TRADITIONAL MEDICINAL-PLANTS OF THAILAND .23. CYTOTOXIC AND ANTIMALARIAL ALKALOIDS FROM THE TUBERS OF STEPHANIA-PIERREI

被引:95
作者
LIKHITWITAYWUID, K
ANGERHOFER, CK
CHAI, HY
PEZZUTO, JM
CORDELL, GA
RUANGRUNGSI, N
机构
[1] UNIV ILLINOIS,COLL PHARM,DEPT MED CHEM & PHARMACOGNOSY,PROGRAM COLLABORAT RES PHARMACEUT SCI,CHICAGO,IL 60612
[2] CHULALONGKORN UNIV,FAC PHARMACEUT SCI,DEPT PHARMACOGNOSY,BANGKOK 5,THAILAND
来源
JOURNAL OF NATURAL PRODUCTS | 1993年 / 56卷 / 09期
关键词
D O I
10.1021/np50099a005
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Biological evaluation of extracts prepared from the tubers of Stephania pierrei revealed cytotoxic and antimalarial activity. During the course of separation, two new aporphine alkaloids, (-)-asimilobine-2-O-beta-D-glucoside [2] and (-)-nordicentrine [8], in addition to twenty-one known isoquinoline alkaloids, were isolated. Each isolate was mainly for cytotoxic and antimalarial activities. It was found that the cytotoxicity of S. pierrei was mainly due to the presence of the aporphine alkaloids containing the 1,2-methylenedioxy group 3-10, whereas the antimalarial activity was attributed to the nonquaternary aporphine alkaloids 1, 3-10 and the tetrahydroprotoberberines possessing a phenolic functionality, 13-15, 18. None of the isolates showed a degree of selectivity comparable to that of antimalarial drugs such as chloroquine, quinine, mefloquine, and artemisinin. Comparison of the alkaloid content of S. pierrei and Stephania erecta strongly suggested separate identities for the two plants.
引用
收藏
页码:1468 / 1478
页数:11
相关论文
共 55 条
[1]   DELTA-POLARIZATION TRANSFER VIA LONG-RANGE COUPLING AS A SIMPLE ONE-DIMENSIONAL NMR TECHNIQUE FOR H-1-C-13 CORRELATION - APPLICATION TO THE DEFINITIVE ASSIGNMENT OF THE SYN AND ANTI C-13 DELTA-RESONANCES OF 2-SUBSTITUTED ADAMANTANES [J].
ABDELSAYED, AN ;
BAUER, L .
TETRAHEDRON LETTERS, 1986, 27 (09) :1003-1006
[2]   NUCLEAR MAGNETIC RESONANCE STUDY OF APORPHINE ALKALOIDS [J].
BAARSCHERS, WH ;
ARNDT, RR ;
DOUGLAS, B ;
PACHLER, K ;
WEISBACH, JA .
JOURNAL OF THE CHEMICAL SOCIETY, 1964, (DEC) :4778-&
[3]   STRUCTURAL CORRELATIONS IN NUCLEAR MAGNETIC RESONANCE SPECTRA OF BISBENZYLISOQUINOLINE AND APORPHINE ALKALOIDS [J].
BICK, IR ;
HARLEYMASON, J ;
SHEPPARD, N ;
VERNENGO, MJ .
JOURNAL OF THE CHEMICAL SOCIETY, 1961, (MAY) :1896-&
[4]   OPIUM ALKALOIDS .2. ISOLATION AND CHARACTERIZATION OF CODAMINE [J].
BROCHMAN.E ;
NIELSEN, B ;
UTZINGER, GE .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1965, 54 (10) :1531-&
[5]  
BROCHMAN.E, 1965, TETRAHEDRON LETT, P1271
[6]  
BROCHMANNHANSSE.E, 1964, PLANTA MED, V12, P328
[7]  
CALDERWOOD JM, 1987, PHYTOCHEMISTRY, V26, P547
[8]  
CASAGRANDE C, 1970, FARMACO-ED SCI, V25, P442
[9]  
CASSELS B. K., 1966, TETRAHEDRON, P485
[10]   STUDIES ON ALKALOIDS OF FORMOSAN LAURACEOUS PLANTS .19. ALKALOIDS OF LINDERA-OLDHAMII-HEMSL .2. [J].
CHEN, IS .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 1977, 24 (01) :41-44