Two new cytotoxic sesquiterpenoids from Eupatorium lindleyanum DC.

被引:22
作者
Huo, J [1 ]
Yang, SP [1 ]
Ding, J [1 ]
Yue, JM [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
关键词
eupalinilides K and L; Eupatorium lindleyanum; sesquiterpenoid;
D O I
10.1111/j.1744-7909.2006.00226.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Two new sesquiterpenoid lactones, namely eupalinilides K and L, were isolated from Eupatorium lindleyanum DC. Their structures were determined by spectral methods, including 1D- and 2D-NMR spectra. Cytotoxic evaluation showed that eupalinilide L exhibited potent cytotoxicity against P-388 and A-549 tumor cell lines with IC50 values of 0.17 and 2.60 mu mol/L, respectively.
引用
收藏
页码:473 / 477
页数:5
相关论文
共 7 条
[1]
Editorial Committee of the Administration Bureau of Traditional Chinese Medicine, 1998, CHIN MAT MED, P839
[2]
Cytotoxic sesquiterpene lactones from Eupatorium lindleyanum [J].
Huo, J ;
Yang, SP ;
Ding, J ;
Yue, JM .
JOURNAL OF NATURAL PRODUCTS, 2004, 67 (09) :1470-1475
[3]
4 NEW GERMACRANOLIDES FROM EUPATORIUM-LINDLEYANUM DC [J].
ITO, K ;
SAKAKIBARA, Y ;
HARUNA, M ;
LEE, KH .
CHEMISTRY LETTERS, 1979, (12) :1469-1472
[4]
EUDESMANOLIDES, TRICHOMATOLIDES B-E, AND A HELIANGOLIDE FROM CALEA-TRICHOMATA [J].
OBER, AG ;
QUIJANO, L ;
FISCHER, NH .
PHYTOCHEMISTRY, 1984, 23 (07) :1439-1443
[5]
CHEMISTRY OF HELIANTHUS .3. SESQUITERPENE LACTONES AND DITERPENE CARBOXYLIC-ACIDS IN HELIANTHUS-NIVEUS SUBSPECIES CANESCENS [J].
OHNO, N ;
MABRY, TJ .
PHYTOCHEMISTRY, 1980, 19 (04) :609-614
[6]
ANTITUMOR AGENTS .109. THE CYTOTOXIC PRINCIPLES OF PSEUDOLARIX-KAEMPFERI - PSEUDOLARIC ACID-A AND ACID-B AND RELATED DERIVATIVES [J].
PAN, DJ ;
LI, ZL ;
HU, CQ ;
CHEN, K ;
CHANG, JJ ;
LEE, KH .
PLANTA MEDICA, 1990, 56 (04) :383-385
[7]
Comparison of the sulforhodamine B assay and the clonogenic assay for in vitro chemoradiation studies [J].
Pauwels, B ;
Korst, AEC ;
de Pooter, CMJ ;
Pattyn, GGO ;
Lambrechts, HAJ ;
Baay, MFD ;
Lardon, F ;
Vermorken, JB .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2003, 51 (03) :221-226