黄芩
细胞毒性T细胞
二萜
传统医学
萜烯
立体化学
医学
化学
生物化学
中医药
替代医学
病理
体外
作者
Trần Thị Hồng Hạnh,Do Hoang Anh,Trần Hồng Quang,Nguyen Quang Trung,Đỗ Thị Thảo,Nguyen The Cuong,Nguyen Thai An,Nguyễn Xuân Cường,Nguyễn Hoài Nam,Phan Văn Kiệm,Châu Văn Minh
标识
DOI:10.1016/j.phytol.2018.11.008
摘要
Abstract Phytochemical investigation of the whole plant of Scutellaria barbata resulted in the isolation of three new neo-clerodane diterpenoids, named scutebarbatolides A-C (1–3), along with six known analogues as 14-deoxy-11,12-didehydroandrographolide (4), scutehenanine H (5), 14β-hydroxyscutolide K (6), scutebata O (7), scutebartines H (8) and I (9). Their structures were elucidated by spectroscopic analyses, including 1D and 2D NMR and mass spectra in comparison with the data reported in the literature. Cytotoxicity of the isolates was evaluated toward five human cancer cell lines, including LNCaP, HepG2, KB, MCF7, and SK-Mel2 cells. Of the isolates, compounds 1 and 6 were shown to have moderate cytotoxicity toward all the cancer cell lines, with IC50 values ranging from 30.8 to 51.1 μM. Our results contribute to more insightful clarification of the use of S. barbata in the prevention and treatment of cancer.
科研通智能强力驱动
Strongly Powered by AbleSci AI