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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:
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.
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页码:1453 / 1461
页数:9
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