Page last updated: 2024-09-04

u-91356 and 7-hydroxy-2-n,n-dipropylaminotetralin

u-91356 has been researched along with 7-hydroxy-2-n,n-dipropylaminotetralin in 2 studies

*7-hydroxy-2-N,N-dipropylaminotetralin: RN given refers to cpd without isomeric designation [MeSH]

Compound Research Comparison

Studies (u-91356)	Trials (u-91356)	Recent Studies (post-2010) (u-91356)	Studies (7-hydroxy-2-n,n-dipropylaminotetralin)	Trials (7-hydroxy-2-n,n-dipropylaminotetralin)	Recent Studies (post-2010) (7-hydroxy-2-n,n-dipropylaminotetralin)
13	0	1	398	0	29

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	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bonifazi, A; Burzynski, C; Donthamsetti, P; Free, RB; Janowsky, A; Javitch, JA; Keck, TM; Kumar, V; Michino, M; Newman, AH; Schweppe, C; Shi, L; Sibley, DR; Zou, MF	1
Bergstrom, DA; Gonzalez, AM; Huang, KX; Kreiss, DS; Sibley, DR; Walters, JR	1

Other Studies

2 other study(ies) available for u-91356 and 7-hydroxy-2-n,n-dipropylaminotetralin

Article	Year
Novel Analogues of (R)-5-(Methylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (Sumanirole) Provide Clues to Dopamine D2/D3 Receptor Agonist Selectivity. Journal of medicinal chemistry, 2016, Apr-14, Volume: 59, Issue:7 Topics: Animals; Benzimidazoles; Binding Sites; Chemistry Techniques, Synthetic; CHO Cells; Cricetulus; Humans; Ligands; Models, Molecular; Molecular Dynamics Simulation; Radioligand Assay; Receptors, Dopamine D2; Receptors, Dopamine D3; Structure-Activity Relationship	2016
Dopamine receptor agonist potencies for inhibition of cell firing correlate with dopamine D3 receptor binding affinities. European journal of pharmacology, 1995, Apr-24, Volume: 277, Issue:2-3 Topics: Aminoquinolines; Animals; Apomorphine; Azepines; Benzothiazoles; Binding, Competitive; CHO Cells; Cricetinae; Dopamine Agonists; Dose-Response Relationship, Drug; Ergolines; Imidazoles; Male; Neurons; Phenethylamines; Piperidines; Pramipexole; Quinolines; Quinpirole; Rats; Rats, Sprague-Dawley; Receptors, Dopamine; Receptors, Dopamine D2; Receptors, Dopamine D3; Structure-Activity Relationship; Substantia Nigra; Tetrahydronaphthalenes; Thiazoles; Thiophenes; Transfection	1995

Article

Year

Novel Analogues of (R)-5-(Methylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (Sumanirole) Provide Clues to Dopamine D2/D3 Receptor Agonist Selectivity.

Journal of medicinal chemistry, 2016, Apr-14, Volume: 59, Issue:7

Topics: Animals; Benzimidazoles; Binding Sites; Chemistry Techniques, Synthetic; CHO Cells; Cricetulus; Humans; Ligands; Models, Molecular; Molecular Dynamics Simulation; Radioligand Assay; Receptors, Dopamine D2; Receptors, Dopamine D3; Structure-Activity Relationship

2016

Dopamine receptor agonist potencies for inhibition of cell firing correlate with dopamine D3 receptor binding affinities.

European journal of pharmacology, 1995, Apr-24, Volume: 277, Issue:2-3

Topics: Aminoquinolines; Animals; Apomorphine; Azepines; Benzothiazoles; Binding, Competitive; CHO Cells; Cricetinae; Dopamine Agonists; Dose-Response Relationship, Drug; Ergolines; Imidazoles; Male; Neurons; Phenethylamines; Piperidines; Pramipexole; Quinolines; Quinpirole; Rats; Rats, Sprague-Dawley; Receptors, Dopamine; Receptors, Dopamine D2; Receptors, Dopamine D3; Structure-Activity Relationship; Substantia Nigra; Tetrahydronaphthalenes; Thiazoles; Thiophenes; Transfection

1995