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Synthesis of 2-alkylthio- N-(quinazolin-2-yl)benzenesulfonamide derivatives: anticancer activity, QSAR studies, and metabolic stability

机译:2-烷硫基的合成 - <重点型=“斜体”> n - (喹唑啉-2-基)苯磺胺酰胺衍生物:抗癌活性,QSAR研究和代谢稳定性

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摘要

A new series of 2-alkylthio- N -(quinazolin-2-yl)benzenesulfonamide derivatives have been synthesized and evaluated in vitro for their antiproliferative activity by MTT assay against cancer cell lines HCT-116, MCF-7, and HeLa as well as the NCI-60 human tumor cell lines screen. In NCI screen, three compounds inhibited approximately 50% growth of RPMI-8226 and A549/ATCC cell lines. The mean of IC~(50)calculated in MTT assays for three tested cell lines was about 45?μM for four compounds. The QSAR allowed finding statistically significant OPLS models for HeLa cell line. Metabolic stability in vitro studies indicated favorable and unfavorable structural elements. The good metabolic stability, with t ~(1/2)higher than 40?min, was observed for three derivatives, which together with their antiproliferative activity and good ADMET profile, makes them good leading structures for further research. Graphical abstract.
机译:已经合成了一种新的2-烷基硫基-N-(喹唑啉-2-基)苯磺胺酰胺衍生物,并通过MTT测定对癌细胞系HCT-116,MCF-7和HELA的抗增殖活性进行抗增殖活性。 NCI-60人肿瘤细胞系筛网。 在NCI筛选中,三种化合物抑制RPMI-8226和A549 / ATCC细胞系的约50%。 对于四个测试细胞系的MTT测定中计算的IC〜(50)的平均值为4个化合物为约45Ωμm。 QSAR允许查找Hela Cell系列的统计显着的OPLS模型。 体外研究的代谢稳定表明了有利和不利的结构元素。 对于三种衍生物观察到高于40Ω分钟的良好的代谢稳定性,与其抗增殖活动和良好的呼叫概况一起,使其成为进一步研究的良好领导结构。 图形概要。

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