Syntheses and cytotoxicity evaluation of bis(indolyl)thiazole, bis(indolyl)pyrazinone and bis(indolyl)pyrazine: analogues of cytotoxic marine bis(indole) alkaloid

Abstract

2,4-Bis(3′-indolyl)thiazoles, 3,5-bis(3′-indolyl)-2(1H)pyrazinone and 3,6-bis(3′-indolyl)pyrazine were synthesized and evaluated for cytotoxic activity against diverse human cancer cell lines by the National Cancer Institute. These compounds demonstrated significant inhibitory effects in the growth of a range of cancer cell lines. 2,4-Bis(3′-indolyl)thiazole displayed selective cytotoxicity against certain leukemia cell lines with GI50 values in the low micromolar range while the substituted derivatives showed a broad spectrum of cytotoxic activity. 3,5-Bis(3′-indolyl)-2(1H)pyrazinone and 3,6-bis[3′-(N-methyl-indolyl)]pyrazine possessed strong inhibitory activity against a wide range of human tumor cell lines. The mechanism of action remained unknown. The results suggested that 2,4-bis(3′-indolyl)thiazoles, 3,5-bis(3′-indolyl)-2(1H)pyrazinone and 3,6-bis[3′-(N-methyl-indolyl)] pyrazine offer potential as lead compounds for the discovery of anticancer agents.