Cytotoxic phenyl polyketides from Hypericum curvisepalum N. Robson

Nat Prod Res. 2023 Nov-Dec;37(22):3815-3820. doi: 10.1080/14786419.2022.2155820. Epub 2022 Dec 12.

Abstract

(±)-Hypecurvone A (1) and B (2), two new undescribed phenyl polyketides, along with seven known analogues (3-9) were isolated from the whole plant of Hypericum curvisepalum. Chiral separation of 1 and 2 yielded two pairs of enantiomers 1a/1b and 2a/2b, respectively. The structures of these compounds were elucidated by extensive spectroscopic analyses and ECD spectra simulations. All isolates exhibited moderate cytotoxicity against human hepatocellular carcinoma SMMC-7721 cells, and compound 3 also showed weak cytotoxicity toward MGC-803 cells. The cytotoxicity of these compounds was found to be related to enhanced mitochondria-mediated apoptosis and inhibition of the G2/M phase of the cell cycle.

Keywords: Hypericum curvisepalum; Phenyl polyketides; cytotoxicity.