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新型具有抗增殖活性的 1,2,4-三嗪衍生物的合成与表征。

Synthesis and characterization of novel 1,2,4-triazine derivatives with antiproliferative activity.

机构信息

Institute of Pharmacy, Martin-Luther-Universität Halle-Wittenberg, 06120 Halle, Germany.

出版信息

Bioorg Med Chem. 2010 Mar 1;18(5):1816-21. doi: 10.1016/j.bmc.2010.01.053. Epub 2010 Jan 25.

Abstract

A series of novel small molecules with a 1,2,4-triazine scaffold was obtained according to a recently published and highly efficient synthetic route. Screening for antiproliferative and cytotoxic activity revealed distinct anticancer effects against the human leukemia cell line K-562 combined with a remarkable low cytotoxicity. All compounds were in agreement with the 'rule-of-five' claims by Lipinski and calculated logP(calc) values were experimentally confirmed (logP(exp)). For the most active compounds, in vitro serum albumin binding was investigated and structure-activity relationships were established.

摘要

根据最近发表的一种高效合成路线,获得了一系列具有 1,2,4-三嗪骨架的新型小分子。对增殖抑制和细胞毒性活性的筛选显示,这些化合物对人白血病细胞系 K-562 具有明显的抗癌作用,同时具有显著的低细胞毒性。所有化合物均符合 Lipinski 的“五规则”要求,计算的 logP(calc) 值得到了实验验证(logP(exp))。对最活跃的化合物进行了体外血清白蛋白结合的研究,并建立了构效关系。

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