Two New N-Oxide Alkaloids from Stemona cochinchinensis

被引:8
|
作者
Lin, Ligen [1 ,2 ]
Bao, Han [1 ]
Wang, Anqi [1 ]
Tang, Chunping [2 ]
Pham-Huu Dien [3 ]
Ye, Yang [2 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau 999078, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[3] Hanoi Natl Univ Educ, Fac Chem, Dept Organ Chem, Hanoi 100000, Vietnam
关键词
Stemona cochinchinensis; Stemonaceae; N-oxide alkaloids; H-1- and C-13-NMR; anti-tussive activity; ROOTS; STEMOCURTISINE; CURTISII;
D O I
10.3390/molecules191220257
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two new N-oxide alkaloids with pyrrolo[1,2-alpha]azepine skeleton, namely isoneostemocochinine-N-oxide (1) and neostemocochinine-N-oxide (2), as well as three known alkaloids with pyrido[1,2-alpha]azepine skeletons, were isolated and identified from the roots of Stemona cochinchinensis (Stemonaceae). The structures of these compounds were elucidated by 1D- and 2D-NMR spectra and other spectroscopic studies. Additionally, the H-1- and C-13-NMR characteristic of N-oxide Stemona alkaloids was summarized. Stemokerrin showed potent anti-tussive activity on citric acid-induced guinea pig model.
引用
收藏
页码:20257 / 20265
页数:9
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