| Literature DB >> 29125222 |
Yi-Xing Chen1, Chao Liu1, Nan Liu2, Ye Wu3, Qing-Jie Zhao1, Hong-Gang Hu1, Xiang Li1, Yan Zou1.
Abstract
As natural-product-derived antibiotics, desotamides A - D and wollamides exhibit growth inhibitory activity against Gram-posivite bacteria (IC50 0.6 - 7 μm) and are noncytotoxic to mammalian cells (IC50 > 30 μm). Herein we firstly report the total synthesis of above two cyclohexapeptides as well as a series of structural variants through solid phase peptide synthesis, of which 3 displayed a 2-fold increase of antibacterial activity when compared with the original peptide 1. This strategy may offer good improvements for the synthesis of other cyclic peptides.Entities:
Keywords: zzm321990SPPSzzm321990; Antibacterial activity; Desotamides; Total synthesis; Wollamides
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Year: 2017 PMID: 29125222 DOI: 10.1002/cbdv.201700414
Source DB: PubMed Journal: Chem Biodivers ISSN: 1612-1872 Impact factor: 2.408