Kahalalide derivatives from the Indian sacoglossan mollusk Elysia grandifolia

被引:108
作者
Ashour, Mohamed
Edrada, RuAngelie
Ebel, Rainer
Wray, Victor
Waetjen, Wim
Padmakumar, K.
Mueller, Werner E. G.
Lin, Wen Han
Proksch, Peter
机构
[1] Univ Dusseldorf, Inst Pharmazeut Biol & Biotechnol, D-40225 Dusseldorf, Germany
[2] Helmholtz Ctr Infect Res, Dept Biol Struct, D-38124 Braunschweig, Germany
[3] Univ Dusseldorf, Inst Toxikol, D-40225 Dusseldorf, Germany
[4] Univ Kerala, Dept Aquat Biol & Fisheries, Ctr Marine Biodivers, Trivandrum 695581, Kerala, India
[5] Univ Mainz, Inst Physiol Chem & Pathobiochem, D-55128 Mainz, Germany
[6] Peking Univ, Natl Res Lab Nat & Biomimet Drugs, Beijing 100083, Peoples R China
[7] Al Azhar Univ, Fac Pharm, Nasr City, Cairo, Egypt
来源
JOURNAL OF NATURAL PRODUCTS | 2006年 / 69卷 / 11期
关键词
D O I
10.1021/np060172v
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Two new cyclic depsipeptide derivatives, kahalalides R (1) and S (2), together with two known congeners, kahalalides F (3) and D (4), were isolated from the Indian sacoglossan mollusk Elysia grandifolia. The structures of the new compounds were unambiguously established on the basis of NMR spectroscopic (H-1, C-13, COSY, HMBC) and mass spectrometric (FABMS, ESIMS, MALDI-TOF/PSD) data, which also included Marfey amino acid analyses. The new derivative kahalalide R was found to exert comparable or even higher cytotoxicity than the potential drug candidate kahalalide F toward the MCF7 human mammary carcinoma cell line.
引用
收藏
页码:1547 / 1553
页数:7
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