| Literature DB >> 20158242 |
Marcelino Gutiérrez1, Kevin Tidgewell, Todd L Capson, Niclas Engene, Alejandro Almanza, Jörg Schemies, Manfred Jung, William H Gerwick.
Abstract
Fractionation of the extract of the marine cyanobacterium Lyngbya majuscula collected from Panama led to the isolation of malyngolide dimer (1). The planar structure of 1 was determined using 1D and 2D NMR spectroscopy and HRESI-TOFMS. The absolute configuration was established by chemical degradation followed by chiral GC-MS analyses and comparisons with an authentic sample of malyngolide seco-acid (4). Compound 1 showed moderate in vitro antimalarial activity against chloroquine-resistant Plasmodium falciparum (W2) (IC(50) = 19 microM) but roughly equivalent toxicity against H-460 human lung cell lines. Furthermore, because the closely related cyanobacterial natural product tanikolide dimer (5) was a potent SIRT2 inhibitor, compound 1 was evaluated in this assay but found to be essentially inactive.Entities:
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Year: 2010 PMID: 20158242 PMCID: PMC2859090 DOI: 10.1021/np9005184
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050