Abstract
A new ketosteroid, 6β,16β-dihydroxycholest-4-en-3-one (1), in addition to the known 6β-hydroxycholest-4-en-3-one (2), 6β-hydroxycholest-4,22-dien-3-one (3) and 16β-hydroxy-5α-cholestan-3,6-dione (4), was isolated from the red alga Jania adhaerens. The structures were assigned on the basis of 1H- and 13C-NMR experiments. The new compound (1) was evaluated for its genotoxic and cytotoxic activities and found to possess protective antigenotoxicity in human peripheral blood cells.
Acknowledgements
The authors are thankful to Mr Zaki El-Assouli for the bioassay analysis. Deanship of Scientific Research (DSR), King Abdulaziz University, is also acknowledged for providing financial support (grant no. 8-003/429). The two anonymous reviewers provided helpful comments on the manuscript.