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Bioorganic & Medicinal Chemistry Letters|December 8, 2004
Optimization of pyrrolidinone based HIV protease inhibitorsRonald G Sherrill, C Webster Andrews, William J Bock, et al.Journal of Medicinal Chemistry|July 31, 2008
Structural basis for the improved drug resistance profile of new generation benzophenone non-nucleoside HIV-1 reverse transcriptase inhibitorsJingshan Ren, Philip P Chamberlain, Anna Stamp, et al.Journal of Medicinal Chemistry|September 29, 2006
A critical assessment of docking programs and scoring functionsGregory L Warren, C Webster Andrews, Anna-Maria Capelli, et al.Bioorganic & Medicinal Chemistry Letters|February 7, 2006
Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: the discovery of GW0385John F Miller, C Webster Andrews, Michael Brieger, et al.Journal of Medicinal Chemistry|November 13, 2004
Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved drug resistance properties. 2George A Freeman, C Webster Andrews Iii, Andrew L Hopkins, et al.Pageof 1