Huynh Quoc-Dung Tran, Phan Thuy-Tien Thi, Liu Ta-Wei, Duong Truc-Ly Thi, Hsu Su-Jung, Kuo Ching-Chuan, Chu Man-Hsiu, Wang Yun-Han, Nguyen Thanh-Vu, Shen Yao-An, Fan Yu-Jui, Nguyen Dang-Khoa, Vo Thanh-Hoa, Lee Ching-Kuo
Ph. D. Program in Clinical Drug Development of Herbal Medicine, College of Pharmacy, Taipei Medical University Taipei 11031 Taiwan
Institute of Pharmaceutical Education and Research, Binh Duong University Thu Dau Mot 820000 Binh Duong Vietnam.
RSC Adv. 2025 Apr 4;15(14):10639-10652. doi: 10.1039/d4ra09007a.
W. T. Wang, a medicinal plant traditionally utilized in herbal remedies, was explored for its cytotoxic properties. Bioassay-guided fractionation led to the discovery of six novel compounds, designated as elatostemanosides I-VI, with their structures elucidated through advanced spectroscopic methods and DP4+ analysis. Among these, compounds 2, 5, and 6 demonstrated moderate cytotoxicity against the human liver cancer cell line HepG2, exhibiting IC values of 18.2 ± 2.1, 32.1 ± 0.4, and 57.6 ± 1.3 µM, respectively. Notably, compound 6 also displayed significant activity against the human breast cancer cell line HCC1806, with an IC value of 35.4 ± 0.3 µM. Mechanistic studies revealed these compounds induced apoptosis by modulating the Bax/Bcl-2 ratio. Furthermore, structure-activity relationship (SAR) analysis underscored the importance of specific functional groups in mediating cytotoxic effects.
传统上用于草药疗法的药用植物W. T. Wang,对其细胞毒性特性进行了研究。生物测定导向的分级分离导致发现了六种新化合物,命名为落新妇苷I - VI,通过先进的光谱方法和DP4 +分析阐明了它们的结构。其中,化合物2、5和6对人肝癌细胞系HepG2表现出中等细胞毒性,IC值分别为18.2±2.1、32.1±0.4和57.6±1.3μM。值得注意的是,化合物6对人乳腺癌细胞系HCC1806也显示出显著活性,IC值为35.4±0.3μM。机制研究表明,这些化合物通过调节Bax/Bcl-2比率诱导细胞凋亡。此外,构效关系(SAR)分析强调了特定官能团在介导细胞毒性作用中的重要性。