New HIV-1 replication inhibitors of the styryquinoline class bearing aroyl/acyl groups at the C-7 position: Synthesis and biological activity-Reference-Cited by-同舟云学术

New HIV-1 replication inhibitors of the styryquinoline class bearing aroyl/acyl groups at the C-7 position: Synthesis and biological activity

Published:2005-09 Issue:18 Volume:15 Page:4019-4022
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Normand-Bayle Marie,Bénard Christophe,Zouhiri Fatima,Mouscadet Jean-François,Leh Hervé,Thomas Claire-Marie,Mbemba Gladys,Desmaële Didier,d’Angelo Jean

Publisher

Elsevier BV

Subject

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

Reference19 articles.

1. New anti-HIV agents and targets

2. HIV-1 integrase inhibitors that compete with the target DNA substrate define a unique strand transfer conformation for integrase

3. A naphthyridine carboxamide provides evidence for discordant resistance between mechanistically identical inhibitors of HIV-1 integrase

4. 2,6-Bis(3,4,5-trihydroxybenzylydene) derivatives of cyclohexanone

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