| Literature DB >> 32250484 |
Daniel Krahn1, Geronimo Heilmann1, Felix C E Vogel2,3, Chrisovalantis Papadopoulos4, Susanne Zweerink1,5, Farnusch Kaschani1, Hemmo Meyer4, Alexander Roesch2, Markus Kaiser1.
Abstract
Natural products (NPs) are an important inspirational source for developing drugs and chemical probes. In 1999, the group of Ōmura reported the constitutional elucidation of zelkovamycin. Although largely unrecognized so far, this NP displays structural similarities as well as differences to the argyrin NP family, a class of peptidic NPs with promising anticancer activities and diverse mode-of-action at the molecular level. By a combination of structure elucidation experiments, the first total synthesis of zelkovamycin and bioassays, the zelkovamycin configuration was determined and its previously proposed molecular structure was revised. The full structure assignment proves zelkovamycin as an additional member of the argyrins with however unique OXPHOS inhibitory properties. Zelkovamycin may therefore not only serve as a new starting point for chemical inhibitors of the OXPHOS system, but also guide customized argyrin NP isolation and biosynthesis studies.Entities:
Keywords: argyrin; bioactivity; cyclopeptides; natural products; zelkovamycin
Year: 2020 PMID: 32250484 DOI: 10.1002/chem.202001577
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236