部分
圆二色性
二维核磁共振波谱
化学
吡啶
消炎药
立体化学
生物
有机化学
药理学
作者
Na Zhang,Yang Xu,Xinyi Yue,Liangliang Xiong,Hua Li,Lixia Chen
出处
期刊:Phytochemistry
[Elsevier BV]
日期:2024-02-07
卷期号:220: 114013-114013
被引量:1
标识
DOI:10.1016/j.phytochem.2024.114013
摘要
Six undescribed alkaloids, neotuberostemonol C (1), dehydrostenines C-D (2–3), tuberostemonines Q-R (10–11), and (6R,8R,8aR)-8-hydroxy-6-methyl-hexahydroindolizin-5-one (32), along with twenty-six known analogues were isolated from the dried roots of Stemona tuberosa Lour. The structures and absolute stereochemistry of these compounds were delineated by extensive spectroscopy (1D NMR, 2D NMR, HRESIMS), quantum chemical calculations of the electronic circular dichroism spectra, and pyridine-induced solvent shifts. Tuberostemonines Q-R (10–11) represent tuberostemonine skeleton alkaloids possessing an α-methyl-γ-butyrolactone moiety attached to C-3. In addition, all these isolated compounds were assayed for their inhibitory activity against LPS-induced NO production in RAW264.7 cells using Griess assay.
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