Suppr超能文献

基于细胞毒性导向从W. T. Wang中分离出落新妇苷I - VI及其细胞毒性活性

Cytotoxicity-guided isolation of elatostemanosides I-VI from W. T. Wang and their cytotoxic activities.

作者信息

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

机构信息

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.

出版信息

RSC Adv. 2025 Apr 4;15(14):10639-10652. doi: 10.1039/d4ra09007a.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd23/11970508/76ec35f3cb06/d4ra09007a-f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验