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4-amido-2-aryl-1,2,4-triazolo[4,3-a]quinoxalin-1-ones as new potent and selective human A3 adenosine receptor antagonists. synthesis, pharmacological evaluation, and ligand-receptor modeling studies.
J Med Chem. 2006 Jun 29;49(13):3916-25. doi: 10.1021/jm060373w.
J Med Chem. 2006.
PMID: 16789747
Synthesis and quantitative structure-activity relationships of selective BCRP inhibitors.
Marighetti F, Steggemann K, Hanl M, Wiese M.
Marighetti F, et al.
ChemMedChem. 2013 Jan;8(1):125-35. doi: 10.1002/cmdc.201200377. Epub 2012 Nov 13.
ChemMedChem. 2013.
PMID: 23150210
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Interactions of the multidrug resistance modulators tariquidar and elacridar and their analogues with P-glycoprotein.
Pajeva IK, Sterz K, Christlieb M, Steggemann K, Marighetti F, Wiese M.
Pajeva IK, et al. Among authors: marighetti f.
ChemMedChem. 2013 Oct;8(10):1701-13. doi: 10.1002/cmdc.201300233. Epub 2013 Aug 13.
ChemMedChem. 2013.
PMID: 23943604
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Scaffold identification of a new class of potent and selective BCRP inhibitors.
Marighetti F, Steggemann K, Karbaum M, Wiese M.
Marighetti F, et al.
ChemMedChem. 2015 Apr;10(4):742-51. doi: 10.1002/cmdc.201402498. Epub 2015 Mar 3.
ChemMedChem. 2015.
PMID: 25735648
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