A new triterpene from Luculia pinciana Hook.

被引:7
作者
Kang, WY
Du, ZZ
Yang, XS
Hao, XJ [1 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources W China, Kunming 650204, Peoples R China
[2] Key Lab Chem Nat Prod Guizhou Prov, Guiyang 550002, Peoples R China
[3] Chinese Acad Sci, Guiyang 550002, Peoples R China
关键词
Luculia pinciana Hook; triterpene; leukaemia cell line;
D O I
10.1080/10286020310001608967
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A new triterpene named luculiaoic acid A (1), showing inhibitory activity of a leukaemia cell line, along with eleven known compounds, has been isolated from the ethyl acetate extract of the stems of Luculia pinciana Hook. All the structures were elucidated on the basis of NMR, MS, and IR methods. The activity to inhibit Staphylococcus aureus and Candida albicans of all compounds showed that ursolic acid inhibits the growth of Staphylococcus aureus with an MIC of 0.5 mg ml(-1) and an MBC of 10 mg ml(-1), and scopletin inhibits Candida albicans with an MIC of 1 mg ml(-1) and an MBC of 5 mg ml(-1).
引用
收藏
页码:91 / 94
页数:4
相关论文
共 16 条
[1]  
*AC SIN ED I BOT K, 1984, IND FLOR YUNN, P1247
[2]   6-PRENYLOXY-7-METHOXYCOUMARIN, A COUMARIN-HEMITERPENE ETHER FROM CARDUUS-TENUIFLORUS [J].
CARDONA, L ;
GARCIA, B ;
PEDRO, JR ;
PEREZ, J .
PHYTOCHEMISTRY, 1992, 31 (11) :3989-3991
[3]  
CONG PZ, 2000, HDB ANAL CHEM, V9, P920
[4]  
GHULAM AM, 1987, PHYTOCHEMISTRY, V26, P225
[5]  
Jin Y. R., 1998, CHIN PHARM J, V33, P402
[6]  
Kang Wenyi, 2002, Zhong Yao Cai, V25, P875
[7]  
Kang WenYi, 2002, Natural Product Research and Development, V14, P40
[8]  
Kang WenYi, 2002, Natural Product Research and Development, V14, P39
[9]  
KAYOKO K, 1993, PHYTOCHEMISTRY, V33, P1475
[10]  
LI CN, 1997, PHYTOCHEMISTRY, V44, P1359