Thieno[2,3-b]pyridines-A new class of multidrug resistance (MDR) modulators

被引:37
|
作者
Krauze, Aivars [1 ]
Grinberga, Signe [1 ]
Krasnova, Laura [1 ]
Adlere, Ilze [1 ]
Sokolova, Elina [1 ]
Domracheva, Ilona [1 ]
Shestakova, Irina [1 ]
Andzans, Zigmars [1 ]
Duburs, Gunars [1 ]
机构
[1] Latvian Inst Organ Synth, LV-1006 Riga, Latvia
关键词
Thieno[2,3-b]pyridine; Multidrug resistance modulators; P-glycoprotein; Multidrug resistance-associated protein; Breast cancer resistance protein; P-GLYCOPROTEIN; DERIVATIVES; INHIBITORS; THIENOPYRIDINE; AGENTS; REVERSAL; PROTEIN; DESIGN; BCRP; ABC;
D O I
10.1016/j.bmc.2014.09.023
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
To identify new potent multidrug resistance modulators, we have synthesized a series of novel thieno[ 2,3-b]pyridines and furo[2,3-b] pyridines, and examined their stucture-activity relationships. All synthesized compounds were tested to determine BCRP1, P-gp, and MRP1 inhibitor activity, and most potent MDR modulators were also screened for their toxicity, cytotoxicity and Ca2+ channel antagonist activity. Among these compounds, thieno[2,3-b] pyridine (6r) was found to exhibit a potent P-gp inhibitory action with EC50 = 0.3 +/- 0.2 mu M, MRP1 inhibitory action with EC50 = 1.1 +/- 0.1 mu M and BCRP1 inhibitory action with EC50 = 0.2 +/- 0.05 mu M and may represent suitable candidate for further pharmacological studies. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5860 / 5870
页数:11
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