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Synthesis of novel 2-alkyl triazole-3-alkyl substituted quinoline derivatives and their cytotoxic activity

机译:新型2-烷基三唑-3-烷基取代喹啉衍生物的合成及其细胞毒性活性

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摘要

The propargyl alcohol on reaction with alkylazides under Sharpless conditions through click chemistry concept gave exclusively 1,4-disubstituted triazoles 2. The compounds 2 were oxidized to aldehydes 3 followed by reaction with aniline resulted Schiff's bases 4. The compounds 4 was further reacted with various aldehydes having ??-hydrogen using molecular iodine as a catalyst and obtained 2-alkyl triazole-3-alkyl substituted quinoline derivatives 5. All the final compounds were screened against four human cancer cell lines (THP-1, Colo205, U937 & HeLa) and promising compounds have been identified. ? 2012 Elsevier Ltd. All rights reserved.
机译:通过点击化学概念在无价值的条件下与烷基氮杂物反应的丙基醇完全产生1,4-二取代的三唑。化合物2被氧化成醛3,然后与苯胺的反应产生的Schiff的碱基4.化合物4进一步与各种反应 使用分子碘作为催化剂的醛与催化剂,得到2-烷基三唑-3-烷基取代的喹啉衍生物5.所有最终化合物均针对四种人癌细胞系(THP-1,Colo205,U937和HeRa)筛选 已经确定了有希望的化合物。 还 2012年elestvier有限公司保留所有权利。

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    Fluoro Organic Division Indian Institute of Chemical Technology Hyderabad 500 607 India;

    Fluoro Organic Division Indian Institute of Chemical Technology Hyderabad 500 607 India;

    Fluoro Organic Division Indian Institute of Chemical Technology Hyderabad 500 607 India;

    Fluoro Organic Division Indian Institute of Chemical Technology Hyderabad 500 607 India;

    Fluoro Organic Division Indian Institute of Chemical Technology Hyderabad 500 607 India;

    Biology Division Indian Institute of Chemical Technology Tarnaka Hyderabad 500 607 India;

    Biology Division Indian Institute of Chemical Technology Tarnaka Hyderabad 500 607 India;

    Fluoro Organic Division Indian Institute of Chemical Technology Hyderabad 500 607 India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

    Alkyl azides; Cytotoxic activity; Jones reagent; Quinoline;

    机译:烷基叠氮化物;细胞毒性活性;琼斯试剂;喹啉;

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