| Literature DB >> 29966871 |
Ru-Yi Jin1, Chu-Yue Zeng2, Xu-Hua Liang3, Xiao-Hong Sun4, Yuan-Fa Liu5, Yan-Yan Wang6, Sha Zhou7.
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.Entities:
Keywords: 1,2,4-Triazole; Biological activity; DFT calculation; Synthesis
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Year: 2018 PMID: 29966871 DOI: 10.1016/j.bioorg.2018.06.030
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275