STRUCTURE AND RELATIVE STEREOCHEMISTRY OF A NEW POLYCYCLIC ALKALOID, ASPARAGAMINE-A, SHOWING ANTI-OXYTOCIN ACTIVITY, ISOLATED FROM ASPARAGUS-RACEMOSUS

被引:49
作者
SEKINE, T
IKEGAMI, F
FUKASAWA, N
KASHIWAGI, Y
AIZAWA, T
FUJII, Y
RUANGRUNGSI, N
MURAKOSHI, I
机构
[1] CHIBA UNIV,FAC PHARMACEUT SCI,INAGE KU,CHIBA 263,JAPAN
[2] TSUMURA & CO,CHIYODA KU,TOKYO 102,JAPAN
[3] CHULALONGKORN UNIV,FAC PHARMACEUT SCI,BANGKOK 10330,THAILAND
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1995年 / 04期
关键词
D O I
10.1039/p19950000391
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The relative stereochemistry of a new cage-type alkaloid, asparagamine A 1. isolated from the roots of Asparagus racemosus Willd. (Liliaceae). has been elucidated by spectroscopic, chemical and single-crystal X-ray analyses. This novel polycyclic pyrrolizidine derivative is both the first alkaloid to be isolated from this genus and also the first pyrrolizidine derivative with carbon substituents at C-5 and C-8. The compound showed anti-oxytocin activity in vitro in a dose of 10(-5)-10(-6) mg cm(-3).
引用
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页码:391 / 393
页数:3
相关论文
共 23 条
[1]  
BEURKENS PT, 1992, DIRDIF PROGRAM SYSTE
[2]  
Burkill IH., 1966, DICT EC PRODUCTS MAL, P264
[3]  
CHEEKE PR, 1988, J ANIM SCI, V66, P2343
[5]  
IKEGAMI F, 1989, CHEM PHARM BULL, V37, P1932
[6]   ENTADAMIDE-C, A SULFUR-CONTAINING AMIDE FROM ENTADA-PHASEOLOIDES [J].
IKEGAMI, F ;
SEKINE, T ;
DUANGTERAPRECHA, S ;
MATSUSHITA, N ;
MATSUDA, N ;
RUANGRUNGSI, N ;
MURAKOSHI, I .
PHYTOCHEMISTRY, 1989, 28 (03) :881-882
[7]  
IKEGAMI F, 1990, J SCI SOC THAILAND, V16, P25
[8]  
LANDGE AB, 1981, INDIAN J CHEM, V8, P588
[9]   POLYFRUCTOSANS OF ASPARAGUS-RACEMOSUS [J].
MADAN, VK .
ZEITSCHRIFT FUR PFLANZENPHYSIOLOGIE, 1972, 68 (03) :272-280
[10]  
MURAKOSHI I, 1993, CHEM PHARM BULL, V41, P388, DOI 10.1248/cpb.41.388