Synthesis and preliminary evaluation of benzimidazole derivatives as antimicrobial agents
Language English Country France Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
12008055
DOI
10.1016/s0223-5234(02)01342-9
PII: S0223523402013429
Knihovny.cz E-resources
- MeSH
- Anti-Bacterial Agents MeSH
- Anti-Infective Agents chemical synthesis pharmacology MeSH
- Aspergillus fumigatus drug effects MeSH
- Benzimidazoles chemical synthesis pharmacology MeSH
- Candida drug effects MeSH
- Magnetic Resonance Spectroscopy MeSH
- Microbial Sensitivity Tests MeSH
- Mycobacterium avium drug effects MeSH
- Mycobacterium kansasii drug effects MeSH
- Mycobacterium drug effects MeSH
- Trichophyton drug effects MeSH
- Trichosporon drug effects MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Anti-Infective Agents MeSH
- Benzimidazoles MeSH
A series of 2-alkylsulphanylbenzimidazoles was synthesised and the compounds were evaluated for their in vitro antimicrobial activity. The structures of the compounds were confirmed by 1H-NMR and IR data, and their purity by elemental analysis. Antimycobacterial activities against Mycobacterium tuberculosis and non-tuberculous mycobacteria as well as antifungal activities against Candida albicans, Candida tropicalis, Candida krusei, Candida glabrata, Trichosporon beigelii, Trichophyton mentagrophytes and Aspergillus fumigatus were expressed as the corresponding MIC values. The substances exhibited appreciable antimycobacterial activity, in particular, against non-tuberculous mycobacteria. The activity of the most active compound in the set, 3,5-dinitro derivative 4t, exceeded that of the standard isoniazide against M. kansasii and M. avium. The antifungal activities of the compounds were relatively low. A weak antifungal effect was observed against the dermatophyte Trichophyton mentagrophytes. None of the compounds showed significant inhibitory activity against yeasts.
References provided by Crossref.org
New antimycobacterial S-alkylisothiosemicarbazones