| Literature DB >> 28090774 |
Naoyuki Kotoku1, Ryosuke Ishida1, Hirokazu Matsumoto1, Masayoshi Arai1, Kazunari Toda1, Andi Setiawan2, Osamu Muraoka3, Motomasa Kobayashi1.
Abstract
Biakamides A-D, novel unusually unique polyketides, were isolated from an Indonesian marine sponge (Petrosaspongia sp.) with a constructed bioassay using PANC-1 human pancreatic cancer cells. Through detailed analyses of the one- and two-dimensional NMR spectra of biakamides, planar chemical structures possessing a terminal thiazole, two N-methyl amides, a chloromethylene, and a substituted butyryl moiety were obtained. After elucidation of the configuration of the secondary alcohol moiety in biakamides A and B, the absolute stereostructures of the two secondary methyl groups in biakamides A-D were determined by the asymmetric total syntheses of all possible stereoisomers from the optically pure monoprotected 2,4-dimethyl-1,5-diol. Biakamides A-D showed selective antiproliferative activities against PANC-1 cells cultured under glucose-deficient conditions in a concentration-dependent manner. The primary mode of action of biakamides was found to be inhibition of complex I in the mitochondrial electron transport chain.Entities:
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Year: 2017 PMID: 28090774 DOI: 10.1021/acs.joc.6b02948
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354