13 articles for H de Vries
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Synthesis and evaluation of N-substituted 2-amino-4,5-diarylpyrimidines as selective adenosine A

Leiden University
When structure-affinity relationships meet structure-kinetics relationships: 3-((Inden-1-yl)amino)-1-isopropyl-cyclopentane-1-carboxamides as CCR2 antagonists.

Leiden University
Design and synthesis of novel small molecule CCR2 antagonists: evaluation of 4-aminopiperidine derivatives.

TBA
Agonists for the adenosine A1 receptor with tunable residence time. A Case for nonribose 4-amino-6-aryl-5-cyano-2-thiopyrimidines.

Leiden University
Structure-kinetic relationships--an overlooked parameter in hit-to-lead optimization: a case of cyclopentylamines as chemokine receptor 2 antagonists.

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

Leiden/Amsterdam Center For Drug Research
A prospective cross-screening study on G-protein-coupled receptors: lessons learned in virtual compound library design.

Radboud University Nijmegen Medical Centre
2-Amino-6-furan-2-yl-4-substituted nicotinonitriles as A2A adenosine receptor antagonists.

Leiden/Amsterdam Center For Drug Research
A series of 2,4-disubstituted quinolines as a new class of allosteric enhancers of the adenosine A3 receptor.

Leiden University
Substituted terphenyl compounds as the first class of low molecular weight allosteric inhibitors of the luteinizing hormone receptor.

Leiden University
Synthesis and biological evaluation of a new series of 2,3,5-substituted [1,2,4]-thiadiazoles as modulators of adenosine A1 receptors and their molecular mechanism of action.

Leiden/Amsterdam Center For Drug Research
Synthesis and biological evaluation of chemokine receptor ligands with 2-benzazepine scaffold.

Universit£T M£Nster
Structure-Affinity Relationships and Structure-Kinetic Relationships of 1,2-Diarylimidazol-4-carboxamide Derivatives as Human Cannabinoid 1 Receptor Antagonists.

Leiden University