-
1
-
-
0026337077
-
The coagulation cascade: Initiation, maintenance, and regulation
-
Davie, E. W.; Fujikawa, K; Kisiel, W. The Coagulation Cascade: Initiation, Maintenance, and Regulation. Biochemistry 1991, 30, 10363-10370.
-
(1991)
Biochemistry
, vol.30
, pp. 10363-10370
-
-
Davie, E.W.1
Fujikawa, K.2
Kisiel, W.3
-
2
-
-
0026102830
-
Thrombin structure and function: Why thrombin is the primary target for antithrombotics
-
Fenton, J. W. H.; Ofosu, F. A.; Moon, D. G.; Maraganore, J. M. Thrombin Structure and Function: Why Thrombin is the Primary Target for Antithrombotics. Blood Coagulation Fibrinolysis 1991, 2, 69-75.
-
(1991)
Blood Coagulation Fibrinolysis
, vol.2
, pp. 69-75
-
-
Fenton, J.W.H.1
Ofosu, F.A.2
Moon, D.G.3
Maraganore, J.M.4
-
3
-
-
0026035523
-
Molecular cloning of a functional thrombin receptor reveals a novel proteolytic mechanism of receptor activation
-
Vu, T.-K. H.; Hung, D. T.; Wheaton, V. I.; Coughlin, S. R. Molecular Cloning of a Functional Thrombin Receptor Reveals a Novel Proteolytic Mechanism of Receptor Activation. Cell 1991, 64, 1057-1068.
-
(1991)
Cell
, vol.64
, pp. 1057-1068
-
-
Vu, T.-K.H.1
Hung, D.T.2
Wheaton, V.I.3
Coughlin, S.R.4
-
4
-
-
0024428222
-
Inhibition of thrombin, a key step in thrombosis
-
Wallis, R. B. Inhibition of Thrombin, a Key Step in Thrombosis. Drugs Today 1989, 9, 596-605.
-
(1989)
Drugs Today
, vol.9
, pp. 596-605
-
-
Wallis, R.B.1
-
5
-
-
0026763390
-
Pharmacologic aspects of the development of selective synthetic thrombin inhibitors as anticoagulants
-
Hauptmann, J.; Markwardt, F. Pharmacologic Aspects of the Development of Selective Synthetic Thrombin Inhibitors as Anticoagulants. Semin. Thromb. Hemostasis 1992, 18, 200-217.
-
(1992)
Semin. Thromb. Hemostasis
, vol.18
, pp. 200-217
-
-
Hauptmann, J.1
Markwardt, F.2
-
6
-
-
0028788077
-
Antithrombotic therapy in patients undergoing coronary angioplasty
-
Popma, J. J.; Coller, B. S.; Ohman, E. M.; Bittl, J. A.; Weitz, J.; Kuntz, R. E.; Leon, M. B. Antithrombotic Therapy in Patients Undergoing Coronary Angioplasty. Chest 1995, 108, 486S-501S.
-
(1995)
Chest
, vol.108
-
-
Popma, J.J.1
Coller, B.S.2
Ohman, E.M.3
Bittl, J.A.4
Weitz, J.5
Kuntz, R.E.6
Leon, M.B.7
-
7
-
-
0026698150
-
Thrombolytic therapy for acute myocardial infarction. A review
-
Granger, C. B.; Califf, R. M.; Topol, E. J. Thrombolytic Therapy for Acute Myocardial Infarction. A Review. Drugs 1992, 3, 293-325.
-
(1992)
Drugs
, vol.3
, pp. 293-325
-
-
Granger, C.B.1
Califf, R.M.2
Topol, E.J.3
-
8
-
-
0027170687
-
Reocclusion following successful thrombolysis
-
Becker, R. C. Reocclusion Following Successful Thrombolysis. Cardiology 1993, 82, 265-273.
-
(1993)
Cardiology
, vol.82
, pp. 265-273
-
-
Becker, R.C.1
-
9
-
-
0023609990
-
Appraisal of various thrombolytic agents in the treatment of acute myocardial infarction
-
Sherry, S. Appraisal of Various Thrombolytic Agents in the Treatment of Acute Myocardial Infarction. Am. J. Med. 1987, 83, 31-46.
-
(1987)
Am. J. Med.
, vol.83
, pp. 31-46
-
-
Sherry, S.1
-
10
-
-
0022635358
-
Acute coronary reocclusion after thrombolysis with recombinant tissue-type plasminogen activator: Prevention by a maintenance infusion
-
Gold, H. K; Leinbach, R. C.; Garabedian, S. M.; Yasuda, T.; Johns, J. A.; Grossbard, E. B.; Palacios, I.; Collen, D. Acute Coronary Reocclusion after Thrombolysis with Recombinant Tissue-type Plasminogen Activator: Prevention by a Maintenance Infusion. Circulation 1987, 73, 347-352.
-
(1987)
Circulation
, vol.73
, pp. 347-352
-
-
Gold, H.K.1
Leinbach, R.C.2
Garabedian, S.M.3
Yasuda, T.4
Johns, J.A.5
Grossbard, E.B.6
Palacios, I.7
Collen, D.8
-
11
-
-
0024670167
-
Fibrin monomer protects thrombin from inactivation by heparin-antithrombin III: Implications for heparin efficacy
-
Hogg, P. J.; Jackson, C. M. Fibrin Monomer Protects Thrombin from Inactivation by Heparin-antithrombin III: Implications for Heparin Efficacy. Proc. Natl. Acad. Sci. U.S.A. 1989, 86, 3619-3623.
-
(1989)
Proc. Natl. Acad. Sci. U.S.A.
, vol.86
, pp. 3619-3623
-
-
Hogg, P.J.1
Jackson, C.M.2
-
12
-
-
0025146426
-
Clot-bound thrombin is protected from inhibition by heparin-antithrombin III but is susceptible to inactivation by antithrombin II-independent inhibitors
-
Weitz, J. I.; Hudoba, M.; Massel, D.; Maraganore, J.; Hirsh, J. Clot-bound Thrombin is Protected from Inhibition by Heparin-Antithrombin III but is Susceptible to Inactivation by Antithrombin II-independent Inhibitors. J. Clin. Invest. 1990, 86, 385-391.
-
(1990)
J. Clin. Invest.
, vol.86
, pp. 385-391
-
-
Weitz, J.I.1
Hudoba, M.2
Massel, D.3
Maraganore, J.4
Hirsh, J.5
-
13
-
-
0001563885
-
Thrombin active site inhibitors
-
Kimball, D. S. Thrombin Active Site Inhibitors. Curr. Pharm. Des. 1995, 1, 441-468.
-
(1995)
Curr. Pharm. Des.
, vol.1
, pp. 441-468
-
-
Kimball, D.S.1
-
14
-
-
0000319455
-
Hirudin is an inhibitor of thrombin
-
Markwardt, F. Hirudin is an Inhibitor of Thrombin. Methods Enzymol. 1970, 19, 924-932.
-
(1970)
Methods Enzymol.
, vol.19
, pp. 924-932
-
-
Markwardt, F.1
-
15
-
-
0022521744
-
Kinetics of the inhibition of thrombin by hirudin
-
Stone, R. S.; Hofsteenge, J. Kinetics of the Inhibition of Thrombin by Hirudin. Biochemistry 1986, 25, 4622-4628.
-
(1986)
Biochemistry
, vol.25
, pp. 4622-4628
-
-
Stone, R.S.1
Hofsteenge, J.2
-
16
-
-
0027409404
-
A player of many parts: The spotlight falls on thrombin structure
-
Stubbs, M. T.; Bode, W. A Player of Many Parts: The Spotlight Falls on Thrombin Structure. Thromb. Res. 1993, 69, 1-58.
-
(1993)
Thromb. Res.
, vol.69
, pp. 1-58
-
-
Stubbs, M.T.1
Bode, W.2
-
17
-
-
44949277731
-
Evidence for thrombin enhancement of fibrin polymerization that is independent of 1st catalytic activity
-
Kaminski, M.; Siebenlist, K. R.; Mosesson, M. W. Evidence for Thrombin Enhancement of Fibrin Polymerization that is Independent of 1st Catalytic Activity. J. Lab. Clin. Med. 1991, 117, 218-225.
-
(1991)
J. Lab. Clin. Med.
, vol.117
, pp. 218-225
-
-
Kaminski, M.1
Siebenlist, K.R.2
Mosesson, M.W.3
-
18
-
-
0024345758
-
Evaluation of the inhibition by heparin and hirudin of coagulation activation during r-tPA-induced thrombolysis
-
Mirshani, M.; Soria, J.; Soria, C.; Faivre, R.; Lu, H.; Courtney, M.; Roitsch, C.; Tripier, D.; Caen, J. P. Evaluation of the Inhibition by Heparin and Hirudin of Coagulation Activation During r-tPA-induced Thrombolysis. Blood 1989, 74, 1025-1030.
-
(1989)
Blood
, vol.74
, pp. 1025-1030
-
-
Mirshani, M.1
Soria, J.2
Soria, C.3
Faivre, R.4
Lu, H.5
Courtney, M.6
Roitsch, C.7
Tripier, D.8
Caen, J.P.9
-
19
-
-
0026102565
-
Reocclusion after thrombolysis: A problem solved by hirudin?
-
Rübsamen, K,; Eschenfelder, V. Reocclusion after Thrombolysis: A Problem Solved by Hirudin? Blood Coagulation Fibrinolysis 1991, 2, 97-100.
-
(1991)
Blood Coagulation Fibrinolysis
, vol.2
, pp. 97-100
-
-
Rübsamen, K.1
Eschenfelder, V.2
-
20
-
-
0025346345
-
Design and characterization of hirulogs: A novel class of bivalent peptide inhibitors of thrombin
-
Maraganore, J. M.; Bourdon, P.; Jablonski, J.; Ramachandran, K. L.; Fenton, J. W. II. Design and Characterization of Hirulogs: A Novel Class of Bivalent Peptide Inhibitors of Thrombin. Biochemistry 1990, 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 J.W. II5
-
21
-
-
0025674180
-
45-65
-
45-65. J. Biol. Chem. 1990, 265, 21698-21703.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 21698-21703
-
-
DiMaio, J.1
Gibbs, B.2
Munn, D.3
Lefebvre, J.4
Ni, F.5
Konishi, Y.6
-
22
-
-
0026743042
-
Hirulog-1 and -B2 thrombin specificity
-
Wittig, J. I.; Bourdon, P.; Maraganore, J. M.; Fenton, J. W. II. Hirulog-1 and -B2 Thrombin Specificity. Biochem. J. 1992, 287, 663-664.
-
(1992)
Biochem. J.
, vol.287
, pp. 663-664
-
-
Wittig, J.I.1
Bourdon, P.2
Maraganore, J.M.3
Fenton J.W. II4
-
23
-
-
0025823257
-
Hirulog peptides with scissile bond replacements resistant to thrombin cleavage
-
Kline, T.; Hammond, C.; Bourdon, P.; Maraganore, J. M. Hirulog Peptides with Scissile Bond Replacements Resistant to Thrombin Cleavage. Biochem. Biophys. Res. Commun. 1991, 177, 1049-1055.
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.177
, pp. 1049-1055
-
-
Kline, T.1
Hammond, C.2
Bourdon, P.3
Maraganore, J.M.4
-
24
-
-
0025906031
-
A new class of potent thrombin inhibitors that incorporates a scissile pseudopeptide bond
-
DiMaio, J.; Ni, F.; Gibbs, B.; Konishi, Y. A New Class of Potent Thrombin Inhibitors that Incorporates a Scissile Pseudopeptide Bond. FEBS Lett. 1991, 282, 47-52.
-
(1991)
FEBS Lett.
, vol.282
, pp. 47-52
-
-
DiMaio, J.1
Ni, F.2
Gibbs, B.3
Konishi, Y.4
-
25
-
-
0026731584
-
Synthesis of a homologous series of ketomethylene arginyl pseudopeptides and application to low molecular weight hirudin-like thrombin inhibitors
-
DiMaio, J.; Gibbs, B.; Lefebvre, J.; Konishi, Y.; Munn, D.; Yue, S. Y.; Hornberger, W. Synthesis of a Homologous Series of Ketomethylene Arginyl Pseudopeptides and Application to Low Molecular Weight Hirudin-like Thrombin Inhibitors. J. Med. Chem. 1992, 35, 3331-3341.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 3331-3341
-
-
DiMaio, J.1
Gibbs, B.2
Lefebvre, J.3
Konishi, Y.4
Munn, D.5
Yue, S.Y.6
Hornberger, W.7
-
26
-
-
0029879577
-
Synthesis, structure, and structure-activity relationships of divalent thrombin inhibitors containing an α-keto-amide transition-state mimetic
-
Krishnan, R.; Tulinsky, A.; Vlasuk, G. P.; Pearson, D.; Vallar, P.; Bergum, P.; Brunck, T. K.; Ripka, W. C. Synthesis, Structure, and Structure-activity Relationships of Divalent Thrombin Inhibitors Containing an α-keto-amide Transition-state Mimetic. Protein Sci. 1996, 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
Bergum, P.6
Brunck, T.K.7
Ripka, W.C.8
-
27
-
-
0020363317
-
Angiotensin converting enzyme inhibitors: Modifications of a tripeptide analogue
-
Meyer, R. F.; Essenburg, A. D.; Smith, R. D.; Kaplan, H. R. Angiotensin Converting Enzyme Inhibitors: Modifications of a Tripeptide Analogue. J. Med. Chem. 1982, 25, 996-999.
-
(1982)
J. Med. Chem.
, vol.25
, pp. 996-999
-
-
Meyer, R.F.1
Essenburg, A.D.2
Smith, R.D.3
Kaplan, H.R.4
-
28
-
-
0021681698
-
Ketomethyldipeptides I. A new class of angiotensin converting enzyme inhibitors
-
Natarajan, S.; Gordon, E. M.; Sabo, E. F.; Godfrey, J. D.; Weller, H. N.; Pluscek, J.; Rom, M. B.; Cushman, D. W. Ketomethyldipeptides I. A New Class of Angiotensin Converting Enzyme Inhibitors. Biochem. Biophys. Res. Commun. 1984, 124, 141-147.
-
(1984)
Biochem. Biophys. Res. Commun.
, vol.124
, pp. 141-147
-
-
Natarajan, S.1
Gordon, E.M.2
Sabo, E.F.3
Godfrey, J.D.4
Weller, H.N.5
Pluscek, J.6
Rom, M.B.7
Cushman, D.W.8
-
29
-
-
0021678342
-
Ketomethyldipeptides II. Effect of modifications of the α-aminoketone portion on inhibition of angiotensin converting enzyme
-
Gordon, E. M.; Natarajan, S.; Pluscek, J.; Weller, H. N.; Godfrey, J. D.; Rom, M. B.; Sabo, E. F.; Engebrecht, J.; Cushman, D. W. Ketomethyldipeptides II. Effect of Modifications of the α-Aminoketone Portion on Inhibition of Angiotensin Converting Enzyme. Biochem. Biophys. Res. Commun. 1984, 124, 148-155.
-
(1984)
Biochem. Biophys. Res. Commun.
, vol.124
, pp. 148-155
-
-
Gordon, E.M.1
Natarajan, S.2
Pluscek, J.3
Weller, H.N.4
Godfrey, J.D.5
Rom, M.B.6
Sabo, E.F.7
Engebrecht, J.8
Cushman, D.W.9
-
30
-
-
0020574211
-
Amino acids and peptides: Part 48. Synthesis of bradykinyl-chloromethane
-
Aplin, B. T.; Christiansen, J.; Young, G. T. Amino acids and Peptides: Part 48. Synthesis of Bradykinyl-chloromethane. Int. J. Pept. Protein Res. 1983, 21, 555-561.
-
(1983)
Int. J. Pept. Protein Res.
, vol.21
, pp. 555-561
-
-
Aplin, B.T.1
Christiansen, J.2
Young, G.T.3
-
31
-
-
0019750662
-
Inactivation of trypsin-like enzymes with peptides of arginine chloromethyl ketone
-
Kettner, C.; Shaw, E. Inactivation of Trypsin-like Enzymes with Peptides of Arginine Chloromethyl Ketone. Methods Enzymol. 1981, 80, 826-842.
-
(1981)
Methods Enzymol.
, vol.80
, pp. 826-842
-
-
Kettner, C.1
Shaw, E.2
-
32
-
-
0001029707
-
Alpha-Ammochloromethyl ketone aus aminosäuren und peptiden als substratanaloge inhibitoren der leucinaminopeptidase
-
Fittkau, S. alpha-Ammochloromethyl ketone aus Aminosäuren und Peptiden als Substratanaloge Inhibitoren der Leucinaminopeptidase. J. Prakt. Chem. 1973, 315, 1037-1044.
-
(1973)
J. Prakt. Chem.
, vol.315
, pp. 1037-1044
-
-
Fittkau, S.1
-
33
-
-
0028818056
-
Synthesis of tight binding inhibitors and their action on the proprotein-processing enzyme furin
-
Angliker, H. Synthesis of Tight Binding Inhibitors and Their Action on the Proprotein-Processing Enzyme Furin. J. Med. Chem. 1995, 38, 4014-4018.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4014-4018
-
-
Angliker, H.1
-
34
-
-
0001018560
-
Aminoketone - Ein beitrag zur synthese optisch aktiver derivate von aminosäuren und peptiden
-
Fittkau, S.; Jahreis, G.; Peters, K.; Baláspiri, L. Aminoketone - Ein Beitrag zur Synthese Optisch Aktiver Derivate von Aminosäuren und Peptiden. J. Prakt. Chem. 1986, 328, 529-538.
-
(1986)
J. Prakt. Chem.
, vol.328
, pp. 529-538
-
-
Fittkau, S.1
Jahreis, G.2
Peters, K.3
Baláspiri, L.4
-
35
-
-
0027372461
-
Peptidyl ammonium methyl ketones as substrate analogue inhibitors of proline specific peptidases
-
Steinmetzer, T.; Silberring, J.; Mrestani-Claus, C.; Fittkau, S.; Demuth, H.-U. Peptidyl Ammonium Methyl Ketones as Substrate Analogue Inhibitors of Proline Specific Peptidases. J. Enzyme Inhib. 1993, 7, 77-85.
-
(1993)
J. Enzyme Inhib.
, vol.7
, pp. 77-85
-
-
Steinmetzer, T.1
Silberring, J.2
Mrestani-Claus, C.3
Fittkau, S.4
Demuth, H.-U.5
-
36
-
-
0024344518
-
Peptide methyl ketones as reversible inhibitors of cysteine proteinases
-
Brömme, D.; Barthels, B.; Kirschke, H.; Fittkau, S. Peptide Methyl Ketones as Reversible Inhibitors of Cysteine Proteinases. J. Enzyme Inhib. 1989, 3, 13-21.
-
(1989)
J. Enzyme Inhib.
, vol.3
, pp. 13-21
-
-
Brömme, D.1
Barthels, B.2
Kirschke, H.3
Fittkau, S.4
-
37
-
-
0028938348
-
Thrombin inhibitors based on keton derivatives of arginine and lysine
-
Jones, D. M.; Atrash, B.; Ryder, H.; Teger-Nilsson, A.-C.; Gyzander, E.; Szelke, M. Thrombin inhibitors Based on Keton Derivatives of Arginine and Lysine. J. Enzyme Inhib. 1995, 9, 43-60.
-
(1995)
J. Enzyme Inhib.
, vol.9
, pp. 43-60
-
-
Jones, D.M.1
Atrash, B.2
Ryder, H.3
Teger-Nilsson, A.-C.4
Gyzander, E.5
Szelke, M.6
-
38
-
-
0023728105
-
The behavior and significance of slow-binding enzyme inhibitors
-
Morrison, J. F.; Walsh, C. T. The Behavior and Significance of Slow-binding Enzyme Inhibitors. Adv. Enzymol. 1988, 61, 201-301.
-
(1988)
Adv. Enzymol.
, vol.61
, pp. 201-301
-
-
Morrison, J.F.1
Walsh, C.T.2
-
39
-
-
0023766115
-
Use of site-directed mutagenesis to investigate the basis for the specificity of hirudin
-
Braun, P. J.; Dennis, S.; Hofsteenge, J.; Stone, S. R. Use of Site-directed Mutagenesis to Investigate the Basis for the Specificity of Hirudin. Biochemistry 1988, 27, 6517-6522.
-
(1988)
Biochemistry
, vol.27
, pp. 6517-6522
-
-
Braun, P.J.1
Dennis, S.2
Hofsteenge, J.3
Stone, S.R.4
-
40
-
-
0025240978
-
Development of MDL 28,050, a small stable antithrombin agent based on a functional domain of the leech protein, hirudin
-
Krstenansky, J. L.; Broersma, R. J.; Owen, T. J.; Payne, M. H.; Yates, M. T.; Mao, S. J. T. Development of MDL 28,050, a Small Stable Antithrombin Agent Based on a Functional Domain of the Leech Protein, Hirudin. Thromb. Haemostasis 1990, 63, 208-214.
-
(1990)
Thromb. Haemostasis
, vol.63
, pp. 208-214
-
-
Krstenansky, J.L.1
Broersma, R.J.2
Owen, T.J.3
Payne, M.H.4
Yates, M.T.5
Mao, S.J.T.6
-
41
-
-
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. 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. 1992, 1, 426-471.
-
(1992)
Protein Sci.
, vol.1
, pp. 426-471
-
-
Bode, W.1
Turk, D.2
Karshikov, A.3
-
42
-
-
0027487088
-
Crystal structure of the complex of human alpha-thrombin and nonhydrolyzable bifunctional inhibitors, hirutonin-2 and hirutonin-6
-
Zdanov, A.; Wu, S.; DiMaio, J.; Konishi, Y.; Li, Y.; Wu, X.; Edwards, B. F. P.; Martin, P. D.; Cygler, M. Crystal Structure of the Complex of Human alpha-Thrombin and Nonhydrolyzable Bifunctional Inhibitors, Hirutonin-2 and Hirutonin-6. Proteins: Struct. Funct. Genet. 1993, 17, 252-265.
-
(1993)
Proteins: Struct. Funct. Genet.
, vol.17
, pp. 252-265
-
-
Zdanov, A.1
Wu, S.2
DiMaio, J.3
Konishi, Y.4
Li, Y.5
Wu, X.6
Edwards, B.F.P.7
Martin, P.D.8
Cygler, M.9
-
43
-
-
0029092861
-
Crystal structure of a peptidyl pyridinium methyl ketone inhibitor with thrombin
-
Rehse, P. H.; Steinmetzer, T.; Li, Y.; Konishi, Y.; Cygler, M. Crystal Structure of a Peptidyl Pyridinium Methyl Ketone Inhibitor with Thrombin. Biochemistry 1995, 34, 11537-11544.
-
(1995)
Biochemistry
, vol.34
, pp. 11537-11544
-
-
Rehse, P.H.1
Steinmetzer, T.2
Li, Y.3
Konishi, Y.4
Cygler, M.5
-
44
-
-
0030598662
-
Tripeptidyl pyridinium methyl ketones as potent active site inhibitors of thrombin
-
Steinmetzer, T.; Konishi, Y. Tripeptidyl Pyridinium Methyl Ketones as Potent Active Site Inhibitors of Thrombin. Bioorg. Med. Chem. Lett. 1996, 6, 1677-1682.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 1677-1682
-
-
Steinmetzer, T.1
Konishi, Y.2
-
45
-
-
0026005785
-
Mechanistic studies on thrombin catalysis
-
Stone, S. R.; Betz, A.; Hofsteenge, J. Mechanistic Studies on Thrombin Catalysis. Biochemistry 1991, 30, 9841-9848.
-
(1991)
Biochemistry
, vol.30
, pp. 9841-9848
-
-
Stone, S.R.1
Betz, A.2
Hofsteenge, J.3
-
46
-
-
33646195474
-
The hydrogen bond in molecular recognition
-
Fersht, A. R. The Hydrogen Bond in Molecular Recognition. Trends Biochem. Sci. 1987, 12, 301-304.
-
(1987)
Trends Biochem. Sci.
, vol.12
, pp. 301-304
-
-
Fersht, A.R.1
-
47
-
-
0027298337
-
Design of a linker for trivalent thrombin inhibitors: Interaction of the main chain of the linker with thrombin
-
Szewczuk, Z.; Gibbs, B. F.; Yue, S. Y.; Purisima, E.; Zdanov, A.; Cygler, M.; Konishi, Y. Design of a Linker for Trivalent Thrombin Inhibitors: Interaction of the Main Chain of the Linker with Thrombin. Biochemistry 1993, 32, 3396-3404.
-
(1993)
Biochemistry
, vol.32
, pp. 3396-3404
-
-
Szewczuk, Z.1
Gibbs, B.F.2
Yue, S.Y.3
Purisima, E.4
Zdanov, A.5
Cygler, M.6
Konishi, Y.7
-
49
-
-
0026786833
-
Conformationally restricted thrombin inhibitors resistant to proteolytic digestion
-
Szewczuk, Z.; Gibbs, B. F.; Yue, S. Y.; Purisima, E. O.; Konishi, Y. Conformationally Restricted Thrombin Inhibitors Resistant to Proteolytic Digestion. Biochemistry 1992, 31, 9132-9140.
-
(1992)
Biochemistry
, vol.31
, pp. 9132-9140
-
-
Szewczuk, Z.1
Gibbs, B.F.2
Yue, S.Y.3
Purisima, E.O.4
Konishi, Y.5
-
51
-
-
0001615524
-
Approaches to the study and analysis of the inhibition of enzymes by slow- and tight-binding inhibitors
-
Morrison, J. F.; Stone, S. R. Approaches to the Study and Analysis of the Inhibition of Enzymes by Slow- and Tight-binding Inhibitors. Comments Mol. Cell. Biophys. 1985, 2, 347-368.
-
(1985)
Comments Mol. Cell. Biophys.
, vol.2
, pp. 347-368
-
-
Morrison, J.F.1
Stone, S.R.2
|