f91 00 • 1 m • ιι 018 · 0-L 'Z i 1VA ZOD m \ plate V 91 00 • ΐ 0LZ · \ ι 0 "8- oio" s 002 1VA 193 plate V 9ΐ 00' ΐ 190 ■ \ ζ 8891 -0997 ooz 1VA ao m \ PJ0XV

ΟΖ'ΑΪ 00 • ΐ 908 • 61 Ζ86Ό- ooz 1VA V3 \ thigh V

8S "9I 00 Ί • 61 99 Γ0 ooz ΊΥΛ N \ V uu ι 019 • 61 n o · o π n * † 7 丄 VA U n

 Intestine V

90 * 91 00 ΐ8 • 61 60, Ί S S'S 661 1VA 3 6Ϊ9Ϊ V

89 'SI 00' ΐ m • 81 639 "Z 661 ΊΥΛ 233 8Ϊ9Ϊ thigh VI 00 • I 968 66ΐ

 Ϊ0'9Ι 00 • I 09Γ8Ι 0167 Z 0 "8 0Ϊ2 ΝΊ3 3 1891 Dish V

00 ■ ΐ 909 · 9Ι 980-n \ · ΟΪ on ΝΊ3 zm 8A9I Thigh V

00 • ΐ 6C8-9I U \ 0 9 '01 on 1D lao 9I 丽 V

Wll 00 • ΐ '91 0S8O- m • 6 012 ΝΊ3 ao 9Α9Ϊ Thigh V

98 · 0 00ΐΐ098 '9ΐ0-80Z8 Oil ΝΊ3 33 Si9I KOXV

22 "81 00 • I ASO'Al 691 Ό ISA • i on ΝΊ3 A9l Thigh V

ΙΓ9ΐ 00 ■ ΐ 992-81 86 £ Ί QU ΝΊ3 vo WOIV 9ΐ 00 ■ ΐ 9Af 6ΐ 908 Ό 'L QU ΝΊ3 N U91 Thigh V

WLI 00 • I 89,0 692 • 6 602 1137 0 0Z9I WOIV

9Γ9Ι 00 • ΐ 869 S9f0 690 • 8 602 nm 0 6991 Thigh V z ^ -fi 00 • ΐ -u 99 06Z 602 zao 8991 Thigh V S'Sl 00 • ΐ-m nai iao Lm Thigh V

91 '91 00 ^ z £ 16Ί 'L nai 3D mi thigh V

6Γ3ΐ 00I L ^ -L m nai ao Q99T Thigh V

Ζ6 · 9ί 00 ο- ssc ■ i 602 nai V3 mi 舰 V

ΖΟ'81 00 ΐ9 · ΐ- S69 • i 60Z nai N zm Marauder V

0Γ6ΐ 00 · \ 800 · οζ ίΠ'Ζ- • 9 m sn 0 Ϊ99Ϊ Plate V

OS'61 00 Ζ68ΌΖ m'z- 880 • L m SAT 3 0991 Thigh V

12 00 068 Ί 1967-m sn ZN 999 thigh V

9f9Z 09 • 0 8 '-• oi m sn 33 9S9I V

00 • ΐ Ζ60ΊΖ 6 09- • 6 m sn ao W0XV ζο'εζ 00 • ΐ 686 0ΐ9'9- • 6 m sn SS91 W0XV

n T ΤΑΙΠ T u

602 00 806 m SAT V3 I99t 舰 V ΙΖ 00 • ΐ llll- • 9 m SAT N 6 9l Thigh V ί600

C9.Z9 / 10 OAV ooz

 C9'9I 00 • ΐ 9 l '9Ϊ 8ΖΖ HZ 0 ZUl Thigh V

29 "9ΐ 00 ΐ S09'8I 988 -S ΠΖ Has 3 1 I Hidden V

Π'ΖΙ 00 291 · Η 062 • 9 flZ 90 60 I Thigh V

ZS'SI 00 • ΐ 8Ζ5-8Ϊ 066 · ΖΪ 0IS ΠΖ 90 80 ”Dish V

00'9Ι 00 ΐ 88Γ6Ι HI Wish vo L0L \ 隐 V ΐ8 · ί 00 Ί 90Γ6Ι flZ N 90 plate V

00 • ΐ 092'ΐΖ • ε UZ 1VA 0 tOAl Thigh V

00 I Ι8 0Ζ n \-\\ ssrs UZ ΊΥΛ 0 80A1 Thigh V

00 Ζ Ζ09 -QZ 992 '8 98' 0 nz 1VA Z d Z0LI Thigh V

00 • ΐ 8Ζ6-6Ι zs oi 63ΐ • 0 z ΊΥΛ 130 \ 0L \ Thigh V

Of 21 00 ι 99Γ6 Z60 • ΐ z 1VA ao 00 Thigh V

66'8I 00 • ΐ ILQ-0Z 96Γ6 'ι U 1VA V3 6691 Thigh V

9Γ8Ϊ 00 • ΐ 989 · 0Ζ S08'8 969 • ε \ Z 1VA N im Thigh V

96'Ζΐ 00 982-61 ΐ 6 I 's l \ l mi 0 9691 Thigh V

80 "SI 00 169-8 9 zu mi 3 S69I Comfort V

ZQ- \ 00 • ΐ 6S6 '0ΖΓ8 l \ l ιαο 691 Marauder V

88.Π 00 Ί 9Ζ9 69S oe • ί III an 133 S691 Thigh V ΐε'Π 00 "ΐ m-zz 20S'6 IS8 • s m an zm Satsu

Π 00 "ΐ 8 9 • 9 zu HI I ao 1691 plate V

96'ZI 00 8ΐΟ · ΐΖ OSS • III an vo 0691 Marauder V

89 'SI 00 Ί966 · 6ΐ Z98'9 991 • 9 zu an N 889Ϊ Thigh V

66'81 00 Ί m oz 9 109 • 9 \\ l 0 2,891 麵 u nnu • D G7 G * G 7 q

 Z90 • 9 people 1J J non T

 ZS 'I 00 Ί 18 -8 Ϊ 968 SZ • 9 ΠΖ kid vo S89I Dish V

00 • ι 818-81 0i6 • 9 uz N S89I Thigh V

8 9Ι 00 • ΐ 099 'Ζΐ Z9S'C 868'8 012 Ί9 0 2891 W0XV

C9.Z9 / 10 OAV 26'9Z 00 • I 6ΪΖ ΑΊ9 vo 隐 V

9 ^ "9Z 00 • ΐ 666'ΖΙ 6Α8-81 M Thigh V

26 · ίΖ 00 • I 906 Όΐ • 81 199 '9- III O i 舰 V

ZL 1Z 00 'I ΐΖ8ΠΠ S S-81 888-LIZ Ha 3 O Al Thigh V

00 • I 398 '6 69, G III DO plate V

6 'LI 00 • ΐ 99 0Ι 9 l6ΐ Ζ96Ό- l \ l ao i Thigh V

00 • I 699 ΊΙ 69Γ81 8ΓΪ- LU vo \ brittle V

00 • ΐ 990'ΖΙ 809 · ί \ m Ό- l \ l ¾HS N ni \ 舰 V

00 99 ΐ Z ZZ -Q- ΑΊ9 0 m \ 丽 πζεζ 00 • ΐ orsi LH · ι \ · ο- ΑΊ9 3 m \ Thigh V

00 8l9'gt 9Z6 gog-o ΑΊ3 VO mi Bandit V

89'61 00 006 ΐ 911 '9ΐ 886 Ό Insert Ί3 N m \ Thigh V

20-81 00 08 · ζ ζπ · π 86Ί m JHX O m \ Thigh V

80 · 81 00 ■ \ • 91 .i 3 in \ Marauder V

6ΐ '81 00 • ΐ 869-Π m -LI 229 * 9 2H3 m \ V

88 '81 00 • ΐ ΠΟ'Ζΐ 69 -LI 99Z m SZO \ Dish V η · \ 00 Ί • 91 '9 m Zld 隐 V

00 • I 8 • 66Ζ • SI \ m m \ Ran

88 1 00 • I 668 * 91 • 91 ταο \ u \ 丽

00 • ΐ US'SI m -LI 912 sao 0ZL \ thigh V 81 00 • ΐ 89Γ2ΐ • 91 m 6UI thigh V

6f ΖΙ 00 • ί 60Z'tl m • 91 8U1 Thigh V

66 ·, τ ι G G G TV bOob 'Τ L in91 n T 7 J \ TT JJ ΤΑ1Π

 L vL Y

86'Si 00 • ΐ 90S '91 989 • 91 968 -S 9ΪΖ aa 9UT V

00 • ΐ 80Γ9Ι 009 • 91 m vo 9UI Thigh V

96'9ΐ 00 • ΐ 192 0S1 'g N eui

C9.Z9 / 10 OAV oi is 00 '■ I 861 ■ ε 9 A-8- III sn 33 9LL \ thigh V

18 · 00 '• I t6S • g m l m-i- III SAT 93 thigh V

00 Ί 629 ■ f 06Z'SI 989 '9- III SAT V3 fLLl V η ^ ζ 00' 'I 908 • g 93ΓΑ- III SAT N Thigh V

00, ΐ 899-5- Ml ΜΊ3 0 m \ Thigh V

If SZ 00 ■ I 900 • L 2Ϊ9-9- Ml 3 QLLl V

66 "tS 0L, 0 06Z • 01 0ΖΓ6- Ml L ^ Ll 丽 V 9S OA • 0 Z90'8 886 1 90 * 6- Ml iao 99 Thigh V u-εε 0Γ0 Α9ΐ • 6 1SS'8- Ml ΝΊ3 CD B9Z1 Thigh V

00 • I fLi zwi- Ml ΝΊ9 mi Thigh V

90'8Ζ 00 • I Α8Ζ8 Ζ8 · 9Ι A9S'9- Ml NO ao Thigh V

00 • I 091 · 8 L0 \ 'SI m-i- Ml N1D V3 Thigh V

00 • I II • 6 Ϊ90-Ml ΝΊΟ N 09 O V mi 00 • I LU • 6 V1V 0 69AI Hidden V

00 • ΐ 98i • 6 8681 V1V 3 89ΖΪ Thigh V

88 00 • I ML 'Π HI \ V1V ao

OfH 00 • I 890 • II 99971 -L- V7V V3 9SZ1 WOXV

00 • ΐ HO • n 60fSI 0S8 * 9- V1ZZ V1V N thigh V o \ -u 00 • ΐ '9ΐ 988'9ΐ 862-9- QZZ SAO O 8SA1 thigh V

S9 00 Ί UO 0980901- OZZ S13 93 Thigh V

00 • ΐ m Ι 60S.8- OZZ SAO 0 Ϊ9ΑΪ thigh V

99 'tZ 00 • I • n 085 * tl OZZ SAD 3 09 Ϊ Dish V t · ι, 7 00' ΐ ZL • ει p 7

 U66 I

 J V J OVL L

 L-H 00I '8ΐ 2SS'9I 0919- QZZ SAO N i Thigh V

00 'ΐ 9ZS'9l Ϊ26-6ΪΖ ΑΊ30 Dish V

68 -SZ 00 • I • SI ΖΠ 'G 61Z 3 thigh V

C9.Z9 / 10 OAV U'OC 00 • i 8 28 oi OHd go 2181 舰 V

99 00 ■ ΐ 060 · 6 80f Π 006 Ό- ou vo πδΐ Thigh V Ζ Ζ 00 • ΐ Ζ66 · 9 6Α0Ό- 03 0ΐ8ΐ PiOXV

Ζ9ΐΖΐΖ 00i 81Γ8 ^ u ou N 608Ϊ V

00 • i Ζ 6 -si ssrz- SAT 0 8081 Restaurant V ι-ιι 00 • i 9281- HZ SAT 3 i Thigh V

68-92 09 • 0 9 · 0Ζ9εε-uz sn ZN 808Ϊ Awake V

0, 0 '9 iors-uz SAT ao ζοδΐ thigh V

OS, 0 m '% \ 6S0'S-SAT ao 1081 bile V wn 00' I 00Ϊ

00 ■ ΐ Ζ69 S6S-HZ SAT 9D 66Ζΐ 舰 V ^ ι 00 so -n 6 ΐ HZ SAT VD mi V

00 90'9 -z ~ HZ SAl N% ί \ Thigh V

00 Ί W 8S6 "0- III NSV 0 plate V

89 "9Z 00 • ΐ 190-i 9 O'Z-m NSV 3 πιι picture

00 • ΐ-m NSV Dutch Restaurant V

06 'S 00' ΐ -n 8 G I NSV iao 06 Thigh V trzs 00 • I 's- II NSV m \ Thigh V

IS '62 00I 08 908908-II NSV go m \ Hidden V

8 9Ζ 00 'ΐ II NSV vo L LI W01V

00 ■ ΐ 'T NSV N Marauder V

00 • ΐ 869 ”9 · 168 · III SAl 0 丽 V

 0 C T 'T T

 UU 96 n unu 666 S person 1 PO 1 T τ u

 ι b9 V J 丄 V

OS • 0 0S8.I 90971 8 '* n- SAl ZN h \ Thigh V

68 2 09 • 0 86ΖΊ 0Ζ9ΊΙ 86 · 6-III SAT mi Dish V

80 'ZS 09 • 0 SSO tlf ΖΪ 889 * 8- III sn ao mi Thigh V

C9.Z9 / 10 OAV Π '9ΐ 00 • ΐ 966'91 893' 6 m • L Ul 0 zm Thigh V

00 • ΐ ISS'91 963 "6 η \ · ι m Ul 0 ini Thigh V 9'9l 00 • ΐ 10 ^ 1 f 9 · ο- m Ul HO 6981 Plate V

96'SI 00 • ΐ 608 0 m Ul ZD 8S8I WOIV

OO'Sl 00 • I Ζ6Ζ · 8 919-\ Ul ΖΏ ZS81 贿

% \ 00 'ΐ 09 · ΐ 62 8 986' I m Ul Zdd 9S81 贿

26'9ΐ 00 • ΐ 8S8-91 98Z "8 99S • \ Ul 3281 Thigh V

16-l 00 Ί 0Α6 ・ 9ΐ 5SI • im Ul ταο n Thigh V

09 · Ί 00 Ί 998'SI 061

00 • ΐ S80'9I 96Γ8 Ϊ80 • 9 m Ul 93 zm Thigh V

OS 'ΐ 00 • ί · 9Ι 889 * 6 9,9 • S u MX V3 mi i¾0XV-i 00 • ΐ 006 · Η (· 0ΐ 98Ζ • 9 m Ul N \ Awake V

2Z'fl 00 288 'SI εΐΖ ί Πί • ε III 7VA 0 i i¾0XV

00 • ΐ-urn ζη III ΊΥΛ 3 贿

00 Ί m-\\ 0 ^ 9 * 81 III 1VA mi V

00 'ΐ 9ΐ0 · 2ΐ 06ΓΖΪ m9 in 9 IDD m \

00 • ΐ 090 -2ΐ in ΊΥΛ Ώ mi Thigh V

99 'tl 00 • ΐ 68ΓΠ Z66'Cill 1VA V3 s W0XV n ^ i 00' ΐ 0 6Η 8S9 'I III 1VA N m \ 瞧

TS'9l 00 • ΐ 986'Π 06Ζ Όΐ 05Ζ Ί m people Ί3 0 o

29 'SI 00 Ί Ζ9Ι · Π LL • \ ΑΊ3 3 6181 麵

If 91 00 • ΐ If ΐΐ III • 0 ΑΊ3 VO 8Τ8Ϊ Thigh V fin "Q T uu ■ τ

 L 1 OTj τ T τ L ΩaΠ U 'τ L τ L 828o- 077

 Person O T O T

 1J N JVUXV

3 ^ -61 00 • ι 99671 ie • 0 QM 0 S18I W0IV

00 • I 982 Όΐ m • o- OU 3 mi Thigh V wu 00 Ί 161 · Π 98Γ0 OU 33 ei8i Thigh V

C9.Z9 / 10 OAV 61 · 0Ζ 00 • ΐ Α0Γ8Ι ΙΠ '8 ζ • SI SAO 3 9A8I Thigh V ΐ6.6

8Α · 8ΐ 00 'ΐ ΐ0 · 8ΐ 691' S ιι \ SI SIO N SA8I Thigh V

ΖΓ8ΐ 00 Ί 98Ζ '0Z 266 * 8 ΊΥΛ 0 ZZ81 舰 V

00 28f '61 tSl 'Si

7VA 3 U81 Thigh V

8 Ι 00 • ΐ ZWU 186 ·, • 6 1VA om thigh V

9Ζ'9ΐ 00 'ΐ m- \ z mn 1VA Ϊ33 6981 Thigh V

00 ■ ΐ ZS9OZ m • 01 ΊΥΛ ao 8981 Thigh V

ZVLI 00 • ΐ Ϊ8 -6Ι 66r 016 • n m 1VA VO 981 舰 V

8 9ΐ 00 • ΐ 983 '8ΐ • n ΊΥΛ N S98T Thigh V

Ζ8'9ΐ 00 • ΐ 06811 68Γ9 • z \ ou 0 ^ 981 PJ0IV

6t'9T 00 • ΐ 69Γ9 • \\ ou sn 3 8981 Thigh V

LfZZ 09 • 0 096 * 01 S69 • SI sn m 6981 Thigh V

00, ΐ OK'Zl 918 • ει ocz sn Ώ 8981 舰 V

06 6 00 00 09 9 998 on m (D Lm Dish V

Ζ 6ΐ 00 • ΐ m • z \ sn 998Ϊ W0IV

8ΐ '9ΐ 00I S96.9 806 SAT ao 9981 舰 V

90'91 00 • ΐ 069-91 u \ • n οεζ sn V3 98I Thigh V

00 Ί 896 '91 880 '8 Α99ΌΪ osz sn N Z98t 舰 V

0 9ΐ 00 • ΐ η \\ \ Ϊ9ΓΑ 398 '8 mi 0 IS81 舰 V

60'91 00 Ί • 6 m mi 3 098 腿 Thigh V

98'8ΐ 00 • I 68Γ6Ϊ 66 '6 699 Όΐ I mi 舰 V

 8S'St 00 Ί 6Sf 6 ΐ 906-66 m mi ao m \ 舰 V

06-l 00 Ί 286 8C9-6 9S6 "8 X vo \ W0IV

Z8'tl 00 • ΐ 81971 8Ϊ9.6 Thigh M mi view V

C9.Z9 / 10 OAV 6 · 00 • ΐ 99S '1 3S6O ΐ86 9ΐ 9SZ ΊΥΛ 93 8061 Thigh V

00 · 6 00 • ΐ 80ΐ ΊΙ ΙίΖ Ul1VA V3 A06I Thigh V ΐΓ8ΐ 00 • I 'ιι Ι869ΐ ssz 1VA N 3061 V

S§ 'LI 00 • ι 916SlTil nz Ul 0 06l W0IV

96 Ι 00 • ΐ 999 "ΖΖ 199 'Ζ96-9Ϊ m 3 S061 Optional

09'SI 00 280 * 61 6 nz HO 1061 Awake

06 'tl 00 • ΐ8 · 6ΐ9Ιΐ9ΐnz MX ZD 0061 Thigh V

ZZ '^ l 00 • ι 8ΐ9'6ϊ ^ ΐΓ6 mi \ nz m 6681 Thigh V O'91 00 • ΐ 188 ΌΖ nz Ul 8681 Thigh V

60 "9ΐ 00 • ΐ 028 ΌΖ ηνοι SZO'91 nz Ul I HO im Thigh V

• 89 'SI 00 • ϊ 6I0 "6 ^ inz Ul iao mi comfort V

ΪΓ9Ϊ 00 • ΐ 90 ^ 31 nz Ul 33 968Ϊ 丽

96'9I 00 61 '1 999' 9 69'9I nz m 93 Sat L-LI 00 19Γ9Ϊ nz V3 mi picture ΐΓδΐ 00 • ΐ 9ΐ m N

86'61 00 • ΐ 61 261 * 9 99S'8I m NSV 0 0681

6Γ6ί 00 • ΐ ν ^ \ NSV 0 6881 V

9 Ζ 00 • ί 109 l NSV saw 9881 Dish V

8ΐ 'ΖΖ 00 • ι 5Z0 "9l 69'91 NSV iao m \ thigh V il' l 00 • ΐ Ζ09'9ΐ 88 9Ϊ m NSV 93 m \

00 'ΐ 80ΓΑΪ 38 "9 6i9'9l m NSV 93 mi hidden V

Zf6I 00 • ΐ 698 · Αΐ LLZ ^ NSV V3 z Plate V Τ υυ ροο ■ τ OP * P

 1 N

 00 • 99S II SAO OS 6 8 thigh V

9ΠΖ 00 • ί SS8-91 0 S'I oortt m SAO 93 8 81 UV

60ΐΖ 00 • ΐ ηζ- ΐ 639 8U'9I m SA3 0 LL \ Thigh V

C9.Z9 / 10 OAV 9Α • 91 00 'Ί i 800 an V3 6261 images fLl 00''ΐS6' 9Z 916 ■ L \ an N im images

ΖΟ • 81 00 '' ΐ i06 -hi U \ 9 96S61 in 0 986Ϊ

U 'LI 00' 'ΐ 69Z 898' 3, 61 0 9S61 Thigh V

00 '■ ι wot 068 • SI ZH3

56 • 61 00, ΐ 6εε6 S69 • 91 LU 2Z3 i W0IV

98 • OZ 00 • I 808 ■ a 168 Όΐ 9il 'LI LU ΖΏ ZS6T 麵

99 Ζ 00 • I, 60 ■ a 91f Οΐ 8S9 • 61 LU mim 0861 麵

19 -QZ 00 Ί LZ92 92f6 921QZ 111 ιαο 6Ζ6Ϊ W0XV

9Z 00 • Im 9.8 Z69 • 91 L Z sao

Z9 • \ z 00, ΐ \ l \ • a ΐΟΖ'ΟΙ Ϊ8Γ8Ϊ LU zao m \ WOIV

68 ΌΖ 00, 1% l 060 * 6 516 ■ L \ zad m \ screen a ■ QZ 00 • i esi 899 '8 \ L \ • 61 LU iU 30 9Ζ6Ϊ screen

• 61 00 • I m-i · 6ΐ LU thigh V u • 81 00 • ΐ 6 S 69Ζ'9 896 · 6ΐ L2Z m vo im

Q8ΐ00 • t n 02Γ9 880 • 02 LU N \ m

U · 6ΐ 00 • ΐ m QZ \ Ζ 0 0Ζ6Ϊ Marauder V

10 • 61 00 • I 880 600 • 9 • OZ 3 6161 Thigh V

66 • 61 OS • 0 fLf 'Π6Ί Z • U 30 Ζΐ6ΐ Thigh V

L6 ■ 61 00 Ί 831 ZZV 8i6 ■ \ ι 9SZ ao 9ΐ6ΐ

A6 • 81 00 'i LLfOZ m VD 9Ι6ΐ Thigh V

10 * 6l 00 'u 1896ΐ N ST6I picture

U • 61 L S lp IVA (J 6 Ιο 1

 96 · 8Ι 00 Ί 3Z6 SOf8ΐ ΊΥΛ3 Π6ΐ Thigh V

62, 8ΐ 00 069 ΊΖ 898 '0 909 • 91 9SZ IVA 0ΐ6ΐ Thigh V

63 • 02 00 OOS'SZ 9SZO- 29ΐ ・ ι \ IVA 133 6061 Thigh V ft'Cio / iodf / xad C9.Z9 / T0 OAV ϋ'6Ι 00 • ΐ 619 • IS 826-61 in dish vo dish V

8Α8ΐ 00 • ΐ • 02 Z6f OZ Plate N U6l Rape V

0Ζ8ΐ 00 • ΐ 6 • IS 9ΖΓΖΖ on 0 0A6I Thigh V ί \ · 8Ι 00 • ι m • OS Z90-9 ΝΊ3 3 6961

9f9 09 • 0 08 • 9Z fiz m ΝΊ3 zm 996Ϊ Plate V

038 OS'O ζηu 0SS * 9 LfH on o tao S961 Satsu

8ΓΠ 03 • 0 • 9Z i mil ΝΊ3 αα 96l Awake V

6Z * Sl 00 310 -82 688 '82 QU ΝΊ3 33 8961 舰 V

9 00 00I 86Z m1D Z96I W0IV

Ι · ι \ 00 • ΐ m • 6Z IQl'ZZ m ΝΊ3 V3 1961 Thigh V

00 • ί 960 '62 09κε 0001Z on ΝΊ9 N 656Ϊ Fragile V

00 • ι 8ΐ6 • OS SAT 0 856Ϊ Fragile V

00 • ΐ 0ZL • z 009 66ΐ · 0Ζ sn 3 L \ Fragile V

00 • 0 908 'LI 9Ι8'9ΐ 6SZ sn ZN SS6I Hall V

Ιί'Π 00 • 0 690 • l -i- 9Ζ0'8ΐ 6S2 sn ao Z361 Marauder V

L9-LI ΟΖΌ • 92 'G 9Z6-8I 68Z SAT (D IS6I W0XV

Ο Αΐ OA • 0 Ζ09 'il sso'o-sn 30 0S61 舰 V

Wl \ 00 690 690 '82 18Γ0 ZI9'6I SAT S3 6 ^ 61 WIV

8f Al 00 • ΐ 606 · 8Ζ 680 · 6Ι VO 8 6I 贿

00 • ΐ 88S'8I N 9 6ΐ

18 * 91 00Im ■ & z m-Li 311 0 S I ΙΪ0ΧΥ

ΟΓΑΙ 00 • ΐ ISill m an 3 麵

¾ V τ ϊ 'ヮ op' T?

 6 τ 1 00 • ΐ 018 n

 δ & 6 d 11 LUJ 670 I η \ 00 • ΐ ZSZ '9Z' 9 868 · an m an 100 ΖΠΙ 麵

00 Ί an ιπι 丽 V

19 Η 00 • ΐ 600 'LI m an ao 0ΠΙ 麵

C9.Z9 / 10 OAV 60Z

 IV9Z OO'I 996 * 9 ^ 2 SV V3 S002 WOXV

6 'SZ OO'I NSV N S002 Thigh V

ΟΟ'ΐ 969 'AS m ras 0 Z00Z Drive V

9f 9Z ΟΟ'ΐ IS9'9 6i9'lZ m Ha 3 Ϊ00Ζ WOIV

6Z OO'I ^ vn 889 -ZZ m ^ as 30 6661 W0IV 5'9Z 0ΟΊ S89'9 Z9f εζ mao 8661 WOIV

Α0 "Ζ OO'I 69Γ9 919'ZZ m vo Lm hidden V Z'U 00 Ί nL '6ϊ6'ΐΖ m N 9661 hidden V

LfU OO'I 129 * 99 S60'8 SS'ZZ m V7V 0 66i woxv L 'Z 0Ο 80S'S m V1V 0 S661 WOIV

WZZ OO'I ^ 68 'ΐ Ϊ6Ϊ' 1 Π V1V ao Z66I woxv tO'CZ OO'I 9'½ ην \ ι 2H V7V V3 1661 WOIV ξΖ'ΖΖ OO'I 988 'SS 6Π ・ ε 680 ・ 0Ζ zn V1V N 6861 WOIV 9 00 · ΐ 998 "81 in an 0 8861 WOIV 6-1 OO'I ίΖ9'ξ 6iO" 6I m an 3 Ζ86Ϊ Thigh V

OO Ζ OO'I zn an ιαα 9861 WOIV

W'OZ 00Ί 9Zf ze m'z an TOO S861 Thigh V

2fZZ OO'I 996 "28 600 ・ Ζ 99'9I zu an 86l Thigh V

32 '02 OO'I οοι · ε 820 1 zu 93 C86I Thigh V

W \ l OO'I 999 -82 IWI \ zu an V3 Z861 WOIV

OO'I '896 * ^ 1998ΐ zu an N 086Ϊ WOIV

ΟΟ'ΐΖ 00ΐ ΐ Z f 9 90 '6ΐ \ u Plate 0 62,61 WOIV

6S "0Z OO'I ZSO'9 ΠΓ6ΐ in 8 6Ϊ WOIV

09 '61 OO'I Ϊ0Π8 6S '81 in i 6I WOIV

ΪΟ'ΖΖ OO'I Z996Ζ 961 '8 69' 6ΐ in mi 130 SA61 WOIV

* 0Z OO'I S08-08 306'81 in thigh 93 Η6Ϊ WOIV

C9.Z9 / 10 OAV OIZ

 80 'SZ 00ΐΐ i z'ie i • 0 m ■-8Ϊ8 m 丛 0 thigh V ΐ6.8 · 00 Ί Lfl • I- m • 9- IIS m AO mz NOXV

8S Ι ΟΟ'ΐ Uf • 81 Olf 8-91S IV 丛 0 1902 woxv

00 Ί font 9 6 • 9 \ n i \-SIS through MO 8S0Z Thigh V 6'SI ΟΟ'ΐ 99Γ92 m • 8 9991 HS through AO z Thigh V

Of 81 ΟΟ'Ϊ 622-92 • 0 89Z • 6-218 丛 0 zm Thigh V

L 'n 00'ΐ Ϊ69ΊΖ 328 • 9 920 US Week MO mz Plate V

Ζ9 · 6 00 * ΐ 9tltl0Ι Z90 • 6 89Z • S_US version MO z plate V

8Z-91 00 'ΐ 880-8 mLL 998' Z 01S through MO s oz NOIV

U l 00'ΐ SZ8 * 6Z0 6i0'8- 60S through MO onz WOIV

9Z'6I 00Ί 16A • 9 900 • S 80S Lm Thigh V

00'ϊ lo es 192-g m '8- L02 through AO noz thigh V ε ι 00Ί 96ε ZZ ^ "0 Ζ8Γ0- 90S week AO 1802 WOIV

6ΐ 'LI 00 088 9Ζ 189 • 0 012 908 Fiber AO Z0Z Thigh V

00 0000 ί 9 Όΐ 126 • 9- fOS AO won

Ζΐ · 9ΐ 00 * 1 • 8 ZU • 6-S02 AO im Dish V

89'91 00ΐ in • 6 S99 • 8- through i view V

99-δΐ 00

HQ ■ L S06 Ί- through 丛 0 i thigh V 8ΐ 00 · ΐ 888 * 98 56S • 0 t m through i thigh V

8ΐ 'OS 00'ΐ 9t8'8S LZQ • 61 9H NSV 10 mi Hidden V

6 '^ 00Ί 69Γ68 8Z9 • 9 30A' LI MSV 0 zm Plate V οι · ιι 00Ί sto • 9 S99 SI NSV D im restaurant V

 7 finn

0 τ L '766 UU [oo L bo 266 "8 IC9 • 61 76 NSV discussion DUU6 1AJ 丄 T V V

00ΐ SIO • 01 68Z • 61 NSV ιαο 800Z V

00Ι 9 O • 6 Ζ9Ϊ • 61 NSV mi thigh V ινη 00Ί 9Z6'98 0 ^ -81 NSV ao mi Dish V

C9.Z9 / 10 OAV Ml

 98 • OZ 00 Ί 891 -SS us • 0-\-fn 丛 0 i Thigh V

02 -ii 00 ■ Ϊ 6It • 0 etc Fiber 0 i Thigh V

6 • 09 00 • 0 i-ii S60 • ΐ 196-91- m through mi 0 mi Thigh V

U • ss 00 • ΐ t60'0Z 9 • 0 801 -91- \ n through 9812

00 • I OIS'9 • 9 91-08 Fiber thigh V u • 6S 00, 1 8Z9-91 661 'ti-689 through 081Z Optional o o

 IS • SZ o o

 00 ■ \ 09Γ8Ι, 9o9 o • 9 080'Ζΐ-888 丛 0 LZU

 9Z • 91 00 ■ \ 9 8 196'ΐ- LIZ through MO uu thigh V

IZ '92 00 928 through m \ Z \ l

18 '00 009.01 • SI 919'-Normal 0 Thigh V

89 Ό200 • I l 821 '-i MO

• 9, 00 • I 008 Ί-Ϊ0 I through m zuz thigh V

99 -6 00 Ί 081 Ι \ \ 厦 丛 0 mz Thigh Vn • S2 00 • I 09S Ι S S '

00 • ΐ m • 0-zo6 -gi- 088 Ring AO mz Parent V

OS * 8 00 • I 8ΖΓ6Ϊ 809 • S oes' ΐ oou Thigh V

99 • 91 00 • I ε · 9ΐ m 'IWW Fiber z Thigh V

ΪΖ • 61 00 • I 8Z8'68 866 'I- m MO z Thigh V

66 • SS 00 • i U9.9I 981 • 9Z through 1602

9S iZ 00 • ΐ 'ST 6I8'8 AO mz Thigh V

OL • SI 00 • I m · ι \ m-\\ Through 丛 0 980Z Thigh V

U • LZ 00 • i LS0 Ί- 98S-9- XV 丛 0 Z 0Z

Π • 900 L VVO 9 A '11 on T ■ 660 丄 Vi¾

 06 · 8Ζ 00 • i 8Z3 • \ i m Fiber 丛 0 9 0Z

S8 •% \ 00 • I 0Z2 'LI Ring M0 Thigh V

9 ^ ■ u 00 • i S 8-61S Thigh V

C9.Z9 / 10 OAV If 00 Ί Ζ ^ Ζ Ι 860 ■ ii 016 ■ 8 UZ Jiang 0 Thigh V

00 • 0 l8'U ΠΖ '6ΐ 6S9 • Ζΐ 69C through O mi V

S6'8t 00 • ΐ III '6ΐ 0S9 • i \ • 61 89S Jiangsu 丛 0 LUZ KOIV

98 'SS 00 • ΐ I MOL • 6 • 61 A9S Ring AO V

00 • ΐ 990 “8ΐ 969 • sim • 61 99S through AO \ m Thigh V

96'8S 00 • ι s ε 9 uro- T O 8022 Thigh V

00 Ί 683 • g m m Plate V

6 9S 00 Ί -z ^ 568 Ό 109-8- V V 丛 mi 0 mi V

00 • 0 m '8 8S6 "n- 丛 0 66IZ N0IV

16 1 00 • I 9S9 "9S 'I 9'0T- through 961Z Thigh V

60 'SS 00 • I SS9-92 • 91 • L 098 Return mi dish V

00 • I 6ΪΓ68 m • 91 • 9 65S through 06IZ Thigh V

Z9'9S 00 • ΐ 8iO * OS LZ • OZ through MO mi hidden V

8A'9S 00 • I 68'I 906 • Π oos • 6-AOS through MO nu V

0S'8Z 00 • ΐ 692 ”69 8 8 Όΐ- 998 丛 V 丛 MO z Thigh V

00 • I fH • 9 99 • 6- 998 f V 丛 AO LIZ Thigh V

19 -82 00 • i 918 "9S L \ Ι Π9 • 6-^ 9S plate 丛 0 plate V

69 * 8Z 00 • I 688 * 28 Z96 'SI • 6-S98 Through 0 mi View V

00 • I 861 S S09 • 91 • _ wish mi marauder V

98-8Z 00 • I ZIO • ZI on • 0 employment mi thigh V

69 3 00 • I 869 · 8Ζ Z 8 • 61 n \ • ι OSS O mz V

20- 200 • ΐ Ζ 928 'I-m through O mz V y o 00 • ΐ 0 b7oo a • \ z 968 • 0- 丄 VA

 00 'ΐ 21VL 9 0 ■ \ z QZf Ί LH through MO nu W0IV 8S 00 Ό LlfQZ eo8 i-m ilO mz V

68 00 • ΐ TOS 'G Z9I O Plate V

C9.Z9 / 10 OAV 99 '00' I 1 -LZ 9ΐ3 "8 968 IVA mz V

U • IS 00, 1 96S through V

Ζ6 • 99 00 • 0 896 '8' S -n through 丛 0% u Plate V

00 • ΐ 89f8 262 IVA 丛 0 z V

8S • i 00 • I fOI -82 96Γ9Ϊ 262 0 mi HOXV

0300 Ί 108 'CI 9U'I εεδ'οι- 168 O mi woxv

Z9S8 00I 9088Ζ 991 'I 068 MO mi W01V

AOSS00 • 0 8A8'9Z 808-0-688 o Dish V

0ΐ 'S 00 Z ^' Ll 299 '9-' zi 丛 0 mi 丽 V

U • SS 00 • I ΐθ 9ΐ sor G S9'8 Mil Bandit V

99 • 68 00 ■ \ 926 '2- 98S 丛 0 mi Bandit V

9Z • 92 00 • \ 8S87 2SS-6 98ε m 丛 0 丽 V

It • 6S 00 • \ 88f 9Z 892 -SI-m mi Marauder V om 00-\ 999 ΌΙ 8S9'9- 86, mm i W01V

00 • \ 900 'l 998' 9- OS'Z Marauder V

S9 '11 00 • I 891 ^ 1 ZU'Q. 96 8-mi dish V

6 • S 00 ■ ΐ 96Γ0- 36Γ6Ϊ 088 mi Dish V

86 Ί9 00 ■ I 0ΐ · 9ΐ i V

68 • 8S 00 • ΐ QL% 'U 69Α * Ζΐ Through LUZ V

93 • Of 00 • I 699 '82 LL2 顺 mi Thigh V

It Sf 00I 689 Otl6 9AS mi WOXV

99 • SS 00 • I 6A9'9S S9i-Ϊ90-Π IV 丛 0 mi

18 • 39 uu u V ending 1 n J, 1

 IL VV yuy VH

 V vLh 0077 TAT A T V

16 "9g 00ΐ ZS9 'S- 9ff' 9 m XV AO zm W0XV

02 00 fl 'i m'zi AO mi

 9ZIS 00 690 "6ΐ 988 * 6 U8 IVM mi WOIV

C9.Z9 / 10 OAV Zf 'Z 00 Ί 98 Γ 6 Ϊ 869 Ί ZZ XVI AO Thigh v

06 '00' 0 SA9-8- 'i through AO 9 hidden v

2119 00-0 9SI 09S'9- ΖΠΊ m ivi thigh v tS'9S 00 'ΐ 68Γ3- Z9f Ό- 6lf through AO 0iC2 woxv

If 19 00'ΐ 980 'SS 86S-Z9'3 8I AO i thigh v

Zl00 6 9- Ofi 'I i through O mz thigh v

ZL-L9 00 '0 8SS'9S 809 "8T- 9l JM 丛 0 \ plate v

Z6- 9 00 '0 686 ε Α8Γ0Ϊ- m 丛 0 m View V er t oo' i 6ΪΓ0Ζ Remains O Plate V

8S'9g 00 '0 O V

99 '^ 9 00' 0 95 6Ϊ ^ 9Όΐ Α9Γ9Ϊ- z mz Plate V

Π'Ζ ^ 00 '0 \\ m 丛 o mz Thigh V

66 S 00 '0 6ΐ6.0 AO z Thigh V

6S "Zt 00 Ί S9f ΐ- 99ΓΖΙ 60 m onz Thigh V

Z6'99 00 '0 808' 9 ■ iM L 丽

08 '9t 00 · ΐ 206- 1 Ζ96'6ΐ 6ΖΓ91 m 丛 o nu thigh V 00' 0 960 * 9 90f 8ΐ 90, m MO mz thigh V

9f 99 00 '0 09 Γ9δ om-work v 丛 O thigh V or 900 · 0 838 "6 80 0Ϊ-through 丛 o mz thigh V

Ι0.600 'I Ϊ8Ζ' St'6 sot through AO mz Thigh V

80 * 8 ^ 00 8 8 ^ * 6 i89'ZI- ZQf through z band V

99 'Z 00' I 89ΐ AT8'S1- lo m AO i Thigh V

99 · 00 9Ζ9'Ζε 290 ^ 1 00, IVA 丛 o Thigh V

01 "IS 00 Ί ΖΖ · 188" 61 9S6'2I 668 m O 0 Ζ8 V V 8 00

9Γ8Ζ 00'ΐ 08Γ6Ϊ UQ-91 i6S Thigh V

C9.Z9 / 10 OAV 9Z ^ f 00 • ΐ 921 • sm MO an wish V

S9'6f 00 • i 969 "Ζ SOZ Ζ osrti in m nn hidden V

00 • 889 506 '1 \\ Vl \ 丛 0 \ m Thigh V

58 '82 00 • ΐ 9 9 '■ u m picture trot 00 • ΐ m A90-91 m 丛 0 麵

00 '89 00 • 0 'AS • s oss'oz- 丛 0 zm hidden

00 ■ I οοε ■ n 019 '869' 9ΐ- Zf through MO mz Hidden V

^ z-n 00 Ί 696 ZllI-in mz thigh V

00 Ί 808 68S'0 SOS'OI o t through 丛 0 z

Zf9f 00 'ϊ • ει 6S 丛 0 Thigh V

01 9 00 • ΐ ss6 ε MO LZH comfort V

00 Ί, Zl • 6 uu thigh V

00 • I 888 • 61 A09 'l Ζ8 · 6ΐ IVA 丛 0 uu Hidden V

8T f 00 • ΐ \ u • L m 'ΐΐ 660 · IV IV AO m Thigh V

8Ζ 00 '0 m Ί-QS6 9ί IVA 0 z thigh V 6 V 00 • ΐ 0Z8 • 9 9A0 9ΐ WOl through m z \ u thigh V

00 '0 991 • L S • ei I9f 91 丛 0 z 丽

S6'Z9 00 ■ 0 m • i 9 8 • 0-00S '

00 Ί 80S • 01 989 • s IVA O Thigh V

00 • ι 9 • Π \ Lf 'T M) oon Thigh V

39-85 00 • 0 Z • Π m IVA MO im Thigh V

99 00 • 0 16Γ8Ϊ MO mi KOIV

00 Ί 966 Of 'fl TOO 967 丄 VA L) T lCo0b7o

 00 m ^ z • 91 060 '6- 9Zf through MO thigh V

00 • ΐ • SI 9iroi-communication 0 S8SZ image

Α800 ・ ΐ '08 in •% \ 609 'Ζΐ-IVA m mi K0IV

C9.Z9 / 10 OAV 912

 90 "6t 00Ί 128 -ει 893 AO Marauder v 60 Oi 00 '0 Z80-08 oir t in' t- Uf woxv i ^-00 '0 199' 6Z 962 ・ Π- OA IV 丛 0 mz Watch v ΐΖ 086.9- 622'1- 69t XVA 丛 0 i thigh v OZ 900 "0 99TS8 ZSI 'L 89 through i woxv 92" 99 00' 0 699 Ζ 6Ό 9Π '8ΐ- A9 Hiring 丛 0 mi woiv 6S'95 ΟΟ' ΐ 998 ^ 99 丛 0 mi hidden v 00 ', 9 00' 0 9ΖΓ9Ϊ 608 "91-S9 wish MO 80 woxv Ζ9" 00 '0 iS6 "9l S96.6- IVA S09Z woxv n ^ f oo '1 22Γ9ΐ m'U m 丛 0 WOIV

00 '0 Ή XV 丛 0 WOIV oo · ΐ 9εΓ6ΐ 8ΙΓ6Ϊ I9 through 丛 0 96K MOIV

88 "i9 00 '0 09, dish V

SS "89 00 '0 Ϊ8Ζ'9 0 0_ 6 ^ IVA AO i OIV ^" S 00' 0 8 ^ IVA 丛 0 im woxv

69 "Z9 00 · Ι ΖΪ9ΊΪ 899-6 Dish 丛 0 nu Thigh V

66 '9 00 Ό L "01 6 · 9 U6 G 9St through \ m Thigh V

16 '6t 00 Ί 69ΐ "6 90Γ6 Hf 9- xvM WOIV

ZO'Lf 00 u ZZ9 "8- Haruka thigh V

00 * 99 00 '0 \ ι \ -ι \ UZ'S through O mi WOIV

66 "S9 00 '0 t60'I-m' \ Z9 Hire 丛 0 Thigh V

L9 'S9 00' 0 ηι S68'3 Ϊ0 0Ϊ- I through mz Thigh V

06 '9 001 S90'6 62S6 0Ζ8ΖΙ09t 丛 丛 0 KOIV

31 '9 00 Ί 9o n 6 ^ through 丛 0 mi WOIV

C9.Z9 / 10 OAV Ill

 9ΓΙΖ 08 • 0 909 • 0- 002, 89α 9N0 z Thigh V

86 2 08 • 0 eu Ί \ 619-CI LffO- 00 890 9N3 08 隐 V

89 -11 08 • 0 SLfLl 86Z 'I m Ί-οο mo mo 6L Z WOIV

08 • 0 6Z9-91 Ϊ9Ι Ί-00Α 89α SN3 z Fragile V

66 "f 2 08 • 0 ιη · η 616 • i- οοζ 89α z woxv

U "82 08 ■ 0 098 'l ZZ \' LI 90 • i- οοζ 89α im i 舰 V

ZQ- \ Z 08 • 0 zn-n 89, • 0 οοζ 89α i Fragile V

St Sog '0 986 Ί Ul • 81 109 ms w Fragile V

Zl-LZ OS'O m-L \ Π Ϊ09 lilS so V

88 "iS OS ■ 0-980 * 91z \ 109 ins zo mi W0IV

SI S 09 -0 69 Ϊ '81 Ϊ 09 ms 10 mz W0XV

68 * 9C OS ■ 0 LU -8 6 6 * 9I 869 • zi 109 ins s i 舰 V

98 'Oi 0 996 "ZZ ΐ9ΐ 619 • \-009 ms 69 Dish V

88 U • 0 -u ^ 9 '81 A60 • l-009 so m 舰 V

9ΐ '8Z Oi'O 65811 839 Ό- 009 ms im R0XV

36 "AZ 02, ■ 0 LZfLl 9ΖΓ0 009 ins 10 mi Dish V

OA • 0 'L \ Z90 • ΐ-009 ms s mi 舰 V

00 • 0 S09 • 81 S8 through mi 隐 V

88 00 • ΐ Z80 * 6l 982 · ι \ Z8 ring 0 0 V 6, 00 • 0 09 A '8- osroi 8i6 "9 I8 through t

00 • I 989 "ΐοο * ε- 001 * 9 08 丛 0 mi Thigh V

60 '00 Ί' 9t 66 ^ '6i 099Z Comfort V

7¾ 'OP

 6? Oil 00 • 0 96S I Uoy L i 819 • LI 01 plate LVhC J 丄 V

89 -t 00 • 0 093 Ό ■ ει 丛 0 Bile V 8S 00 • 0 8 9 "92 0ΖΓ0- • SI AO mz Thigh V

88 'S9 00 • 0 i'h m • π-s through MO 8SSZ 舰 V

C9.Z9 / 10 OAV ATOM 700 1 1 ^ ππ, ώυο 190 22.58

ATOM N nRo MR o ώ n so 22. 33

ATOM. I ο ο 1 Ru, fi u o Πu u-ou 22. 74

ATOM ί u w 7 ίfiS 1 fi u * u ou u.ow 24.34

ATO 7ΠΠ, 7 qi n n u. Roou 31.92

ATOM 2587 01 D68 700 -4.067 18.929 16.566 0.80 32.72

ATOM 2588 02 D68 700 »4.645 18.509 18.933 0.80 32.63

ATOM 2589 Nl D68 700 -2.603 19.797 18.345 0.80 31.40

ATOM 2590 CP1 D68 700 -1.602 20.297 17.391 0.80 31.68 Industrial availability

 In the present invention, a new partial structure that interacts with the S1 pocket of trypsin-type serine protease was found, and a trypsin-type serine protease inhibitor was created using the same. The trypsin-type serine protease inhibitor has superior oral absorbability compared to a conventionally known compound having a partial structure that interacts with the S1 pocket through ionic binding to Asp189. It can be a protease inhibitor.

Claims

The scope of the claims

1. The following general formula (1) or (2)

(Wherein, R ¹ and R ² represent a hydrogen atom, (1- （3 alkyl group, halogen atom, C 2 —C 3 alkenyl group or ethenyl group, and R ³ and R ⁴ represent a hydrogen atom , a hydroxyl group or an amino group, X _P X _2, X ₃ and X ₄ represents CH or N, Y _t and Y ₂ represents CH or New, Y ₃ is shown Nyuita, the Ο or S A method of inhibiting a trypsin-type serine protease by allowing a compound having a group represented by the formula to act on trypsin-type serine protease, and entering the S1 pocket of the trypsin-type serine protease.

2. The following general formula (3) or (4)

(Wherein, R ¹ and R ² represent a hydrogen atom, (: 1-〇3 alkyl group, halogen atom, C 2 —C 3 alkenyl group or ethynyl group, and R ³ and R ⁴ represent a hydrogen atom XX ₂ , X ₃ and X ₄ represent CH or N, and Y ₂ represents CH or 、, Υ ₃ represents ΝΗ, 0 or S, Α and Β represents a sulfonyl group, a carbonyl group, a methylene group, an oxygen atom, a zeo atom or a nitrogen atom.) A compound having a group represented by the formula: A method for inhibiting trypsin-type serine protease by entering the S1 pocket of serine protease.

 3. A compound that inhibits a trypsin-type serine protease, wherein the compound enters the S1 pocket of a trypsin-type serine protease and is represented by the general formula (1) or (2) according to claim 1 or the general formula according to claim 2. A compound having a group represented by the formula (3) or (4).

4. A group represented by the general formula (1) or (2) described in claim 1 or the general formula (3) or (4) described in claim 2 (where R ¹ and R ² are hydrogen atoms ), Wherein the group is

 1) A 1a 190, Va l 213 and Ty r 228,

2) Ser 90, Va 1 213 and T yr 228, 3) Serl 90, Thr 213 and Tyr 228,

 4) A la 90, Va 1 213 and Ph e 228,

 5) Th r l 90, T h r 213 and T y r 228,

 6) A la 90, I 1 e 213 and T y r 228,

 7) S e r l 90, I 1 e 213 and Ty r 228,

 8) G l y l 90, T h r 213 and T y r 228, or

 9) Th r l 90, T h r 213 and T y r 228

A compound that inhibits the trypsin serine protease by entering the S1 box of the trypsin serine protease having any one of the above amino acid residues.

5. A group represented by the general formula (1) or (2) described in claim 1 or the general formula (3) or (4) described in claim 2 (where R ¹ and R ² are hydrogen atoms Is not a compound having the formula:

 1) A 1 a 190, Va 1213 and Ty r 228,

 2) S er l 90, V a 1213 and T y r 228,

 3) S er l 90, T h r 213 and T y r 228,

 4) A 1a 190, Va 1 213 and Ph e 228,

 5) Th r l 90, T h r 213 and T y r 228,

 6) A la 90, I 1 e 213 and Ty r 228,

 7) S e r l 90, I 1 e 213 and Ty r 228,

 8) G 1 y 190, T h r 213 and T y r 228, or

 9) Th r l 90, T h r 213 and T y r 228

A compound that enters the S1 box of a trypsin-type serine protease having any one of the above amino acid residues and interacts with those amino acid residues to inhibit the trypsin-type serine protease.

6. The general formula (1) or (2) according to claim 1 or the one according to claim 2 A compound having a group represented by the general formula (3) or (4) (wherein R ¹ and R ² are not hydrogen atoms),

 1) A 1 a 190, V a 1 213 and Ty r 228, or

 2) S e r l 90, V a 1 213 and T y r 228

A compound that enters the S1 box of a trypsin-type serine protease having any one of the above amino acid residues and interacts with those amino acid residues to inhibit the trypsin-type serine protease.

 7. It has a group represented by the general formula (1) or (2) according to claim 1 or the general formula (3) or (4) according to claim 2, and the group is activated blood coagulation. A compound that exerts an inhibitory effect on activated blood coagulation factor X by entering the S1 pocket of factor X.

8. A group represented by the general formula (1) or (2) described in claim 1 or the general formula (3) or (4) described in claim 2 (where R ¹ and R ² are hydrogen atoms A compound that has an inhibitory effect on activated blood coagulation factor X when the group enters the S1 pocket of activated blood coagulation factor X.

9. A group represented by the general formula (1) or (2) described in claim 1 or the general formula (3) or (4) described in claim 2 (where R ¹ and R ² are hydrogen atoms Not activated), and the group enters the S1 pocket of activated blood coagulation factor X and activates blood coagulation factor X by interacting with A1a190, Va1213 and Tyr228. A compound that exhibits an inhibitory action.

 10. A medicament comprising, as an active ingredient, a compound that inhibits trypsin serine protease by the method according to claim 1 or 2.

 11. A medicament comprising the compound according to claim 3 as an active ingredient.

 12. A trypsin-type serine protease inhibitor comprising, as an active ingredient, a compound that inhibits trypsin-type serine protease by the method of claim 1 or 2.

13. A trypsin-type serine protein comprising the compound according to claim 3 as an active ingredient. Thease inhibitor.

 1. An active blood coagulation factor comprising the compound according to claim 7 as an active ingredient;

15. A crystal of a complex of a compound that inhibits trypsin serine protease and the trypsin serine protease according to the method of claim 1 or 2.

 16. A method of using a computer to screen a drug that is expected to inhibit a trypsin-type serine protease by using data obtained by X-ray analysis of the crystal according to claim 15. .