| Literature DB >> 18444683 |
Marcelino Gutiérrez1, Takashi L Suyama, Niclas Engene, Joshua S Wingerd, Teatulohi Matainaho, William H Gerwick.
Abstract
Cancer cell toxicity-guided fractionation of extracts of the Papua New Guinea marine cyanobacteria Lyngbya majuscula and Lyngbya sordida led to the isolation of apratoxin D (1). Compound 1 contains the same macrocycle as apratoxins A and C but possesses the novel 3,7-dihydroxy-2,5,8,10,10-pentamethylundecanoic acid as the polyketide moiety. The planar structures and stereostructures of compound 1 were determined by extensive 1D and 2D NMR and MS data analyses and by comparison with the spectroscopic data of apratoxins A and C. Apratoxin D (1) showed potent in vitro cytotoxicity against H-460 human lung cancer cells with an IC 50 value of 2.6 nM.Entities:
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Year: 2008 PMID: 18444683 DOI: 10.1021/np800121a
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050