Isolation, structure determination, and biological activity of dolastatin 12 and lyngbyastatin I from Lyngbya majuscula Schizothrix calcicola cyanobacterial assemblages

被引:104
作者
Harrigan, GG
Yoshida, WY
Moore, RE
Nagle, DG
Park, PU
Biggs, J
Paul, VJ [1 ]
Mooberry, SL
Corbett, TH
Valeriote, FA
机构
[1] Univ Hawaii Manoa, Dept Chem, Honolulu, HI 96822 USA
[2] Univ Guam, Marine Lab, UOG Stn, Mangilao, GU 96923 USA
[3] Univ Hawaii, Canc Res Ctr Hawaii, Honolulu, HI 96813 USA
[4] Wayne State Univ, Karmanos Canc Ctr, Detroit, MI 48201 USA
[5] Wayne State Univ, Dept Internal Med, Detroit, MI 48201 USA
来源
JOURNAL OF NATURAL PRODUCTS | 1998年 / 61卷 / 10期
关键词
D O I
10.1021/np9801211
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Lyngbyastatin 1 (1a), a new cytotoxic analogue of dolastatins 12 (2a) and 11 (4), was isolated as an inseparable mixture with its C-15 epimer (1b) from extracts of a Lyngbya majuscula/Schizothrix calcicola assemblage and a L. majuscula strain collected near Guam. Dolastatin 12 (2a) was also encountered as an inseparable mixture with its C-15 epimer (2b) in L, majuscula/S. calcicola assemblages. At least one of the compounds in each mixture appeared to exist in solution as a mixture of slowly interconverting conformers resulting in broadened signals in H-1 NMR spectra. Structure elucidation therefore relied principally on mass spectroscopy and chemical degradation studies. Both 1ab and 2ab proved toxic with only marginal or no antitumor activity when tested against colon adenocarcinoma #38 or mammary adenocarcinoma #16/C. Both 1ab and 2ab were shown to be potent disrupters of cellular microfilament networks.
引用
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页码:1221 / 1225
页数:5
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