Ring-substituted 8-hydroxyquinoline-2-carboxanilides as potential antimycobacterial agents
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
26183541
DOI
10.1016/j.bmc.2015.06.047
PII: S0968-0896(15)00541-6
Knihovny.cz E-resources
- Keywords
- 8-Hydroxyquinolines, In vitro antimycobacterial activity, In vitro cytotoxicity, MTT assay, Structure–activity relationships,
- MeSH
- Anti-Bacterial Agents chemistry pharmacology MeSH
- Cell Line MeSH
- Humans MeSH
- Microbial Sensitivity Tests MeSH
- Mycobacterium avium drug effects MeSH
- Mycobacterium tuberculosis drug effects metabolism MeSH
- Oxyquinoline chemistry MeSH
- Drug Evaluation, Preclinical methods MeSH
- Toxicity Tests MeSH
- Structure-Activity Relationship * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Oxyquinoline MeSH
In this study, a series of twenty-two ring-substituted 8-hydroxyquinoline-2-carboxanilides was prepared and characterized. Primary in vitro screening of the synthesized compounds was performed against Mycobacterium tuberculosis H37Ra, Mycobacterium avium complex and M. avium subsp. paratuberculosis. Some of the tested compounds showed the antimycobacterial activity against M. avium subsp. paratuberculosis comparable with or higher than that of rifampicin. 8-Hydroxy-N-[3-(trifluoromethyl)phenyl]- and 8-hydroxy-N-[4-(trifluoromethyl)phenyl]quinoline-2-carboxamide showed MIC=24 μM against all tested mycobacterial strains. 3-Methoxyphenyl- and 3-methylphenyl derivatives expressed MIC=27 or 29 μM also against all the tested strains. Their activity against M. avium subsp. paratuberculosis was 4-fold higher than that of rifampicin. 2-Bromophenyl- and 2-(trifluoromethyl)phenyl derivatives had MIC=23 or 24 μM against M. tuberculosis. A significant decrease of mycobacterial cell metabolism (viability of M. tuberculosis H37Ra) was observed using MTT assay. Screening of cytotoxicity of the compounds was performed using the THP-1 cells, and no significant lethal effect was observed up to tested concentration 30 μM. The structure-activity relationships are discussed.
Department of Biological Sciences Cork Institute of Technology Bishopstown Cork Ireland
Global Change Research Centre AS CR Belidla 986 4a 603 00 Brno Czech Republic
References provided by Crossref.org
Design, Synthesis, and Anticancer and Antibacterial Activities of Quinoline-5-Sulfonamides
Trifluoromethylcinnamanilide Michael Acceptors for Treatment of Resistant Bacterial Infections
Design, Synthesis and Antimicrobial Properties of New Tetracyclic Quinobenzothiazine Derivatives
Synthesis and Spectrum of Biological Activities of Novel N-arylcinnamamides
Proline-Based Carbamates as Cholinesterase Inhibitors
N-Alkoxyphenylhydroxynaphthalenecarboxamides and Their Antimycobacterial Activity