Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Scott I. Klein"'
Autor:
Scott I. Klein, M. Jonathan Rudolph, Carl R. Illig, Ehab Khalil, Farah Ali, John C. Spurlino, Renee L. DesJarlais, Carl Crysler, Philip E. Morris, J. M. Kilpatrick, Richard Soll, Y. Sudhakara Babu, Nalin L. Subasinghe, Roger F. Bone, Maxwell D. Cummings
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 14:3043-3047
Activation of the classical pathway of complement has been implicated in disease states such as hereditary angioedema, ischemia-reperfusion injury and acute transplant rejection. The trypsin-like serine protease C1s represents a pivotal upstream poin
Publikováno v:
European Journal of Medicinal Chemistry. 32:833-839
Summary A series of nonpeptide fibrinogen receptor antagonists based upon the tetrapeptide Arg-Gly-Asp-Arg were prepared. These relatively simple derivatives incorporate a high degree of conformational flexibility that was anticipated to allow them t
Autor:
Rose D'Alisa, Bruce F. Molino, Scott I. Klein, Jeffrey M Dener, Robert J. Leadley, Charles Kasiewski, Christopher T. Dunwiddie, Charles J. Gardner
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:2225-2230
A series of analogs were prepared based on the known thrombin inhibitor PPACK, in which the D-Phe-Pro dipeptide has been replaced by trans-4-O-benzyl hydroxyproline. One of these analogs is a more potent inhibitor of thrombin, and is more selective,
Autor:
Robert J. Leadley, Bruce F. Molino, Scott I. Klein, Jeffrey S Dener, Christopher T. Dunwiddie, Ralph D. Sabatino, Mark Czekaj, Valeria Chu
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:1403-1408
Structure-activity relationships developed from work with peptide based fibrinogen receptor antagonists have been successfully applied to the development of simple and highly potent nonpeptide agents of the same class.
Autor:
Rose D'Alisa, Scott I. Klein, Jeffrey M Dener, Bruce F. Molino, Charles Kasiewski, Charles J. Gardner, Robert J. Leadley, Christopher T. Dunwiddie
Publikováno v:
ChemInform. 28
A series of analogs were prepared based on the known thrombin inhibitor PPACK, in which the D-Phe-Pro dipeptide has been replaced by trans-4-O-benzyl hydroxyproline. One of these analogs is a more potent inhibitor of thrombin, and is more selective,
Autor:
Mark Czekaj, Valeria Chu, Karen D. Brown, Scott I. Klein, Dennis J. Colussi, Robert J. Leadley, Christopher Heran, Ross Bentley, Charles Kasiewski, Mark H. Perrone, Suzanne Morgan, Jeffrey S. Bostwick
Publikováno v:
European journal of pharmacology. 389(2-3)
Coagulation factor Xa is the sole enzyme responsible for activating the zymogen prothrombin to thrombin, resulting in fibrin generation, platelet activation, and subsequent thrombus formation. Our objective was to evaluate the antithrombotic efficacy
Autor:
Charles Kasiewski, Scott I. Klein, Mark Czekaj, Valeria Chu, Karen D. Brown, Jeffrey S. Bostwick, Vincent Windisch, Christopher T. Dunwiddie, Ross Bentley, Bruce F. Molino, Charles J. Gardner, Ralph D. Sabatino, Robert J. Leadley, Mark H. Perrone
Publikováno v:
Journal of medicinal chemistry. 41(14)
The integrin receptor recognition sequence Arg-Gly-Asp was successfully used as a template from which to develop a series of potent, selective, orally active, peptide-based fibrinogen receptor antagonists with a long duration of action. Simple modifi
Autor:
Karen S. Brown, Mark H Perrone, Alfred P. Spada, Valeria Chu, Christopher L. Heran, Mark Czekaj, Scott A. Bolton, Guertin Kevin R, Scott I. Klein, Robert J. Leadley, Christopher T. Dunwiddie, Dennis Colussi, Charles J. Gardner, Daniel L. Cheney, Suzanne R. Morgan
Publikováno v:
Journal of medicinal chemistry. 41(4)
The discovery and some of the basic structure-activity relationships of a series of novel nonpeptide inhibitors of blood coagulation Factor Xa is described. These inhibitors are functionalized beta-alanines, exemplified by 2a. Docking experiments pla
Autor:
Robert J. Leadley, Christopher T. Dunwiddie, Scott I. Klein, Jeffrey S. Bostwick, Ralph D. Sabatino, Charles Kasiewski, Valeria Chu, Mark H. Perrone, Jacquelynn J. Cook
Publikováno v:
Thrombosis research. 82(6)
RG13965, a pseudotetrapeptide analogue of Arg-Gly-Asp (RGD), inhibited collagen-induced dog, monkey, human, hamster, mouse, and pig platelet aggregation in vitro with IC 50 values of 3.7, 4.6, 6.3, 126, 136 and 1600 μM, respectively. RG13965 (3, 10,
Autor:
Scott I. Klein, Jacquelynn J. Cook, Zaverio M. Ruggeri, Bruce F. Molino, Mark Czekaj, Valeria Chu, Charles Kasiewski, Jeffrey S. Bostwick
Publikováno v:
Peptides 1992 ISBN: 9789401046466
Peptides 1992
Peptides 1992
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75897ed5e33a4636008842a82f191484
https://doi.org/10.1007/978-94-011-1470-7_288
https://doi.org/10.1007/978-94-011-1470-7_288