Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Eugene C. Amparo"'
Autor:
Eugene C. Amparo, Srinivas K. Chunduru, Ariamala Gopalsamy, Christopher A. Benetatos, Lori E. Miller, Tandy L. Draper, Christopher J. Burns, Matthew G. LaPorte, Lara K. Leister, Torsten Herbertz, Dorothy C. Young, Stephen M. Condon, Blackledge Charles W, Gerry Rhodes, Alison R. Hussey
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:2968-2973
We describe the structure-activity relationship of the C1-group of pyrano[3,4-b]indole based inhibitors of HCV NS5B polymerase. Further exploration of the allosteric binding site led to the discovery of the significantly more potent compound 12.
Autor:
Matthew R. Wright, John M. Fevig, Richard S. Alexander, Mimi L. Quan, Ruth R. Wexler, Patrick Y.S. Lam, Bruce J. Aungst, Pancras C. Wong, Joseph M. Luettgen, Shuaige Wang, Donald J. P. Pinto, Robert M. Knabb, Michael J. Orwat, Angela Smallwood, Joseph Cacciola, Eugene C. Amparo, Karen A. Rossi, Li Liang
Publikováno v:
Journal of Medicinal Chemistry. 44:566-578
Factor Xa (fXa) plays a critical role in the coagulation cascade, serving as the point of convergence of the intrinsic and extrinsic pathways. Together with nonenzymatic cofactor Va and Ca2+ on the phospholipid surface of platelets or endothelial cel
Autor:
Vicki L. Nienaber, Eugene C. Amparo
Publikováno v:
Journal of the American Chemical Society. 118:6807-6810
The 2.0 A resolution crystal structure of the retro-binding natural product nazumamide A (NAZA) complexed with human thrombin is presented. The crystal structure shows that the retro-binding nazumamide A is noncleavable and extends into the prime end
Autor:
Diane Cebzanov, C. Faust, D. Ortlip, Lessen Thomas A, L. Leister, Thomas R. Bailey, Dorothy C. Young, Christopher J. Burns, Srinivas K. Chunduru, Eugene C. Amparo, Theodore J. Nitz, M.G. LaPorte
Publikováno v:
Bioorganicmedicinal chemistry letters. 16(1)
A novel series of selective HCV NS5B RNA dependent RNA polymerase inhibitors has been disclosed. These compounds contain an appropriately substituted tetrahydrobenzothiophene scaffold. This communication will detail the SAR and activities of this ser
Autor:
Ruth R. Wexler, Eugene C. Amparo, Joseph M. Luettgen, Celia Dominguez, Daniel E. Duffy, Pancras C. Wong, Richard S. Alexander, Qi Han, Robert A. Galemmo, Robert M. Knabb, Jeongsook M. Park
Publikováno v:
Bioorganicmedicinal chemistry letters. 9(7)
Thrombin, a serine protease, plays a central role in the initiation of thrombotic events. We report the design, synthesis, and antithrombotic efficacy of XU817 (7), a nonpeptide 5-(amidino) indole thrombin inhibitor. Utilizing the co-crystal structur