Viracept (Nelfinavir Mesylate, AG1343):  A Potent, Orally Bioavailable Inhibitor of HIV-1 Protease

Stephen W. Kaldor(General Atomics (United States)), Vincent J. Kalish(Eli Lilly (United States)), Jay F. Davies(General Atomics (United States)), Bhasker V. Shetty(General Atomics (United States)), James E. Fritz(Eli Lilly (United States)), Krzysztof Appelt(Eli Lilly (United States)), Jeffrey A. Burgess(Eli Lilly (United States)), Kristina Campanale(General Atomics (United States)), Nickolay Y. Chirgadze(General Atomics (United States)), David K. Clawson(Eli Lilly (United States)), Bruce A. Dressman(Eli Lilly (United States)), Steven D. Hatch(Eli Lilly (United States)), Deborah A. Khalil(General Atomics (United States)), Maha Kosa(General Atomics (United States)), Penny P. Lubbehusen(General Atomics (United States)), Mark A. Muesing(Eli Lilly (United States)), Amy K. Patick(General Atomics (United States)), Siegfried Reich(General Atomics (United States)), Kenneth S.E. Su(General Atomics (United States)), John H. Tatlock(Eli Lilly (United States))
Journal of Medicinal Chemistry
November 1, 1997
Cited by 619Open Access
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Abstract

Using a combination of iterative structure-based design and an analysis of oral pharmacokinetics and antiviral activity, AG1343 (Viracept, nelfinavir mesylate), a nonpeptidic inhibitor of HIV-1 protease, was identified. AG1343 is a potent enzyme inhibitor (Ki = 2 nM) and antiviral agent (HIV-1 ED50 = 14 nM). An X-ray cocrystal structure of the enzyme-AG1343 complex reveals how the novel thiophenyl ether and phenol-amide substituents of the inhibitor interact with the S1 and S2 subsites of HIV-1 protease, respectively. In vivo studies indicate that AG1343 is well absorbed orally in a variety of species and possesses favorable pharmacokinetic properties in humans. AG1343 (Viracept) has recently been approved for marketing for the treatment of AIDS.


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