| Literature DB >> 32987133 |
Sarra Bekri1, Florie Desriac2, Magalie Barreau3, Thomas Clamens3, Thibault Gallavardin4, Patricia Le Nahenec-Martel4, Julien Vieillard4, Yazid Datoussaid5, Noureddine Choukchou-Braham5, Olivier Lesouhaitier3, Xavier Franck4, Stéphane Leleu6.
Abstract
The synthesis of new cadiolide analogues was carried out using a one-pot multi component synthesis. The antibacterial activity of these molecules was evaluated on standard and antibiotic resistant bacterial strains chosen for their involvement in human health or in food-born poisoning. Four molecules have shown good activities with MICs of 2 μg/mL-1. The introduction of an indole group or the conversion of the lactone into lactam have highlighted two new families of molecules with promising antibacterial activity. In addition, most of these active molecules are devoid of cytotoxic activity against keratinocyte cells.Entities:
Keywords: Antibacterial; Antibiotic-resistance; Cadiolide analogues; Natural products
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Year: 2020 PMID: 32987133 DOI: 10.1016/j.bmcl.2020.127580
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823