In Search of a Novel Anti-HIV Drug:  Multidisciplinary Coordination in the Discovery of 4-[[4-[[4-[(1<i>E</i>)-2-Cyanoethenyl]-2,6-dimethylphenyl]amino]-2- pyrimidinyl]amino]benzonitrile (R278474, Rilpivirine)

Paul A. J. Janssen(Johnson & Johnson (United States)), Paul Lewi(Johnson & Johnson (United States)), Eddy Arnold(Johnson & Johnson (United States)), Frits Daeyaert(Johnson & Johnson (United States)), Marc R. de Jonge(Johnson & Johnson (United States)), Jan Heeres(Johnson & Johnson (United States)), Luc Koymans(Johnson & Johnson (United States)), Maarten Vinkers(Johnson & Johnson (United States)), Jérôme Guillemont(Johnson & Johnson (United States)), Élisabeth Pasquier(Johnson & Johnson (United States)), Mike Kukla(Johnson & Johnson (United States)), D.W. Ludovici(Johnson & Johnson (United States)), Koen Andries(Johnson & Johnson (United States)), Marie‐Pierre de Béthune(Johnson & Johnson (United States)), Rudi Pauwels(Johnson & Johnson (United States)), Kalyan Das(Johnson & Johnson (United States)), Art D. Clark(Johnson & Johnson (United States)), Yulia Volovik Frenkel(Johnson & Johnson (United States)), Stephen H. Hughes(Johnson & Johnson (United States)), Bart Medaer(Johnson & Johnson (United States)), Fons De Knaep(Johnson & Johnson (United States)), Hilde Bohets(Johnson & Johnson (United States)), Fred De Clerck(Johnson & Johnson (United States)), Ann Lampo(Johnson & Johnson (United States)), Peter Williams(Johnson & Johnson (United States)), Paul Stoffels(Johnson & Johnson (United States))
Journal of Medicinal Chemistry
November 6, 2004
Cited by 342

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.


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