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噻吩的吡唑基 - 噻唑衍生物的合成、表征、生物活性及计算研究

Synthesis, characterization, biological activities, and computational studies of pyrazolyl-thiazole derivatives of thiophene.

作者信息

Bhagwat Seema K, Pawar Tushar Janardan, Kulkarni Sayali A, Patil Amar A, More Rahul Ashokrao, Jimenez-Halla J Oscar C, Alvarado-Salazar Juan Andres, Olivares-Romero Jose Luis, Muteeb Ghazala, Delgado-Alvarado Enrique, Patil Sachin V

机构信息

Department of Chemistry, Research Centre HPT Arts and RYK Science College (Affiliated to S. P. Pune University) Nashik 422005 Maharashtra India.

Red de Estudios Moleculares Avanzados, Campus III, Instituto de Ecología, A. C. Carretera Antigua a Coatepec 351 91073 Xalapa Veracruz Mexico.

出版信息

RSC Adv. 2024 Dec 10;14(52):39004-39016. doi: 10.1039/d4ra06228k. eCollection 2024 Dec 3.

Abstract

This study reports the synthesis, characterization, and biological evaluation of a series of pyrazolyl-thiazole derivatives of thiophene. Seven compounds were synthesized and characterized using NMR spectroscopy and mass spectrometry. The antimicrobial activities of these derivatives were evaluated against various bacterial (, , , ) and fungal strains (, , , ), demonstrating significant inhibition zones and low minimum inhibitory concentrations (MIC). In addition, the compounds exhibited notable antioxidant activities in DPPH and hydroxyl radical scavenging assays. Computational studies, including density functional theory (DFT) calculations and molecular docking simulations, were performed to understand the electronic properties and binding interactions of the synthesized compounds with biological targets. The molecular docking results supported the experimental findings, highlighting the potential of these pyrazolyl-thiazole derivatives as multifunctional therapeutic agents with both antimicrobial and antioxidant properties.

摘要

本研究报告了一系列噻吩基吡唑基噻唑衍生物的合成、表征及生物学评价。合成了七种化合物,并利用核磁共振光谱和质谱对其进行了表征。评估了这些衍生物对各种细菌(、、、)和真菌菌株(、、、)的抗菌活性,显示出显著的抑菌圈和低最低抑菌浓度(MIC)。此外,这些化合物在DPPH和羟基自由基清除试验中表现出显著的抗氧化活性。进行了包括密度泛函理论(DFT)计算和分子对接模拟在内的计算研究,以了解合成化合物的电子性质及其与生物靶点的结合相互作用。分子对接结果支持了实验结果,突出了这些吡唑基噻唑衍生物作为具有抗菌和抗氧化特性的多功能治疗剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43d9/11629146/5f5f6c834c9f/d4ra06228k-s1.jpg

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