Antibacterial effect of substituted 4-quinazolyl-hydrazines and their arylhydrazones determined by a modified microdilution method
Language English Country United States Media print
Document type Comparative Study, Journal Article
PubMed
8768252
DOI
10.1007/bf02818517
Knihovny.cz E-resources
- MeSH
- Anti-Bacterial Agents chemistry pharmacology MeSH
- Quinazolines chemistry pharmacology MeSH
- Enterococcus faecalis drug effects MeSH
- Escherichia coli drug effects MeSH
- Hydrazines chemistry pharmacology MeSH
- Microbial Sensitivity Tests * MeSH
- Microchemistry MeSH
- Pseudomonas aeruginosa drug effects MeSH
- Staphylococcus aureus drug effects MeSH
- Structure-Activity Relationship MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Quinazolines MeSH
- Hydrazines MeSH
Eight 4-quinazolylhydrazines and eleven their arylhydrazones have been tested for antibacterial effects and for structure-activity relationships by a modified microdilution method. The derivative 6-chloro-2-morpholino-4-quinazolyl-5'-nitro-2'-furylhydrazone++ + had the highest antibacterial effect, the MIC values being 100 mg/L for E. faecalis, 250 mg/L for S. aureus, 200 mg/L for P. aeruginosa and 350 mg/L for E. coli. The most effective derivatives were those with the benzene ring substituted with chlorine or methyl group in position 6 or 8 and with pyrimidine ring substituted with a secondary amine in position 2. The modified microdilution method did not give rise to any statistically significant deviations in the MIC values for ampicillin in comparison with reported reference collection values.
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