Synthesis, characterization, DFT calculations, antimicrobial activity, molecular docking, and ADMET study of new pyrazole-carboxamide derivatives

被引:1
|
作者
Roby, Othmane [1 ]
Kadiri, Fatima Zahra [2 ]
Moutaouakil, Mohamed [1 ]
Ousaid, Fatima Ez-zahra [3 ]
Saddik, Rafik [1 ]
Aboulmouhajir, Aziz [1 ]
Alzahrani, Abdullah Yahya [4 ]
Tighadouini, Said [1 ]
机构
[1] Hassan II Univ, Fac Sci Ain Chock, Lab Organ Synth Extract & Valorizat, BP 5366, Casablanca, Morocco
[2] Hassan II Univ, Fac Sci Ain Chock, Lab Immunol & Biodivers, BP 5366, Casablanca, Morocco
[3] Hassan II Univ, Fac Sci Ain Chock, Hlth & Environm Lab, BP 5366, Casablanca, Morocco
[4] King Khalid Univ, Fac Sci & Arts, Dept Chem, Mohail Assir, Saudi Arabia
关键词
Pyrazole-carboxamide; One-pot synthesis; Antimicrobial activity; DFT; Docking; ADMETox; ANTIBACTERIAL;
D O I
10.1016/j.molstruc.2024.140400
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An efficient one-step synthesis of carboxamides from pyrazole acid was achieved using thionyl chloride as an activating agent. Thirteen new pyrazole carboxamide derivatives were synthesized and characterized through spectroscopic and spectrometric techniques. These compounds were evaluated for antifungal activity against Candida albicans, Aspergillus brasiliensis, and Saccharomyces cerevisiae. Notably, compounds R5, R11, and R 13 showed significant antifungal efficacy, while none exhibited antibacterial activity against Escherichia coli. To further our understanding, a computational DFT analysis revealed crucial information about the structure, electronic proprieties, and reactivity of these materials. The experimental results were supported by molecular docking analysis, reinforcing the validity of the results. Extending our exploration, an analysis of the pharmacokinetic properties and toxicity by ADMET profiling confirmed the safe use of these newly synthesized compounds, paving the way for promising applications in the medical field.
引用
收藏
页数:17
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