Jing Yang, Xi-Yu Pan, Wen-Yao Su, Shu-Miao Gu, Ge-Ping Xu, Liang-Fei Wu, Qing Gao, Meng-Lian Wang, Yan-Hui Fu, Yan-Ping Liu
The stems (including barks and woods) and leaves of Ficus altissima Blume were chemically studied. This work caused the discovery of a new isoflavone, ficusaltissine A (1), alongside seven recognised analogues (2-8). Ficusaltissine A (1) was fully characterised by spectral methods and the recognised isolates (2-8) were assigned by reference to published spectral data. The in vitro antiproliferative effects of compounds 1-8 were assessed against a panel of five human cancer cell lines. The tested isoflavones showed strong growth‑suppressive properties. A range of 0.22 ± 0.03 to 16.58 ± 0.16 μM was obtained for the IC50 values of compounds 1-8. Notably, ficusaltissine A (1) exhibited superior potency against HL-60 cells (IC50 = 0.22 ± 0.03 μM), surpassing the reference drug doxorubicin (IC50 = 0.32 ± 0.05 μM). These findings indicated that these these isoflavones derived from F. altissima were an exciting source for the development of new anticancer drug scaffolds.