-
1
-
-
2442674610
-
-
American Heart Association: Dallas, Texas. American Heart Association
-
American Heart Association: Heart Disease and Stroke Statistics - 2005 Update. Dallas, Texas. American Heart Association (2004).
-
(2004)
Heart Disease and Stroke Statistics - 2005 Update
-
-
-
2
-
-
0035383645
-
Coagulation Factor Xa inhibition: Biological background and rationale
-
LEADLEY RJ: Coagulation Factor Xa inhibition: biological background and rationale. Curr. Top. Med. Chem. (2001) 1:151-159.
-
(2001)
Curr. Top. Med. Chem.
, vol.1
, pp. 151-159
-
-
Leadley, R.J.1
-
6
-
-
10744220641
-
Structure-based design of novel guanidine/benzamidine mimics: Potent and orally bioavailable Factor Xa inhibitors as novel anticoagulants
-
LAM PY, CLARK CG, LI R et al.: Structure-based design of novel guanidine/benzamidine mimics: potent and orally bioavailable Factor Xa inhibitors as novel anticoagulants. J. Med. Chem. (2003) 46:4405-4418.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 4405-4418
-
-
Lam, P.Y.1
Clark, C.G.2
Li, R.3
-
7
-
-
4644221541
-
The race to an orally active Factor Xa inhibitor: Recent advances
-
QUAN ML, SMALLHEER JM: The race to an orally active Factor Xa inhibitor: recent advances. Curr. Opin. Drug Disc. Dev. (2004) 7:460-469.
-
(2004)
Curr. Opin. Drug Disc. Dev.
, vol.7
, pp. 460-469
-
-
Quan, M.L.1
Smallheer, J.M.2
-
8
-
-
0028265990
-
Dibasic (amidinoaryl)propanoic acid derivatives as novel blood coagulation Factor Xa inhibitors
-
NAGAHARA T, YOKOYAMA Y, INAMURA K et al.: Dibasic (amidinoaryl)propanoic acid derivatives as novel blood coagulation Factor Xa inhibitors. J. Med. Chem. (1994) 37:1200-1207.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1200-1207
-
-
Nagahara, T.1
Yokoyama, Y.2
Inamura, K.3
-
9
-
-
0037150191
-
First experience with direct Factor Xa inhibition in patients with stable coronary disease: A pharmacokinetic and pharmacodynamic evaluation
-
DYKE CK, BECKER RC, KLEIMAN NS et al.: First experience with direct Factor Xa inhibition in patients with stable coronary disease: a pharmacokinetic and pharmacodynamic evaluation. Circulation (2002) 105:2385-2391.
-
(2002)
Circulation
, vol.105
, pp. 2385-2391
-
-
Dyke, C.K.1
Becker, R.C.2
Kleiman, N.S.3
-
10
-
-
4644316833
-
Initial experience with Factor Xa inhibition in percutaneous coronary intervention: The XaNADU-PIC Pilot
-
ALEXANDER JH, DYKE CK, YANG H et al.: Initial experience with Factor Xa inhibition in percutaneous coronary intervention: the XaNADU-PIC Pilot. J. Thromb. Haemost. (2004) 2:234-241.
-
(2004)
J. Thromb. Haemost.
, vol.2
, pp. 234-241
-
-
Alexander, J.H.1
Dyke, C.K.2
Yang, H.3
-
11
-
-
0035865785
-
Discovery of 1-[3-(aminomethyl)phenyl]-N-[3-fluoro- 2′-(methylsulfonyl)-[1,1′-biphenyl]-4-yl]-3- (trifluoromethyl)-1H-pyrazole-5-carboxamide (DPC-423), a highly potent, selective, and orally bioavailable inhibitor of blood coagulation Factor Xa
-
PINTO DJ, ORWAT MJ, WANG S et al.: Discovery of 1-[3-(aminomethyl)phenyl]-N-[3-fluoro- 2′-(methylsulfonyl)-[1,1′-biphenyl]-4-yl]-3- (trifluoromethyl)-1H-pyrazole-5-carboxamide (DPC-423), a highly potent, selective, and orally bioavailable inhibitor of blood coagulation Factor Xa. J. Med. Chem. (2001) 44:566-578.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 566-578
-
-
Pinto, D.J.1
Orwat, M.J.2
Wang, S.3
-
12
-
-
0036387145
-
Nonpeptide Factor Xa inhibitors: DPC423, a highly potent and orally bioavailable pyrazole antithrombotic agent
-
WONG PC, PINTO DJ, KNABB RM: Nonpeptide Factor Xa inhibitors: DPC423, a highly potent and orally bioavailable pyrazole antithrombotic agent. Cardiovasc. Drug Rev. (2002) 20:137-152.
-
(2002)
Cardiovasc. Drug Rev.
, vol.20
, pp. 137-152
-
-
Wong, P.C.1
Pinto, D.J.2
Knabb, R.M.3
-
13
-
-
20144374942
-
Discovery of 1-(3′-aminobenzisoxazol-5′-yl)-3- trifluoromethyl-N-[2-fluoro-4-[(2′-dimethylaminomethyl) imidazol-1-yl]phenyl]-1H-pyrazole-5-carboxyamide hydrochloride (razaxaban), a highly potent, selective, and orally bioavailable Factor Xa inhibitor
-
QUAN ML, LAM PY, HAN Q et al.: Discovery of 1-(3′-aminobenzisoxazol-5′-yl)-3- trifluoromethyl-N-[2-fluoro-4-[(2′-dimethylaminomethyl) imidazol-1-yl]phenyl]-1H-pyrazole-5-carboxyamide hydrochloride (razaxaban), a highly potent, selective, and orally bioavailable Factor Xa inhibitor. J. Med. Chem. (2005) 48:1729-1744.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1729-1744
-
-
Quan, M.L.1
Lam, P.Y.2
Han, Q.3
-
14
-
-
11244325810
-
A Phase II randomized, double-blind, five-arm, parallel-group, dose-response study of a new oral directly-acting Factor Xa inhibitor, razaxaban, for the prevention of deep vein thrombosis in knee replacement surgery - On behalf of the razaxaban investigators
-
Abst 41
-
LASSEN MR. DAVIDSON BL, GALLUS A et al.: A Phase II randomized, double-blind, five-arm, parallel-group, dose-response study of a new oral directly-acting Factor Xa inhibitor, razaxaban, for the prevention of deep vein thrombosis in knee replacement surgery - on behalf of the razaxaban investigators. Blood (2003) 102: Abst 41.
-
(2003)
Blood
, vol.102
-
-
Lassen, M.R.1
Davidson, B.L.2
Gallus, A.3
-
15
-
-
24944536065
-
Discovery of the novel antithrombotic agent 5-chloro-N-({(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl) phenyl]-1,3-oxazolidin-5-yl}methyl)thiophene-2-carboxamide (BAY 59-7939): An oral, direct Factor Xa inhibitor
-
ROEHRIG S, STRAUB A, POHLMANN J et al.: Discovery of the novel antithrombotic agent 5-chloro-N-({(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl) phenyl]-1,3-oxazolidin-5-yl}methyl)thiophene-2-carboxamide (BAY 59-7939): an oral, direct Factor Xa inhibitor. J. Med. Chem. (2005) 48:5900-5908.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 5900-5908
-
-
Roehrig, S.1
Straub, A.2
Pohlmann, J.3
-
16
-
-
33144456514
-
An oral, direct Factor Xa inhibitor - BAY 59-7939 - For prophylaxis against aenous ahromboembolism after total knee replacement: A dose-ranging study
-
Sydney, Australia Abstract 02573
-
TURPIE AC, FISHER WD, BAUER K et al.: An oral, direct Factor Xa inhibitor - BAY 59-7939 - for prophylaxis against aenous ahromboembolism after total knee replacement: a dose-ranging study. International Society for Thrombosis and Hacmostasis. Sydney, Australia (2005) Abstract 02573.
-
(2005)
International Society for Thrombosis and Hacmostasis
-
-
Turpie, A.C.1
Fisher, W.D.2
Bauer, K.3
-
17
-
-
0037124199
-
Optimization of the β-aminoester class of Factor Xa inhibitors. Part 1: P4 and side-chain modifications for improved in vitro potency
-
CZEKAJ M, KLEIN SI, GUERTIN KR et al.: Optimization of the β-aminoester class of Factor Xa inhibitors. Part 1: P4 and side-chain modifications for improved in vitro potency. Bioorg. Med. Chem. Lett. (2002) 12:1667-1670.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1667-1670
-
-
Czekaj, M.1
Klein, S.I.2
Guertin, K.R.3
-
18
-
-
0037124202
-
Optimization of the β-aminoester class of Factor Xa inhibitors. Part 2: Identification of FXV673 as a potent and selective inhibitor with excellent in vivo anticoagulant activity
-
GUERTIN KR, GARDNER CJ, KLEIN SI et al.: Optimization of the β-aminoester class of Factor Xa inhibitors. Part 2: Identification of FXV673 as a potent and selective inhibitor with excellent in vivo anticoagulant activity. Bioorg. Med. Chem. Lett. (2002) 12:1671-1674.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1671-1674
-
-
Guertin, K.R.1
Gardner, C.J.2
Klein, S.I.3
-
19
-
-
0035880858
-
Pharmacological characterization of a novel Factor Xa inhibitor, FXV673
-
CHU V, BROWN K, COLUSSI D et al.: Pharmacological characterization of a novel Factor Xa inhibitor, FXV673. Thromb. Res. (2001) 103:309-324.
-
(2001)
Thromb. Res.
, vol.103
, pp. 309-324
-
-
Chu, V.1
Brown, K.2
Colussi, D.3
-
20
-
-
0034887402
-
Antithrombotic efficacy of a novel Factor Xa inhibitor, FXV673, in a canine model of coronary artery thrombolysis
-
REBELLO SS, BENTLEY RG, MORGAN SR et al.: Antithrombotic efficacy of a novel Factor Xa inhibitor, FXV673, in a canine model of coronary artery thrombolysis. Br. J. Pharmacol. (2001) 133:1190-1198.
-
(2001)
Br. J. Pharmacol.
, vol.133
, pp. 1190-1198
-
-
Rebello, S.S.1
Bentley, R.G.2
Morgan, S.R.3
-
21
-
-
0034914281
-
Role of short-term inhibition of Factor Xa by FXV673 in arterial passivation: A study in a chronic model of thrombosis in conscious dogs
-
REBELLO SS, KASIEWSKI CJ, WANG W et al.: Role of short-term inhibition of Factor Xa by FXV673 in arterial passivation: a study in a chronic model of thrombosis in conscious dogs. J. Cardiovasc. Pharmacol. (2001) 38:288-297.
-
(2001)
J. Cardiovasc. Pharmacol.
, vol.38
, pp. 288-297
-
-
Rebello, S.S.1
Kasiewski, C.J.2
Wang, W.3
-
22
-
-
0346992348
-
Direct thrombin inhibitors for anticoagulation
-
NUTESCU EA, WITTKOWSKY AK: Direct thrombin inhibitors for anticoagulation. Ann. Pharmacother. (2004) 38:99-109.
-
(2004)
Ann. Pharmacother.
, vol.38
, pp. 99-109
-
-
Nutescu, E.A.1
Wittkowsky, A.K.2
-
23
-
-
0034658164
-
Solid-phase parallel synthesis of azarene pyrrolidinones as Factor Xa inhibitors
-
GONG Y, BECKER M, CHOI-SLEDESKI YM et al.: Solid-phase parallel synthesis of azarene pyrrolidinones as Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2000) 10:1033-1036.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 1033-1036
-
-
Gong, Y.1
Becker, M.2
Choi-Sledeski, Y.M.3
-
24
-
-
0037468474
-
Discovery of an orally efficacious inhibitor of coagulation Factor Xa which incorporates a neutral P1 ligand
-
CHOI-SLEDESKI YM, KEARNEY R, POLI G et al.: Discovery of an orally efficacious inhibitor of coagulation Factor Xa which incorporates a neutral P1 ligand. J. Med. Chem. (2003) 46:681-684.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 681-684
-
-
Choi-Sledeski, Y.M.1
Kearney, R.2
Poli, G.3
-
25
-
-
0034976145
-
Recent advances in Factor Xa inhibitors
-
BETZ A: Recent advances in Factor Xa inhibitors. Expert Opin. Ther. Patents (2001) 11:1007-1017.
-
(2001)
Expert Opin. Ther. Patents
, vol.11
, pp. 1007-1017
-
-
Betz, A.1
-
26
-
-
0037468471
-
Molecular structures of human Factor Xa complexed with ketopiperazine inhibitors: Preference for a neutral group in the S1 pocket
-
MAIGNAN S, GUILLOTEAU JP, CHOI-SLEDESKI YM et al.: Molecular structures of human Factor Xa complexed with ketopiperazine inhibitors: preference for a neutral group in the S1 pocket. J. Med. Chem. (2003) 46:685-690.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 685-690
-
-
Maignan, S.1
Guilloteau, J.P.2
Choi-Sledeski, Y.M.3
-
27
-
-
18344396419
-
Benzimidazoles and isosteric compounds as potent and selective Factor Xa inhibitors
-
HE W, HANNEY B, MYERS MR et al.: Benzimidazoles and isosteric compounds as potent and selective Factor Xa inhibitors. Bioorg. Med. Chem Lett. (2002) 12:919-922.
-
(2002)
Bioorg. Med. Chem Lett.
, vol.12
, pp. 919-922
-
-
He, W.1
Hanney, B.2
Myers, M.R.3
-
28
-
-
0035383371
-
The design of competitive, small molecule inhibitors of coagulation Factor Xa
-
PAULS HW, EWING WR: The design of competitive, small molecule inhibitors of coagulation Factor Xa. Curr. Top. Med. Chem. (2001) 1:83-100.
-
(2001)
Curr. Top. Med. Chem.
, vol.1
, pp. 83-100
-
-
Pauls, H.W.1
Ewing, W.R.2
-
29
-
-
0141954082
-
Recent advances in the discovery and development of direct coagulation Factor Xa inhibitors
-
GOULD WR, LEADLEY RJ: Recent advances in the discovery and development of direct coagulation Factor Xa inhibitors. Curr. Pharm. Design (2003) 9:2337-2347.
-
(2003)
Curr. Pharm. Design
, vol.9
, pp. 2337-2347
-
-
Gould, W.R.1
Leadley, R.J.2
-
30
-
-
2342452009
-
Novel Factor Xa inhibitors based on a benzoic acid scaffold incorporating a neutral P1 ligand
-
NAZARÉ M, MATTER H, KLINGLER O et al.: Novel Factor Xa inhibitors based on a benzoic acid scaffold incorporating a neutral P1 ligand. Bioorg. Med. Chem. Lett. (2004) 14:2801-2805.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 2801-2805
-
-
Nazaré, M.1
Matter, H.2
Klingler, O.3
-
31
-
-
18344364519
-
Structural requirements for Factor Xa inhibition by 3-oxybenzamides with neutral P1 substituents: Combining X-ray crystallography, 3D-QSAR, and tailored scoring functions
-
MATTER H, WILL DW, NAZARÉ M et al.: Structural requirements for Factor Xa inhibition by 3-oxybenzamides with neutral P1 substituents: combining X-ray crystallography, 3D-QSAR, and tailored scoring functions. J. Med. Chem. (2005) 48:3290-3312.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 3290-3312
-
-
Matter, H.1
Will, D.W.2
Nazaré, M.3
-
32
-
-
3142682251
-
Factor Xa inhibitors based on a 2-carboxyindole scaffold: SAR of neutral P1 substituents
-
NAZARÉ M, ESSRICH M, WILL DW et al.: Factor Xa inhibitors based on a 2-carboxyindole scaffold: SAR of neutral P1 substituents. Bioorg. Med. Chem. Lett. (2004) 14:4191-4195.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 4191-4195
-
-
Nazaré, M.1
Essrich, M.2
Will, D.W.3
-
33
-
-
22244460783
-
Probing the subpockets of Factor Xa reveals two binding modes for inhibitors based on a 2-carboxyindole scaffold: A study combining structure-activity relationship and X-ray crystallography
-
NAZARÉ M, WILL DW, MATTER H et al.: Probing the subpockets of Factor Xa reveals two binding modes for inhibitors based on a 2-carboxyindole scaffold: a study combining structure-activity relationship and X-ray crystallography. J. Med. Chem. (2005) 48:4511-4525.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 4511-4525
-
-
Nazaré, M.1
Will, D.W.2
Matter, H.3
-
34
-
-
3142727707
-
Novel Factor Xa inhibitors based on a 2-carboxyindole scaffold: SAR of P4 substituents in combination with a neutral P1 ligand
-
NAZARÉ M, ESSRICH M, WILL DW et al.: Novel Factor Xa inhibitors based on a 2-carboxyindole scaffold: SAR of P4 substituents in combination with a neutral P1 ligand. Bioorg. Med. Chem Lett. (2004) 14:4197-4201.
-
(2004)
Bioorg. Med. Chem Lett.
, vol.14
, pp. 4197-4201
-
-
Nazaré, M.1
Essrich, M.2
Will, D.W.3
-
35
-
-
33144462374
-
Discovery of the novel antithrombotic agent BAY 59-7939, an orally active, direct Factor Xa inhibitor
-
228th ACS National Meeting. Philadelphia, USA MEDI-156
-
ROEHRIG S, STRAUB A, POHLMANN J et al.: Discovery of the novel antithrombotic agent BAY 59-7939, an orally active, direct Factor Xa inhibitor. 228th ACS National Meeting. Philadelphia, USA (2004) MEDI-156.
-
(2004)
-
-
Roehrig, S.1
Straub, A.2
Pohlmann, J.3
-
36
-
-
22844442726
-
In vitro and in vivo studies of the novel antithrombotic agent BAY 59-7939 - An oral, direct Factor Xa inhibitor
-
PERZBORN E, STRASSBURGER J, POHLMANN J et al.: In vitro and in vivo studies of the novel antithrombotic agent BAY 59-7939 - an oral, direct Factor Xa inhibitor. J. Thromb. Haemost. (2005) 3:514-521.
-
(2005)
J. Thromb. Haemost.
, vol.3
, pp. 514-521
-
-
Perzborn, E.1
Strassburger, J.2
Pohlmann, J.3
-
37
-
-
24944439340
-
Multiple dose escalation study investigating the pharmacodynamics, safety, and pharmacokinetics of BAY 59-7939 an oral, direct Factor Xa inhibitor in healthy male subjects
-
KUBITZA D, BECKA M, WENSING G et al.: Multiple dose escalation study investigating the pharmacodynamics, safety, and pharmacokinetics of BAY 59-7939 an oral, direct Factor Xa inhibitor in healthy male subjects. Blood (2003) 102:811a.
-
(2003)
Blood
, vol.102
-
-
Kubitza, D.1
Becka, M.2
Wensing, G.3
-
38
-
-
24944439340
-
Single dose escalation study investigating the pharmacodynamics, safety, and pharmacokinetics of BAY 59-7939 an oral, direct Factor Xa inhibitor in healthy male subjects
-
KUBITZA D, BECKA M, WENSING G et al.: Single dose escalation study investigating the pharmacodynamics, safety, and pharmacokinetics of BAY 59-7939 an oral, direct Factor Xa inhibitor in healthy male subjects. Blood (2003) 102:813a.
-
(2003)
Blood
, vol.102
-
-
Kubitza, D.1
Becka, M.2
Wensing, G.3
-
39
-
-
0035383215
-
Discovery of the Factor Xa inhibitor, ZK 807834 (CI-1031)
-
LIGHT DR, GUILFORD WJ: Discovery of the Factor Xa inhibitor, ZK 807834 (CI-1031). Curr. Top. Med. Chem. (2001) 1:121-136.
-
(2001)
Curr. Top. Med. Chem.
, vol.1
, pp. 121-136
-
-
Light, D.R.1
Guilford, W.J.2
-
40
-
-
0034193505
-
Design, synthesis, and in vitro biological activity of indole-based Factor Xa inhibitors
-
ARNAIZ DO, ZHAO Z, LIANG A et al.: Design, synthesis, and in vitro biological activity of indole-based Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2000) 10:957-961.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 957-961
-
-
Arnaiz, D.O.1
Zhao, Z.2
Liang, A.3
-
41
-
-
0034194347
-
Design, synthesis, and in vitro biological activity of benzimidazole based Factor Xa inhibitors
-
ZHAO Z, ARNAIZ DO, GRIEDEL B et al.: Design, synthesis, and in vitro biological activity of benzimidazole based Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2000) 10:963-966.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 963-966
-
-
Zhao, Z.1
Arnaiz, D.O.2
Griedel, B.3
-
42
-
-
18344368811
-
Design and synthesis of aminophenol-base Factor Xa inhibitors
-
WU S, GUILFORD WJ, CHOU Y-L et al.: Design and synthesis of aminophenol-base Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2002) 12:1307-1310.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1307-1310
-
-
Wu, S.1
Guilford, W.J.2
Chou, Y.-L.3
-
43
-
-
0037328153
-
Structure-activity relationships of substituted benzothiophene-anthranilamide Factor Xa inhibitors
-
CHOU Y-L, DAVEY DD, EAGEN KA et al.: Structure-activity relationships of substituted benzothiophene-anthranilamide Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2003) 13:507-511.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 507-511
-
-
Chou, Y.-L.1
Davey, D.D.2
Eagen, K.A.3
-
44
-
-
0037207123
-
Crystal structures of two potent nonamidine inhibitors bound to Factor Xa
-
ADLER M, KOCHANNY MJ, YE B et al.: Crystal structures of two potent nonamidine inhibitors bound to Factor Xa. Biochemistry (2002) 41:15514-15523.
-
(2002)
Biochemistry
, vol.41
, pp. 15514-15523
-
-
Adler, M.1
Kochanny, M.J.2
Ye, B.3
-
45
-
-
0035382790
-
The design and synthesis of noncovalent Factor Xa inhibitors
-
QUAN ML, WEXLER RR: The design and synthesis of noncovalent Factor Xa inhibitors. Curr. Top. Med. Chem. (2001) 1:137-149.
-
(2001)
Curr. Top. Med. Chem.
, vol.1
, pp. 137-149
-
-
Quan, M.L.1
Wexler, R.R.2
-
46
-
-
20144363496
-
Antithrombotic effects of razaxaban, an orally-active Factor Xa inhibitor, in rabbit models of thrombosis
-
Abst 3011
-
WONG PC, WATSON CA, CRAIN EJ et al.: Antithrombotic effects of razaxaban, an orally-active Factor Xa inhibitor, in rabbit models of thrombosis. Blood (2003) 102: Abst 3011.
-
(2003)
Blood
, vol.102
-
-
Wong, P.C.1
Watson, C.A.2
Crain, E.J.3
-
47
-
-
0037325621
-
Nonbenzamidine tetrazole derivatives as Factor Xa inhibitors
-
QUAN ML, ELLIS CD, HE MY: Nonbenzamidine tetrazole derivatives as Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2003) 13:369-373.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 369-373
-
-
Quan, M.L.1
Ellis, C.D.2
He, M.Y.3
-
48
-
-
0037463812
-
Nonbenzamidine isoxazoline derivatives as Factor Xa inhibitors
-
QUAN ML, ELLIS CD, HE MY et al.: Nonbenzamidine isoxazoline derivatives as Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2003) 13:1023-1028.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1023-1028
-
-
Quan, M.L.1
Ellis, C.D.2
He, M.Y.3
-
49
-
-
33144459966
-
Ketene aminals based lactam derivatives as novel class of orally bioavailable FXa inhibitors
-
226th ACS National Meeting. New York, USA MEDI-81
-
SHI Y, SITKOFF D, ZHANG J et al.: Ketene aminals based lactam derivatives as novel class of orally bioavailable FXa inhibitors. 226th ACS National Meeting. New York, USA (2003) MEDI-81.
-
(2003)
-
-
Shi, Y.1
Sitkoff, D.2
Zhang, J.3
-
50
-
-
2342635946
-
Orally active Factor Xa inhibitors: 4,5,6,7-tetrahydrothiarzolo[5,4-c]pyridine derivatives
-
HAGINOYA N, KOBAYASHI S, KOMORIYA S et al.: Orally active Factor Xa inhibitors: 4,5,6,7-tetrahydrothiarzolo[5,4-c]pyridine derivatives. Bioorg. Med. Chem. Lett. (2004 14:2935-2939.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 2935-2939
-
-
Haginoya, N.1
Kobayashi, S.2
Komoriya, S.3
-
51
-
-
4744376263
-
Synthesis and conformational analysis of a non-amidine Factor Xa inhibitor that incorporates 5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine as S4 binding element
-
HAGINOYA N, KOBAYASHI S, KOMORIYA S et al.: Synthesis and conformational analysis of a non-amidine Factor Xa inhibitor that incorporates 5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine as S4 binding element. J. Med. Chem. (2004) 47:5167-5182.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 5167-5182
-
-
Haginoya, N.1
Kobayashi, S.2
Komoriya, S.3
-
52
-
-
4644228993
-
Design, synthesis, and biological activity of non-amidine Factor Xa inhibitors containing pyridine N-oxide and 2-carbamoylthiazole units
-
HAGINOYA N, KOBAYASHI S, KOMORIYA S et al.: Design, synthesis, and biological activity of non-amidine Factor Xa inhibitors containing pyridine N-oxide and 2-carbamoylthiazole units. Bioorg. Med. Chem. Lett. (2004) 12:5579-5586.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 5579-5586
-
-
Haginoya, N.1
Kobayashi, S.2
Komoriya, S.3
-
53
-
-
21144453825
-
Design, synthesis, and biological activity of non-basic compounds as Factor Xa inhibitors: SAR study of S1 and aryl binding sites
-
KOMORIYA S, HAGINOYA N, KOBAYASHI S et al.: Design, synthesis, and biological activity of non-basic compounds as Factor Xa inhibitors: SAR study of S1 and aryl binding sites. Bioorg. Med. Chem. Lett. (2005) 13:3927-3954.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3927-3954
-
-
Komoriya, S.1
Haginoya, N.2
Kobayashi, S.3
-
54
-
-
33144465540
-
Anthranilamide inhibitors of Factor Xa
-
229th ACS National Meeting. San Diego, USA MEDI-246
-
MENDEL D, MARQUART AL, JOSEPH S et al.: Anthranilamide inhibitors of Factor Xa. 229th ACS National Meeting. San Diego, USA (2005). MEDI-246.
-
(2005)
-
-
Mendel, D.1
Marquart, A.L.2
Joseph, S.3
-
55
-
-
17844385569
-
New anticoagulants: Beyond heparin, low-molecular-weight heparin and warfain
-
BATES SM, WEITZ JI: New anticoagulants: beyond heparin, low-molecular-weight heparin and warfain. Br. J. Pharmacol. (2005) 144:1017-1028.
-
(2005)
Br. J. Pharmacol.
, vol.144
, pp. 1017-1028
-
-
Bates, S.M.1
Weitz, J.I.2
-
56
-
-
0035848391
-
The design of phenylglycine containing benzamidine carboxamides as potent and selective inhibitors of Factor Xa
-
JONES SD, LIEBESCHUETZ JW, MORGAN PJ et al.: The design of phenylglycine containing benzamidine carboxamides as potent and selective inhibitors of Factor Xa. Bioorg. Med. Chem. Lett. (2001) 11:733-736.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 733-736
-
-
Jones, S.D.1
Liebeschuetz, J.W.2
Morgan, P.J.3
-
57
-
-
33144464604
-
Bicyclic S1-binding constructs in a series of phenyl glycine-based inhibitors of human Factor Xa
-
224th ACS National Meeting. Boston, USA MEDI-284
-
MASTERS JJ, WEBER WW, FRANCISKOVICH JB et al.: Bicyclic S1-binding constructs in a series of phenyl glycine-based inhibitors of human Factor Xa. 224th ACS National Meeting. Boston, USA (2002) MEDI-284.
-
(2002)
-
-
Masters, J.J.1
Weber, W.W.2
Franciskovich, J.B.3
-
58
-
-
12444250679
-
A four component coupling strategy for the synthesis of E-phenylglycinamide-derived non-covalent Factor Xa inhibitors
-
SHEEHAN SM, MASTERS JJ, WILEY MR et al.: A four component coupling strategy for the synthesis of E-phenylglycinamide-derived non-covalent Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2003) 13:2255-2259.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2255-2259
-
-
Sheehan, S.M.1
Masters, J.J.2
Wiley, M.R.3
-
59
-
-
33144475211
-
Non-aromatic E-amino acid-derived inhibitors of human FXa
-
228th ACS National Meeting. Philadelphia, USA MEDI-252
-
WILEY MR, SMITH SM, BASTIAN JA et al.: Non-aromatic E-amino acid-derived inhibitors of human FXa. 228th ACS National Meeting. Philadelphia, USA (2004) MEDI-252.
-
(2004)
-
-
Wiley, M.R.1
Smith, S.M.2
Bastian, J.A.3
-
60
-
-
33144473894
-
SAR investigation of heteroatom containing non-arylglycine inhibitors of human fXa
-
228th ACS National Meeting. Philadelphia, USA MEDI-254
-
WILEY MR, BASTIAN JA, SALL DJ et al.: SAR investigation of heteroatom containing non-arylglycine inhibitors of human fXa. 228th ACS National Meeting. Philadelphia, USA (2004) MEDI-254.
-
(2004)
-
-
Wiley, M.R.1
Bastian, J.A.2
Sall, D.J.3
-
61
-
-
33144471275
-
1,2-Aminoethanol-derived non-covalent Factor Xa inhibitors
-
226th ACS National Meeting. New York, USA MEDI-357
-
SHEEHAN SM, WATSON BM, WILEY MR et al.: 1,2-Aminoethanol-derived non-covalent Factor Xa inhibitors. 226th ACS National Meeting. New York, USA (2003) MEDI-357.
-
(2003)
-
-
Sheehan, S.M.1
Watson, B.M.2
Wiley, M.R.3
-
62
-
-
0141768350
-
A general synthesis of 1-aryl carbamoyl-2-alkyl-4-aryl substituted semicarbazides as nonbasic Factor Xa inhibitors
-
MEDERSKI WW, GERMANN M: A general synthesis of 1-aryl carbamoyl-2-alkyl-4-aryl substituted semicarbazides as nonbasic Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2003) 13:3715-3718.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3715-3718
-
-
Mederski, W.W.1
Germann, M.2
-
63
-
-
2942527396
-
Halothiophene benzimidazoles as P1 surrogates of inhibitors of blood coagulation Factor Xa
-
MEDERSKI WW, DORSCH D, ANZALI S et al.: Halothiophene benzimidazoles as P1 surrogates of inhibitors of blood coagulation Factor Xa. Bioorg. Med. Chem. Lett. (2004) 14:3763-3769.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 3763-3769
-
-
Mederski, W.W.1
Dorsch, D.2
Anzali, S.3
-
64
-
-
7044274358
-
Chlorothiophenecarboxamides as P1 surrogates of inhibitors of blood coagulation Factor Xa
-
MEDERSKI WWKR, CEZANNE B, VAN AMSTERDAM C et al.: Chlorothiophenecarboxamides as P1 surrogates of inhibitors of blood coagulation Factor Xa. Bioorg. Med. Chem. Lett. (2004) 14:5817-5822.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 5817-5822
-
-
Mederski, W.W.K.R.1
Cezanne, B.2
van Amsterdam, C.3
-
65
-
-
33144472472
-
Novel solubilizing S4-residues for Factor Xa inhibitors: Synthesis and structure-activity relationships of 1-aryl-2-imino-pyrrolidine and -piperidine derivatives
-
228th ACS National Meeting. Philadelphia, USA MEDI-253
-
CEZANNE B, DORSCH D, MEDERSKI WW et al.: Novel solubilizing S4-residues for Factor Xa inhibitors: synthesis and structure-activity relationships of 1-aryl-2-imino-pyrrolidine and -piperidine derivatives. 228th ACS National Meeting. Philadelphia, USA (2004) MEDI-253.
-
(2004)
-
-
Cezanne, B.1
Dorsch, D.2
Mederski, W.W.3
-
66
-
-
0037013433
-
Design, synthesis, and SAR of substituted acrylamides as Factor Xa inhibitors
-
SONG Y, CLIZBE L, BHAKTA C et al.: Design, synthesis, and SAR of substituted acrylamides as Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2002) 12:1511-1515.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1511-1515
-
-
Song, Y.1
Clizbe, L.2
Bhakta, C.3
-
67
-
-
0037025465
-
Substituted arylamides as Factor Xa inhibitors: Improving bioavailability by P1 modification
-
SONG Y, CLIZBE L, BHAKTA C et al.: Substituted arylamides as Factor Xa inhibitors: improving bioavailability by P1 modification. Bioorg. Med. Chem. Lett. (2002) 12:2043-2046.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 2043-2046
-
-
Song, Y.1
Clizbe, L.2
Bhakta, C.3
-
68
-
-
0037212871
-
Design and synthesis of Factor Xa inhibitors and their prodrugs
-
SONG Y, CLIZBE L, BHAKTA C et al.: Design and synthesis of Factor Xa inhibitors and their prodrugs. Bioorg. Med. Chem. Lett. (2003) 13:297-300.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 297-300
-
-
Song, Y.1
Clizbe, L.2
Bhakta, C.3
-
69
-
-
0037124198
-
Design, synthesis, and biological activity of novel non-amidine Factor Xa inhibitors. Part 1: Structure-activity relationships of the substituted 1-(2-napthyl)-1H-pyrazole-5-carboxylamides
-
JIA ZJ, WU Y, HUANG W et al.: Design, synthesis, and biological activity of novel non-amidine Factor Xa inhibitors. Part 1: structure-activity relationships of the substituted 1-(2-napthyl)-1H-pyrazole-5-carboxylamides. Bioorg. Med. Chem. Lett. (2002) 12:1651-1655.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1651-1655
-
-
Jia, Z.J.1
Wu, Y.2
Huang, W.3
-
70
-
-
10744224048
-
1-(2-Napthyl)-1H-pyrazole-5-carboxylamides as potent Factor Xa inhibitors. Part 2: A survey of P4 motifs
-
JIA ZJ, WU Y, HUANG W et al.: 1-(2-Napthyl)-1H-pyrazole-5-carboxylamides as potent Factor Xa inhibitors. Part 2: a survey of P4 motifs. Bioorg. Med. Chem. Lett. (2004) 14:1221-1227.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 1221-1227
-
-
Jia, Z.J.1
Wu, Y.2
Huang, W.3
-
71
-
-
10744221472
-
1-(2-Napthyl)- 1H-pyrazole-5-carboxylamides as potent Factor Xa inhibitors. Part 3: Design, synthesis, and SAR of orally bioavailable benzamidine-P4 inhibitors
-
JIA ZJ, WU Y, HUANG W et al.: 1-(2-Napthyl)- 1H-pyrazole-5-carboxylamides as potent Factor Xa inhibitors. Part 3: design, synthesis, and SAR of orally bioavailable benzamidine-P4 inhibitors. Bioorg. Med. Chem. Lett. (2004) 14:1229-1234.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 1229-1234
-
-
Jia, Z.J.1
Wu, Y.2
Huang, W.3
-
72
-
-
0037124195
-
Design, synthesis, and SAR of monobenzamidines and aminoisoquinolines as Factor Xa inhibitors
-
ZHANG P, ZUCKETT JF, WOOLFREY J et al.: Design, synthesis, and SAR of monobenzamidines and aminoisoquinolines as Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2002) 12:1657-1661.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1657-1661
-
-
Zhang, P.1
Zuckett, J.F.2
Woolfrey, J.3
-
73
-
-
10744220835
-
Design, synthesis, and SAR of anthranilamide-based Factor Xa inhibitors incorporating substituted biphenyl P4 motifs
-
ZHANG P. BAO L, ZUCKETT JF et al.: Design, synthesis, and SAR of anthranilamide-based Factor Xa inhibitors incorporating substituted biphenyl P4 motifs. Bioorg. Med. Chem. Lett. (2004) 14:983-987.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 983-987
-
-
Zhang, P.1
Bao, L.2
Zuckett, J.F.3
-
74
-
-
10744219996
-
Design, synthesis, and SAR of anthranilamide-based Factor Xa inhibitors with improved functional activity
-
ZHANG P, BAO L, ZUCKETT JF et al.: Design, synthesis, and SAR of anthranilamide-based Factor Xa inhibitors with improved functional activity. Bioorg. Med. Chem. Lett. (2004) 14:989-993.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 989-993
-
-
Zhang, P.1
Bao, L.2
Zuckett, J.F.3
-
75
-
-
11144357441
-
N,N-Dialkylated 4-(4-arylsulfonylpiperazine-1-carbonyl)-benzamidines and 4-((4-arylsulfonyl)-2-oxo-piperazin-1-ylmethyl)-benzamides as potent Factor Xa inhibitors
-
JIA ZJ, SU T, ZUCKETT JF et al.: N,N-Dialkylated 4-(4-arylsulfonylpiperazine-1-carbonyl)-benzamidines and 4-((4-arylsulfonyl)-2-oxo-piperazin-1-ylmethyl)-benzamides as potent Factor Xa inhibitors. Bioorg. Med. Chem. Lett. (2004) 14:2073-2078.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 2073-2078
-
-
Jia, Z.J.1
Su, T.2
Zuckett, J.F.3
-
76
-
-
0034761462
-
Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as Factor Xa inhibitor
-
NISHIDA H, MIYAZAKI Y, KITAMURA Y et al.: Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as Factor Xa inhibitor. Chem. Pharm. Bull. (2001) 49:1237-1244.
-
(2001)
Chem. Pharm. Bull.
, vol.49
, pp. 1237-1244
-
-
Nishida, H.1
Miyazaki, Y.2
Kitamura, Y.3
-
77
-
-
19044367143
-
Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as a Factor Xa inhibitor II. Substituent effect on biological activities
-
NISHIDA H, MIYAZAKI Y, MUKAIHIRA T et al.: Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as a Factor Xa inhibitor II. Substituent effect on biological activities. Chem. Pharm. Bull. (2002) 50:1187-1194.
-
(2002)
Chem. Pharm. Bull.
, vol.50
, pp. 1187-1194
-
-
Nishida, H.1
Miyazaki, Y.2
Mukaihira, T.3
-
78
-
-
4644358773
-
Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as Factor Xa inhibitors III. Effect of ring opening of piperazinone moiery on inhibition
-
NISHIDA H, MIYAZAKI Y, MUKAIHIRA T et al.: Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as Factor Xa inhibitors III. Effect of ring opening of piperazinone moiery on inhibition. Chem. Pharm. Bull. (2004) 52:459-462.
-
(2004)
Chem. Pharm. Bull.
, vol.52
, pp. 459-462
-
-
Nishida, H.1
Miyazaki, Y.2
Mukaihira, T.3
-
79
-
-
4644261286
-
Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as Factor Xa inhibitors IV. A series of new derivatives containing a spiro[5H-oxazolo[3,2-a]pyrazine-2(3H), 4′-piperidin]-5-one skeleton
-
NISHIDA H, MUKAIHIRA T, SAITOH F et al.: Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as Factor Xa inhibitors IV. A series of new derivatives containing a spiro[5H-oxazolo[3,2-a]pyrazine-2(3H), 4′-piperidin]-5-one skeleton. Chem. Pharm. Bull. (2004) 52:406-412.
-
(2004)
Chem. Pharm. Bull.
, vol.52
, pp. 406-412
-
-
Nishida, H.1
Mukaihira, T.2
Saitoh, F.3
-
80
-
-
33144474261
-
Design, synthesis and biological activities of new potent Factor Xa inhibitor
-
228th ACS National Meeting. Philadelphia, USA MEDI-251
-
NISHIDA H, MUKAIHIRA T, SAITOH F et al.: Design, synthesis and biological activities of new potent Factor Xa inhibitor. 228th ACS National Meeting. Philadelphia, USA (2004), MEDI-251.
-
(2004)
-
-
Nishida, H.1
Mukaihira, T.2
Saitoh, F.3
-
81
-
-
0034597606
-
Rational design, synthesis, and biological activity of benzoxazinones as novel Factor Xa inhibitors
-
DUDLEY DA, BUNKER AM, CHI L et al.: Rational design, synthesis, and biological activity of benzoxazinones as novel Factor Xa inhibitors. J. Med. Chem. (2000) 43:4063-4070.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 4063-4070
-
-
Dudley, D.A.1
Bunker, A.M.2
Chi, L.3
-
82
-
-
3242776164
-
Design, synthesis and biological activity of potent and selective inhibitors of blood coagulation Factor Xa
-
WILLARDSEN JA, DUDLEY DA, CODY WL et al.: Design, synthesis and biological activity of potent and selective inhibitors of blood coagulation Factor Xa. J. Med. Chem. (2004) 47:4089-4099.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 4089-4099
-
-
Willardsen, J.A.1
Dudley, D.A.2
Cody, W.L.3
-
83
-
-
18344374666
-
The discovery of YM-60828: A potent, selective and orally-bioavailable Factor Xa inhibitor
-
HIRAYAMA F, KOSHIO H, KATAYAMA N et al.: The discovery of YM-60828: a potent, selective and orally-bioavailable Factor Xa inhibitor. Bioorg. Med. Chem. (2002) 10:1509-1523.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 1509-1523
-
-
Hirayama, F.1
Koshio, H.2
Katayama, N.3
-
84
-
-
0031823861
-
Antithrombotic effect of YM-75466 is separated from its effect on bleeding time and coagulation time
-
SATO K, KAKU S, HIRAYAMA F et al.: Antithrombotic effect of YM-75466 is separated from its effect on bleeding time and coagulation time. Eur. J. Pharmacol. (1998) 352:59-63.
-
(1998)
Eur. J. Pharmacol.
, vol.352
, pp. 59-63
-
-
Sato, K.1
Kaku, S.2
Hirayama, F.3
-
85
-
-
0032577589
-
Antithrombotic effectS of YM-75466 in three thrombosis models in guinea pigs
-
SATO K, KAWASAKI T, HISAMICHI N et al.: Antithrombotic effectS of YM-75466 in three thrombosis models in guinea pigs. Eur. J. Pharmacol. (1998) 350:87-91.
-
(1998)
Eur. J. Pharmacol.
, vol.350
, pp. 87-91
-
-
Sato, K.1
Kawasaki, T.2
Hisamichi, N.3
-
86
-
-
0036285561
-
Design, synthesis and biological activity of YM-60828 derivatives: Potent and orally-bioavailable Factor Xa inhibitors based on naphthoanilide and naphthalensulfonanilide templates
-
HIRAYAMA F, KOSHIO H, ISHIHARA T et al.: Design, synthesis and biological activity of YM-60828 derivatives: potent and orally-bioavailable Factor Xa inhibitors based on naphthoanilide and naphthalensulfonanilide templates. Bioorg. Med. Chem. (2002) 10:2597-2610.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 2597-2610
-
-
Hirayama, F.1
Koshio, H.2
Ishihara, T.3
-
87
-
-
0037295132
-
Design, synthesis and biological activity of YM-60828 derivatives. Part 2: Potent and orally-bioavailable Factor Xa inhibitors based on benzothiadiazine-4-one template
-
HIRAYAMA F, KOSHIO H, KATAYAMA N et al.: Design, synthesis and biological activity of YM-60828 derivatives. Part 2: potent and orally-bioavailable Factor Xa inhibitors based on benzothiadiazine-4-one template. Bioorg. Med. Chem. (2003) 11:367-381.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 367-381
-
-
Hirayama, F.1
Koshio, H.2
Katayama, N.3
-
88
-
-
11144353708
-
Synthesis and biological activity of novel 1,4-diazepane derivatives as Factor Xa inhibitor with potent anticoagulant and antithrombotic activity
-
KOSHIO H, HIRAYAMA F, ISHIHARA T et al.: Synthesis and biological activity of novel 1,4-diazepane derivatives as Factor Xa inhibitor with potent anticoagulant and antithrombotic activity Bioorg. Med. Chem. (2004) 12:2179-2191.
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 2179-2191
-
-
Koshio, H.1
Hirayama, F.2
Ishihara, T.3
-
89
-
-
20244385921
-
Synthesis and biological activity of novel 1,2-disubstituted benzene derivatives as Factor Xa inhibitors
-
KOSHIO H, HIRAYAMA F, ISHIHARA T et al.: Synthesis and biological activity of novel 1,2-disubstituted benzene derivatives as Factor Xa inhibitors. Bioorg. Med. Chem. (2005) 13:1305-1323.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 1305-1323
-
-
Koshio, H.1
Hirayama, F.2
Ishihara, T.3
|