首页> 外文期刊>Archiv der Pharmazie >Synthesis and cytotoxicity of bis-1,3,4-oxadiazoles and bis-pyrazoles derived from 1,4-bis(5-thio-4-substituted-1,2,4-triazol-3-yl)-butane and their DNA binding studies.
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Synthesis and cytotoxicity of bis-1,3,4-oxadiazoles and bis-pyrazoles derived from 1,4-bis(5-thio-4-substituted-1,2,4-triazol-3-yl)-butane and their DNA binding studies.

机译:1,4-双(5-硫-4-取代-1,2,4-三唑-3-基)丁烷衍生的双-1,3,4-恶二唑和双吡唑及其DNA的合成和细胞毒性绑定研究。

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摘要

A new series of 1,4-bis[5-(5-mercapto-1,3,4-oxadiazol-2-yl-methyl)-thio-4-substituted-1,2,4-triaz ol-3-yl]-butane 7-12 and 1,4-bis[5-(1-oxo-1-(3,5 dimethyl pyrazol-1-yl)-methyl)-thio-4-substitued-1,2,4-triazol-3-yl]-butane 13-18 were prepared from 1,4-bis(5[hydrazinocarbonylmethylthio]-4-substituted-1,2,4-triazol-3-yl) butane based derivativess were synthesized 1-6. All the synthesized compounds were characterized by IR, NMR and Mass spectral studies. The synthesized compounds 7-18 were screened for in-vitro cytotoxicity potential using the standard MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay against a panel of three human cancer cell lines: Lung carcinoma A-549, colon carcinoma HT-29 and breast cancer MDA MB-231. DNA binding studies were conducted for three potent molecules by absorption titration method.
机译:1,4-双[5-(5-巯基-1,3,4-恶二唑-2-基-甲基)-硫代-4-取代的1,2,4-三唑--3-基的新系列]-丁烷7-12和1,4-双[5-(1-氧-1-(3,5二甲基吡唑-1-基)-甲基)-硫代-4-取代-1,2,4-三唑由1,4-双(5 [肼基羰基甲硫基] -4-取代的1,2,4-三唑-3-基)丁烷基衍生物合成1-6,制备了-3--3-基]-丁烷13-18。所有合成的化合物都通过IR,NMR和质谱研究进行了表征。使用标准的MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑鎓溴化物)测定法针对一组三种人类癌细胞系筛选合成的化合物7-18的体外细胞毒性:肺癌A-549,结肠癌HT-29和乳腺癌MDA MB-231。通过吸收滴定法对三种有效分子进行了DNA结合研究。

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