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

被引:515
作者
Kaldor, SW
Kalish, VJ
Davies, JF
Shetty, BV
Fritz, JE
Appelt, K
Burgess, JA
Campanale, KM
Chirgadze, NY
Clawson, DK
Dressman, BA
Hatch, SD
Khalil, DA
Kosa, MB
Lubbehusen, PP
Muesing, MA
Patick, AK
Reich, SH
Su, KS
Tatlock, JH
机构
[1] AGOURON PHARMACEUT INC,SAN DIEGO,CA 92121
[2] ELI LILLY & CO,LILLY RES LABS,INDIANAPOLIS,IN 46285
关键词
D O I
10.1021/jm9704098
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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, 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.
引用
收藏
页码:3979 / 3985
页数:7
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