Unité Associée au CNRS, UMR 8076, Faculté de Pharmacie, 5, rue J.-B. Clément, 92290 Chatenay-Malabry, France.
Abstract:
Novel variants of HIV-1 replication inhibitors of the styrylquinoline class harboring aroyl/acyl group at the C-7 position have been synthesized. In sharp contrast with styrylquinolines bearing a carboxylic acid group at C-7, these compounds proved to be inactive toward HIV-1 integrase in in vitro assays.