-
1
-
-
0023242324
-
Thrombosis and atherosclerosis: Regulatory role of interactions among blood components and endothelium
-
Scharf, R.E., Harker, L.A. Thrombosis and atherosclerosis: Regulatory role of interactions among blood components and endothelium. Blut 1987, 55: 131-44.
-
(1987)
Blut
, vol.55
, pp. 131-144
-
-
Scharf, R.E.1
Harker, L.A.2
-
2
-
-
0025006615
-
Atherosclerotic plaque rupture and thrombosis. Evolving concepts
-
Fuster, V., Stein, B., Ambrose, J.A., Badimon, L., Badimon, J.J., Chesebro, J.H. Atherosclerotic plaque rupture and thrombosis. Evolving concepts. Circulation 1990, 82: II47-59.
-
(1990)
Circulation
, vol.82
-
-
Fuster, V.1
Stein, B.2
Ambrose, J.A.3
Badimon, L.4
Badimon, J.J.5
Chesebro, J.H.6
-
3
-
-
0031801933
-
Syndromes of thrombosis and hypercoagulability. Congenital and acquired causes of thrombosis
-
Bick, R.L., Kaplan, H. Syndromes of thrombosis and hypercoagulability. Congenital and acquired causes of thrombosis. Med Clin North Am 1998, 82: 409-58.
-
(1998)
Med Clin North Am
, vol.82
, pp. 409-458
-
-
Bick, R.L.1
Kaplan, H.2
-
4
-
-
0002661387
-
New antithrombotic drugs: A perspective
-
Fareed, J., Hoppensteadt, D., Bick, R.L. New antithrombotic drugs: A perspective. Curr Opin Cardiovasc Pulm Renal Invest Drugs 1999, 1: 40-55.
-
(1999)
Curr Opin Cardiovasc Pulm Renal Invest Drugs
, vol.1
, pp. 40-55
-
-
Fareed, J.1
Hoppensteadt, D.2
Bick, R.L.3
-
5
-
-
0032505039
-
Clinical potential of antithrombotic drugs in coronary syndromes
-
Turpie, A.G. Clinical potential of antithrombotic drugs in coronary syndromes. Am J Cardiol 1998, 82: 11-4L.
-
(1998)
Am J Cardiol
, vol.82
-
-
Turpie, A.G.1
-
6
-
-
0031802256
-
Current recommendations for warfarin therapy. Use and monitoring
-
Triplett, D.A. Current recommendations for warfarin therapy. Use and monitoring. Med Clin North Am 1998, 82: 601-11.
-
(1998)
Med Clin North Am
, vol.82
, pp. 601-611
-
-
Triplett, D.A.1
-
7
-
-
0342869489
-
Development of pharmacological adjuncts to coronary angioplasty for the prevention of restenosis
-
Douglas, S.A., Feuerstein, G.Z. Development of pharmacological adjuncts to coronary angioplasty for the prevention of restenosis. Curr Res Vasc Dis 1998, 3: 39-58.
-
(1998)
Curr Res Vasc Dis
, vol.3
, pp. 39-58
-
-
Douglas, S.A.1
Feuerstein, G.Z.2
-
8
-
-
0025224552
-
Platelet membrane glycoproteins: Functions in cellular interactions
-
Kieffer, N., Phillips, D.R. Platelet membrane glycoproteins: Functions in cellular interactions. Annu Rev Cell Biol 1990, 6: 329-57.
-
(1990)
Annu Rev Cell Biol
, vol.6
, pp. 329-357
-
-
Kieffer, N.1
Phillips, D.R.2
-
9
-
-
0031729333
-
New antithrombotic agents
-
Weitz, J.I., Hirsh, J. New antithrombotic agents. Chest 1998, 114: 715-27S.
-
(1998)
Chest
, vol.114
-
-
Weitz, J.I.1
Hirsh, J.2
-
10
-
-
0026569416
-
Comparison of subcutaneous standard low-molecular weight heparin with intravenous standard heparin in proximal deep-vein thrombosis
-
Prandoni, P., Lensing, A., Buller, H. et al. Comparison of subcutaneous standard low-molecular weight heparin with intravenous standard heparin in proximal deep-vein thrombosis. Lancet 1992, 339: 441-5.
-
(1992)
Lancet
, vol.339
, pp. 441-445
-
-
Prandoni, P.1
Lensing, A.2
Buller, H.3
-
11
-
-
0003011102
-
The development of low molecular weight heparins for clinical use
-
M. et al. (Eds.). Leuven University Press: Leuven
-
Hirsh, J., Levine, M. The development of low molecular weight heparins for clinical use. In: Thrombosis and Haemostasis. Verstraete, M. et al. (Eds.). Leuven University Press: Leuven 1987, 425-48.
-
(1987)
Thrombosis and Haemostasis. Verstraete
, pp. 425-448
-
-
Hirsh, J.1
Levine, M.2
-
12
-
-
0027424531
-
Cell mediated events that control blood coagulation and vascular injury
-
Esmon, C.T. Cell mediated events that control blood coagulation and vascular injury. Ann Rev Cell Biol 1993, 9: 1-26.
-
(1993)
Ann Rev Cell Biol
, vol.9
, pp. 1-26
-
-
Esmon, C.T.1
-
13
-
-
0342632392
-
Update on glycoprotein IIb/IIIa inhibitors
-
Subbarao, V., Phillips, J., Stouffer, G.A. Update on glycoprotein IIb/IIIa inhibitors. Curr Opin Cardiovasc Pulm Renal Invest Drugs 1999, 1: 56-62.
-
(1999)
Curr Opin Cardiovasc Pulm Renal Invest Drugs
, vol.1
, pp. 56-62
-
-
Subbarao, V.1
Phillips, J.2
Stouffer, G.A.3
-
14
-
-
0033378391
-
Strategies and progress towards the ideal orally active thrombin inhibitor
-
Rewinkel, J.B.M., Adang, A.E.P. Strategies and progress towards the ideal orally active thrombin inhibitor. Curr Pharm Des 1999, 5: 1043-75.
-
(1999)
Curr Pharm Des
, vol.5
, pp. 1043-1075
-
-
Rewinkel, J.B.M.1
Adang, A.E.P.2
-
15
-
-
0030217867
-
Radioimmunoassay method for DX-9065a, an anticoagulant agent. Development, evaluation and application to human plasma
-
Murayama, N., Tanaka, S., Kikuchi, T., Nakaoka, M., Sudo, K. Radioimmunoassay method for DX-9065a, an anticoagulant agent. Development, evaluation and application to human plasma. J Pharm Biomed Anal 1996, 14: 1435-45.
-
(1996)
J Pharm Biomed Anal
, vol.14
, pp. 1435-1445
-
-
Murayama, N.1
Tanaka, S.2
Kikuchi, T.3
Nakaoka, M.4
Sudo, K.5
-
16
-
-
0033573790
-
Platelet GPIIb-IIIa blockers
-
Topol, E.J., Byzova, T.V., Plow, E.F. Platelet GPIIb-IIIa blockers. Lancet 1999, 353: 227-31.
-
(1999)
Lancet
, vol.353
, pp. 227-231
-
-
Topol, E.J.1
Byzova, T.V.2
Plow, E.F.3
-
17
-
-
0031838598
-
Thrombin and factor Xa inhibitors
-
Kaiser, B. Thrombin and factor Xa inhibitors. Drugs Fut 1998, 23: 423-36.
-
(1998)
Drugs Fut
, vol.23
, pp. 423-436
-
-
Kaiser, B.1
-
18
-
-
0030693694
-
Small-molecule direct thrombin inhibitors
-
Wiley, M., Fisher, M.J. Small-molecule direct thrombin inhibitors. Exp Opin Ther Pat 1997, 7: 1265-82.
-
(1997)
Exp Opin Ther Pat
, vol.7
, pp. 1265-1282
-
-
Wiley, M.1
Fisher, M.J.2
-
19
-
-
0001808999
-
Factor Xa inhibitors: Today and beyond
-
Walenga, J.M., Jeske, W.P., Hoppensteadt, D., Kaiser, B. Factor Xa inhibitors: Today and beyond. Curr Opin Cardiovasc Pulm Renal Invest Drugs 1999, 1: 13-27.
-
(1999)
Curr Opin Cardiovasc Pulm Renal Invest Drugs
, vol.1
, pp. 13-27
-
-
Walenga, J.M.1
Jeske, W.P.2
Hoppensteadt, D.3
Kaiser, B.4
-
20
-
-
0029775681
-
RGD and other recognition sequences for integrins
-
Ruoslahti, E. RGD and other recognition sequences for integrins. Ann Rev Cell Dev Biol 1996, 12: 697-715.
-
(1996)
Ann Rev Cell Dev Biol
, vol.12
, pp. 697-715
-
-
Ruoslahti, E.1
-
22
-
-
0017648045
-
Primary structure of human prethrombin 2 and α-thrombin
-
Butrowski, R.J., Elion, J., Downing, M.R., Mann, K.G. Primary structure of human prethrombin 2 and α-thrombin. J Biol Chem 1977, 252: 4942-57.
-
(1977)
J Biol Chem
, vol.252
, pp. 4942-4957
-
-
Butrowski, R.J.1
Elion, J.2
Downing, M.R.3
Mann, K.G.4
-
23
-
-
0026475194
-
Low molecular weight non-peptide fibrinogen receptor antagonists
-
Alig, L., Edenhofer, A., Hadváry, P. et al. Low molecular weight non-peptide fibrinogen receptor antagonists. J Med Chem 1992, 35: 4393-407.
-
(1992)
J Med Chem
, vol.35
, pp. 4393-4407
-
-
Alig, L.1
Edenhofer, A.2
Hadváry, P.3
-
24
-
-
0026563721
-
A strategy for a rational approach to designing synthetic selective inhibitors
-
Hijikata-Okunomiya, A., Okamoto, S. A strategy for a rational approach to designing synthetic selective inhibitors. Semin Thromb Hemost 1992, 18: 135-49.
-
(1992)
Semin Thromb Hemost
, vol.18
, pp. 135-149
-
-
Hijikata-Okunomiya, A.1
Okamoto, S.2
-
25
-
-
0028269097
-
DX-9065a, a new synthetic, potent anticoagulant and selective inhibitor for factor Xa
-
Hara, T., Yokoyama, A., Ishihara, H., Yokoyama, Y., Nagahara, T., Iwamoto, M. DX-9065a, a new synthetic, potent anticoagulant and selective inhibitor for factor Xa. Thromb Haemost 1994, 71: 314-9.
-
(1994)
Thromb Haemost
, vol.71
, pp. 314-319
-
-
Hara, T.1
Yokoyama, A.2
Ishihara, H.3
Yokoyama, Y.4
Nagahara, T.5
Iwamoto, M.6
-
26
-
-
0001334658
-
Design principles for orally bioavailable drugs
-
Navia, M.A., Chaturvedi, P.R. Design principles for orally bioavailable drugs. DDT 1996, 1: 179-89.
-
(1996)
DDT
, vol.1
, pp. 179-189
-
-
Navia, M.A.1
Chaturvedi, P.R.2
-
27
-
-
0000312699
-
Physicochemical and drug-delivery considerations for oral drug unavailability
-
Chan, O.H., Stewart, B.H. Physicochemical and drug-delivery considerations for oral drug unavailability. DDT 1996, 1: 461-73.
-
(1996)
DDT
, vol.1
, pp. 461-473
-
-
Chan, O.H.1
Stewart, B.H.2
-
28
-
-
0342437513
-
Improvement of oral peptide bioavailability: Peptidomimetics and prodrug strategies
-
Pauletti, G.M., Gangwar, S., Siahaan, T.J., Aubé, J., Borchardt, R.T. Improvement of oral peptide bioavailability: Peptidomimetics and prodrug strategies. Adv Drug Deliv Rev 1997, 27: 235-56.
-
(1997)
Adv Drug Deliv Rev
, vol.27
, pp. 235-256
-
-
Pauletti, G.M.1
Gangwar, S.2
Siahaan, T.J.3
Aubé, J.4
Borchardt, R.T.5
-
29
-
-
0031024171
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C.A., Lombardo, F., Dominy, B.W., Feeney, P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv Drug Deliv Rev 1997, 23: 3-25.
-
(1997)
Adv Drug Deliv Rev
, vol.23
, pp. 3-25
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
30
-
-
0032585545
-
Evaluation of dynamic polar molecular surface area as predictor of drug absorption: Comparison with other computational and experimental predictors
-
Palm, K., Luthman, K., Ungell, A.L. et al. Evaluation of dynamic polar molecular surface area as predictor of drug absorption: Comparison with other computational and experimental predictors. J Med Chem 1998, 41: 5382-92.
-
(1998)
J Med Chem
, vol.41
, pp. 5382-5392
-
-
Palm, K.1
Luthman, K.2
Ungell, A.L.3
-
31
-
-
0032714220
-
Polar molecular surface as a dominating determinant for oral absorption and brain penetration of drugs
-
Kelder, J., Grootenhuis, P.D.J., Bayada, D.M., Delbressine, L.P.C., Ploemen, J.-P. Polar molecular surface as a dominating determinant for oral absorption and brain penetration of drugs. Pharm Res 1999, 16: 1514-9.
-
(1999)
Pharm Res
, vol.16
, pp. 1514-1519
-
-
Kelder, J.1
Grootenhuis, P.D.J.2
Bayada, D.M.3
Delbressine, L.P.C.4
Ploemen, J.-P.5
-
32
-
-
0030946942
-
Molecular determinants of recognition for the intestinal peptide carrier
-
Swaan, P.W., Tukker, J.J. Molecular determinants of recognition for the intestinal peptide carrier. J Pharm Sci 1997, 86: 596-602.
-
(1997)
J Pharm Sci
, vol.86
, pp. 596-602
-
-
Swaan, P.W.1
Tukker, J.J.2
-
33
-
-
0026713248
-
The ideal antithrombotic drug
-
Sixma, J.J., de Groot, P.G. The ideal antithrombotic drug. Thromb Res 1992, 67: 305-11.
-
(1992)
Thromb Res
, vol.67
, pp. 305-311
-
-
Sixma, J.J.1
De Groot, P.G.2
-
34
-
-
0033056269
-
Eptifibatide
-
Goa, K.L., Noble, S. Eptifibatide. Drugs 1999, 57: 439-62.
-
(1999)
Drugs
, vol.57
, pp. 439-462
-
-
Goa, K.L.1
Noble, S.2
-
35
-
-
0031849692
-
Eptifibatide
-
Scarborough, R.M. Eptifibatide. Drugs Fut 1998, 23: 585-90.
-
(1998)
Drugs Fut
, vol.23
, pp. 585-590
-
-
Scarborough, R.M.1
-
36
-
-
9344236530
-
Orally active fibrinogen antagonists. 2. Amidoximes as pro-drugs of amidines
-
Weller, T., Alig, L., Beresini, M. et al. Orally active fibrinogen antagonists. 2. Amidoximes as pro-drugs of amidines. J Med Chem 1996, 39: 3139-47.
-
(1996)
J Med Chem
, vol.39
, pp. 3139-3147
-
-
Weller, T.1
Alig, L.2
Beresini, M.3
-
37
-
-
0033535522
-
Orally active isoxazoline glycoprotein IIb/IIIa antagonists with extended duration of action
-
Olson, R.E., Sielecki, T.M., Wityak, J. et al. Orally active isoxazoline glycoprotein IIb/IIIa antagonists with extended duration of action. J Med Chem 1999, 42: 1178-92.
-
(1942)
J Med Chem 1999
, pp. 1178-1192
-
-
Olson, R.E.1
Sielecki, T.M.2
Wityak, J.3
-
39
-
-
0032509964
-
Novel non-peptide fibrinogen antagonists. 1. Synthesis and glycoprotein IIb-IIIa antagonistic activities of 1,3,4-trisubstituted 2-oxopiperazine derivatives incorporating side-chain functions of the RGDF peptide
-
Sugihara, H., Fukushi, H., Miyawaki, T. et al. Novel non-peptide fibrinogen antagonists. 1. Synthesis and glycoprotein IIb-IIIa antagonistic activities of 1,3,4-trisubstituted 2-oxopiperazine derivatives incorporating side-chain functions of the RGDF peptide. J Med Chem 1998, 41: 489-502.
-
(1998)
J Med Chem
, vol.41
, pp. 489-502
-
-
Sugihara, H.1
Fukushi, H.2
Miyawaki, T.3
-
40
-
-
0031984477
-
Effects of melagatran, a new low-molecular-weight thrombin inhibitor, on thrombin and fibrinolytic enzymes
-
Gustafsson, D., Antonsson, T., Bylund, R. et al. Effects of melagatran, a new low-molecular-weight thrombin inhibitor, on thrombin and fibrinolytic enzymes. Thromb Haemost 1998, 79: 110-8.
-
(1998)
Thromb Haemost
, vol.79
, pp. 110-118
-
-
Gustafsson, D.1
Antonsson, T.2
Bylund, R.3
-
41
-
-
0033008172
-
Pharmacokinetics and pharmacodynamics of melagatran, a novel synthetic LMW thrombin inhibitor, in patients with acute DVT
-
Eriksson, H., Eriksson, U.G., Frison, L. et al. Pharmacokinetics and pharmacodynamics of melagatran, a novel synthetic LMW thrombin inhibitor, in patients with acute DVT. Thromb Haemost 1999, 81: 358-63.
-
(1999)
Thromb Haemost
, vol.81
, pp. 358-363
-
-
Eriksson, H.1
Eriksson, U.G.2
Frison, L.3
-
42
-
-
4243268786
-
Proteinase inhibition as a drug discovery strategy: Tackling the challenges of absorption, clearance and selectivity
-
Sept 6-10, Edinburgh
-
McElroy, A. Proteinase inhibition as a drug discovery strategy: Tackling the challenges of absorption, clearance and selectivity. 15th Int Symp Med Chem (Sept 6-10, Edinburgh) 1998, I-4.
-
(1998)
15th Int Symp Med Chem
-
-
McElroy, A.1
-
43
-
-
0028988227
-
Synthesis and characterisation of novel thrombin inhibitors based on 4-amidinophenylalanine
-
Reers, M., Koschinsky, R., Dickneite, G., Hoffmann, D., Czech, J., Strüber W. Synthesis and characterisation of novel thrombin inhibitors based on 4-amidinophenylalanine. J Enzyme Inhib 1995, 9: 61-72.
-
(1995)
J Enzyme Inhib
, vol.9
, pp. 61-72
-
-
Reers, M.1
Koschinsky, R.2
Dickneite, G.3
Hoffmann, D.4
Czech, J.5
Strüber, W.6
-
44
-
-
0003857101
-
Inhibition of thrombin by derivatives of the dipeptide aspartic acid-amidinophenylalanine
-
Strüber W., Koschinsky, R., Kolar et al. Inhibition of thrombin by derivatives of the dipeptide aspartic acid-amidinophenylalanine. Pept Chem Struct Biol 1994, 13: 643-5.
-
(1994)
Pept Chem Struct Biol
, vol.13
, pp. 643-645
-
-
Strüber, W.1
Koschinsky, R.2
Kolar3
-
45
-
-
0030667455
-
Inhibition of thrombin generation in plasma by inhibitors of factor Xa
-
Prada, D., Svendsen, L., Sturzebecher, J. Inhibition of thrombin generation in plasma by inhibitors of factor Xa. Thromb Haemost 1997, 78: 1215-9.
-
(1997)
Thromb Haemost
, vol.78
, pp. 1215-1219
-
-
Prada, D.1
Svendsen, L.2
Sturzebecher, J.3
-
46
-
-
0029112614
-
Antithrombotic effects of orally active synthetic antagonist of activated factor Xa in nonhuman primates
-
Yokoyama, T., Kelly, A.B., Marzec, U.M., Hanson, S.R., Kunitada, S., Harker, L.A. Antithrombotic effects of orally active synthetic antagonist of activated factor Xa in nonhuman primates. Circulation 1995, 92: 485-91.
-
(1995)
Circulation
, vol.92
, pp. 485-491
-
-
Yokoyama, T.1
Kelly, A.B.2
Marzec, U.M.3
Hanson, S.R.4
Kunitada, S.5
Harker, L.A.6
-
47
-
-
0031793092
-
Comparison of the anticoagulant and antithrombotic effects of YM-75466, a novel orally-active factor Xa inhibitor, and warfarin in mice
-
Sato, K., Taniuchi, Y., Kawasaki, T. et al. Comparison of the anticoagulant and antithrombotic effects of YM-75466, a novel orally-active factor Xa inhibitor, and warfarin in mice. Jpn J Pharmacol 1998, 78: 191-7.
-
(1998)
Jpn J Pharmacol
, vol.78
, pp. 191-197
-
-
Sato, K.1
Taniuchi, Y.2
Kawasaki, T.3
-
48
-
-
0031888018
-
Biochemical and pharmacological characterization of YM-60828, a newly synthesized and orally active inhibitor of human factor Xa
-
Taniuchi, Y., Sakai, Y., Hisamichi, N. et al. Biochemical and pharmacological characterization of YM-60828, a newly synthesized and orally active inhibitor of human factor Xa. Thromb Haemost 1998, 79: 543-8.
-
(1998)
Thromb Haemost
, vol.79
, pp. 543-548
-
-
Taniuchi, Y.1
Sakai, Y.2
Hisamichi, N.3
-
49
-
-
0032416061
-
Orbofiban acetate
-
Merlos, M., Leeson, P.A., Castaner, J. Orbofiban acetate. Drugs Fut 1998, 23: 1190-8.
-
(1998)
Drugs Fut
, vol.23
, pp. 1190-1198
-
-
Merlos, M.1
Leeson, P.A.2
Castaner, J.3
-
50
-
-
8044235823
-
Novelnonpeptideantiplateletglycoprotein IIa/IIIb receptor antagonist, DMP754: Receptor binding affinity and specificity
-
Mousa, S.A. et al. Novelnonpeptideantiplateletglycoprotein IIa/IIIb receptor antagonist, DMP754: Receptor binding affinity and specificity. Coron Artery Dis 1996, 7: 767-74.
-
(1996)
Coron Artery Dis
, vol.7
, pp. 767-774
-
-
Mousa, S.A.1
-
51
-
-
0031856736
-
Orally active isoxazoline GPIIb/IIIa antagonists
-
Mousa, S.A., Wityak, J. Orally active isoxazoline GPIIb/IIIa antagonists. Cardiovasc Drug Rev 1998, 16: 48-61.
-
(1998)
Cardiovasc Drug Rev
, vol.16
, pp. 48-61
-
-
Mousa, S.A.1
Wityak, J.2
-
52
-
-
0029067684
-
Potent in vitro and in vivo inhibitors of platelet aggregation based upon the Arg-Gly-Asp sequence of fribinogen. (Aminobenzamidine)succinyl (ABAS) series of orally active fribinogen receptor antagonists
-
Zablocki, J.A., Rico, J.G., Garland, R.B. et al. Potent in vitro and in vivo inhibitors of platelet aggregation based upon the Arg-Gly-Asp sequence of fribinogen. (Aminobenzamidine)succinyl (ABAS) series of orally active fribinogen receptor antagonists. J Med Chem 1995, 38: 2378-94.
-
(1995)
J Med Chem
, vol.38
, pp. 2378-2394
-
-
Zablocki, J.A.1
Rico, J.G.2
Garland, R.B.3
-
54
-
-
0342869483
-
Structural analysis of thrombin inhibitors utilizing a phenyl-based peptide mimetic
-
March 29-April 2, Dallas Abst MEDI 198
-
Spurlino, J.C., Lu, T., Illig, C., Soll, R.M., Bone, R. Structural analysis of thrombin inhibitors utilizing a phenyl-based peptide mimetic. 215th ACS Natl Meet (March 29-April 2, Dallas) 1998, Abst MEDI 198.
-
(1998)
215th ACS Natl Meet
-
-
Spurlino, J.C.1
Lu, T.2
Illig, C.3
Soll, R.M.4
Bone, R.5
-
56
-
-
0033594506
-
Secondary structure peptide mimetics: Design, synthesis, and evaluation of β-strand thrombin inhibitors
-
Boatman, P.D., Ogbu, C.O., Eguchi, M. et al. Secondary structure peptide mimetics: Design, synthesis, and evaluation of β-strand thrombin inhibitors. J Med Chem 1999, 42: 1367-75.
-
(1999)
J Med Chem
, vol.42
, pp. 1367-1375
-
-
Boatman, P.D.1
Ogbu, C.O.2
Eguchi, M.3
-
57
-
-
0344629348
-
Synthetic inhibitors of thrombin and factor Xa: From bench to bedside
-
Hauptmann, J., Sturzebecher, J. Synthetic inhibitors of thrombin and factor Xa: From bench to bedside. Thromb Res 1999, 93: 203-41.
-
(1999)
Thromb Res
, vol.93
, pp. 203-241
-
-
Hauptmann, J.1
Sturzebecher, J.2
-
58
-
-
0024328497
-
Synthetic inhibitors of bovine factor Xa and thrombin. Comparison of their anticoagulant efficiency
-
Sturzebecher, J., Sturzebecher, U., Vieweg, H., Wagner, G., Hauptmann, J., Markwardt, F. Synthetic inhibitors of bovine factor Xa and thrombin. Comparison of their anticoagulant efficiency. Thromb Res 1989, 54: 245-52.
-
(1989)
Thromb Res
, vol.54
, pp. 245-252
-
-
Sturzebecher, J.1
Sturzebecher, U.2
Vieweg, H.3
Wagner, G.4
Hauptmann, J.5
Markwardt, F.6
-
59
-
-
0033615024
-
Design and synthesis of isoxazoline derivatives as factor Xa inhibitors. 2
-
Quan, M.L., Ellis, C.D., Liauw, A.Y. et al. Design and synthesis of isoxazoline derivatives as factor Xa inhibitors. 2. J Med Chem 1999, 42: 2760-73.
-
(1999)
J Med Chem
, vol.42
, pp. 2760-2773
-
-
Quan, M.L.1
Ellis, C.D.2
Liauw, A.Y.3
-
60
-
-
0032570258
-
Discovery of a novel, potent, and specific family of factor Xa inhibitors via combinatorial chemistry
-
Ostrem, J.A., Al-Obeidi, F.A., Safar, P., et al. Discovery of a novel, potent, and specific family of factor Xa inhibitors via combinatorial chemistry. Biochemistry 1998, 37: 1053-9.
-
(1998)
Biochemistry
, vol.37
, pp. 1053-1059
-
-
Ostrem, J.A.1
Al-Obeidi, F.A.2
Safar, P.3
-
61
-
-
0027373464
-
The effects of two synthetic glycoprotein IIb/IIIa antagonists, Ro 43-8857 and L-700,462, on platelet aggregation and bleeding in guinea-pigs and dogs: Evidence that Ro 43-8857 is orally active
-
Cook, N.S., Bruttger, O., Pally, C., Hagenbach, A. The effects of two synthetic glycoprotein IIb/IIIa antagonists, Ro 43-8857 and L-700,462, on platelet aggregation and bleeding in guinea-pigs and dogs: Evidence that Ro 43-8857 is orally active. Thromb Haemost 1993, 70: 838-47.
-
(1993)
Thromb Haemost
, vol.70
, pp. 838-847
-
-
Cook, N.S.1
Bruttger, O.2
Pally, C.3
Hagenbach, A.4
-
62
-
-
0029150503
-
Non-peptide GPIIb/IIIa inhibitors. 7. Design and synthesis of a potent, orally active fibrinogen receptor antagonist
-
Duggan, M.E., Naylor-Olsen, A.M., Perkins, J.J. et al. Non-peptide GPIIb/IIIa inhibitors. 7. Design and synthesis of a potent, orally active fibrinogen receptor antagonist. J Med Chem 1995, 38: 3332-41.
-
(1995)
J Med Chem
, vol.38
, pp. 3332-3341
-
-
Duggan, M.E.1
Naylor-Olsen, A.M.2
Perkins, J.J.3
-
63
-
-
0033168403
-
Non-peptide GPIIb/IIIa inhibitors. 20. Centrally constrained thienothiophene alpha-sulfonamides are potent, long acting in vivo inhibitors of platelet aggregation
-
Egbertson, M.S., Cook, J.J., Bednar, B. et al. Non-peptide GPIIb/IIIa inhibitors. 20. Centrally constrained thienothiophene alpha-sulfonamides are potent, long acting in vivo inhibitors of platelet aggregation. J Med Chem 1999, 42: 2409-21.
-
(1999)
J Med Chem
, vol.42
, pp. 2409-2421
-
-
Egbertson, M.S.1
Cook, J.J.2
Bednar, B.3
-
64
-
-
0029775672
-
Potent, selective, orally active 3-oxo-1,4-benzodiazepine GPIIb/IIIa integrin antagonists
-
Samanen, J.M., Ali, F.E., Barton, L.S. et al. Potent, selective, orally active 3-oxo-1,4-benzodiazepine GPIIb/IIIa integrin antagonists. J Med Chem 1996, 39: 4867-70.
-
(1996)
J Med Chem
, vol.39
, pp. 4867-4870
-
-
Samanen, J.M.1
Ali, F.E.2
Barton, L.S.3
-
66
-
-
0029031716
-
Design and evaluation of nonpeptide fibrinogen γ-chain based GPIIb/IIIa antagonists
-
Hoekstra, W.J., Beavers, M.P., Andrade-Gordon, P. et al. Design and evaluation of nonpeptide fibrinogen γ-chain based GPIIb/IIIa antagonists. J Med Chem 1995, 38: 1582-92.
-
(1995)
J Med Chem
, vol.38
, pp. 1582-1592
-
-
Hoekstra, W.J.1
Beavers, M.P.2
Andrade-Gordon, P.3
-
67
-
-
0346485500
-
A polar pharmacophore for oral bioavailability in thrombin inhibitors
-
Sept 6-10, Edinburgh Abst P.157.
-
Adang, A.E.P., van Dinther, T.G., Visser, A. et al. A polar pharmacophore for oral bioavailability in thrombin inhibitors. EFMC 15th Int Symp Med Chem (Sept 6-10, Edinburgh) 1998, Abst P.157.
-
(1998)
EFMC 15th Int Symp Med Chem
-
-
Adang, A.E.P.1
Van Dinther, T.G.2
Visser, A.3
-
68
-
-
0342434890
-
4-Aminopyridine and related heterocycles as Pi residues in selective thrombin inhibitors
-
Sept 7-10, Cambridge
-
von der Saal, W. 4-Aminopyridine and related heterocycles as Pi residues in selective thrombin inhibitors. 9th RCS-SCI Med Chem Symp (Sept 7-10, Cambridge) 1997.
-
(1997)
9th RCS-SCI Med Chem Symp
-
-
Von Der Saal, W.1
-
69
-
-
16144365754
-
Enzyme fexibility, solvent and "weak" interactions characterize thrombin-ligand interactions: Implications for drug design
-
Engh, R.A., Brandstetter, H., Sucher, G. et al. Enzyme fexibility, solvent and "weak" interactions characterize thrombin-ligand interactions: Implications for drug design. Structure 1996, 4: 1353-62.
-
(1996)
Structure
, vol.4
, pp. 1353-1362
-
-
Engh, R.A.1
Brandstetter, H.2
Sucher, G.3
-
70
-
-
0032493403
-
Diarylsulfonamides as selective, non-peptidic thrombin inhibitors
-
Weber, I.R., Neidlein, R., von der Saal, W. et al. Diarylsulfonamides as selective, non-peptidic thrombin inhibitors. Bioorg Med Chem Lett 1998, 8: 1613-8.
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 1613-1618
-
-
Weber, I.R.1
Neidlein, R.2
Von Der Saal, W.3
-
71
-
-
15444357642
-
Design and synthesis of a series of potent and orally bioavailable noncovalent thrombin inhibitors that utilize nonbasic groups in the P1 position
-
Tucker, T.J., Brady, S.F., Lumma, W.C. et al. 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: 3210-9.
-
(1998)
J Med Chem
, vol.41
, pp. 3210-3219
-
-
Tucker, T.J.1
Brady, S.F.2
Lumma, W.C.3
-
72
-
-
15144357944
-
Efficacious, orally bioavailable thrombin inhibitors based on 3-aminopyridinone or 3-aminopyrazinone acetamide peptidomimetic templates
-
Sanderson, P.E.J., Lyle, E.A., Cutrona, K.J. et al. Efficacious, orally bioavailable thrombin inhibitors based on 3-aminopyridinone or 3-aminopyrazinone acetamide peptidomimetic templates. J Med Chem 1998, 41: 4466-74.
-
(1998)
J Med Chem
, vol.41
, pp. 4466-4474
-
-
Sanderson, P.E.J.1
Lyle, E.A.2
Cutrona, K.J.3
-
73
-
-
0002710966
-
Discovery of a highly selective, orally bioavailable, direct thrombin inhibitor, LB30057
-
Kim, I.-C., Oh, Y.S., Yun, M. et al. Discovery of a highly selective, orally bioavailable, direct thrombin inhibitor, LB30057. Circulation 1997, 96: 1-41.
-
(1997)
Circulation
, vol.96
, pp. 1-41
-
-
Kim, I.-C.1
Oh, Y.S.2
Yun, M.3
-
74
-
-
19244385909
-
Discovery of LB30057, a benzamidrazone-based selective, oral thrombin inhibitor
-
Oh, Y.S., Yun, M., Hwang, S.Y. et al. Discovery of LB30057, a benzamidrazone-based selective, oral thrombin inhibitor. Bioorg Med Chem Lett 1998, 8: 631-4.
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 631-634
-
-
Oh, Y.S.1
Yun, M.2
Hwang, S.Y.3
-
75
-
-
0033523711
-
Design, synthesis and testing of amino-bicycloaryl based orally bioavailable thrombin inhibitors
-
Rewinkel, J.B.M., Lucas, H., Smit, M.J. et al. Design, synthesis and testing of amino-bicycloaryl based orally bioavailable thrombin inhibitors. Bioorg Med Chem Lett 1999, 9: 2837-42.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 2837-2842
-
-
Rewinkel, J.B.M.1
Lucas, H.2
Smit, M.J.3
-
76
-
-
0033583555
-
The discovery of orally available thrombin inhibitors: Optimisation of the P1 pharmacophore
-
Ambler, J., Bentley, D., Brown, L. et al. The discovery of orally available thrombin inhibitors: Optimisation of the P1 pharmacophore. Bioorg Med Chem Lett 1999, 9: 1103-8.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 1103-1108
-
-
Ambler, J.1
Bentley, D.2
Brown, L.3
-
77
-
-
0033530140
-
Aminoisoquinolines: Design and synthesis of an orally active benzamidine isostere for the inhibition of factor Xa
-
Choi-Sledeski, Y.M., Becker, M.R., Green, D.M. et al. Aminoisoquinolines: Design and synthesis of an orally active benzamidine isostere for the inhibition of factor Xa. Bioorg Med Chem Lett 1999, 9: 2539-44.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 2539-2544
-
-
Choi-Sledeski, Y.M.1
Becker, M.R.2
Green, D.M.3
-
78
-
-
0343304509
-
Rational design of novel, potent and highly selective factor Xa inhibitors
-
Sept 5-8, Cambridge
-
Young, S.C., Brady, L., Jones, S.D. et al. Rational design of novel, potent and highly selective factor Xa inhibitors. 10th RSC-SCI Med Chem Symp (Sept 5-8, Cambridge) 1999.
-
(1999)
10th RSC-SCI Med Chem Symp
-
-
Young, S.C.1
Brady, L.2
Jones, S.D.3
-
79
-
-
0343443219
-
Potent noncovalent thrombin inhibitors that utilize the unique amino acid D-dicyclohexylalanine in the P3 position. Implications on oral bioavailability and antithrombotic efficacy
-
Tucker, T.J., Lumma, W.C., Lewis, S.D. et al 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: 1565-9.
-
(1997)
J Med Chem
, vol.40
, pp. 1565-1569
-
-
Tucker, T.J.1
Lumma, W.C.2
Lewis, S.D.3
-
80
-
-
0032492707
-
Solid phase synthesis of benzylamine-derived sulfonamide library
-
Kim, S., Hong, C.Y., Lee, E.J., Koh, J.S. Solid phase synthesis of benzylamine-derived sulfonamide library. Bioorg Med Chem Lett 1998, 8: 735-8.
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 735-738
-
-
Kim, S.1
Hong, C.Y.2
Lee, E.J.3
Koh, J.S.4
-
81
-
-
0032558536
-
Benzylamine-based selective and orally bioavailable inhibitors of thrombin
-
Lee, K., Jung, W-H., Park, C.W. et al. Benzylamine-based selective and orally bioavailable inhibitors of thrombin. Bioorg Med Chem Lett 1998, 8: 2563-8.
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 2563-2568
-
-
Lee, K.1
Jung, W.-H.2
Park, C.W.3
-
82
-
-
0033535401
-
1-Aminoisoquinoline as benzamidine isoster in the design and synthesis of orally active thrombin inhibitors
-
Rewinkel, J.B.M., Lucas, H., van Galen, P.J.M. et al. 1-Aminoisoquinoline as benzamidine isoster in the design and synthesis of orally active thrombin inhibitors. Bioorg Med Chem Lett 1999, 9: 685-90.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 685-690
-
-
Rewinkel, J.B.M.1
Lucas, H.2
Van Galen, P.J.M.3
-
85
-
-
0342872079
-
Profound and sustained inhibition of platelet aggregation by fradafiban, a nonpeptide platelet glycoprotein IIb/IIIa antagonist, and its orally active pro-drug, lefradafiban, in men
-
Müller, T.H., Weisenberger, H., Brickl, R. et al. Profound and sustained inhibition of platelet aggregation by fradafiban, a nonpeptide platelet glycoprotein IIb/IIIa antagonist, and its orally active pro-drug, lefradafiban, in men. Circulation 1997, 96: 1130-8.
-
(1997)
Circulation
, vol.96
, pp. 1130-1138
-
-
Müller, T.H.1
Weisenberger, H.2
Brickl, R.3
-
86
-
-
0030731809
-
Antagonism of the GPIIb/IIIa receptor with the nonpetidic molecule B/BU52: Inhibition of platelet aggregation in vitro and antithrombotic efficacy in vivo
-
Guth, B.D., Seewaldt-Becker, E., Himmelsbach, F. et al. Antagonism of the GPIIb/IIIa receptor with the nonpetidic molecule B/BU52: Inhibition of platelet aggregation in vitro and antithrombotic efficacy in vivo. J Cardiovasc Pharmacol 1997, 30: 261-72.
-
(1997)
J Cardiovasc Pharmacol
, vol.30
, pp. 261-272
-
-
Guth, B.D.1
Seewaldt-Becker, E.2
Himmelsbach, F.3
-
87
-
-
0030882379
-
New orally active non-peptide fibrinogen receptor (GpIIb-IIIa) antagonists: Indentification of ethyl 3-N-[4-[4-[[amino[(ethyoxycarbonyl)imino]methyl]phenyl]-1,3-thiazl-2-yl]-N-[1- [(ethoxycarbonyl)methyl]-piperid-4-yl]amino]propionate (SR 121787) as a potent and long-acting antithrombotic agent
-
Badorc, A., Bordes, M-F., de Cointet, P. et al. New orally active non-peptide fibrinogen receptor (GpIIb-IIIa) antagonists: Indentification of ethyl 3-[N-[4-[4-[[amino[(ethyoxycarbonyl)imino]methyl]phenyl]-1,3-thiazl-2-yl]-N-[1- [(ethoxycarbonyl)methyl]-piperid-4-yl]amino]propionate (SR 121787) as a potent and long-acting antithrombotic agent. J Med Chem 1997, 40: 3393-401.
-
(1997)
J Med Chem
, vol.40
, pp. 3393-3401
-
-
Badorc, A.1
Bordes, M.-F.2
De Cointet, P.3
-
88
-
-
0342434888
-
-
WO 9723499
-
Antonsson, T., Gustafsson, D., Hoffmann, K., Nystrom, J., Sorensen, H., Sellen, M. Preparation of peptide derivatives as prodrugs of thrombin inhibitors. WO 9723499.
-
Preparation of Peptide Derivatives as Prodrugs of Thrombin Inhibitors
-
-
Antonsson, T.1
Gustafsson, D.2
Hoffmann, K.3
Nystrom, J.4
Sorensen, H.5
Sellen, M.6
-
90
-
-
0033535387
-
Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 4. SAR studies on the conformationally restricted C3-side chain of hydroxybenzo[b]thiophenes
-
Takeuchi, K., Kohn, T.J., Sail, D.J. et al. Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 4. SAR studies on the conformationally restricted C3-side chain of hydroxybenzo[b]thiophenes. Bioorg Med Chem Lett 1999, 9: 759-64.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 759-764
-
-
Takeuchi, K.1
Kohn, T.J.2
Sail, D.J.3
-
91
-
-
0033535402
-
Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 2. Side chain optimisation and demonstration of in vivo efficacy
-
Zhang, M., Bailey, D.L., Bastian, J.A. et al. Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 2. Side chain optimisation and demonstration of in vivo efficacy. Bioorg Med Chem Lett 1999, 9: 775-80.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 775-780
-
-
Zhang, M.1
Bailey, D.L.2
Bastian, J.A.3
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