首页> 外文期刊>Der Pharma Chemica: journal for medicinal chemistry, pharmaceutical chemistry and computational chemistry >Synthesis and antitumor activity of some new N-substituted-sulfonyl, 1,2,4-triazole, N-substituted-benzylidene and pyrrole derivatives attached to 4-(benzo[d]thiazol-2-yl)benzohydrazide
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Synthesis and antitumor activity of some new N-substituted-sulfonyl, 1,2,4-triazole, N-substituted-benzylidene and pyrrole derivatives attached to 4-(benzo[d]thiazol-2-yl)benzohydrazide

机译:与4-(苯并[d]噻唑-2-基)苯并酰肼连接的一些新的N-取代磺酰基,1,2,4-三唑,N-取代亚苄基和吡咯衍生物的合成及抗肿瘤活性

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摘要

Some N-substituted-sulfonyl, 1,2,4-triazole, N-substituted-benzylidene and pyrrole derivatives attached to 4-(benzo[d]thiazol-2-yl)benzohydrazide were prepared starting from oaminothiophenol 1 by reacting with different electrophilic and nucleophilic reagents. Some of the newly synthesized compounds have been evaluated for their potential cytotoxicity against breast cancer cell line (MCF7), compound 12a exhibited the highest activity.
机译:从邻氨基苯硫酚1开始,通过与不同的亲电试剂反应,制备了一些与4-(苯并[d]噻唑-2-基)苯并酰肼连接的N-取代的磺酰基,1,2,4-三唑,N-取代的亚苄基和吡咯衍生物和亲核试剂。已经评估了一些新合成的化合物对乳腺癌细胞系(MCF7)的潜在细胞毒性,化合物12a表现出最高的活性。

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