首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Thee-component, one-pot synthesis of hexahydroazepino [3,4-b]indole and tetrahydro-1H-pyrido[3,4-b]indole derivatives and evaluation of their cytotoxicity
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Thee-component, one-pot synthesis of hexahydroazepino [3,4-b]indole and tetrahydro-1H-pyrido[3,4-b]indole derivatives and evaluation of their cytotoxicity

机译:一锅法合成六氢氮杂环庚烷[3,4-b]吲哚和四氢-1H-吡啶并[3,4-b]吲哚衍生物及其细胞毒性

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摘要

A three-component, four-center Ugi reaction has been developed to produce a novel class of 2-aryl-3-oxo-hexahydroazepino[3,4-b]indole and 2-aryl-3-oxo-tetrahydro-1H-pyrido[3,4-b]indole derivatives in good to high yields. A few of them exhibit moderate cytotoxicity against various cancer cell lines such as HeLa (human epithelial cervical cancer), A549 (human lung carcinoma epithelial), DU145 (human prostate carcinoma epithelial) and MCF-7 (human breast adenocarcinoma). (C) 2014 Published by Elsevier Ltd.
机译:已经开发了一种三组分,四中心的Ugi反应,以产生一类新型的2-芳基-3-氧代-六氢氮杂环庚烷[3,4-b]吲哚和2-芳基-3-氧代-四氢-1H-吡啶基[3,4-b]吲哚衍生物的产率高至高。它们中的一些对各种癌细胞系表现出中等的细胞毒性,例如HeLa(人类上皮宫颈癌),A549(人类肺癌上皮),DU145(人类前列腺癌上皮)和MCF-7(人类乳腺腺癌)。 (C)2014由Elsevier Ltd.出版

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