Article ID: c16-00743
A phytochemical fractionation of a methanol extract of Ophiopogon japonicus tubers led to the isolation of a new homoisoflavanone, homoisopogon A (1), and three new homoisoflavanes, homoisopogon B–D (2–4). Their chemical structures were elucidated by mass, NMR, and CD spectroscopic methods. Homoisopogon A (1) exhibited potent cytotoxicity against LU-1, KB, and SK-Mel-2 cancer cells with IC50 values ranging from 0.51 to 0.66 μM.