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Indinavir analogues with blocked metabolism sites as HIV protease inhibitors with improved pharmacological profiles and high potency against PI-Resistant viral strains

Authors :
Cheng, Yuan
Zhang, Fengqi
Rano, Thomas A.
Lu, Zhijian
Schleif, William A.
Gabryelski, Lori
Olsen, David B.
Stahlhut, Mark
Rutkowski, Carrie A.
Lin, Jiunn H.
Jin, Lixia
Emini, Emilio A.
Chapman, Kevin T.
Tata, James R.
Source :
Bioorganic & Medicinal Chemistry Letters. Sep2002, Vol. 12 Issue 17, p2419. 4p.
Publication Year :
2002

Abstract

Indinavir analogues with blocked metabolism sites show highly improved pharmacokinetic profiles in animals. The cis-aminochromanol substituted analogues exhibited excellent potency against both the wild-type (NL4-3) virus and protease inhibitor-resistant HIV strains. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
0960894X
Volume :
12
Issue :
17
Database :
Academic Search Index
Journal :
Bioorganic & Medicinal Chemistry Letters
Publication Type :
Academic Journal
Accession number :
7854458
Full Text :
https://doi.org/10.1016/S0960-894X(02)00424-9