12 articles for T Mulder-Krieger
The following articles (labelled with PubMed ID or TBD) are for your review
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Synthesis and evaluation of N-substituted 2-amino-4,5-diarylpyrimidines as selective adenosine A

Leiden University
Structure-kinetics relationships of Capadenoson derivatives as adenosine A1 receptor agonists.

Leiden University
Identifying novel adenosine receptor ligands by simultaneous proteochemometric modeling of rat and human bioactivity data.

Leiden/Amsterdam Center For Drug Research
2-Amino-6-furan-2-yl-4-substituted nicotinonitriles as A2A adenosine receptor antagonists.

Leiden/Amsterdam Center For Drug Research
A new generation of adenosine receptor antagonists: from di- to trisubstituted aminopyrimidines.

Leiden/Amsterdam Center For Drug Research
A series of ligands displaying a remarkable agonistic-antagonistic profile at the adenosine A1 receptor.

Leiden/Amsterdam Center For Drug Research
New, non-adenosine, high-potency agonists for the human adenosine A2B receptor with an improved selectivity profile compared to the reference agonist N-ethylcarboxamidoadenosine.

University of Leiden
A series of 2,4-disubstituted quinolines as a new class of allosteric enhancers of the adenosine A3 receptor.

Leiden University
2,6,8-trisubstituted 1-deazapurines as adenosine receptor antagonists.

Leiden/Amsterdam Center For Drug Research
2,6-disubstituted and 2,6,8-trisubstituted purines as adenosine receptor antagonists.

Leiden/Amsterdam Center For Drug Research
2,4,6-trisubstituted pyrimidines as a new class of selective adenosine A1 receptor antagonists.

Leiden/Amsterdam Center For Drug Research
Discovery and Kinetic Profiling of 7-Aryl-1,2,4-triazolo[4,3-a]pyridines: Positive Allosteric Modulators of the Metabotropic Glutamate Receptor 2.

Leiden University