Design and Efficient Synthesis of Novel 4,5-Dimethylthiazole-Hydrazone Derivatives and their Anticancer Activity
作者:Asaf Evrim Evren、Leyla Yurttaş、Büşra Ekselli、Onur Aksoy、Gülşen Akalin-Çiftçi
DOI:10.2174/1570180817999201022192937
日期:2021.4
this purpose, our research group designed and synthesized novel 4,5-dimethyl thiazole-hydrazone derivatives which were tested against cancer and normal cell lines to understand the structureactivity relationship (SAR). Methods: The lead compounds were obtained by reacting 2-(substituted aryl-2-ylmethylene) hydrazin-1-carbothioamide with 3-chloro-2-butanone derivatives. The structural elucidation of the
背景:最近,研究人员已警告各种癌症类型的死亡率增加。而且,由于晚期或错误的诊断和/或不足的治疗方法,肺腺癌和神经胶质瘤类型是世界健康的迫在眉睫的问题。为此,我们的研究小组设计并合成了新颖的4,5-二甲基噻唑-衍生物,并对其进行了抗癌和正常细胞株测试,以了解其结构活性关系(SAR)。方法:通过使2-(取代的芳基-2-基亚甲基)肼-1-碳硫酰胺与3-氯-2-丁酮衍生物反应制得先导化合物。通过1 H-NMR,13 C-NMR和LC / MS-IT-TOF光谱和元素分析进行化合物的结构阐明。体外测试了合成的化合物对A549人肺腺癌和C6大鼠神经胶质瘤细胞的抗癌活性,并研究了诱导细胞死亡的途径。此外,完成了对活性化合物的对接研究,以了解SAR。