Structure, absolute configuration and cytotoxicity of compounds isolated from Decaschistia harmandii

In this work, we report the isolation and structure characterization of four compounds from ethyl acetate extract of the aerial part of D. harmandii for the first time. Especially, the absolute configuration of dimer stilbene ampelopsin F was successfully established upon circular dichroism (ECD) data. Besides, the cytotoxic properties of these compounds was also investigated on the cancer cell lines.