Ultrasound assisted rapid synthesis, biological evaluation, and molecular docking study of new 1,2,3-triazolyl pyrano[2,3-c]pyrazoles as antifungal and antioxidant agent

被引:18
作者
Khare, Smita P. [1 ]
Deshmukh, Tejshri R. [1 ]
Sangshetti, Jaiprakash N. [2 ]
Khedkar, Vijay M. [3 ]
Shingate, Bapurao B. [1 ]
机构
[1] Dr Babasaheb Ambedkar Marathwada Univ, Dept Chem, Aurangabad 431004, MH, India
[2] YB Chavan Coll Pharm, Dept Pharmaceut Chem, Aurangabad, MH, India
[3] Shri Vile Parle Kelavani Mandals Inst Pharm, Dept Pharmaceut Chem, Dhule, MH, India
关键词
POT MULTICOMPONENT SYNTHESIS; ANTIMICROBIAL ACTIVITIES; TRIAZOLE DERIVATIVES; EFFICIENT SYNTHESIS; FACILE SYNTHESIS; DESIGN; PYRANOPYRAZOLES; INHIBITORS; CHEMISTRY; GREEN;
D O I
10.1080/00397911.2019.1631849
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In search of new generation of triazole based antifungal agents, synthesis of series of new 1,2,3-triazolyl pyrano[2,3-c]pyrazoles under ultrasonic irradiation using NaHCO3 has been reported. The bioevaluation results indicate that, the compounds 7c, 7d, 7e, 7f, and 7i displayed excellent antifungal activity with lower MIC <= 25 mu g/mL. Most of the compounds from the series showed potent antioxidant activity with a lower IC50 value in the range 09.39 +/- 0.42-14.97 +/- 0.24 mu g/mL, in comparison to butylated hydroxyl toluene (BHT). Molecular docking studies against potential target sterol 14 alpha-demethylase (CYP51) was also performed and showed excellent binding affinity with the target enzyme. Moreover, in silico ADME study shows that the derivatives could serve as drug like molecules for further drug development in clinical research.
引用
收藏
页码:2521 / 2537
页数:17
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