Literature DB >> 17533131

Structure-activity relationships of novel N-acyloxy-1,4-dihydropyridines as P-glycoprotein inhibitors.

Burkhardt Voigt1, Claudius Coburger, Joséf Monár, Andreas Hilgeroth.   

Abstract

Series of novel N-acyloxy-1,4-dihydropyridines have been synthesized and evaluated as P-glycoprotein inhibitors in an in vitro assay to estimate their potential to act as multidrug resistance modulators in cancer cells. Structure-activity relationships are discussed and prove a significant and regiospecific influence of certain functional groups.

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Year:  2007        PMID: 17533131     DOI: 10.1016/j.bmc.2007.05.036

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  2 in total

1.  Synthetic Utility of Epoxides for Chiral Functionalization of Isoxazoles.

Authors:  Jared K Nelson; Christopher T Burns; Miles P Smith; Brendan Twamley; N R Natale
Journal:  Tetrahedron Lett       Date:  2008-05-05       Impact factor: 2.415

2.  Fluorescent probes of the isoxazole-dihydropyridine scaffold: MDR-1 binding and homology model.

Authors:  Monika I Szabon-Watola; Sarah V Ulatowski; Kathleen M George; Christina D Hayes; Scott A Steiger; Nicholas R Natale
Journal:  Bioorg Med Chem Lett       Date:  2013-12-04       Impact factor: 2.823

  2 in total

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