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The Thai Journal of Pharmaceutical Sciences

Abstract

A new class of non-peptide analogues in chromone series, were synthesized as potential HIV-1 protease inhibitors. The general structure of compounds consists of chromone nucleus with different substituents at position 2, 3, 7, and 8. The in vitro inhibit...

Publisher

Faculty of Pharmaceutical Sciences, Chulalongkorn University

First Page

155

Last Page

164

Included in

Pharmacology Commons

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