Microcionamides A and B, bioactive peptides from the philippine sponge Clathria (Thalysias) abietina.
Author(s)
Davis, Rohan A.
Mangalindan, Gina C.
Bojo, Zenaida P.
Antemano, Rowena R.
Rodriguez, Nell O.
Concepcion, Gisela P.
Samson, Shiela C.
Guzman, Dennis
Cruz, Lourdes J.
Tasdemir, Deniz
Harper, Mary Kay
Feng, Xidong
Carter, Guy T.
Ireland, Chris M.
Griffith University Author(s)
Year published
2004
Metadata
Show full item recordAbstract
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 ...
View more >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.
View less >
View more >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.
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Journal Title
Journal of Organic Chemistry
Volume
69
Publisher URI
Copyright Statement
© 2004 American Chemical Society. Self-archiving of the author-manuscript version is not yet supported by this publisher.
Subject
Medicinal and Biomolecular Chemistry
Organic Chemistry