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新型2,5-二取代-1,3,4-恶二唑衍生物的合成、表征及生物学评价

Synthesis, characterization and biological evaluation of novel 2,5 substituted-1,3,4 oxadiazole derivatives.

作者信息

Kavitha Selvaraj, Kannan Kulanthai, Gnanavel Sadhasivam

机构信息

Department of Chemistry, Government College of Engineering, Salem 11, Tamil Nadu, India.

出版信息

Saudi Pharm J. 2017 Mar;25(3):337-345. doi: 10.1016/j.jsps.2016.07.004. Epub 2016 Aug 1.

Abstract

In the present study, a series of 3-(5-cyclohexyl-1,3,4-oxadiazol-2-yl)-N-substituted aniline have been synthesized by multistep reaction scheme. Benzohydrazide was used as the starting material. The structures of all synthesized compounds are characterized and confirmed by FT-IR, H and C NMR and mass spectral studies with the intention of developing the novel biologically active compounds. All title synthetic compounds were screened for their antidiabetic, anti-inflammatory and anticancer activities.

摘要

在本研究中,通过多步反应方案合成了一系列3-(5-环己基-1,3,4-恶二唑-2-基)-N-取代苯胺。以苯甲酰肼为起始原料。通过傅里叶变换红外光谱(FT-IR)、氢核磁共振(H NMR)、碳核磁共振(C NMR)和质谱研究对所有合成化合物的结构进行了表征和确认,旨在开发新型生物活性化合物。对所有标题合成化合物进行了抗糖尿病、抗炎和抗癌活性筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8eaf/5357090/ea225394b655/fx1.jpg

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