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

被引:83
|
作者
Krauth, Fabian [1 ]
Dahse, Hans-Martin [2 ]
Ruettinger, Hans-Hermann [1 ]
Frohberg, Petra [1 ]
机构
[1] Univ Halle Wittenberg, Inst Pharm, D-06120 Halle, Germany
[2] HKI, Leibniz Inst Nat Prod Res & Infect Biol, D-07745 Jena, Germany
关键词
1,2,4-triazin-5-ones; Small molecules; Leukemia; K-562; Rule-of-five; log P; Imatinib; Serum albumin binding; HUMAN SERUM-ALBUMIN; 5-LIPOXYGENASE INHIBITORS; ARYLHYDRAZONIC ACIDS; PROTEIN-BINDING; AGENTS; DRUGS; IDENTIFICATION; ANTIBACTERIAL; AMIDRAZONES; CYCLIZATION;
D O I
10.1016/j.bmc.2010.01.053
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 log P(calc) values were experimentally confirmed (log P(exp)). For the most active compounds, in vitro serum albumin binding was investigated and structure-activity relationships were established. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1816 / 1821
页数:6
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