| Literature DB >> 15176844 |
Rohan A Davis1, Gina C Mangalindan, Zenaida P Bojo, Rowena R Antemano, Nell O Rodriguez, Gisela P Concepcion, Shiela C Samson, Dennis de Guzman, Lourdes J Cruz, Deniz Tasdemir, Mary Kay Harper, Xidong Feng, Guy T Carter, Chris M Ireland.
Abstract
Microcionamides A (1) and B (2) have been isolated from the Philippine marine sponge Clathria (Thalysias) abietina. These new linear peptides are cyclized via a cystine moiety and have their C-terminus blocked by a 2-phenylethylenamine group. Their total structures, including absolute stereochemistry, were determined by a combination of spectral and chemical methods. Compound 1 was shown to slowly isomerize about the C-36/C-37 double bond when stored in DMSO. Microcionamides A (1) and B (2) exhibited significant cytotoxicity against the human breast tumor cells lines MCF-7 and SKBR-3 and displayed inhibitory activity against Mycobacterium tuberculosis H(37)Ra.Entities:
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Year: 2004 PMID: 15176844 DOI: 10.1021/jo040129h
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354