Synthesis and HIV-1 integrase inhibitory activities of caffeic acid dimers derived from Salvia officinalis

The synthesis of two caffeoyl-coumarin conjugates, derived from sagecoumarin, has been accomplished, starting from ferulic acid, isoferulic acid and sesamol. Both compounds exhibited potent inhibitory activities at micromolar concentrations against HIV-1 integrase in 3′-end processing reaction but were less effective against HIV-1 replication in a single-round infection assay of HeLa-β-gal-CD4+ cells.

Two caffeoyl-coumarin conjugates derived from sagecoumarin were synthesized and exhibited potent micromolar inhibitory potencies against HIV-1 integrase in 3′-end processing reaction but were less effective against HIV-1 replication.Figure optionsDownload as PowerPoint slide