“An Overview On Biological Behavior Of Benzotriazole: Synthesis And Docking Study On Its Versatile Biological Activities”

Somashekhar Metri, Divya Shirke, Vishal Babar, Shivanand Kolageri
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Abstract

The practice of medicinal chemistry is devoted to the discovery and development of new chemical agents for treating diseases. Triazoles are obtained by a slight modification of azole ring and similar or improved activities as well as fewer adverse effects are reported for triazole derivatives several advantages are the notable attraction for using benzotriazole moiety-dependent methodologies, in my research work I synthesized various derivatives of n-(1h-benzotriazol-6-yl)-benzamide from Benzene 1,2,4-triamine and benzoic acid with high yield and the synthesized derivatives characterized by FT-IR spectrum, H1 NMR spectrum, and mass spectrum data of synthesized derivatives compounds of benzotriazole Scheme analysis proves that resultant compounds n-(1h-benzotriazol-6-yl)-benzamide derivatives. The molecular docking studies validated the outcome results from the anti-inflammatory and antiarthritic agents and signifies the potential of these derivatives as crystal structure of C-terminus of voltage-gated sodium channel in complex (PDB ID:4DCK) and COX 2 Inhibitor (PDB ID:1CX2) inhibitors. So, these compounds can be modified further for the development of new anti-inflammatory and antiarthritic agents. This study strongly suggests that most of molecules synthesized in this study may indeed be promising drug candidates with interesting pharmacological profile and most of these derivatives could be a fruitful for further development of better anti-inflammatory and antiarthritic activity.
"苯并三唑生物行为概述:关于其多种生物活性的合成和 Docking 研究"
药物化学致力于发现和开发治疗疾病的新化学制剂。在我的研究工作中,我从苯 1.2,4-三胺和苯甲酸中合成了 n-(1h-苯并三唑-6-基)-苯甲酰胺的各种衍生物、通过傅立叶变换红外光谱、H1 NMR 光谱和苯并三唑合成衍生物的质谱数据,对合成的衍生物进行了表征。分子对接研究验证了抗炎剂和抗关节炎剂的结果,并表明这些衍生物具有作为电压门控钠通道 C 端晶体结构复合物(PDB ID:4DCK)和 COX 2 抑制剂(PDB ID:1CX2)抑制剂的潜力。因此,可以对这些化合物进行进一步改造,以开发新的抗炎和抗关节炎药物。这项研究有力地表明,本研究中合成的大多数分子可能确实是具有有趣药理特征的有前途的候选药物,而且这些衍生物中的大多数可能在进一步开发更好的抗炎和抗关节炎活性方面取得丰硕成果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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