Comparison of the binding and functional properties of two structurally different D2 dopamine receptor subtype selective compounds

Keyphrases

• 2,3-dihydroquinazoline-4(1H)-one 25%
• Adenylyl Cyclase 50%
• Aripiprazole 25%
• Binding Properties 100%
• Binding Selectivity 75%
• Cell-based 25%
• Channel Activation 25%
• Chemical Classes 25%
• Computer Modeling 25%
• D2 Dopamine Receptor 100%
• D2 Receptor 50%
• D2-like 25%
• D3 Dopamine Receptor 100%
• D3 Receptor 25%
• Dopamine Receptor 100%
• ERK2 25%
• Functional Properties 100%
• G Protein-coupled 25%
• GIRK Channel 25%
• Imaging Agents 25%
• In Vivo Imaging 25%
• Indol 25%
• Indole Analogues 25%
• Inhibition Assay 50%
• Intrinsic Efficacy 25%
• Methoxy 25%
• Methoxyphenyl 25%
• Methyl 25%
• Methylthiol 25%
• Modeling Techniques 25%
• Neutral Antagonist 25%
• Partial Agonist 25%
• Pharmaceutics 25%
• Phenyl 25%
• Piperidin-4-ol 25%
• Potassium 25%
• Receptor Binding 25%
• Receptor Subtypes 25%
• Selective Ligands 50%
• Substituted Phenyl 25%
• Subtype Selectivity 100%

Pharmacology, Toxicology and Pharmaceutical Science

• Adenylate Cyclase 50%
• Aripiprazole 25%
• Binding Selectivity 75%
• Dopamine 3 Receptor 50%
• Dopamine Receptor D2 100%
• G Protein Coupled Inwardly Rectifying Potassium Channel 25%
• Guanine Nucleotide Binding Protein 25%
• Indole 50%
• Isotopes of Potassium 25%
• Mitogen Activated Protein Kinase 3 25%
• Partial Agonist 25%
• Piperazine 25%
• Receptor 75%
• Receptor Subtype 100%

Biochemistry, Genetics and Molecular Biology

• Adenylate Cyclase 50%
• Agonist 25%
• Aripiprazole 25%
• D2-Like Receptor 25%
• Dopamine Receptor 25%
• Dopamine Receptor D2 100%
• Dopamine Receptor D3 50%
• G Protein 25%
• G Protein-Coupled Inwardly-Rectifying Potassium Channel 25%
• Mitogen-Activated Protein Kinase 25%
• Receptor Binding 25%
• Wild Type 25%