-
1
-
-
34347260916
-
-
st American Chemical Society National Meeting, April 1-5, 2001, San Diego, CA; American Chemical Society: Washington, DC, 2001; Abstract MEDI-128.
-
st American Chemical Society National Meeting, April 1-5, 2001, San Diego, CA; American Chemical Society: Washington, DC, 2001; Abstract MEDI-128.
-
-
-
-
2
-
-
34347241977
-
-
st American Chemical Society National Meeting, April 1-5, 2001, San Diego, CA; American Chemical Society: Washington, DC 2001; Abstract MEDI-16.
-
st American Chemical Society National Meeting, April 1-5, 2001, San Diego, CA; American Chemical Society: Washington, DC 2001; Abstract MEDI-16.
-
-
-
-
3
-
-
0001111615
-
Direct factor Xa inhibitors
-
1st ed; Sasahara, A. A, Loscalzo, J, Eds, Marcel Dekker: New York
-
Vlasuk, G. P. Direct factor Xa inhibitors. In New Therapeutic Agents in Thrombosis and Thrombolysis, 1st ed; Sasahara, A. A., Loscalzo, J., Eds.; Marcel Dekker: New York, 1997; pp 261-283.
-
(1997)
New Therapeutic Agents in Thrombosis and Thrombolysis
, pp. 261-283
-
-
Vlasuk, G.P.1
-
4
-
-
0027932365
-
Direct thrombin inhibitors in cardiovascular medicine
-
(a) Lefkovits, J.; Topol, E. Direct thrombin inhibitors in cardiovascular medicine. Circulation 1994, 90, 1522-1568.
-
(1994)
Circulation
, vol.90
, pp. 1522-1568
-
-
Lefkovits, J.1
Topol, E.2
-
5
-
-
0027959329
-
Effects of synthetic thrombin inhibitor argatroban on fibrin or clot-incorporated thrombin: Comparison with heparin and recombinant hirudin
-
(b) Berry, C. N.; Girardot, C.; Lecoffre, C.; Lunven, C. Effects of synthetic thrombin inhibitor argatroban on fibrin or clot-incorporated thrombin: comparison with heparin and recombinant hirudin. Thromb. Haemost. 1994, 72, 381-386 .
-
(1994)
Thromb. Haemost
, vol.72
, pp. 381-386
-
-
Berry, C.N.1
Girardot, C.2
Lecoffre, C.3
Lunven, C.4
-
6
-
-
0026598494
-
Thrombin-specific inhibition by and slow cleavage of hirulog-1
-
(c) Wittig, J. I.; Bourdon, P.; Brezniak, D. V.; Maraganore, J. M.; Fenton, J. W., II. Thrombin-specific inhibition by and slow cleavage of hirulog-1. Biochem. J. 1992, 283, 737-43.
-
(1992)
Biochem. J
, vol.283
, pp. 737-743
-
-
Wittig, J.I.1
Bourdon, P.2
Brezniak, D.V.3
Maraganore, J.M.4
Fenton II, J.W.5
-
7
-
-
0026073345
-
Hirudin interruption of heparin-resistant arterial thrombus formation in baboons
-
(d) Kelly, A. G.; Marzee, W. M.; Krupski, W.; Bass, A.; Cadroy, Y.; Hanson, S. R.; Harker, L. A. Hirudin interruption of heparin-resistant arterial thrombus formation in baboons. Blood 1991, 77, 1006-1012.
-
(1991)
Blood
, vol.77
, pp. 1006-1012
-
-
Kelly, A.G.1
Marzee, W.M.2
Krupski, W.3
Bass, A.4
Cadroy, Y.5
Hanson, S.R.6
Harker, L.A.7
-
8
-
-
0028094869
-
Therapeutic level of anticoagulation with Warfarin in patients with mechanical prosthetic heart valves; review of literature and recommendations based on International Normalized Ratio
-
(a) Stein, P. D.; Grandison, D.; Hua, T. A. Therapeutic level of anticoagulation with Warfarin in patients with mechanical prosthetic heart valves; review of literature and recommendations based on International Normalized Ratio. Postgrad. Med. 1994, 70 (Suppl. 1), S72-S83.
-
(1994)
Postgrad. Med
, vol.70
, Issue.SUPPL. 1
-
-
Stein, P.D.1
Grandison, D.2
Hua, T.A.3
-
9
-
-
0027958326
-
The International Normalized Ratio. A guide to understanding and correcting its problems
-
(b) Hirsh, J.; Poller, L. The International Normalized Ratio. A guide to understanding and correcting its problems. Arch. Int. Med. 1994, 154, 282-288.
-
(1994)
Arch. Int. Med
, vol.154
, pp. 282-288
-
-
Hirsh, J.1
Poller, L.2
-
10
-
-
0037962878
-
Factor Xa inhibitors: Today and beyond
-
(a) Walenga, J. M.; Jeske, W. P.; Hoppensteadt, D.; Fareed, J. Factor Xa inhibitors: Today and beyond. Curr. Opin. Invest. Drugs 2003, 4, 272-281.
-
(2003)
Curr. Opin. Invest. Drugs
, vol.4
, pp. 272-281
-
-
Walenga, J.M.1
Jeske, W.P.2
Hoppensteadt, D.3
Fareed, J.4
-
11
-
-
0036180835
-
-
Kaiser, B. Factor Xa - A promising target for drug development. Cell Mol. Life Sci. 2002, 59, 189-192.
-
(b) Kaiser, B. Factor Xa - A promising target for drug development. Cell Mol. Life Sci. 2002, 59, 189-192.
-
-
-
-
12
-
-
0037231552
-
The dynamics of thrombin formation
-
(a) Mann, K. G.; Butenas, S.; Brummel, K. The dynamics of thrombin formation. Arterioscler. Thromb. Vasc. Biol. 2003, 23, 17-25.
-
(2003)
Arterioscler. Thromb. Vasc. Biol
, vol.23
, pp. 17-25
-
-
Mann, K.G.1
Butenas, S.2
Brummel, K.3
-
13
-
-
0037239007
-
Evaluation of the pharmacological properties and clinical results of the synthetic pentasaccharide (fondaparinux)
-
(b) Samama, M. M.; Gerotziafas, G. T. Evaluation of the pharmacological properties and clinical results of the synthetic pentasaccharide (fondaparinux). Thromb. Res. 2003, 109, 1-11.
-
(2003)
Thromb. Res
, vol.109
, pp. 1-11
-
-
Samama, M.M.1
Gerotziafas, G.T.2
-
14
-
-
0036897444
-
Nonpeptide factor Xa inhibitors III: Effects of DPC423, an orally-active pyrazole antithrombotic agent, on arterial thrombosis in rabbits
-
(a) Wong, P. C.; Crain, E. J.; Watson, C. A.; Zaspel, A. M.; Wright, M. R.; Lam, P. Y. S.; Pinto, D. J.; Wexler, R. R.; Knabb, R. M. Nonpeptide factor Xa inhibitors III: Effects of DPC423, an orally-active pyrazole antithrombotic agent, on arterial thrombosis in rabbits. J. Pharmacol. Exp. Ther. 2002, 303, 993-1000.
-
(2002)
J. Pharmacol. Exp. Ther
, vol.303
, pp. 993-1000
-
-
Wong, P.C.1
Crain, E.J.2
Watson, C.A.3
Zaspel, A.M.4
Wright, M.R.5
Lam, P.Y.S.6
Pinto, D.J.7
Wexler, R.R.8
Knabb, R.M.9
-
15
-
-
0035824736
-
The antithrombotic effects of CI-1031 (ZK-807834) and enoxaparin in a canine electrolytic injury model of arterial and venous thrombosis
-
(b) McClanahan, T. B.; Hicks, G. W.; Morrison, A. L.; Peng, Y. W.; Janiczek-Dolphin, N.; Mertz, T. E.; Sullivan, M. E.; Morser, J.; Juneau, P. L.; Leadley, R. The antithrombotic effects of CI-1031 (ZK-807834) and enoxaparin in a canine electrolytic injury model of arterial and venous thrombosis. Eur. J. Pharmacol. 2001, 432, 187-194.
-
(2001)
Eur. J. Pharmacol
, vol.432
, pp. 187-194
-
-
McClanahan, T.B.1
Hicks, G.W.2
Morrison, A.L.3
Peng, Y.W.4
Janiczek-Dolphin, N.5
Mertz, T.E.6
Sullivan, M.E.7
Morser, J.8
Juneau, P.L.9
Leadley, R.10
-
16
-
-
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
-
(c) Rebello, S. S.; Kasiewski, C. J.; Wang, W.; Bentley, R. G.; Morgan, S. R.; Chu, V.; Colussi, D.; Brown, K.; Perrone, M. H.; Leadley, R. J. 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
Bentley, R.G.4
Morgan, S.R.5
Chu, V.6
Colussi, D.7
Brown, K.8
Perrone, M.H.9
Leadley, R.J.10
-
17
-
-
0034696927
-
Antithrombotic and hemostatic capacity of factor Xa versus thrombin inhibitors in models of venous and arteriovenous thrombosis
-
(d) Sinha, U.; Ku, P.; Malinowski, J.; Zhu, B. Y.; Scarborough, R. M.; Marlowe, C. K.; Wong, P. W.; Lin, P. H.; Hollenbach, S. J. Antithrombotic and hemostatic capacity of factor Xa versus thrombin inhibitors in models of venous and arteriovenous thrombosis. Eur. J. Pharmacol. 2000, 395, 51-59.
-
(2000)
Eur. J. Pharmacol
, vol.395
, pp. 51-59
-
-
Sinha, U.1
Ku, P.2
Malinowski, J.3
Zhu, B.Y.4
Scarborough, R.M.5
Marlowe, C.K.6
Wong, P.W.7
Lin, P.H.8
Hollenbach, S.J.9
-
18
-
-
0032750094
-
Pharmacodynamic activity and antithrombotic efficacy of RPR120844, a novel inhibitor of coagulation factor Xa
-
(e) Leadley, R. J., Jr.; Morgan, S. R.; Bentley, R.; Bostwick, J. S.; Kasiewski, C. J.; Heran, C.; Chu, V.; Brown, K.; Moxey, P.; Ewing, W. R.; Pauls, H.; Spada, A. P.; Perrone, M. H.; Dunwiddie, C. T. Pharmacodynamic activity and antithrombotic efficacy of RPR120844, a novel inhibitor of coagulation factor Xa. J. Cardiovasc. Pharmacol. 1999, 34, 791-799.
-
(1999)
J. Cardiovasc. Pharmacol
, vol.34
, pp. 791-799
-
-
Leadley Jr., R.J.1
Morgan, S.R.2
Bentley, R.3
Bostwick, J.S.4
Kasiewski, C.J.5
Heran, C.6
Chu, V.7
Brown, K.8
Moxey, P.9
Ewing, W.R.10
Pauls, H.11
Spada, A.P.12
Perrone, M.H.13
Dunwiddie, C.T.14
-
19
-
-
0031964032
-
Antithrombotic effects of YM-60828, a newly synthesized factor Xa inhibitor, in rat thrombosis models and its effects on bleeding time
-
(f) Sato, K.; Kawasaki, T.; Hisamichi, N.; Taniuchi, Y.; Hirayama, F.; Koshio, H.; Matsumoto, Y. Antithrombotic effects of YM-60828, a newly synthesized factor Xa inhibitor, in rat thrombosis models and its effects on bleeding time. Br. J. Pharmacol. 1998, 123, 92-96.
-
(1998)
Br. J. Pharmacol
, vol.123
, pp. 92-96
-
-
Sato, K.1
Kawasaki, T.2
Hisamichi, N.3
Taniuchi, Y.4
Hirayama, F.5
Koshio, H.6
Matsumoto, Y.7
-
20
-
-
0035383645
-
Coagulation factor Xa inhibition: Biological background and rationale
-
(a) Leadley, R. J., Jr. 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 Jr., R.J.1
-
21
-
-
0344629348
-
Synthetic inhibitors of thrombin and factor Xa: From bench to bedside
-
(b) Hauptmann, J.; Stuerzebecher, J. Synthetic inhibitors of thrombin and factor Xa: From bench to bedside. Thromb. Res. 1999, 93, 203-241.
-
(1999)
Thromb. Res
, vol.93
, pp. 203-241
-
-
Hauptmann, J.1
Stuerzebecher, J.2
-
22
-
-
4644221541
-
The race to an orally active factor Xa inhibitor: Recent advances
-
Reviews: a
-
Reviews: (a) Quan, M. L.; Smallheer, J. M. The race to an orally active factor Xa inhibitor: Recent advances. Curr. Opin. Drug Discovery Dev. 2004, 7, 460-469.
-
(2004)
Curr. Opin. Drug Discovery Dev
, vol.7
, pp. 460-469
-
-
Quan, M.L.1
Smallheer, J.M.2
-
23
-
-
0141954082
-
Recent advances in the discovery and development of direct coagulation factor Xa inhibitors
-
(b) Gould, W. R.; Leadley, R. J. Recent advances in the discovery and development of direct coagulation factor Xa inhibitors. Curr. Pharm. Des. 2003, 9, 2337-2347.
-
(2003)
Curr. Pharm. Des
, vol.9
, pp. 2337-2347
-
-
Gould, W.R.1
Leadley, R.J.2
-
24
-
-
0035004409
-
Perspectives on factor Xa inhibition
-
(c) Rai, R.; Sprengler, P. A.; Elrod, K. C.; Young, W. B. Perspectives on factor Xa inhibition. Curr. Med. Chem. 2001, 8, 101-109.
-
(2001)
Curr. Med. Chem
, vol.8
, pp. 101-109
-
-
Rai, R.1
Sprengler, P.A.2
Elrod, K.C.3
Young, W.B.4
-
25
-
-
0002362826
-
Anticoagulants: Inhibitors of thrombin and factor Xa
-
(d) Sanderson, P. E. J. Anticoagulants: Inhibitors of thrombin and factor Xa. Ann. Rep. Med. Chem. 2001, 36, 79-88.
-
(2001)
Ann. Rep. Med. Chem
, vol.36
, pp. 79-88
-
-
Sanderson, P.E.J.1
-
26
-
-
3042749886
-
Factor Xa inhibitors: Recent advances in anticoagulant agents
-
(e) Zhu, B. Y.; Scarborough, R. M. Factor Xa inhibitors: Recent advances in anticoagulant agents. Ann. Rep. Med. Chem., 2000, 35, 83-102.
-
(2000)
Ann. Rep. Med. Chem
, vol.35
, pp. 83-102
-
-
Zhu, B.Y.1
Scarborough, R.M.2
-
27
-
-
0033859659
-
New advances in the discovery of thrombin and factor Xa inhibitors
-
(f) Vacca, J. P. New advances in the discovery of thrombin and factor Xa inhibitors. Curr. Opin. Chem. Biol. 2000, 4, 394-400.
-
(2000)
Curr. Opin. Chem. Biol
, vol.4
, pp. 394-400
-
-
Vacca, J.P.1
-
28
-
-
0032831727
-
Progress in the design of inhibitors of coagulation factor Xa
-
(g) Ewing, W. R.; Pauls, H. W.; Spada, A. P. Progress in the design of inhibitors of coagulation factor Xa. Drugs Future 1999, 24, 771-787.
-
(1999)
Drugs Future
, vol.24
, pp. 771-787
-
-
Ewing, W.R.1
Pauls, H.W.2
Spada, A.P.3
-
29
-
-
33750497430
-
-
Young, R. J.; Campbell, M.; Borthwick, A. D.; Brown, D.; Burns-Kurtis, C. L.; Chan, C.; Convery, M. A.; Crowe, M. C.; Dayal, S.; Diallo, H.; Kelly, H. A.; King, N. P.; Kleanthous, S.; Mason, A. M.; Mordaunt, J. E.; Patel, C.; Pateman, A. J.; Senger, S.; Shah, G. P.; Smith, P. W.; Watson, N. S.; Weston, H. E.; Zhou, P. Structure- and property-based design of factor Xa inhibitors: Pyrrolidin-2-ones with acyclic alanyl amides as P4 motifs. Bioorg. Med. Chem. Lett. 2006, 16, 5953-5957.
-
(a) Young, R. J.; Campbell, M.; Borthwick, A. D.; Brown, D.; Burns-Kurtis, C. L.; Chan, C.; Convery, M. A.; Crowe, M. C.; Dayal, S.; Diallo, H.; Kelly, H. A.; King, N. P.; Kleanthous, S.; Mason, A. M.; Mordaunt, J. E.; Patel, C.; Pateman, A. J.; Senger, S.; Shah, G. P.; Smith, P. W.; Watson, N. S.; Weston, H. E.; Zhou, P. Structure- and property-based design of factor Xa inhibitors: Pyrrolidin-2-ones with acyclic alanyl amides as P4 motifs. Bioorg. Med. Chem. Lett. 2006, 16, 5953-5957.
-
-
-
-
30
-
-
33745123026
-
-
Pinto, D. J. P.; Orwat, M. J.; Quan, M. L.; Han, Q.; Galemmo, R. A., Jr.; Amparo, E.; Wells, B.; Ellis, C.; He, M. Y.; Alexander, R. S.; Rossi, K. A.; Smallwood, A.; Wong, P. C.; Luettgen, J.M.; Rendina, A. R.; Knabb, R. M.; Mersinger, L.; Kettner, C.; Bai, S.; He, K.; Wexler, R. R.; Lam, P. Y. S. 1-[3-Aminobenzisoxazol-5′-yl]-3-trifluoromethyl-6-[2′-(3-(R) -hydroxy-N-pyrrolidinyl)methyl-[1,1′]-biphen-4-yl]-1,4,5, 6-tetrahydropyrazolo-[3,4-c]-pyridin-7-one (BMS-740808), a highly potent, selective, efficacious, and orally bioavailable inhibitor of blood coagulation factor Xa. Bioorg. Med. Chem. Lett. 2006, 16, 4141-4147.
-
(b) Pinto, D. J. P.; Orwat, M. J.; Quan, M. L.; Han, Q.; Galemmo, R. A., Jr.; Amparo, E.; Wells, B.; Ellis, C.; He, M. Y.; Alexander, R. S.; Rossi, K. A.; Smallwood, A.; Wong, P. C.; Luettgen, J.M.; Rendina, A. R.; Knabb, R. M.; Mersinger, L.; Kettner, C.; Bai, S.; He, K.; Wexler, R. R.; Lam, P. Y. S. 1-[3-Aminobenzisoxazol-5′-yl]-3-trifluoromethyl-6-[2′-(3-(R) -hydroxy-N-pyrrolidinyl)methyl-[1,1′]-biphen-4-yl]-1,4,5, 6-tetrahydropyrazolo-[3,4-c]-pyridin-7-one (BMS-740808), a highly potent, selective, efficacious, and orally bioavailable inhibitor of blood coagulation factor Xa. Bioorg. Med. Chem. Lett. 2006, 16, 4141-4147.
-
-
-
-
31
-
-
24944536065
-
-
Roehrig, S.; Straub, A.; Pohlmann, J.; Lampe, T.; Pernerstorfer, J.; Schlemmer, K. H.; Reinemer, P.; Perzborn, E. 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.
-
(c) Roehrig, S.; Straub, A.; Pohlmann, J.; Lampe, T.; Pernerstorfer, J.; Schlemmer, K. H.; Reinemer, P.; Perzborn, E. 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.
-
-
-
-
32
-
-
20144374942
-
-
Quan, M. L.; Lam, P. Y. S.; Han, Q.; Pinto, D. J. P.; He, M. Y.; Li, R.; Ellis, C. D.; Clark, C. G.; Teleha, C. A.; Sun, J. H.; Alexander, R. S.; Bai, S.; Luettgen, J. M.; Knabb, R. M.; Wong, P. C.; Wexler, R. R. 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.
-
(d) Quan, M. L.; Lam, P. Y. S.; Han, Q.; Pinto, D. J. P.; He, M. Y.; Li, R.; Ellis, C. D.; Clark, C. G.; Teleha, C. A.; Sun, J. H.; Alexander, R. S.; Bai, S.; Luettgen, J. M.; Knabb, R. M.; Wong, P. C.; Wexler, R. R. 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.
-
-
-
-
33
-
-
4744376263
-
-
Haginoya, N.; Kobayashi, S.; Komoriya, S.; Yoshino, T.; Suzuki, M.; Shimada, T.; Watanabe, K.; Hirokawa, Y.; Furugori, T.; Nagahara, T. 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.
-
(e) Haginoya, N.; Kobayashi, S.; Komoriya, S.; Yoshino, T.; Suzuki, M.; Shimada, T.; Watanabe, K.; Hirokawa, Y.; Furugori, T.; Nagahara, T. 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.
-
-
-
-
34
-
-
4644228993
-
Design, synthesis and biological activity of non-amidine factor Xa inhibitors containing pyridine N-oxide and 2-carbamoylthiazole units
-
(f) Haginoya, N.; Kobayashi, S.; Komoriya, S.; Yoshino, T.; Nagata, T.; Hirokawa, Y.; Nagahara, T. Design, synthesis and biological activity of non-amidine factor Xa inhibitors containing pyridine N-oxide and 2-carbamoylthiazole units. Bioorg. Med. Chem. 2004, 12, 5579-5586.
-
(2004)
Bioorg. Med. Chem
, vol.12
, pp. 5579-5586
-
-
Haginoya, N.1
Kobayashi, S.2
Komoriya, S.3
Yoshino, T.4
Nagata, T.5
Hirokawa, Y.6
Nagahara, T.7
-
35
-
-
3142682251
-
Factor Xa inhibitors based on a 2-carboxyindole scaffold: SAR of neutral P1 substituents
-
(g) Nazare, M.; Essrich, M.; Will, D. W.; Matter, H.; Ritter, K.; Urmann, M.; Bauer, A.; Schreuder, H.; Dudda, A.; Czech, J.; Lorenz, M.; Laux, V.; Wehner, V. 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
-
-
Nazare, M.1
Essrich, M.2
Will, D.W.3
Matter, H.4
Ritter, K.5
Urmann, M.6
Bauer, A.7
Schreuder, H.8
Dudda, A.9
Czech, J.10
Lorenz, M.11
Laux, V.12
Wehner, V.13
-
36
-
-
3142727707
-
Novel factor Xa inhibitors based on a 2-carboxyindole scaffold: SAR of P4 substituents in combination with a neutral P1 ligand
-
(h) Nazare, M.; Essrich, M.; Will, D. W.; Matter, H.; Ritter, K.; Urmann, M.; Bauer, A.; Schreuder, H.; Czech, J.; Lorenz, M.; Laux, V.; Wehner, V. 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
-
-
Nazare, M.1
Essrich, M.2
Will, D.W.3
Matter, H.4
Ritter, K.5
Urmann, M.6
Bauer, A.7
Schreuder, H.8
Czech, J.9
Lorenz, M.10
Laux, V.11
Wehner, V.12
-
37
-
-
10744220835
-
Design, synthesis and SAR of anthranilamide-based factor Xa inhibitors incorporating substituted biphenyl P4 motifs
-
(i) Zhang, P.; Bao, L.; Zuckett, J. F.; Goldman, E. A.; Jia, Z. J.; Arfsten, A.; Edwards, S.; Sinha, U.; Hutchaleelaha, A.; Park, G.; Lambing, J. L.; Hollenbach, S. J.; Scarborough, R. M.; Zhu, B. Y. 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
Goldman, E.A.4
Jia, Z.J.5
Arfsten, A.6
Edwards, S.7
Sinha, U.8
Hutchaleelaha, A.9
Park, G.10
Lambing, J.L.11
Hollenbach, S.J.12
Scarborough, R.M.13
Zhu, B.Y.14
-
38
-
-
0037468474
-
Discovery of an orally efficacious inhibitor of coagulation factor Xa which incorporates a neutral P1 ligand
-
(j) Choi-Sledeski, Y. M.; Kearney, R.; Poli, G.; Pauls, H.; Gardner, C.; Gong, Y.; Becker, M.; Davis, R.; Spada, A.; Liang, G.; Chu, V.; Brown, K.; Collussi, D.; Leadley, R., Jr.; Rebello, S.; Moxey, P.; Morgan, S.; Bentley, R.; Kasiewski, C.; Maignan, S.; Guilloteau, J.-P.; Mikol, V. 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
Pauls, H.4
Gardner, C.5
Gong, Y.6
Becker, M.7
Davis, R.8
Spada, A.9
Liang, G.10
Chu, V.11
Brown, K.12
Collussi, D.13
Leadley Jr., R.14
Rebello, S.15
Moxey, P.16
Morgan, S.17
Bentley, R.18
Kasiewski, C.19
Maignan, S.20
Guilloteau, J.-P.21
Mikol, V.22
more..
-
39
-
-
0034213954
-
Non-amidine-containing 1,2-dibenzamidobenzene inhibitors of human factor Xa with potent anticoagulant and antithrombotic activity
-
(k) Masters, J. J.; Franciskovich, J. B.; Tinsley, J. M.; Campbell, C.; Craft, T. J.; Froelich, L. L.; Gifford-Moore, D. S.; Hay, L. A.; Herron, D. K.; Klimkowski, V. J.; Kurz, K. D.; Metz, J. T.; Ratz, A. M.; Shuman, R. T.; Smith, G. F.; Smith, T.; Towner, R. D.; Wiley, M. R.; Wilson, A.; Yee, Y. K. Non-amidine-containing 1,2-dibenzamidobenzene inhibitors of human factor Xa with potent anticoagulant and antithrombotic activity. J. Med. Chem. 2000, 43, 2087-2092.
-
(2000)
J. Med. Chem
, vol.43
, pp. 2087-2092
-
-
Masters, J.J.1
Franciskovich, J.B.2
Tinsley, J.M.3
Campbell, C.4
Craft, T.J.5
Froelich, L.L.6
Gifford-Moore, D.S.7
Hay, L.A.8
Herron, D.K.9
Klimkowski, V.J.10
Kurz, K.D.11
Metz, J.T.12
Ratz, A.M.13
Shuman, R.T.14
Smith, G.F.15
Smith, T.16
Towner, R.D.17
Wiley, M.R.18
Wilson, A.19
Yee, Y.K.20
more..
-
40
-
-
17444438416
-
1,2-Dibenzamidobenzene inhibitors of human factor Xa
-
(l) Herron, D. K.; Goodson, T., Jr.; Wiley, M. R.; Weir, L. C.; Kyle, J. A.; Yee, Y. K.; Tebbe, A. L.; Tinsley, J. M.; Mendel, D.; Masters, J. J.; Franciskovich, J. B.; Sawyer, J. S.; Beight, D. W.; Ratz, A. M.; Milot, G.; Hall, S. E.; Klimkowski, V. J.; Wikel, J. H.; Eastwood, B. J.; Towner, R. D.; Gifford-Moore, D. S.; Craft, T. J.; Smith, G. F. 1,2-Dibenzamidobenzene inhibitors of human factor Xa. J. Med. Chem. 2000, 43, 859-872.
-
(2000)
J. Med. Chem
, vol.43
, pp. 859-872
-
-
Herron, D.K.1
Goodson Jr., T.2
Wiley, M.R.3
Weir, L.C.4
Kyle, J.A.5
Yee, Y.K.6
Tebbe, A.L.7
Tinsley, J.M.8
Mendel, D.9
Masters, J.J.10
Franciskovich, J.B.11
Sawyer, J.S.12
Beight, D.W.13
Ratz, A.M.14
Milot, G.15
Hall, S.E.16
Klimkowski, V.J.17
Wikel, J.H.18
Eastwood, B.J.19
Towner, R.D.20
Gifford-Moore, D.S.21
Craft, T.J.22
Smith, G.F.23
more..
-
41
-
-
0037328153
-
Structure-activity relationships of substituted benzothiophene-anthranilamide factor Xa inhibitors
-
(a) Chou, Y. L.; Davey, D. D.; Eagen, K. A.; Griedel, B. D.; Karanjawala, R.; Phillips, G. B.; Sacchi, K. L.; Shaw, K. J.; Wu, S. C.; Lentz, D.; Liang, A.; Trinh, L.; Morrissey, M. M.; Kochanny, M. J. 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
Griedel, B.D.4
Karanjawala, R.5
Phillips, G.B.6
Sacchi, K.L.7
Shaw, K.J.8
Wu, S.C.9
Lentz, D.10
Liang, A.11
Trinh, L.12
Morrissey, M.M.13
Kochanny, M.J.14
-
42
-
-
0038065501
-
Discovery and characterization of a potent and selective non-amidine inhibitor of human factor Xa
-
(b) Liang, A. M.; Light, D. R.; Kochanny, M.; Trinh, L.; Rumennik, G.; Lentz, D.; Post, J.; Morser, J.; Snider, M. Discovery and characterization of a potent and selective non-amidine inhibitor of human factor Xa. Biochem. Pharmacol. 2003, 65, 1407-1418.
-
(2003)
Biochem. Pharmacol
, vol.65
, pp. 1407-1418
-
-
Liang, A.M.1
Light, D.R.2
Kochanny, M.3
Trinh, L.4
Rumennik, G.5
Lentz, D.6
Post, J.7
Morser, J.8
Snider, M.9
-
43
-
-
33846617308
-
Substituted thiophene-anthranilamides as potent inhibitors of human factor Xa
-
Kochanny, M. J.; Adler, M.; Ewing, J.; Griedel, B. D.; Ho, E.; Karanjawala, R.; Lee, W.; Lentz, D.; Liang, A. M.; Morrissey, M. M.; Phillips, G. B.; Post, J.; Sacchi, K. L.; Sakata, S. T.; Subramanyam, B.; Vergona, R.; Walters, J.; White, K. A.; Whitlow, M.; Ye, B.; Zhao, Z.; Shaw, K. J. Substituted thiophene-anthranilamides as potent inhibitors of human factor Xa. Bioorg. Med. Chem. 2007, 15, 2127-2146.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 2127-2146
-
-
Kochanny, M.J.1
Adler, M.2
Ewing, J.3
Griedel, B.D.4
Ho, E.5
Karanjawala, R.6
Lee, W.7
Lentz, D.8
Liang, A.M.9
Morrissey, M.M.10
Phillips, G.B.11
Post, J.12
Sacchi, K.L.13
Sakata, S.T.14
Subramanyam, B.15
Vergona, R.16
Walters, J.17
White, K.A.18
Whitlow, M.19
Ye, B.20
Zhao, Z.21
Shaw, K.J.22
more..
-
44
-
-
0034624694
-
-
2-Aroylanthramlamide inhibitors of human factor Xa. J. Med. Chem. 2000, 43, 873-882.
-
2-Aroylanthramlamide inhibitors of human factor Xa. J. Med. Chem. 2000, 43, 873-882.
-
-
-
-
45
-
-
0035939308
-
Neutral inhibitors of the serine protease factor Xa
-
(b) Shrader, W. D.; Young, W. B.; Sprengeler, P. A.; Sangalang, J. C.; Elrod, K.; Carr, G. Neutral inhibitors of the serine protease factor Xa. Bioorg. Med. Chem. Lett. 2001, 11, 1801-1804.
-
(2001)
Bioorg. Med. Chem. Lett
, vol.11
, pp. 1801-1804
-
-
Shrader, W.D.1
Young, W.B.2
Sprengeler, P.A.3
Sangalang, J.C.4
Elrod, K.5
Carr, G.6
-
46
-
-
10744219996
-
Design, synthesis and SAR of anthranilamide-based factor Xa inhibitors with improved functional activity
-
(c) Zhang, P.; Bao, L.; Zuckett, J. F.; Jia, Z. J.; Woolfrey, J.; Arfsten, A.; Edwards, S.; Sinha, U.; Hutchaleelaha, A.; Lambing, J. L.; Hollenbach, S. J.; Scarborough, R. M.; Zhu, B. Y. 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
Jia, Z.J.4
Woolfrey, J.5
Arfsten, A.6
Edwards, S.7
Sinha, U.8
Hutchaleelaha, A.9
Lambing, J.L.10
Hollenbach, S.J.11
Scarborough, R.M.12
Zhu, B.Y.13
-
47
-
-
0343443219
-
Potent noncovalent thrombin inhibitors that utilize the unique amino acid D-dicyclohexylalanine in the P3 position. Implications on oral bioavailability and antithrombotic efficacy
-
See references 10i, 10k, 11a, 12, 13c, and the following: a
-
See references 10i, 10k, 11a, 12, 13c, and the following: (a) Tucker, T. J.; Lumma, W. C.; Lewis, S. D.; Gardell, S. J.; Lucas, B. J.; Baskin, E. P.; Woltmann, R.; Lynch, J. J.; Lyle, E. A.; Appleby, S. D.; Chen, I.-W.; Dancheck, K. B.; Vacca, J. P. Potent noncovalent thrombin inhibitors that utilize the unique amino acid D-dicyclohexylalanine in the P3 position. Implications on oral bioavailability and antithrombotic efficacy. J. Med. Chem. 1997, 40, 1565-1569.
-
(1997)
J. Med. Chem
, vol.40
, pp. 1565-1569
-
-
Tucker, T.J.1
Lumma, W.C.2
Lewis, S.D.3
Gardell, S.J.4
Lucas, B.J.5
Baskin, E.P.6
Woltmann, R.7
Lynch, J.J.8
Lyle, E.A.9
Appleby, S.D.10
Chen, I.-W.11
Dancheck, K.B.12
Vacca, J.P.13
-
48
-
-
15444357642
-
-
Tucker, T. J.; Brady, S. F.; Lumma, W. C.; Lewis, S. D.; Gardell, S. J.; Naylor-Olsen, A. M.; Yan, Y.; Sisko, J. T.; Stauffer, K. J.; Lucas, B. J.; Lynch, J. J.; Cook, J. J.; Stranieri, M. T.; Holahan, M. A.; Lyle, E. A.; Baskin, E. P.; Chen, I. W.; Dancheck, K. B.; Krueger, J. A.; Cooper, C. M.; Vacca, J. P. Design and synthesis of a series of potent and orally bioavailable noncovalent thrombin inhibitors that utilize nonbasic groups in the P1 position. J. Med. Chem. 1998, 41, 3210-3219.
-
(b) Tucker, T. J.; Brady, S. F.; Lumma, W. C.; Lewis, S. D.; Gardell, S. J.; Naylor-Olsen, A. M.; Yan, Y.; Sisko, J. T.; Stauffer, K. J.; Lucas, B. J.; Lynch, J. J.; Cook, J. J.; Stranieri, M. T.; Holahan, M. A.; Lyle, E. A.; Baskin, E. P.; Chen, I. W.; Dancheck, K. B.; Krueger, J. A.; Cooper, C. M.; Vacca, J. P. Design and synthesis of a series of potent and orally bioavailable noncovalent thrombin inhibitors that utilize nonbasic groups in the P1 position. J. Med. Chem. 1998, 41, 3210-3219.
-
-
-
-
49
-
-
0017570846
-
A new sensitive and highly specific chromogenic peptide substrate for factor Xa
-
Aurell, L.; Friberger, P.; Karlsson, G.; Claeson, G. A new sensitive and highly specific chromogenic peptide substrate for factor Xa. Thromb. Res. 1977, 11, 595-609.
-
(1977)
Thromb. Res
, vol.11
, pp. 595-609
-
-
Aurell, L.1
Friberger, P.2
Karlsson, G.3
Claeson, G.4
-
50
-
-
34347215008
-
-
Although this method has a shortcoming in that active metabolites could alter results, the speed at which we were able to generate data to influence the design process outweighed this shortcoming
-
Although this method has a shortcoming in that active metabolites could alter results, the speed at which we were able to generate data to influence the design process outweighed this shortcoming.
-
-
-
-
51
-
-
34347268694
-
-
Arnaiz, D. O, Chou, Y. L, Griedel, B. D, Karanjawala, R. E, Kochanny, M. J, Lee, W, Liang, A. M, Morrissey, M. M, Phillips, G. B, Sacchi, K. L, Sakata, S. T, Shaw, K. J, Snider, R. M, Wu, S. C, Ye, B, Zhao, Z. ortho-Anthranilamide derivatives as anticoagulants. U.S. Patent 6,140,351, October 31, 2000
-
Arnaiz, D. O.; Chou, Y. L.; Griedel, B. D.; Karanjawala, R. E.; Kochanny, M. J.; Lee, W.; Liang, A. M.; Morrissey, M. M.; Phillips, G. B.; Sacchi, K. L.; Sakata, S. T.; Shaw, K. J.; Snider, R. M.; Wu, S. C.; Ye, B.; Zhao, Z. ortho-Anthranilamide derivatives as anticoagulants. U.S. Patent 6,140,351, October 31, 2000.
-
-
-
-
52
-
-
0037468471
-
Molecular structures of human factor Xa complexed with ketopiperazine inhibitors: Preference for a neutral group in the S1 pocket
-
See reference 10c and the following: a
-
See reference 10c and the following: (a) Maignan, S.; Guilloteau, J. P.; Choi-Sledeski, Y. M.; Becker, M. R.; Ewing, W. R.; Pauls, H. W.; Spada, A. P.; Mikol, V. 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
Becker, M.R.4
Ewing, W.R.5
Pauls, H.W.6
Spada, A.P.7
Mikol, V.8
-
53
-
-
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
-
(b) Nazare, M.; Will, D. W.; Matter, H.; Schreuder, H.; Ritter, K.; Urmann, M.; Essrich, M.; Bauer, A.; Wagner, M.; Czech, J.; Lorenz, M.; Laux, V.; Wehner, V. 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
-
-
Nazare, M.1
Will, D.W.2
Matter, H.3
Schreuder, H.4
Ritter, K.5
Urmann, M.6
Essrich, M.7
Bauer, A.8
Wagner, M.9
Czech, J.10
Lorenz, M.11
Laux, V.12
Wehner, V.13
-
54
-
-
33646567824
-
The discovery of glycine and related amino acid-based factor Xa inhibitors
-
(c) Kohrt, J. T.; Filipiski, K. J.; Cody, W. L.; Bigge, C. F.; La, F.; Welch, K.; Dahring, T.; Bryant, J. W.; Leonard, D.; Bolton, G.; Narasimhan, L.; Zhang, E.; Peterson, J. T.; Haarer, S.; Sahasrabudhe, V.; Janiczek, N.; Desiraju, S.; Hena, M.; Fiakpui, C.; Saraswat, N.; Sharma, R.; Sun, S.; Maiti, S. N.; Leadley, R.; Edmunds, J. J. The discovery of glycine and related amino acid-based factor Xa inhibitors. Bioorg. Med. Chem. 2006, 14, 4379-4392.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 4379-4392
-
-
Kohrt, J.T.1
Filipiski, K.J.2
Cody, W.L.3
Bigge, C.F.4
La, F.5
Welch, K.6
Dahring, T.7
Bryant, J.W.8
Leonard, D.9
Bolton, G.10
Narasimhan, L.11
Zhang, E.12
Peterson, J.T.13
Haarer, S.14
Sahasrabudhe, V.15
Janiczek, N.16
Desiraju, S.17
Hena, M.18
Fiakpui, C.19
Saraswat, N.20
Sharma, R.21
Sun, S.22
Maiti, S.N.23
Leadley, R.24
Edmunds, J.J.25
more..
-
55
-
-
0036523422
-
pH-Dependent binding modes observed in trypsin crystals: Lessons for structure-based drug design
-
Stubbs, M. T.; Reyda, S.; Dullweber, F.; Moller, M.; Klebe, G.; Dorsch, D.; Mederski, W. W.; Wurziger, H. pH-Dependent binding modes observed in trypsin crystals: Lessons for structure-based drug design. ChemBioChem 2002, 3, 246-249.
-
(2002)
ChemBioChem
, vol.3
, pp. 246-249
-
-
Stubbs, M.T.1
Reyda, S.2
Dullweber, F.3
Moller, M.4
Klebe, G.5
Dorsch, D.6
Mederski, W.W.7
Wurziger, H.8
-
56
-
-
0035194282
-
Engineering inhibitors highly selective for the S1 sites of Ser190 trypsin-like serine protease drug targets
-
(a) Katz, B. A.; Sprengeler, P. A.; Luong, C.; Verner, E.; Elrod, K.; Kirtley, M.; Jane, J.; Spencer, J. R.; Breitenbucher, J. G.; Hui, H.; McGee, D.; Allen, D.; Martelli, A.; Mackman, R. L. Engineering inhibitors highly selective for the S1 sites of Ser190 trypsin-like serine protease drug targets. Chem. Biol. 2001, 8, 1107-1121.
-
(2001)
Chem. Biol
, vol.8
, pp. 1107-1121
-
-
Katz, B.A.1
Sprengeler, P.A.2
Luong, C.3
Verner, E.4
Elrod, K.5
Kirtley, M.6
Jane, J.7
Spencer, J.R.8
Breitenbucher, J.G.9
Hui, H.10
McGee, D.11
Allen, D.12
Martelli, A.13
Mackman, R.L.14
-
57
-
-
0035829469
-
Exploiting subsite S1 of trypsin-like serine proteases for selectivity: Potent and selective inhibitors of urokinase-type plasminogen activator
-
(b) Mackman, R. L.; Katz, B. A.; Breitenbucher, J. G.; Hui, H. C.; Verner, E.; Luong, C.; Liu, L.; Sprengeler, P. A. Exploiting subsite S1 of trypsin-like serine proteases for selectivity: Potent and selective inhibitors of urokinase-type plasminogen activator. J. Med. Chem. 2001, 44, 3856-3871.
-
(2001)
J. Med. Chem
, vol.44
, pp. 3856-3871
-
-
Mackman, R.L.1
Katz, B.A.2
Breitenbucher, J.G.3
Hui, H.C.4
Verner, E.5
Luong, C.6
Liu, L.7
Sprengeler, P.A.8
-
58
-
-
0037207123
-
-
A detailed discussion of the crystal structure of compound 13a bound to fXa is described elsewhere: Adler, M.; Kochanny, M. J.; Ye, B.; Rumennik, G.; Light, D. R.; Biancalana, S.; Whitlow, M. Crystal structures of two potent nonamidine inhibitors bound to factor Xa. Biochemistry 2002, 41, 15514-15523.
-
A detailed discussion of the crystal structure of compound 13a bound to fXa is described elsewhere: Adler, M.; Kochanny, M. J.; Ye, B.; Rumennik, G.; Light, D. R.; Biancalana, S.; Whitlow, M. Crystal structures of two potent nonamidine inhibitors bound to factor Xa. Biochemistry 2002, 41, 15514-15523.
-
-
-
-
59
-
-
0035382791
-
The use of 3D structure data in the design of specific factor Xa inhibitors
-
(a) Maignan, S.; Mikol, V. The use of 3D structure data in the design of specific factor Xa inhibitors. Curr. Top. Med. Chem. 2001, 1, 161-174.
-
(2001)
Curr. Top. Med. Chem
, vol.1
, pp. 161-174
-
-
Maignan, S.1
Mikol, V.2
-
60
-
-
0034680369
-
Preparation, characterization, and the crystal structure of the inhibitor ZK-807834 (CI-1031) complexed with factor Xa
-
(b) Adler, M.; Davey, D. D.; Phillips, G. B.; Kim, S.-H.; Jancarik, J.; Rumennik, G.; Light, D. R.; Whitlow, M. Preparation, characterization, and the crystal structure of the inhibitor ZK-807834 (CI-1031) complexed with factor Xa. Biochemistry 2000, 39, 12534-12542.
-
(2000)
Biochemistry
, vol.39
, pp. 12534-12542
-
-
Adler, M.1
Davey, D.D.2
Phillips, G.B.3
Kim, S.-H.4
Jancarik, J.5
Rumennik, G.6
Light, D.R.7
Whitlow, M.8
-
61
-
-
0019752371
-
Assay of coagulation proteases using peptide chromogenic and fluorogenic substrates
-
Lottenberg, R.; Christensen, U.; Jackson, C. M.; Coleman, P. L. Assay of coagulation proteases using peptide chromogenic and fluorogenic substrates. Methods Enzymol. 1981, 80, 341-361.
-
(1981)
Methods Enzymol
, vol.80
, pp. 341-361
-
-
Lottenberg, R.1
Christensen, U.2
Jackson, C.M.3
Coleman, P.L.4
-
62
-
-
0025683260
-
Tick anticoagulant peptide: Kinetic analysis of the recombinant inhibitor with blood coagulation factor Xa
-
(a) Jordan, S. P.; Waxman, L.; Smith, D. E.; Vlasuk, G. P. Tick anticoagulant peptide: kinetic analysis of the recombinant inhibitor with blood coagulation factor Xa. Biochem. 1990, 29, 11095-11100.
-
(1990)
Biochem
, vol.29
, pp. 11095-11100
-
-
Jordan, S.P.1
Waxman, L.2
Smith, D.E.3
Vlasuk, G.P.4
-
63
-
-
0014454095
-
Kinetics of the reversible inhibition of enzyme-catalysed reactions by tight-binding inhibitors
-
(b) Morrison, J. F. Kinetics of the reversible inhibition of enzyme-catalysed reactions by tight-binding inhibitors. Biochim. Biophys. Acta 1969, 185, 269-286.
-
(1969)
Biochim. Biophys. Acta
, vol.185
, pp. 269-286
-
-
Morrison, J.F.1
|