Structure-activity relationships of some 4-quinazolylthiosemicarbazides and their triazolo derivatives
Language English Country United States Media print
Document type Journal Article
PubMed
8549994
DOI
10.1007/bf02814064
Knihovny.cz E-resources
- MeSH
- Anti-Bacterial Agents chemical synthesis chemistry pharmacology MeSH
- Bacteria drug effects MeSH
- Microbial Sensitivity Tests MeSH
- Semicarbazides chemical synthesis chemistry pharmacology MeSH
- Triazoles chemical synthesis chemistry pharmacology MeSH
- Structure-Activity Relationship MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Semicarbazides MeSH
- Triazoles MeSH
Eight 4-quinazolylthiosemicarbazides and nine of their structural analogues have been tested for antibacterial effects and for structure activity relationships. 9-Chloro-5-morpholino-1,2,4-triazolo[4,3-c]quinazoline-3-thione has demonstrated the highest antibacterial effect (MIC of 1 mg/L for E. coli and P. mirabilis and < 1 mg/L for S. aureus and B. subtilis). The most effective derivatives have the carbon aromatic ring substituted with chlorine and the pyrimidine ring with morpholine or with secondary amine group.
See more in PubMed
Z Allg Mikrobiol. 1972;12(5):355-64 PubMed
Arch Pharm (Weinheim). 1990 Oct;323(10):833-6 PubMed
J Med Chem. 1991 Jan;34(1):38-46 PubMed
J Chem Technol Biotechnol. 1992;53(4):329-36 PubMed
J Med Chem. 1986 Nov;29(11):2403-9 PubMed
Antibacterial effects of trisubstituted quinazoline derivatives
Antibacterial effect of some 2,6-disubstituted 4-anilinoquinazolines