Stereoisomers of Cyclic Urea HIV-1 Protease Inhibitors: Synthesis and Binding Affinities
Author:
Affiliation:
1. DuPont Merck Pharmaceutical Company, P.O. Box 80500, Wilmington, Delaware 19880-0500
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm980255b
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1. Regulation of MHC Class I Transport by the Molecular Chaperone, Calnexin (p88, IP90)
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3. Cyclic HIV-1 Protease Inhibitors Derived from Mannitol: Synthesis, Inhibitory Potencies, and Computational Predictions of Binding Affinities
4. L-687,908, a potent hydroxyethylene containing HIV protease inhibitor
5. Symmetry-based inhibitors of HIV protease. Structure-activity studies of acylated 2,4-diamino-1,5-diphenyl-3-hydroxypentane and 2,5-diamino-1,6-diphenylhexane-3,4-diol
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