A new denudatine type C20-diterpenoid alkaloid from Aconitum sinchiangense W. T. Wang

被引:15
作者
Samanbay, Ahmatbeck [1 ,2 ]
Zhao, Bo [2 ,3 ]
Aisa, Haji Akber [2 ,3 ]
机构
[1] Xinjiang Med Univ, Coll Pharm, Urumqi, Peoples R China
[2] Chinese Acad Sci, Xinjiang Tech Inst Phys & Chem, Key Lab Plants Resources & Chem Arid Zone, Urumqi, Peoples R China
[3] Chinese Acad Sci, Xinjiang Tech Inst Phys & Chem, State Key Lab Basis Xinjiang Indigenous Med Plant, Urumqi, Peoples R China
基金
中国科学院西部之光基金;
关键词
Aconitum sinchiangense W; T; Wang; diterpenoid alkaloids; sinchianine; denudatine-type; DITERPENOID ALKALOIDS; ROOTS;
D O I
10.1080/14786419.2017.1410814
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A new denudatine-type C-20-diterpenoid alkaloid, designated as sinchianine (1), together with eight known diterpenoid alkaloids, 12-acetyl-12-epi-napelline (2), 12-epi-napelline (3), neoline (4), talatisamine (5), 14-O-acetylsenbusine A (6) and benzoylaconine (7), songorine (8) and aconitine (9), were isolated from the whole herb of Aconitum sinchiangense W. T. Wang. Their structures were elucidated on the basis of extensive spectroscopic analyses (NMR and HR-ESI-MS) and comparison with data reported in the literature. [GRAPHICS] .
引用
收藏
页码:2319 / 2324
页数:6
相关论文
共 24 条
[1]   ALKALOIDS OF ACONITUM-COLUMBIANUM NUTT [J].
BOIDO, V ;
EDWARDS, OE ;
HANDA, KL ;
KOLT, RJ ;
PURUSHOTHAMAN, KK .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1984, 62 (04) :778-784
[2]   A new C20-diterpenoid alkaloid from Aconitum soongaricum var. pubescens [J].
Chen, Lin ;
Shan, Lianhai ;
Xu, Wenliang ;
Zhang, Jifa ;
Huang, Shuai ;
Zhou, Xianli .
NATURAL PRODUCT RESEARCH, 2017, 31 (05) :523-528
[3]  
CHEN ZG, 1987, HETEROCYCLES, V26, P1455
[4]  
Fuente G, 1989, S STR HETEROCYCLES, V29, P1577, DOI [10.3987/COM-89-5006, DOI 10.3987/COM-89-5006]
[5]   New alkaloids from Aconitum taipaicum and their cytotoxic activities [J].
Guo, Zeng-Jun ;
Xu, Ying ;
Zhang, Hui ;
Li, Meng-Yi ;
Xi, Ke .
NATURAL PRODUCT RESEARCH, 2014, 28 (03) :164-168
[6]   ISOLATION AND IDENTIFICATION OF 4 NORDITERPENOID ALKALOIDS FROM PROCESSED AND UNPROCESSED ROOT TUBERS OF ACONITUM-FEROX [J].
HANUMAN, JB ;
KATZ, A .
JOURNAL OF NATURAL PRODUCTS, 1993, 56 (06) :801-809
[7]  
HANUMAN JB, 1994, PHYTOCHEMISTRY, V36, P1527, DOI 10.1016/S0031-9422(00)89756-3
[8]   PHARMACEUTICAL STUDIES ON ACONITUM ROOTS .13. STRUCTURE OFHOKBUSINE-A AND HOKBUSINE-B DITERPENIC ALKALOIDS OF ACONITUM-CARMICHAELI ROOTS FROM JAPAN [J].
HIKINO, H ;
KUROIWA, Y ;
KONNO, C .
JOURNAL OF NATURAL PRODUCTS, 1983, 46 (02) :178-182
[9]   C-13 NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY IN THE ELUCIDATION OF STRUCTURES OF DITERPENOID ALKALOIDS [J].
JOSHI, BS ;
WUNDERLICH, JK ;
PELLETIER, SW .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1987, 65 (01) :99-103
[10]   A 16,17-EPOXY C-20-DITERPENOID ALKALOID FROM ACONITUM-DELPHINIFOLIUM [J].
KULATHAIVEL, P ;
BENN, MH .
PHYTOCHEMISTRY, 1988, 27 (12) :3998-3999