| Literature DB >> 24639892 |
Daniel P Canterbury1, Kristen E N Scott2, Ozora Kubo1, Rolf Jansen3, John L Cleveland2, Glenn C Micalizio1.
Abstract
A synthesis of C11-desmethoxy soraphen A1α is described that proceeds in just 14 steps from readily available starting materials. This natural product analog was identified as a target of interest in a program aimed at identifying novel natural product-inspired inhibitors of acetyl-CoA carboxylase (ACC) as potential anticancer therapeutics. While describing the most efficient synthesis of a soraphen A1α analog (total syntheses of the natural product have been reported that proceed in 25 to ≥40 linear steps), we also present data supporting the conclusion that C11-heteroatom functionality is a beneficial but unnecessary structural characteristic of soraphen A1α analogs for inhibiting ACC.Entities:
Keywords: Soraphen A; acetyl-CoA carboxylase (ACC); function-oriented synthesis; polyketide synthesis
Year: 2013 PMID: 24639892 PMCID: PMC3951358 DOI: 10.1021/ml400377p
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345