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BMS 232632

Known as: 232632, BMS, BMS-232632, BMS232632 
National Institutes of Health

Papers overview

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Review
2008
Review
2008
Recommendations for a highly active antiretroviral therapy (HAART) in either pretreated patients or symptomatic patients with an… Expand
2003
2003
A selective, accurate, and reproducible LC-MS-MS assay was developed for the determination of the HIV protease inhibitor… Expand
2003
2003
A selective, accurate, and reproducible LC/MS/MS assay was developed and validated for the determination of the HIV protease… Expand
Review
2002
Review
2002
  • P. Piliero
  • Expert opinion on investigational drugs
  • 2002
  • Corpus ID: 20374074
The introduction of HIV-1 protease inhibitors in 1995 ushered in the era of highly active antiretroviral therapy. For the first… Expand
Highly Cited
2002
Highly Cited
2002
ABSTRACT The in vitro inhibition of wild-type human immunodeficiency virus (HIV) by combinations of lopinavir and six other… Expand
2001
2001
BMS-232632 is a potent human immunodeficiency type 1 (HIV-1) protease inhibitor with a half-life that allows for once-daily… Expand
  • figure 1
  • figure 2
2001
2001
  • G. Witherell
  • Current opinion in investigational drugs
  • 2001
  • Corpus ID: 21294499
BMS-232632, an azapeptide HIV protease inhibitor, is in development by Bristol-Myers Squibb (BMS), under license from Novartis… Expand
Highly Cited
2000
Highly Cited
2000
ABSTRACT BMS-232632 is an azapeptide human immunodeficiency virus type 1 (HIV-1) protease (Prt) inhibitor that exhibits potent… Expand
Highly Cited
2000
Highly Cited
2000
  • Yi-Fei Gong, B. Robinson, +5 authors Pin-fang Lin
  • Antimicrobial Agents and Chemotherapy
  • 2000
  • Corpus ID: 39162240
ABSTRACT BMS-232632 is an azapeptide human immunodeficiency virus (HIV) type 1 (HIV-1) protease inhibitor that displays potent… Expand