| Literature DB >> 31756025 |
Ansley M Nemeth1, Akash K Basak1, Alexander W Weig1, Santiana A Marrujo1, William T Barker1, Leigh A Jania2, Tyler A Hendricks1, Ashley E Sullivan1, Patrick M O'Connor1, Roberta J Melander1, Beverly H Koller2, Christian Melander1.
Abstract
Infections caused by multidrug-resistant (MDR) bacteria, particularly Gram-negative bacteria, are an escalating global health threat. Often clinicians are forced to administer the last-resort antibiotic colistin; however, colistin resistance is becoming increasingly prevalent, giving rise to the potential for a situation in which there are no treatment options for MDR Gram-negative infections. The development of adjuvants that circumvent bacterial resistance mechanisms is a promising orthogonal approach to the development of new antibiotics. We recently disclosed that the known IKK-β inhibitor IMD-0354 potently suppresses colistin resistance in several Gram-negative strains. In this study, we explore the structure-activity relationship (SAR) between the IMD-0354 scaffold and colistin resistance suppression, and identify several compounds with more potent activity than the parent against highly colistin-resistant strains of Acinetobacter baumannii and Klebsiella pneumoniae.Entities:
Keywords: Gram-negative bacteria; adjuvants; antibiotic resistance; colistin
Mesh:
Substances:
Year: 2019 PMID: 31756025 PMCID: PMC6982545 DOI: 10.1002/cmdc.201900560
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466