| Literature DB >> 15771434 |
Paul A J Janssen1, Paul J Lewi, Eddy Arnold, Frits Daeyaert, Marc de Jonge, Jan Heeres, Luc Koymans, Maarten Vinkers, Jérôme Guillemont, Elisabeth Pasquier, Mike Kukla, Don Ludovici, Koen Andries, Marie-Pierre de Béthune, Rudi Pauwels, Kalyan Das, Art D Clark, Yulia Volovik Frenkel, Stephen H Hughes, Bart Medaer, Fons De Knaep, Hilde Bohets, Fred De Clerck, Ann Lampo, Peter Williams, Paul Stoffels.
Abstract
Ideally, an anti-HIV drug should (1) be highly active against wild-type and mutant HIV without allowing breakthrough; (2) have high oral bioavailability and long elimination half-life, allowing once-daily oral treatment at low doses; (3) have minimal adverse effects; and (4) be easy to synthesize and formulate. R278474, a new diarylpyrimidine (DAPY) non-nucleoside reverse transcriptase inhibitor (NNRTI), appears to meet these criteria and to be suitable for high compliance oral treatment of HIV-1 infection. The discovery of R278474 was the result of a coordinated multidisciplinary effort involving medicinal chemists, virologists, crystallographers, molecular modelers, toxicologists, analytical chemists, pharmacists, and many others.Entities:
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Year: 2005 PMID: 15771434 DOI: 10.1021/jm040840e
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446