Viracept (nelfinavir mesylate, AG1343): a potent, orally bioavailable inhibitor of HIV-1 protease

SW Kaldor, VJ Kalish, JF Davies… - Journal of medicinal …, 1997 - ACS Publications
SW Kaldor, VJ Kalish, JF Davies, BV Shetty, JE Fritz, K Appelt, JA Burgess, KM Campanale…
Journal of medicinal chemistry, 1997ACS Publications
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
(K i= 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 …
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.
ACS Publications