Feng Wan-Bi, Liu Ming-Shang, Zheng Tong-Xin, Lin Zi-Xin, Xu Hai-Wei, Cai Hai-Tao, Zhang Yu-Bo, Bai Jia-Lue, Yang Mao-Xun, Luo Hui, Li Xiao-San
Guangdong Engineering Technology Research Center for the Development and Utilization of Mangrove Wetland Medicinal Resources, Zhangjiang Key Laboratory of R&D Marine Microbial Resources in the Beibu Gulf Rim, and the School of Ocean and Tropical Medicine, Guangdong Medical University, Zhanjiang, Guangdong, 524023, China.
Zhanjiang Central Hospital, Guangdong Medical University, Zhanjiang, Guangdong, 524023, China.
Fitoterapia. 2025 Oct;186:106840. doi: 10.1016/j.fitote.2025.106840. Epub 2025 Aug 19.
Phytochemical investigation of the 95 % ethanol extract of the tubers of Hemsleya chinensis led to the isolation of five previously undescribed cucurbitane-type triterpenoids (1-5, named hemslyencins G-K), along with five known analogues (6-10). The structures of these compounds were elucidated through comprehensive spectroscopic analysis (UV, IR, HR-ESI-MS, 1D and 2D NMR data). Compounds 1, 2, 7, 9, and 10 are characterized as 24‑oxygenated cucurbitane-type triterpenoids, were rarely found in the genus Hemsleya. The cytotoxic activities of 1-10 were evaluated against MCF-7, HCT-116, HeLa, and HepG2 cancer cell lines, in which compounds 1 and 8-10 exhibited significant cytotoxic activities with the value of 0.382-13.77 μM. Further mechanism studies displayed that compound 1 dose-dependently induced apoptosis and caused G0/G1 phase cell cycle arrest in MCF-7 cells.