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PMID: 10813954 Published · ppublish English Journal Article

Peloruside A: a potent cytotoxic macrolide isolated from the new zealand marine sponge Mycale sp.

The Journal of organic chemistry ·Vol. 65 ·No. 2 ·2000-01-28 ·Pages 445-9

West LM, Northcote PT, Battershill CN

Abstract

A novel, polyoxygenated, pyranose ring containing 16-membered macrolide peloruside A (1) exhibiting cytotoxic activity in the nanomolar range was isolated from the New Zealand marine sponge Mycale sp. The structure of 1 and relative stereochemistry of the 10 stereogenic centers were determined on a 3 mg sample using a variety of spectroscopic methods. Compound 1 was isolated along with the previously reported cytotoxins mycalamide A (2) and pateamine (3) from a single specimen of this sponge.

MeSH Terms
Animals Antineoplastic Agents/chemistry,isolation & purification Bridged Bicyclo Compounds, Heterocyclic/chemistry,isolation & purification Lactones/chemistry,isolation & purification Magnetic Resonance Spectroscopy Molecular Structure Porifera/chemistry Stereoisomerism
Chemicals
Antineoplastic Agents Bridged Bicyclo Compounds, Heterocyclic Lactones peloruside A
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
West L M
School of Chemical and Physical Sciences, Victoria, University of Wellington, New Zealand.
Northcote P T
Battershill C N
Article Info
Journal
The Journal of organic chemistry
Abbr.
J Org Chem
ISSN
0022-3263
Published
2000-01-28
Pages
445-9
Language
English
Region
United States
NLM ID
2985193R
Subset
IM
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