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新型2,4-二氨基-1,3,5-三嗪衍生物的合成、结构表征及抗肿瘤活性

Synthesis, structural characterization and antitumor activity of novel 2,4-diamino-1,3,5-triazine derivatives.

作者信息

Brzozowski Z, Saczewski F, Gdaniec M

机构信息

Department of Chemical Technology of Drugs, Medical University of Gdańsk, Poland.

出版信息

Eur J Med Chem. 2000 Dec;35(12):1053-64. doi: 10.1016/s0223-5234(00)01194-6.

Abstract

The syntheses, structural elucidation based on NMR spectroscopy and X-ray analysis of 8 as well as antitumor activities of novel 2,4-diamino-1,3,5-triazine derivatives 5 and 7-22 are described. Screenings performed at NCI showed that most derivatives possessed a moderate to strong growth inhibition activity on various tumor panel cell lines between 0.148 and 56.2 microM concentrations. 2-Amino-6-bromomethyl-4-(3,5,5-trimethyl-2-pyrazoline)-1,3,5-triazine 11 showed the most potent antitumor activity with the mean midpoint values of log(10) GI50, log(10) TGI50 and log(10) LC50 of all tests equal to -5.26, -4.81 and -4.37, respectively and therefore, it can be considered as a lead structure for further development of anticancer agents.

摘要

本文描述了新型2,4-二氨基-1,3,5-三嗪衍生物5以及7-22的合成、基于核磁共振光谱和X射线分析的结构解析,以及其抗肿瘤活性。美国国立癌症研究所(NCI)进行的筛选表明,大多数衍生物在0.148至56.2微摩尔浓度之间对各种肿瘤细胞系具有中度至强的生长抑制活性。2-氨基-6-溴甲基-4-(3,5,5-三甲基-2-吡唑啉)-1,3,5-三嗪11表现出最强的抗肿瘤活性,所有测试的log(10) GI50、log(10) TGI50和log(10) LC50的平均中点值分别为-5.26、-4.81和-4.37,因此,它可被视为进一步开发抗癌药物的先导结构。

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