Discovery and SAR studies of a novel class of cytotoxic 1,4-disubstituted piperidines via Ugi reaction

被引：10

作者：

de Castro, Sonia ^{[1
]}

Camarasa, Maria-Jose ^{[1
]}

Balzarini, Jan ^{[2
]}

Velazquez, Sonsoles ^{[1
]}

机构：

[1] CSIC, Inst Quim Med, E-28006 Madrid, Spain

[2] Katholieke Univ Leuven, Rega Inst Med Res, B-3000 Leuven, Belgium

来源：

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY | 2014年 / 83卷

关键词：

Disubstituted piperidines; Ugi reaction; Anticancer; Structure-activity relationships; MULTICOMPONENT REACTIONS; 4-COMPONENT REACTION; CHEMISTRY; KETONES; ANTIBACTERIAL; CONDENSATION; DERIVATIVES;

D O I：

10.1016/j.ejmech.2014.06.026

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

Herein we report a novel class of 1,4-disubstituted piperidines as potential anticancer agents. One-step and efficient synthesis of a structurally diverse library of piperidine-based analogs with five points of diversity has been developed using the Ugi four-component reaction. A structure-activity relationship (SAR) study showed that the presence of a benzyl or a Boc group at the N-1 position together with two or three aromatic groups at the C-4 position of the piperidine ring are important for optimal cytostatic properties. Compounds 20, 22, 27 and 29 were found to be the most potent with a 50% inhibitory concentration (IC50) ranging between 3 and 9.5 mu M in the cancer cell lines evaluated. The NCI60 screen confirmed this 50% cytostatic concentration range for compound 20, irrespective of the nature of the tumor cell lines evaluated. The NCI COMPARE algorithm did not show any significant correlation between the growth inhibition profile of compound 20 with the NCI database compound profiles suggesting a potential novel mechanism of action. (C) 2014 Elsevier Masson SAS. All rights reserved.

引用

收藏

页码：174 / 189

页数：16

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