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European Journal of Medicinal Chemistry
|
August 26, 2017
Synthesis and biological investigation of 2,4-substituted quinazolines as highly potent inhibitors of breast cancer resistance protein (ABCG2)
Michael K Krapf, Jennifer Gallus, Michael Wiese
Biochimica Et Biophysica Acta. Biomembranes
|
November 5, 2016
Pyrrolopyrimidine derivatives and purine analogs as novel activators of Multidrug Resistance-associated Protein 1 (MRP1, ABCC1)
Sven Marcel Schmitt, Katja Stefan, Michael Wiese
Journal of Medicinal Chemistry
|
March 5, 2016
Pyrrolopyrimidine Derivatives as Novel Inhibitors of Multidrug Resistance-Associated Protein 1 (MRP1, ABCC1)
Sven Marcel Schmitt, Katja Stefan, Michael Wiese
Molecular Informatics
|
July 29, 2016
A Microarray Tool Provides Pathway and GO Term Analysis
Martin Koch, Hans-Dieter Royer, Michael Wiese
Chemmedchem
|
January 5, 2008
Identification of putative binding sites of P-glycoprotein based on its homology model
Christoph Globisch, Ilza K Pajeva, Michael Wiese
Bioorganic & Medicinal Chemistry
|
November 25, 2011
Investigation of chalcones and benzochalcones as inhibitors of breast cancer resistance protein
Kapil Juvale, Veronika F S Pape, Michael Wiese
Chemmedchem
|
March 5, 2015
Scaffold identification of a new class of potent and selective BCRP inhibitors
Federico Marighetti, Kerstin Steggemann, Maria Karbaum, et al.
Chemmedchem
|
November 15, 2012
Synthesis and quantitative structure-activity relationships of selective BCRP inhibitors
Federico Marighetti, Kerstin Steggemann, Markus Hanl, et al.
International Journal of Clinical Pharmacology and Therapeutics
|
December 25, 2012
Are low molecular weight heparins able to sensitize chemoresistant tumor cells?
Daniel P Stölting, Ulrich Jaehde, Michael Wiese, et al.
Journal of Medicinal Chemistry
|
August 5, 2018
2,4,6-Substituted Quinazolines with Extraordinary Inhibitory Potency toward ABCG2
Michael K Krapf, Jennifer Gallus, Vigneshwaran Namasivayam, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 119) with videos related to
Sort By:
Page
of 12
European Journal of Medicinal Chemistry
|
August 26, 2017
Synthesis and biological investigation of 2,4-substituted quinazolines as highly potent inhibitors of breast cancer resistance protein (ABCG2)
Michael K Krapf, Jennifer Gallus, Michael Wiese
Biochimica Et Biophysica Acta. Biomembranes
|
November 5, 2016
Pyrrolopyrimidine derivatives and purine analogs as novel activators of Multidrug Resistance-associated Protein 1 (MRP1, ABCC1)
Sven Marcel Schmitt, Katja Stefan, Michael Wiese
Journal of Medicinal Chemistry
|
March 5, 2016
Pyrrolopyrimidine Derivatives as Novel Inhibitors of Multidrug Resistance-Associated Protein 1 (MRP1, ABCC1)
Sven Marcel Schmitt, Katja Stefan, Michael Wiese
Molecular Informatics
|
July 29, 2016
A Microarray Tool Provides Pathway and GO Term Analysis
Martin Koch, Hans-Dieter Royer, Michael Wiese
Chemmedchem
|
January 5, 2008
Identification of putative binding sites of P-glycoprotein based on its homology model
Christoph Globisch, Ilza K Pajeva, Michael Wiese
Bioorganic & Medicinal Chemistry
|
November 25, 2011
Investigation of chalcones and benzochalcones as inhibitors of breast cancer resistance protein
Kapil Juvale, Veronika F S Pape, Michael Wiese
Chemmedchem
|
March 5, 2015
Scaffold identification of a new class of potent and selective BCRP inhibitors
Federico Marighetti, Kerstin Steggemann, Maria Karbaum, et al.
Chemmedchem
|
November 15, 2012
Synthesis and quantitative structure-activity relationships of selective BCRP inhibitors
Federico Marighetti, Kerstin Steggemann, Markus Hanl, et al.
International Journal of Clinical Pharmacology and Therapeutics
|
December 25, 2012
Are low molecular weight heparins able to sensitize chemoresistant tumor cells?
Daniel P Stölting, Ulrich Jaehde, Michael Wiese, et al.
Journal of Medicinal Chemistry
|
August 5, 2018
2,4,6-Substituted Quinazolines with Extraordinary Inhibitory Potency toward ABCG2
Michael K Krapf, Jennifer Gallus, Vigneshwaran Namasivayam, et al.
Page
of 12