HIV-1 protease and HIV-1 integrase inhibitory substances from Eclipta prostrata

The bioassay-guided fractionation for anti-HIV-1 integrase activity led to the isolation of six compounds from the whole plant extract of Eclipta prostrata extract. They were identified as 5-hydroxymethyl-(2,2':5',2'')terthienyl tiglate (1), 5-hydroxymethyl-(2,2':5',2'')-terthienyl agelate (2), 5-hydroxymethyl-(2,2':5',2'')-terthienyl acetate (3), ecliptal (4), orobol (5) and wedelolactone (6). Of these, compound 6 showed the highest activity against HIV-1 integrase (IN) with an IC50 value of 4.0 +/- 0.2 mu M, followed by compound 5(IC50 = 8.1 0.5 mu M), whereas the four terthiophene compounds (1-4) were inactive (IC50 > 100 mu M). Regarding HIV-1 protease (PR) inhibitory activity, compound 1 exhibited appreciable activity against HIV-1 PR with an IC, of 58.3 +/- 0.8 gm, followed by compound 4(IC50 = 83.3 +/- 1.6 mu M) and compound 3 (IC50 = 93.7 +/- 0.8 mu M), while compounds 2, 5 and 6 were inactive against HIV-1 PR (IC50 > 100 mu M). This is the first report of anti-HIV-1 IN activities for wedelolactone (6), a coumarin derivative, and orobol (5), an isoflavone derivative. This study supports the use of E. prostrata in AIDS patients, which is in accord with its traditional use by Thai traditional doctors for curing blood related diseases. Copyright (c) 2007 John Wiley & Sons, Ltd.