-
1
-
-
77957669137
-
Novel anticoagulant therapy: principle and practice
-
Mousa SA, (2010) Novel anticoagulant therapy: principle and practice. Methods Mol Biol 663: 157-179.
-
(2010)
Methods Mol Biol
, vol.663
, pp. 157-179
-
-
Mousa, S.A.1
-
2
-
-
80051834654
-
Novel oral anticoagulants: focus on stroke prevention and treatment of venous thrombo-embolism
-
Steffel J, Braunwald E, (2011) Novel oral anticoagulants: focus on stroke prevention and treatment of venous thrombo-embolism. Eur Heart J 32: 1968-1976.
-
(2011)
Eur Heart J
, vol.32
, pp. 1968-1976
-
-
Steffel, J.1
Braunwald, E.2
-
3
-
-
68349093744
-
Novel anticoagulants in clinical development: focus on factor Xa and direct thrombin inhibitors
-
Steffel J, Luscher TF, (2009) Novel anticoagulants in clinical development: focus on factor Xa and direct thrombin inhibitors. J Cardiovasc Med (Hagerstown) 10: 616-623.
-
(2009)
J Cardiovasc Med (Hagerstown)
, vol.10
, pp. 616-623
-
-
Steffel, J.1
Luscher, T.F.2
-
4
-
-
10344241475
-
Progress in the design of low molecular weight thrombin inhibitors
-
Srivastava S, Goswami LN, Dikshit DK, (2005) Progress in the design of low molecular weight thrombin inhibitors. Med Res Rev 25: 66-92.
-
(2005)
Med Res Rev
, vol.25
, pp. 66-92
-
-
Srivastava, S.1
Goswami, L.N.2
Dikshit, D.K.3
-
5
-
-
0024431034
-
The refined 1.9 Å crystal structure of human alpha-thrombin: interaction with D-Phe-Pro-Arg chloromethylketone and significance of the Tyr-Pro-Pro-Trp insertion segment
-
Bode W, Mayr I, Baumann U, Huber R, Stone SR, et al. (1989) The refined 1.9 Å crystal structure of human alpha-thrombin: interaction with D-Phe-Pro-Arg chloromethylketone and significance of the Tyr-Pro-Pro-Trp insertion segment. EMBO J 8: 3467-3475.
-
(1989)
EMBO J
, vol.8
, pp. 3467-3475
-
-
Bode, W.1
Mayr, I.2
Baumann, U.3
Huber, R.4
Stone, S.R.5
-
6
-
-
0027756155
-
The synthesis and anticoagulant activity of novel peptidylfluoroalkanes
-
Neises B, Tarnus C, Broersma RJ, Bald C, Remy JM, et al. (1993) The synthesis and anticoagulant activity of novel peptidylfluoroalkanes. Adv Exp Med Biol 340: 185-188.
-
(1993)
Adv Exp Med Biol
, vol.340
, pp. 185-188
-
-
Neises, B.1
Tarnus, C.2
Broersma, R.J.3
Bald, C.4
Remy, J.M.5
-
7
-
-
0025346345
-
Design and characterization of hirulogs: a novel class of bivalent peptide inhibitors of thrombin
-
Maraganore JM, Bourdon P, Jablonski J, Ramachandran KL, Fenton JW 2nd, (1990) Design and characterization of hirulogs: a novel class of bivalent peptide inhibitors of thrombin. Biochemistry 29: 7095-7101.
-
(1990)
Biochemistry
, vol.29
, pp. 7095-7101
-
-
Maraganore, J.M.1
Bourdon, P.2
Jablonski, J.3
Ramachandran, K.L.4
Fenton 2nd, J.W.5
-
8
-
-
0026091628
-
Structure of the hirugen and hirulog 1 complexes of alpha-thrombin
-
Skrzypczak-Jankun E, Carperos VE, Ravichandran KG, Tulinsky A, Westbrook M, et al. (1991) Structure of the hirugen and hirulog 1 complexes of alpha-thrombin. J Mol Biol 221: 1379-1393.
-
(1991)
J Mol Biol
, vol.221
, pp. 1379-1393
-
-
Skrzypczak-Jankun, E.1
Carperos, V.E.2
Ravichandran, K.G.3
Tulinsky, A.4
Westbrook, M.5
-
9
-
-
0025837452
-
Crystallographic analysis at 3.0-Å resolution of the binding to human thrombin of four active site-directed inhibitors
-
Banner DW, Hadvary P, (1991) Crystallographic analysis at 3.0-Å resolution of the binding to human thrombin of four active site-directed inhibitors. J Biol Chem 266: 20085-20093.
-
(1991)
J Biol Chem
, vol.266
, pp. 20085-20093
-
-
Banner, D.W.1
Hadvary, P.2
-
10
-
-
0019891328
-
Potent inhibition of thrombin by the newly synthesized arginine derivative No. 805. The importance of stereo-structure of its hydrophobic carboxamide portion
-
Okamoto S, Hijikata A, Kikumoto R, Tonomura S, Hara H, et al. (1981) Potent inhibition of thrombin by the newly synthesized arginine derivative No. 805. The importance of stereo-structure of its hydrophobic carboxamide portion. Biochem Biophys Res Commun 101: 440-446.
-
(1981)
Biochem Biophys Res Commun
, vol.101
, pp. 440-446
-
-
Okamoto, S.1
Hijikata, A.2
Kikumoto, R.3
Tonomura, S.4
Hara, H.5
-
11
-
-
79958131485
-
Heparin-induced thrombocytopenia: present and future
-
Cuker A, (2011) Heparin-induced thrombocytopenia: present and future. J Thromb Thrombolysis 31: 353-366.
-
(2011)
J Thromb Thrombolysis
, vol.31
, pp. 353-366
-
-
Cuker, A.1
-
12
-
-
79952062775
-
Argatroban in the management of heparin-induced thrombocytopenia
-
Babuin L, Pengo V, (2010) Argatroban in the management of heparin-induced thrombocytopenia. Vasc Health Risk Manag 6: 813-819.
-
(2010)
Vasc Health Risk Manag
, vol.6
, pp. 813-819
-
-
Babuin, L.1
Pengo, V.2
-
13
-
-
41949116970
-
Clinical pharmacokinetics and pharmacodynamics of the oral direct thrombin inhibitor dabigatran etexilate
-
Stangier J, (2008) Clinical pharmacokinetics and pharmacodynamics of the oral direct thrombin inhibitor dabigatran etexilate. Clin Pharmacokinet 47: 285-295.
-
(2008)
Clin Pharmacokinet
, vol.47
, pp. 285-295
-
-
Stangier, J.1
-
14
-
-
84855611604
-
Dabigatran in atrial fibrillation: pharmacology and clinical trials
-
Ezekowitz M, Nagarakanti R, (2011) Dabigatran in atrial fibrillation: pharmacology and clinical trials. J Interv Card Electrophysiol 32: 173-180.
-
(2011)
J Interv Card Electrophysiol
, vol.32
, pp. 173-180
-
-
Ezekowitz, M.1
Nagarakanti, R.2
-
15
-
-
0037171819
-
Structure-based design of novel potent nonpeptide thrombin inhibitors
-
Hauel NH, Nar H, Priepke H, Ries U, Stassen J-M, et al. (2002) Structure-based design of novel potent nonpeptide thrombin inhibitors. J Med Chem 45: 1757-1766.
-
(2002)
J Med Chem
, vol.45
, pp. 1757-1766
-
-
Hauel, N.H.1
Nar, H.2
Priepke, H.3
Ries, U.4
Stassen, J.-M.5
-
16
-
-
0020073364
-
Design and synthesis of peptide inhibitors of blood coagulations
-
Bajusz S, Szell E, Barabas E, Bagdy D, (1982) Design and synthesis of peptide inhibitors of blood coagulations. Folia Haematol Int Mag Klin Morphol Blutforsch 109: 16-21.
-
(1982)
Folia Haematol Int Mag Klin Morphol Blutforsch
, vol.109
, pp. 16-21
-
-
Bajusz, S.1
Szell, E.2
Barabas, E.3
Bagdy, D.4
-
17
-
-
42149143441
-
Thrombostatin FM compounds: direct thrombin inhibitors - mechanism of action in vitro and in vivo
-
Nieman MT, Burke F, Warnock M, Zhou Y, Sweigart J, et al. (2008) Thrombostatin FM compounds: direct thrombin inhibitors - mechanism of action in vitro and in vivo. J Thromb Haemost 6: 837-845.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 837-845
-
-
Nieman, M.T.1
Burke, F.2
Warnock, M.3
Zhou, Y.4
Sweigart, J.5
-
18
-
-
6344247582
-
The preparation and characterization of novel peptide antagonists to thrombin and factor VIIa and activation of protease-activated receptor 1
-
Nieman MT, Warnock M, Hasan AAK, Mahdi F, Lucchesi BR, et al. (2004) The preparation and characterization of novel peptide antagonists to thrombin and factor VIIa and activation of protease-activated receptor 1. J Pharmacol Exp Ther 311: 492-501.
-
(2004)
J Pharmacol Exp Ther
, vol.311
, pp. 492-501
-
-
Nieman, M.T.1
Warnock, M.2
Hasan, A.A.K.3
Mahdi, F.4
Lucchesi, B.R.5
-
19
-
-
33845535102
-
Synthesis of novel peptide inhibitors of thrombin-induced platelet activation
-
Burke FM, Warnock M, Schmaier AH, Mosberg HI, (2006) Synthesis of novel peptide inhibitors of thrombin-induced platelet activation. Chem Biol Drug Des 68: 235-238.
-
(2006)
Chem Biol Drug Des
, vol.68
, pp. 235-238
-
-
Burke, F.M.1
Warnock, M.2
Schmaier, A.H.3
Mosberg, H.I.4
-
20
-
-
71449097054
-
Structure-based design of residue 1 analogs of the direct thrombin inhibitor pentapeptide FM 19
-
Girnys EA, Sobczyk-Kojiro K, Mosberg HI, (2010) Structure-based design of residue 1 analogs of the direct thrombin inhibitor pentapeptide FM 19. Chem Biol Drug Des 75: 35-39.
-
(2010)
Chem Biol Drug Des
, vol.75
, pp. 35-39
-
-
Girnys, E.A.1
Sobczyk-Kojiro, K.2
Mosberg, H.I.3
-
21
-
-
79951723419
-
Design, synthesis and SAR of a series of 1,3,5-trisubstituted benzenes as thrombin inhibitors
-
Isaacs RCA, Newton CL, Cutrona KJ, Mercer SP, Payne LS, et al. (2011) Design, synthesis and SAR of a series of 1,3,5-trisubstituted benzenes as thrombin inhibitors. Bioorg Med Chem Lett 21: 1536-1540.
-
(2011)
Bioorg Med Chem Lett
, vol.21
, pp. 1536-1540
-
-
Isaacs, R.C.A.1
Newton, C.L.2
Cutrona, K.J.3
Mercer, S.P.4
Payne, L.S.5
-
22
-
-
73449121150
-
Structure-based drug design strategies in medicinal chemistry
-
Andricopulo AD, Salum LB, Abraham DJ, (2009) Structure-based drug design strategies in medicinal chemistry. Curr Top Med Chem 9: 771-790.
-
(2009)
Curr Top Med Chem
, vol.9
, pp. 771-790
-
-
Andricopulo, A.D.1
Salum, L.B.2
Abraham, D.J.3
-
23
-
-
77949405791
-
Successful applications of computer aided drug discovery: moving drugs from concept to the clinic
-
Talele TT, Khedkar SA, Rigby AC, (2010) Successful applications of computer aided drug discovery: moving drugs from concept to the clinic. Curr Top Med Chem 10: 127-141.
-
(2010)
Curr Top Med Chem
, vol.10
, pp. 127-141
-
-
Talele, T.T.1
Khedkar, S.A.2
Rigby, A.C.3
-
24
-
-
0028114289
-
Antigenic mimicry of natural L-peptides with retro-inverso-peptidomimetics
-
Guichard G, Benkirane N, Zeder-Lutz G, van Regenmortel MH, Briand JP, et al. (1994) Antigenic mimicry of natural L-peptides with retro-inverso-peptidomimetics. Proc Natl Acad Sci U S A 91: 9765-9769.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 9765-9769
-
-
Guichard, G.1
Benkirane, N.2
Zeder-Lutz, G.3
van Regenmortel, M.H.4
Briand, J.P.5
-
25
-
-
0026493575
-
Structure of the hirulog 3-thrombin complex and nature of the S′ subsites of substrates and inhibitors
-
Qiu X, Padmanabhan KP, Carperos VE, Tulinsky A, Kline T, et al. (1992) Structure of the hirulog 3-thrombin complex and nature of the S′ subsites of substrates and inhibitors. Biochemistry 31: 11689-11697.
-
(1992)
Biochemistry
, vol.31
, pp. 11689-11697
-
-
Qiu, X.1
Padmanabhan, K.P.2
Carperos, V.E.3
Tulinsky, A.4
Kline, T.5
-
26
-
-
78651087716
-
Crystallization and preliminary crystallographic characterization of three peptidic inhibitors in complex with α-thrombin
-
Figueiredo AC, Clement CC, Philipp M, Pereira PJB, (2011) Crystallization and preliminary crystallographic characterization of three peptidic inhibitors in complex with α-thrombin. Acta Crystallogr Sect F Struct Biol Cryst Commun 67: 54-58.
-
(2011)
Acta Crystallogr Sect F Struct Biol Cryst Commun
, vol.67
, pp. 54-58
-
-
Figueiredo, A.C.1
Clement, C.C.2
Philipp, M.3
Pereira, P.J.B.4
-
27
-
-
34447508216
-
Phaser crystallographic software
-
McCoy AJ, Grosse-Kunstleve RW, Adams PD, Winn MD, Storoni LC, et al. (2007) Phaser crystallographic software. J Appl Crystallogr 40: 658-674.
-
(2007)
J Appl Crystallogr
, vol.40
, pp. 658-674
-
-
McCoy, A.J.1
Grosse-Kunstleve, R.W.2
Adams, P.D.3
Winn, M.D.4
Storoni, L.C.5
-
28
-
-
8644252551
-
Enantiomerically pure thrombin inhibitors for exploring the molecular-recognition features of the oxyanion hole
-
Schärer K, Morgenthaler M, Seiler P, Diederich F, Banner D, et al. (2004) Enantiomerically pure thrombin inhibitors for exploring the molecular-recognition features of the oxyanion hole. Helv Chim Acta 87: 2517-2538.
-
(2004)
Helv Chim Acta
, vol.87
, pp. 2517-2538
-
-
Schärer, K.1
Morgenthaler, M.2
Seiler, P.3
Diederich, F.4
Banner, D.5
-
30
-
-
76449098262
-
PHENIX: a comprehensive Python-based system for macromolecular structure solution
-
Adams PD, Afonine PV, Bunkoczi G, Chen VB, Davis IW, et al. (2010) PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr D Biol Crystallogr 66: 213-221.
-
(2010)
Acta Crystallogr D Biol Crystallogr
, vol.66
, pp. 213-221
-
-
Adams, P.D.1
Afonine, P.V.2
Bunkoczi, G.3
Chen, V.B.4
Davis, I.W.5
-
31
-
-
33646260450
-
Optimal description of a protein structure in terms of multiple groups undergoing TLS motion
-
Painter J, Merritt EA, (2006) Optimal description of a protein structure in terms of multiple groups undergoing TLS motion. Acta Crystallogr D Biol Crystallogr 62: 439-450.
-
(2006)
Acta Crystallogr D Biol Crystallogr
, vol.62
, pp. 439-450
-
-
Painter, J.1
Merritt, E.A.2
-
32
-
-
33645158291
-
TLSMD web server for the generation of multi-group TLS models
-
Painter J, Merritt EA, (2006) TLSMD web server for the generation of multi-group TLS models. J Appl Cryst 39: 109-111.
-
(2006)
J Appl Cryst
, vol.39
, pp. 109-111
-
-
Painter, J.1
Merritt, E.A.2
-
33
-
-
79956150472
-
New synthetic thrombin inhibitors: molecular design and experimental verification
-
Sinauridze EI, Romanov AN, Gribkova IV, Kondakova OA, Surov SS, et al. (2011) New synthetic thrombin inhibitors: molecular design and experimental verification. PLoS ONE 6: e19969.
-
(2011)
PLoS ONE
, vol.6
-
-
Sinauridze, E.I.1
Romanov, A.N.2
Gribkova, I.V.3
Kondakova, O.A.4
Surov, S.S.5
-
34
-
-
0027050807
-
The refined 1.9-Å X-ray crystal structure of D-Phe-Pro-Arg chloromethylketone-inhibited human alpha-thrombin: structure analysis, overall structure, electrostatic properties, detailed active-site geometry, and structure-function relationships
-
Bode W, Turk D, Karshikov A, (1992) The refined 1.9-Å X-ray crystal structure of D-Phe-Pro-Arg chloromethylketone-inhibited human alpha-thrombin: structure analysis, overall structure, electrostatic properties, detailed active-site geometry, and structure-function relationships. Protein Sci 1: 426-471.
-
(1992)
Protein Sci
, vol.1
, pp. 426-471
-
-
Bode, W.1
Turk, D.2
Karshikov, A.3
-
35
-
-
0032505172
-
Rational design, synthesis, and X-ray structure of selective noncovalent thrombin inhibitors
-
Wagner J, Kallen J, Ehrhardt C, Evenou J-P, Wagner D, (1998) Rational design, synthesis, and X-ray structure of selective noncovalent thrombin inhibitors. J Med Chem 41: 3664-3674.
-
(1998)
J Med Chem
, vol.41
, pp. 3664-3674
-
-
Wagner, J.1
Kallen, J.2
Ehrhardt, C.3
Evenou, J.-P.4
Wagner, D.5
-
36
-
-
0036293418
-
The methyl group of N[alpha](Me)Arg-containing peptides disturbs the active-site geometry of thrombin, impairing efficient cleavage
-
Friedrich R, Steinmetzer T, Huber R, Stürzebecher J, Bode W, (2002) The methyl group of N[alpha](Me)Arg-containing peptides disturbs the active-site geometry of thrombin, impairing efficient cleavage. J Mol Biol 316: 869-874.
-
(2002)
J Mol Biol
, vol.316
, pp. 869-874
-
-
Friedrich, R.1
Steinmetzer, T.2
Huber, R.3
Stürzebecher, J.4
Bode, W.5
-
37
-
-
0031580204
-
Human alpha-thrombin inhibition by the highly selective compounds N-ethoxycarbonyl-D-Phe-Pro-alpha-azaLys p-nitrophenyl ester and N-carbobenzoxy-Pro-alpha-azaLys p-nitrophenyl ester: A kinetic, thermodynamic and X-ray crystallographic study
-
De Simone G, Balliano G, Milla P, Gallina C, Giordano C, et al. (1997) Human alpha-thrombin inhibition by the highly selective compounds N-ethoxycarbonyl-D-Phe-Pro-alpha-azaLys p-nitrophenyl ester and N-carbobenzoxy-Pro-alpha-azaLys p-nitrophenyl ester: A kinetic, thermodynamic and X-ray crystallographic study. J Mol Biol 269: 558-569.
-
(1997)
J Mol Biol
, vol.269
, pp. 558-569
-
-
de Simone, G.1
Balliano, G.2
Milla, P.3
Gallina, C.4
Giordano, C.5
-
38
-
-
0029088844
-
Crystal structure of human alpha-thrombin complexed with hirugen and p-amidinophenylpyruvate at 1.6 Å resolution
-
Chen ZG, Li Y, Mulichak AM, Lewis SD, Shafer JA, (1995) Crystal structure of human alpha-thrombin complexed with hirugen and p-amidinophenylpyruvate at 1.6 Å resolution. Arch Biochem Biophys 322: 198-203.
-
(1995)
Arch Biochem Biophys
, vol.322
, pp. 198-203
-
-
Chen, Z.G.1
Li, Y.2
Mulichak, A.M.3
Lewis, S.D.4
Shafer, J.A.5
-
39
-
-
0029879577
-
Synthesis, structure, and structure-activity relationships of divalent thrombin inhibitors containing an alpha-keto-amide transition-state mimetic
-
Krishnan R, Tulinsky A, Vlasuk GP, Pearson D, Vallar P, et al. (1996) Synthesis, structure, and structure-activity relationships of divalent thrombin inhibitors containing an alpha-keto-amide transition-state mimetic. Protein Sci 5: 422-433.
-
(1996)
Protein Sci
, vol.5
, pp. 422-433
-
-
Krishnan, R.1
Tulinsky, A.2
Vlasuk, G.P.3
Pearson, D.4
Vallar, P.5
-
40
-
-
0029965611
-
Crystal structures of thrombin with thiazole-containing inhibitors: probes of the S1′ binding site
-
Matthews JH, Krishnan R, Costanzo MJ, Maryanoff BE, Tulinsky A, (1996) Crystal structures of thrombin with thiazole-containing inhibitors: probes of the S1′ binding site. Biophys J 71: 2830-2839.
-
(1996)
Biophys J
, vol.71
, pp. 2830-2839
-
-
Matthews, J.H.1
Krishnan, R.2
Costanzo, M.J.3
Maryanoff, B.E.4
Tulinsky, A.5
-
41
-
-
0033594326
-
Bound structures of novel P3-P1′ beta-strand mimetic inhibitors of thrombin
-
St Charles R, Matthews JH, Zhang E, Tulinsky A, (1999) Bound structures of novel P3-P1′ beta-strand mimetic inhibitors of thrombin. J Med Chem 42: 1376-1383.
-
(1999)
J Med Chem
, vol.42
, pp. 1376-1383
-
-
St Charles, R.1
Matthews, J.H.2
Zhang, E.3
Tulinsky, A.4
-
42
-
-
0034092880
-
Design of P1′ and P3′ residues of trivalent thrombin inhibitors and their crystal structures
-
Slon-Usakiewicz JJ, Sivaraman J, Li Y, Cygler M, Konishi Y, (2000) Design of P1′ and P3′ residues of trivalent thrombin inhibitors and their crystal structures. Biochemistry 39: 2384-2391.
-
(2000)
Biochemistry
, vol.39
, pp. 2384-2391
-
-
Slon-Usakiewicz, J.J.1
Sivaraman, J.2
Li, Y.3
Cygler, M.4
Konishi, Y.5
|