| Literature DB >> 25311564 |
Aivars Krauze1, Signe Grinberga2, Laura Krasnova2, Ilze Adlere2, Elina Sokolova2, Ilona Domracheva2, Irina Shestakova2, Zigmars Andzans2, Gunars Duburs2.
Abstract
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 structure-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 Ca(2+) 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 μM, MRP1 inhibitory action with EC50 = 1.1 ± 0.1 μM and BCRP1 inhibitory action with EC50 = 0.2 ± 0.05 μM and may represent suitable candidate for further pharmacological studies.Entities:
Keywords: Breast cancer resistance protein; Multidrug resistance modulators; Multidrug resistance-associated protein; P-glycoprotein; Thieno[2,3-b]pyridine
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Year: 2014 PMID: 25311564 DOI: 10.1016/j.bmc.2014.09.023
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641