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Separacenes A-D, Novel Polyene Polyols from the Marine Actinomycete, Streptomyces sp.

Authors
Bae, MunhyungKim, HeegyuShin, YoonhoKim, Byung YongLee, Sang KookOh, Ki-BongShin, JongheonOh, Dong-Chan
Issue Date
Aug-2013
Publisher
MDPI
Keywords
marine actinomycete; polyene polyol; cytotoxicity; isocitrate lyase
Citation
MARINE DRUGS, v.11, no.8, pp.2882 - 2893
Journal Title
MARINE DRUGS
Volume
11
Number
8
Start Page
2882
End Page
2893
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/83315
DOI
10.3390/md11082882
ISSN
1660-3397
Abstract
Separacenes A-D (1-4), novel polyene polyols, were isolated from Streptomyces sp. collected from the southern area of Jeju Island, Korea. The chemical structures of 1-4 were established by NMR, mass, UV, and IR spectroscopy as well as the modified Mosher's method. Separacenes A-B (1-2), which share an identical planar structure but possess different relative configurations, bear tetraene units flanked by two diol moieties, whereas the stereoisomeric separacenes C-D (3-4) possess a triene moiety between two diol substructures. Separacenes A-D each contain a terminal olefinic methylene. Separacene A displayed inhibitory activity against Candida albicans isocitrate lyase and weak cytotoxicity against both the colon carcinoma cell line HCT-116 and the lung cancer cell line A549.
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