首页> 美国卫生研究院文献>Springer Open Choice >Synthesis of 5-arylidine amino-134-thiadiazol-2-(N-substituted benzyol)sulphonamides endowed with potent antioxidants and anticancer activity induces growth inhibition in HEK293 BT474 and NCI-H226 cells
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Synthesis of 5-arylidine amino-134-thiadiazol-2-(N-substituted benzyol)sulphonamides endowed with potent antioxidants and anticancer activity induces growth inhibition in HEK293 BT474 and NCI-H226 cells

机译:具有强效抗氧化剂和抗癌活性的5-芳基氨基-134-噻二唑-2-(N-取代的苯甲醛)磺酰胺的合成诱导HEK293BT474和NCI-H226细胞的生长抑制

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摘要

AbstractA series of imines 5-amino-1,3,4-thiadiazol-2-[(N-substituted benzyol)]sulphonamide derivatives were synthesized from various aromatic aldehydes and substituted with benzoyl acetazolamides under different reaction conditions and were evaluated for their antioxidant and free radical scavenging, antimitotic activity by Allium cepa meristem root model and cytotoxicity activity against HEK 293 (human epidermal kidney cell line), BT474 (breast cancer cell line) and NCI-H226 (lung cancer cell line) by MTT assay. Some of the synthesized compounds showed moderately potent cytotoxicity compared to indisulam.
机译:摘要从各种芳族醛中合成了一系列亚胺5-氨基-1,3,4-噻二唑-2-[(N-取代的苯甲醛)]磺酰胺衍生物,并在不同的反应条件下用苯甲酰基乙酰唑酰胺取代,并对其抗氧化剂和抗氧化剂进行了评估。通过MTT法测定洋葱清除能力,洋葱头皮分生组织根模型的抗有丝分裂活性以及对HEK 293(人表皮肾细胞系),BT474(乳腺癌细胞系)和NCI-H226(肺癌细胞系)的细胞毒性活性。与靛蓝相比,一些合成的化合物显示出中等有效的细胞毒性。

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