Design, synthesis and QSAR studies on N-aryl heteroarylisopropanolamines, a new class of non-peptidic HIV-1 protease inhibitors-Reference-Cited by-同舟云学术

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Design, synthesis and QSAR studies on N-aryl heteroarylisopropanolamines, a new class of non-peptidic HIV-1 protease inhibitors

Published:2002-08 Issue:8 Volume:10 Page:2511-2526
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Di Santo Roberto,Costi Roberta,Artico Marino,Massa Silvio,Ragno Rino,Marshall Garland R.,La Colla Paolo

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference29 articles.

1. 5 Inhibitors of HIV Proteinase

2. Crystal structures of HIV-1 protease-inhibitor complexes

3. Rational Design of Peptide-Based HIV Proteinase Inhibitors

4. ABT-538 is a potent inhibitor of human immunodeficiency virus protease and has high oral bioavailability in humans.

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