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Zygosporamide, a cytotoxic cyclic depsipeptide from the marine-derived fungus Zygosporium masonii

Cited 46 time in Web of Science Cited 56 time in Scopus
Authors

Oh, Dong-Chan; Jensen, Paul R.; Fenical, William

Issue Date
2006-11
Publisher
Elsevier BV
Citation
Tetrahedron Letters, Vol.47 No.48, pp.8625-8628
Abstract
Zygosporamide (1), a new cyclic pentadepsipeptide, was isolated from the seawater-based fermentation broth of a marine-derived fungus identified as Zygosporium masonii. The structure of 1, which is composed of alpha-hydroxyleucic acid and both D-and L-amino acids, was determined by combined spectral and chemical methods. Despite a simple structure, zygosporamide illustrated significant cytotoxicity in the NCI's 60 cell line panel (median GI(50) = 9-1 mu M), with highly enhanced selectivity against the CNS cancer cell line SF-268 (GI(50) = 6.5 nM) and the renal cancer cell line RXF 393 (GI(50) <= 5.0 nM). (c) 2006 Elsevier Ltd. All rights reserved.
ISSN
0040-4039
URI
https://hdl.handle.net/10371/208522
DOI
https://doi.org/10.1016/j.tetlet.2006.08.113
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Chemical biology of natural products, Drug discovery from microbial natural products, Study of insect-microbial symbiosis, 미생물 유래 생리활성 천연물 발굴, 천연물 구조 분석

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