Page last updated: 2024-08-16

sulpiride and 5-hydroxy-1-methyl-2--(di-n-propylamino)tetralin methyl ether

sulpiride has been researched along with 5-hydroxy-1-methyl-2--(di-n-propylamino)tetralin methyl ether in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Emaduddin, M; Takeuchi, H	1
Fu, D; Javitch, JA; Lin, H; Strange, PG; Wilson, J	1

Other Studies

2 other study(ies) available for sulpiride and 5-hydroxy-1-methyl-2--(di-n-propylamino)tetralin methyl ether

Article	Year
Lineweaver-Burk analysis for the blocking effects of mammalian dopamine receptor antagonists on dopamine-induced currents in Achatina giant neurones. General pharmacology, 1996, Volume: 27, Issue:7 Topics: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; 8-Hydroxy-2-(di-n-propylamino)tetralin; Animals; Dopamine; Dopamine Antagonists; Dopamine D2 Receptor Antagonists; Ganglia, Invertebrate; In Vitro Techniques; Membrane Potentials; Neurons; Patch-Clamp Techniques; Receptors, Dopamine; Receptors, Dopamine D1; Snails; Sulpiride	1996
Mechanisms of inverse agonism of antipsychotic drugs at the D(2) dopamine receptor: use of a mutant D(2) dopamine receptor that adopts the activated conformation. Journal of neurochemistry, 2001, Volume: 77, Issue:2 Topics: 1-Methyl-3-isobutylxanthine; 8-Hydroxy-2-(di-n-propylamino)tetralin; Animals; Antipsychotic Agents; Apomorphine; Binding, Competitive; Bromocriptine; Butaclamol; Chlorpromazine; CHO Cells; Clozapine; Colforsin; Cricetinae; Cricetulus; Cyclic AMP; Dopamine Agonists; Dopamine Antagonists; Dopamine D2 Receptor Antagonists; Dose-Response Relationship, Drug; GTP-Binding Proteins; Haloperidol; Humans; Macromolecular Substances; Mutagenesis, Site-Directed; Phenethylamines; Piperidines; Protein Binding; Protein Conformation; Radioligand Assay; Receptors, Dopamine D2; Recombinant Fusion Proteins; Sodium; Spiperone; Structure-Activity Relationship; Sulpiride; Transfection; Tyramine	2001

Article

Year

Lineweaver-Burk analysis for the blocking effects of mammalian dopamine receptor antagonists on dopamine-induced currents in Achatina giant neurones.

General pharmacology, 1996, Volume: 27, Issue:7

Topics: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; 8-Hydroxy-2-(di-n-propylamino)tetralin; Animals; Dopamine; Dopamine Antagonists; Dopamine D2 Receptor Antagonists; Ganglia, Invertebrate; In Vitro Techniques; Membrane Potentials; Neurons; Patch-Clamp Techniques; Receptors, Dopamine; Receptors, Dopamine D1; Snails; Sulpiride

1996

Mechanisms of inverse agonism of antipsychotic drugs at the D(2) dopamine receptor: use of a mutant D(2) dopamine receptor that adopts the activated conformation.

Journal of neurochemistry, 2001, Volume: 77, Issue:2

Topics: 1-Methyl-3-isobutylxanthine; 8-Hydroxy-2-(di-n-propylamino)tetralin; Animals; Antipsychotic Agents; Apomorphine; Binding, Competitive; Bromocriptine; Butaclamol; Chlorpromazine; CHO Cells; Clozapine; Colforsin; Cricetinae; Cricetulus; Cyclic AMP; Dopamine Agonists; Dopamine Antagonists; Dopamine D2 Receptor Antagonists; Dose-Response Relationship, Drug; GTP-Binding Proteins; Haloperidol; Humans; Macromolecular Substances; Mutagenesis, Site-Directed; Phenethylamines; Piperidines; Protein Binding; Protein Conformation; Radioligand Assay; Receptors, Dopamine D2; Recombinant Fusion Proteins; Sodium; Spiperone; Structure-Activity Relationship; Sulpiride; Transfection; Tyramine

2001