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SF 5 - and SCF 3 -substituted tetrahydroquinoline compounds as potent bactericidal agents against multidrug-resistant persister Gram-positive bacteria.

Authors :
Onyedibe KI
Dayal N
Sintim HO
Source :
RSC medicinal chemistry [RSC Med Chem] 2021 Aug 10; Vol. 12 (11), pp. 1879-1893. Date of Electronic Publication: 2021 Aug 10 (Print Publication: 2021).
Publication Year :
2021

Abstract

Bacteria persister cells are immune to most antibiotics and hence compounds that are active against persister bacteria are needed. We screened a chemical library of SF <subscript>5</subscript> - and SCF <subscript>3</subscript> -substituted tetrahydroquinoline compounds, synthesized via the Povarov reaction, for antibacterial activity and identified active compounds that displayed good activities against many Gram-positive bacteria, including persisters. The most potent of these compounds, HSD1835 , inhibited the growth of drug-resistant Gram-positive bacterial pathogens (including clinical strains) at concentrations ranging from 1 μg mL <superscript>-1</superscript> to 4 μg mL <superscript>-1</superscript> . Several of the SCF <subscript>3</subscript> - and SF <subscript>5</subscript> -containing compounds were active against methicillin-resistant Staphylococcus aureus (MRSA) and against the two most fatal strains of vancomycin-resistant Enterococcus (VRE), VRE faecalis and VRE faecium . The compounds showed bactericidal activity against stationary phase persister MRSA in time-kill assays. Mechanistic studies showed that HSD1835 acts by disrupting bacterial membranes. Scanning electron microscopy (SEM) was used to confirm bacterial membrane disruption. Interestingly, in a 30 day serial exposure experiment, MRSA remained susceptible to low-dose HSD1835 whilst resistance to ciprofloxacin and mupirocin emerged by day 10. Analogs of HSD1835 , which did not bear the SF <subscript>5</subscript> or SCF <subscript>3</subscript> moieties, were inactive against bacteria. Recent reports (G. A. Naclerio, N. S. Abutaleb, K. I. Onyedibe, M. N. Seleem and H. O. Sintim, RSC Med. Chem. 2020, 11 , 102-110 and G. A. Naclerio, N. S. Abutaleb, D. Li, M. N. Seleem and H. O. Sintim, J. Med. Chem. 2020, 63 (20), 11934-11944) also demonstrated that adding the SF <subscript>5</subscript> or SCF <subscript>3</subscript> groups to a different scaffold (oxadiazoles) enhanced the antibacterial properties of the compounds, so it appears that these groups are privileged moieties that enhance the antimicrobial activities of compounds.<br />Competing Interests: There is no conflict of interest.<br /> (This journal is © The Royal Society of Chemistry.)

Details

Language :
English
ISSN :
2632-8682
Volume :
12
Issue :
11
Database :
MEDLINE
Journal :
RSC medicinal chemistry
Publication Type :
Academic Journal
Accession number :
34825185
Full Text :
https://doi.org/10.1039/d1md00211b