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Peloruside A: a potent cytotoxic macrolide isolated from the new zealand marine sponge Mycale sp.
- Source :
-
The Journal of organic chemistry [J Org Chem] 2000 Jan 28; Vol. 65 (2), pp. 445-9. - Publication Year :
- 2000
-
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.
- Subjects :
- Animals
Antineoplastic Agents chemistry
Bridged Bicyclo Compounds, Heterocyclic chemistry
Lactones chemistry
Magnetic Resonance Spectroscopy
Molecular Structure
Stereoisomerism
Antineoplastic Agents isolation & purification
Bridged Bicyclo Compounds, Heterocyclic isolation & purification
Lactones isolation & purification
Porifera chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0022-3263
- Volume :
- 65
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- The Journal of organic chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 10813954
- Full Text :
- https://doi.org/10.1021/jo991296y