Jatrophane Diterpenes from Euphorbia esula as Antiproliferative Agents and Potent Chemosensitizers to Overcome Multidrug Resistance

被引:43
|
作者
Vasas, Andrea [1 ]
Sulyok, Edvard [1 ]
Redei, Dora [1 ]
Forgo, Peter [1 ]
Szabo, Pal [2 ]
Zupko, Istvan [3 ]
Berenyi, Agnes [3 ]
Molnar, Joseph [4 ]
Hohmann, Judit [1 ]
机构
[1] Univ Szeged, Dept Pharmacognosy, H-6720 Szeged, Hungary
[2] Hungarian Acad Sci, Inst Chem, Chem Res Ctr, H-1525 Budapest, Hungary
[3] Univ Szeged, Dept Pharmacodynam & Biopharm, H-6720 Szeged, Hungary
[4] Univ Szeged, Dept Med Microbiol & Immunobiol, H-6720 Szeged, Hungary
来源
JOURNAL OF NATURAL PRODUCTS | 2011年 / 74卷 / 06期
基金
匈牙利科学研究基金会;
关键词
MACROCYCLIC DITERPENE; POLYESTERS; ESTERS; CONSTITUENTS; PRINCIPLES; MODULATORS; IRRITANT; BINDING; FAMILY;
D O I
10.1021/np200202h
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Phytochemical study of whole, undried plants of Euphorbia esula led to the isolation of six new (1-6) jatrophane diterpene polyesters, named esulatins H-M, together with the known compounds 2 alpha,3 beta,5 alpha,7 beta,15 beta-pentaacetoxy-9 alpha-nicotinoyloxyjatropha-6(17),11-dien-14-one (7), salicinolide (8), and euphosalicin (9). The structures and relative configuration of 1-6 were established on the basis of extensive spectroscopic analysis, including HRESIMS and one- and two-dimensional NMR techniques. All these compounds, together with diterpenes (10-14) isolated previously from this plant, were evaluated for their antiproliferative activity against HeLa, Ishikawa, and MCF7 cells. The multidrug-resistance-reversing activities were also investigated on L5178 mouse lymphoma cells transfected with the pHa MDR1/A retrovinis DNA. Preliminary structure-activity relationship data are discussed.
引用
收藏
页码:1453 / 1461
页数:9
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