Keyphrases
Subtype Selectivity
100%
D3 Dopamine Receptor
100%
Dopamine Receptor
100%
D2 Dopamine Receptor
100%
Binding Properties
100%
Functional Properties
100%
Binding Selectivity
75%
D2 Receptor
50%
Adenylyl Cyclase
50%
Inhibition Assay
50%
Selective Ligands
50%
ERK2
25%
Cell-based
25%
Channel Activation
25%
D3 Receptor
25%
Phenyl
25%
Receptor Binding
25%
Methoxyphenyl
25%
Receptor Subtypes
25%
Potassium
25%
Methyl
25%
In Vivo Imaging
25%
Chemical Classes
25%
Indol
25%
Methoxy
25%
Partial Agonist
25%
Pharmaceutics
25%
D2-like
25%
G Protein-coupled
25%
Neutral Antagonist
25%
Imaging Agents
25%
2,3-dihydroquinazoline-4(1H)-one
25%
Aripiprazole
25%
Methylthiol
25%
GIRK Channel
25%
Modeling Techniques
25%
Piperidin-4-ol
25%
Intrinsic Efficacy
25%
Substituted Phenyl
25%
Computer Modeling
25%
Indole Analogues
25%
Pharmacology, Toxicology and Pharmaceutical Science
Dopamine Receptor D2
100%
Receptor Subtype
100%
Receptor
75%
Binding Selectivity
75%
Dopamine 3 Receptor
50%
Indole
50%
Adenylate Cyclase
50%
Mitogen Activated Protein Kinase 3
25%
Piperazine
25%
Partial Agonist
25%
Guanine Nucleotide Binding Protein
25%
Aripiprazole
25%
Isotopes of Potassium
25%
G Protein Coupled Inwardly Rectifying Potassium Channel
25%
Biochemistry, Genetics and Molecular Biology
Dopamine Receptor D2
100%
Dopamine Receptor D3
50%
Adenylate Cyclase
50%
Agonist
25%
Wild Type
25%
Receptor Binding
25%
Mitogen-Activated Protein Kinase
25%
Aripiprazole
25%
G Protein-Coupled Inwardly-Rectifying Potassium Channel
25%
Dopamine Receptor
25%
D2-Like Receptor
25%
G Protein
25%