Structure–Activity Relationships of Tariquidar Analogs as Multidrug Resistance Modulators

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Structure–Activity Relationships of Tariquidar Analogs as Multidrug Resistance Modulators

Journal Title: The AAPS Journal - Year 2009, Vol 11, Issue 3

Abstract

The review summarizes the most recent achievements in structure–activity relationship (SAR) studies of tariquidar and its analogs. Tariquidar is one of the most promising representatives of the third generation of multidrug resistance (MDR) modulators created so far. This fact determines the strong interest of different research groups in the development of tariquidar-like structures as selective inhibitors of MDR transporters in resistant human cancer cells. After the discovery of tariquidar, a number of analogs have been synthesized and pharmacologically tested, thus supplying good data for comprehensive analyses of their structure–activity relationships. In the review, the structural and pharmacological data of newly synthesized tariquidar-like compounds are first presented. Next, the main achievements in the SAR studies are described focusing on two main transport proteins: P-glycoprotein and breast cancer resistance protein. The reported results are discussed from the point of view of their significance and importance for future directions in the rational design of effective MDR modulators.

Authors and Affiliations

Ilza K. Pajeva, Michael Wiese

Keywords

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The online version of this article (doi:10.1208/s12248-014-9669-5) contains supplementary material, which is available to authorized users.

EP ID EP681495
DOI 10.1208/s12248-009-9118-z
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