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British Journal of Pharmacology
|
February 14, 2012
Functional efficacy of adenosine A₂A receptor agonists is positively correlated to their receptor residence time
Dong Guo, Thea Mulder-Krieger, Adriaan P IJzerman, et al.
Biochemical Pharmacology
|
August 12, 2009
The endocannabinoid 2-arachidonylglycerol is a negative allosteric modulator of the human A3 adenosine receptor
J Robert Lane, Margot W Beukers, Thea Mulder-Krieger, et al.
Chembiochem : a European Journal of Chemical Biology
|
August 30, 2017
A New Class of Fluorinated A<sub>2A</sub> Adenosine Receptor Agonist with Application to Last-Step Enzymatic [<sup>18</sup> F]Fluorination for PET Imaging
Phillip T Lowe, Sergio Dall'Angelo, Thea Mulder-Krieger, et al.
European Journal of Medicinal Chemistry
|
October 9, 2016
Synthesis and evaluation of N-substituted 2-amino-4,5-diarylpyrimidines as selective adenosine A<sub>1</sub> receptor antagonists
Georgios Alachouzos, Eelke B Lenselink, Thea Mulder-Krieger, et al.
Chemmedchem
|
October 25, 2011
Substructure-based virtual screening for adenosine A2A receptor ligands
Eelke van der Horst, Rianne van der Pijl, Thea Mulder-Krieger, et al.
Bioorganic & Medicinal Chemistry
|
February 25, 2005
Synthesis and biological evaluation of 2-aminothiazoles and their amide derivatives on human adenosine receptors. Lack of effect of 2-aminothiazoles as allosteric enhancers
Anikó Göblyös, Sabrina Neves Santiago, Daniele Pietra, et al.
British Journal of Pharmacology
|
January 31, 2006
Allosteric modulation, thermodynamics and binding to wild-type and mutant (T277A) adenosine A1 receptors of LUF5831, a novel nonadenosine-like agonist
Laura H Heitman, Thea Mulder-Krieger, Ronald F Spanjersberg, et al.
Journal of Medicinal Chemistry
|
May 12, 2006
2,6-disubstituted and 2,6,8-trisubstituted purines as adenosine receptor antagonists
Lisa C W Chang, Ronald F Spanjersberg, Jacobien K von Frijtag Drabbe Künzel, et al.
Journal of Medicinal Chemistry
|
February 16, 2007
2,6,8-trisubstituted 1-deazapurines as adenosine receptor antagonists
Lisa C W Chang, Jacobien K von Frijtag Drabbe Künzel, Thea Mulder-Krieger, et al.
European Journal of Medicinal Chemistry
|
July 27, 2015
Structure-kinetics relationships of Capadenoson derivatives as adenosine A1 receptor agonists
Julien Louvel, Dong Guo, Marjolein Soethoudt, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
British Journal of Pharmacology
|
February 14, 2012
Functional efficacy of adenosine A₂A receptor agonists is positively correlated to their receptor residence time
Dong Guo, Thea Mulder-Krieger, Adriaan P IJzerman, et al.
Biochemical Pharmacology
|
August 12, 2009
The endocannabinoid 2-arachidonylglycerol is a negative allosteric modulator of the human A3 adenosine receptor
J Robert Lane, Margot W Beukers, Thea Mulder-Krieger, et al.
Chembiochem : a European Journal of Chemical Biology
|
August 30, 2017
A New Class of Fluorinated A<sub>2A</sub> Adenosine Receptor Agonist with Application to Last-Step Enzymatic [<sup>18</sup> F]Fluorination for PET Imaging
Phillip T Lowe, Sergio Dall'Angelo, Thea Mulder-Krieger, et al.
European Journal of Medicinal Chemistry
|
October 9, 2016
Synthesis and evaluation of N-substituted 2-amino-4,5-diarylpyrimidines as selective adenosine A<sub>1</sub> receptor antagonists
Georgios Alachouzos, Eelke B Lenselink, Thea Mulder-Krieger, et al.
Chemmedchem
|
October 25, 2011
Substructure-based virtual screening for adenosine A2A receptor ligands
Eelke van der Horst, Rianne van der Pijl, Thea Mulder-Krieger, et al.
Bioorganic & Medicinal Chemistry
|
February 25, 2005
Synthesis and biological evaluation of 2-aminothiazoles and their amide derivatives on human adenosine receptors. Lack of effect of 2-aminothiazoles as allosteric enhancers
Anikó Göblyös, Sabrina Neves Santiago, Daniele Pietra, et al.
British Journal of Pharmacology
|
January 31, 2006
Allosteric modulation, thermodynamics and binding to wild-type and mutant (T277A) adenosine A1 receptors of LUF5831, a novel nonadenosine-like agonist
Laura H Heitman, Thea Mulder-Krieger, Ronald F Spanjersberg, et al.
Journal of Medicinal Chemistry
|
May 12, 2006
2,6-disubstituted and 2,6,8-trisubstituted purines as adenosine receptor antagonists
Lisa C W Chang, Ronald F Spanjersberg, Jacobien K von Frijtag Drabbe Künzel, et al.
Journal of Medicinal Chemistry
|
February 16, 2007
2,6,8-trisubstituted 1-deazapurines as adenosine receptor antagonists
Lisa C W Chang, Jacobien K von Frijtag Drabbe Künzel, Thea Mulder-Krieger, et al.
European Journal of Medicinal Chemistry
|
July 27, 2015
Structure-kinetics relationships of Capadenoson derivatives as adenosine A1 receptor agonists
Julien Louvel, Dong Guo, Marjolein Soethoudt, et al.
Page
of 3