Improved P1/P1‘ Substituents for Cyclic Urea Based HIV-1 Protease Inhibitors: Synthesis, Structure−Activity Relationship, and X-ray Crystal Structure Analysis
Author:
Affiliation:
1. The 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/jm960839i
Reference27 articles.
1. L-735,524: The Design of a Potent and Orally Bioavailable HIV Protease Inhibitor
2. ABT-538 is a potent inhibitor of human immunodeficiency virus protease and has high oral bioavailability in humans.
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