| Literature DB >> 12502348 |
Hendrik Luesch1, Wesley Y Yoshida, George G Harrigan, James P Doom, Richard E Moore, Valerie J Paul.
Abstract
A Palauan collection of the marine cyanobacterium Lyngbya sp., which had already afforded diverse peptide-based cytotoxins, also yielded a new glycoside macrolide exhibiting slight cytotoxicity. The compound was termed lyngbyaloside B (1) due to its structural analogy to the previously isolated lyngbyaloside (2). Lyngbyaloside B (1) appears to be only the third glycoside macrolide and second brominated compound of its kind from a marine cyanobacterium. Its gross structure was determined by a combination of NMR spectroscopy and mass spectrometric techniques. The relative stereochemistry for the 12 stereocenters is proposed on the basis of proton-proton spin-coupling constants and ROESY data.Entities:
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Year: 2002 PMID: 12502348 DOI: 10.1021/np0202879
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050