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首页> 外文期刊>Letters in drug design & discovery >Synthesis & Characterization of 2-(substituted-phenyl)acetohydrazide Analogs, 1,3,4-oxadiazoles, and 1,2,4-triazine Ring Systems: A Novel Class of Potential Analgesic and Anti-Inflammatory Agents
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Synthesis & Characterization of 2-(substituted-phenyl)acetohydrazide Analogs, 1,3,4-oxadiazoles, and 1,2,4-triazine Ring Systems: A Novel Class of Potential Analgesic and Anti-Inflammatory Agents

机译:2-(取代-苯基)乙酰肼类似物,1,3,4-恶二唑和1,2,4-三嗪环系统的合成与表征:一类新型的镇痛药和消炎药

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摘要

The new series of 2-(substituted-phenyl)acetohydrazides analogs, S-alkylated 5-substituted-1,3,4-oxadiazoles-2-thione derivatives and 5-arylidene-3-substituted-1,2,4-triazines have been synthesized in good yields and characterized by IR, NMR, mass spectral and elemental analyses. All the synthesized compounds 4(a-d), 5(a-d), 7(a-b), and 8(a-f) are evaluated for their in vitro DPPH scavenging, antimicrobial activity, in vivo analgesic, anti-inflammatory activities. The results of the anti-inflammatory activity are supported by molecular docking study with mouse COX-1 (PDB ID: 2CZT) and COX-2 (PDB ID: 3LN1) enzymes to predict their putative interactions. Among all the assays conducted, the compounds 5-(4-bromophenyl)-3-(naphthalen-2-ylmethyl)-1,2,4-triazine (4d) and 2-{[5-(diphenylmethyl)-1,3,4-oxadiazol-2-yl] sulfanyl}-N-(pyrazin-2-yl) acetamide (8a) have emerged as the most potent molecules.
机译:新系列的2-(取代-苯基)乙酰肼类似物,S-烷基化的5-取代的1,3,4-恶二唑-2-硫酮衍生物和5-芳基-3-取代的1,2,4-三嗪合成得率很高,并通过IR,NMR,质谱和元素分析进行​​了表征。评价所有合成的化合物4(a-d),5(a-d),7(a-b)和8(a-f)的体外DPPH清除能力,抗微生物活性,体内止痛,抗炎活性。抗炎活性的结果得到了与小鼠COX-1(PDB ID:2CZT)和COX-2(PDB ID:3LN1)酶的分子对接研究的支持,以预测其假定的相互作用。在进行的所有测定中,化合物5-(4-溴苯基)-3-(萘-2-基甲基)-1,2,4-三嗪(4d)和2-{[5-(二苯甲基)-1,3 1,4-恶二唑-2-基]硫烷基} -N-(吡嗪-2-基)乙酰胺(8a)已成为最有效的分子。

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