| Literature DB >> 26031409 |
Holger Hoffmann1, Herbert Kogler1,2, Winfried Heyse1, Hans Matter1, Michael Caspers1, Dietmar Schummer1,3, Christine Klemke-Jahn1, Armin Bauer1, Geraldine Penarier4, Laurent Debussche4, Mark Brönstrup5,6.
Abstract
Microbial natural products are a rich source of bioactive molecules to serve as drug leads and/or biological tools. We investigated a little-explored myxobacterial genus, Nannocystis sp., and discovered a novel 21-membered macrocyclic scaffold that is composed of a tripeptide and a polyketide part with an epoxyamide moiety. The relative and absolute configurations of the nine stereocenters was determined by NMR spectroscopy, molecular dynamics calculations, chemical degradation, and X-ray crystallography. The compound, named nannocystin A (1), was found to inhibit cell proliferation at low nanomolar concentrations through the early induction of apoptosis. The mode of action of 1 could not be matched to that of standard drugs by transcriptional profiling and biochemical experiments. An initial investigation of the structure-activity relationship based on seven analogues demonstrated the importance of the epoxide moiety for high activity.Entities:
Keywords: antiproliferative agents; apoptosis; drug discovery; natural products; structure elucidation
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Year: 2015 PMID: 26031409 DOI: 10.1002/anie.201411377
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336