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Synthesis and multi-spectroscopic DNA binding study of 1,3,4-oxadiazole and 1,3,4-thiadiazole derivatives of fatty acid

机译:1,3,4-恶二唑和1,3,4-噻二唑脂肪酸衍生物的合成及多光谱DNA结合研究

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摘要

A facile and convenient synthesis of a series of fatty acid derivatives of 1,3,4-oxadiazole and 1,3,4-thiadiazole has been described. The key step of this protocol is the cyclization of acyl thiosemicarbazides via iodobenzene diacetate and methanesulfonic acid under mild conditions. The newly synthesized compounds were characterized by FT-IR, (HNMR)-H-1, (CNMR)-C-13 and mass spectral study. The binding affinity of 5-(pentadecyl)-N-propenyl-1,3,4-oxadiazol-2-amine (3a) and 5-(heptadecyl)-2-amino-1,3,4-thiadiazole (6a) with CT-DNA has been evaluated by UV, fluorescence, Circular Dichroism (CD) and thermal denaturation studies. It has been found that these small and planer heteroaromatic compounds are capable of binding to the minor groove region of DNA. (C) 2015 Elsevier B.V. All rights reserved.
机译:已经描述了容易且方便地合成一系列1,3,4-恶二唑和1,3,4-噻二唑的脂肪酸衍生物。该协议的关键步骤是在温和条件下通过碘代苯二乙酸酯和甲磺酸环化环硫代氨基脲。通过FT-IR,(HNMR)-H-1,(CNMR)-C-13和质谱研究对新合成的化合物进行表征。 5-(十五烷基)-N-丙烯基-1,3,4-恶二唑-2-胺(3a)和5-(十七烷基-2-氨基-1,3,4-噻二唑(6a)与CT-DNA已通过紫外线,荧光,圆二色性(CD)和热变性研究进行了评估。已经发现这些小的且平面的杂芳族化合物能够结合到DNA的小沟区域。 (C)2015 Elsevier B.V.保留所有权利。

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