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Bioorg Med Chem 2010 Mar 15;18(6):2135-40

SAR and molecular mechanism study of novel acylhydrazone compounds targeting HIV-1 CA.

Jin Y, Tan Z, He M, Tian B, Tang S, Hewlett I, Yang M

Abstract

We synthesized a series of acylhydrazone compounds bearing naturally occurring amino acids' side chains as HIV assembly inhibitors. Biological evaluation indicated that the compounds had anti-SIV and capsid assembly inhibitory activities. The structure-activity relationship (SAR) study showed that compounds bearing proper aromatic side chains had potential antiviral activities. The molecular modeling experiments revealed the molecular mechanism that they could bind to CA in the same manner as CAP-1 and occupy two more grooves.


Category: Journal Article
PubMed ID: #20188575
Includes FDA Authors from Scientific Area(s): Biologics
Entry Created: 2011-10-04 Entry Last Modified: 2012-08-29
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