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Design, synthesis, biological activities and DFT calculation of novel 1,2,4-triazole Schiff base derivatives
- Source :
- Bioorganic Chemistry. 80:253-260
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- Series of 1,2,4-triazole Schiff bases (2a-2d, 2f-2h and 3a-3h) have been designed and synthesized. The structure of title compounds was confirmed on the basis of their spectral data and elemental analysis. All the target compounds were screened for their in vitro antifungal activity and antibacterial activity. Two of the tested compounds (2a and 2b) exhibited significant antifungal activity against most fungi, especially compound 2a showed better antifungal activity than triadimefon. Meanwhile, the antibacterial activity assay also indicated compound 2a exhibited excellent antibacterial activities comparable to chloramphenicol. The SAR manifested no substitution at position 5 of the triazole ring caused an increase in activity, and 3-phenoxy phenyl group introduced in 1,2,4-triazole scaffold can enhance the antibacterial activity. The DFT calculation indicated triazole ring, S atom and benzene ring in both of the 2a and 3a make a major contribution to the activity.
- Subjects :
- Staphylococcus aureus
Antifungal Agents
Molecular Conformation
Triazole
Pythium
Microbial Sensitivity Tests
Crystallography, X-Ray
010402 general chemistry
Ring (chemistry)
01 natural sciences
Biochemistry
Structure-Activity Relationship
chemistry.chemical_compound
Drug Discovery
Escherichia coli
Phenyl group
Structure–activity relationship
Molecular Biology
Density Functional Theory
Schiff Bases
Schiff base
010405 organic chemistry
Chemistry
Organic Chemistry
Fungi
1,2,4-Triazole
Biological activity
Triazoles
Combinatorial chemistry
Anti-Bacterial Agents
0104 chemical sciences
Drug Design
Antibacterial activity
Subjects
Details
- ISSN :
- 00452068
- Volume :
- 80
- Database :
- OpenAIRE
- Journal :
- Bioorganic Chemistry
- Accession number :
- edsair.doi.dedup.....dd26cb2474cedfc70fdc997191c09625
- Full Text :
- https://doi.org/10.1016/j.bioorg.2018.06.030