1h-3-benzazepin-7-ol, 8-bromo-2,3,4,5-tetrahydro-3-methyl-5-phenyl- and apomorphine

1h-3-benzazepin-7-ol, 8-bromo-2,3,4,5-tetrahydro-3-methyl-5-phenyl- has been researched along with apomorphine in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19902 (40.00)18.7374
1990's2 (40.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
George, SR; Guan, HC; Laurier, LG; Ng, G; Niznik, HB; O'Dowd, BF; Seeman, P; Sunahara, RK; Torchia, J; Van Tol, HH1
Alberts, I; Harding, WW; Juarez, R; Karki, A; Namballa, HK1
Chang, JP; Peter, RE; Wong, AO; Yu, KL1
Barone, FC; Fine, CF; Fowler, PJ; Grous, M; Lombardi, DM; Ormsbee, HS; Phyall, WB; Rush, JA1
Molloy, AG; Waddington, JL1

Other Studies

5 other study(ies) available for 1h-3-benzazepin-7-ol, 8-bromo-2,3,4,5-tetrahydro-3-methyl-5-phenyl- and apomorphine

ArticleYear
Cloning of the gene for a human dopamine D5 receptor with higher affinity for dopamine than D1.
    Nature, 1991, Apr-18, Volume: 350, Issue:6319

    Topics: Amino Acid Sequence; Animals; Base Sequence; Binding, Competitive; Blotting, Northern; Brain; Cell Line; Cell Membrane; Cloning, Molecular; Dopamine; Humans; Kinetics; Molecular Sequence Data; Molecular Weight; Oligonucleotide Probes; Rats; Receptors, Dopamine; Receptors, Dopamine D1; Receptors, Dopamine D5; RNA, Messenger; Sequence Homology, Nucleic Acid; Transfection

1991
Identification of C10 nitrogen-containing aporphines with dopamine D
    Bioorganic & medicinal chemistry letters, 2020, 04-15, Volume: 30, Issue:8

    Topics: Aporphines; Dopamine Agonists; Dose-Response Relationship, Drug; Humans; Ligands; Molecular Docking Simulation; Molecular Structure; Receptors, Dopamine D1; Receptors, Dopamine D5; Structure-Activity Relationship

2020
Differential actions of dopamine receptor subtypes on gonadotropin and growth hormone release in vitro in goldfish.
    Neuroendocrinology, 1990, Volume: 51, Issue:6

    Topics: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; Animals; Apomorphine; Cells, Cultured; Cyprinidae; Domperidone; Dopamine Antagonists; Ergolines; Female; Goldfish; Gonadotropins, Pituitary; Growth Hormone; Male; Perfusion; Pituitary Gland; Pituitary Hormone-Releasing Hormones; Quinpirole; Receptors, Dopamine; Receptors, Dopamine D1; Receptors, Dopamine D2

1990
DA1 receptor mediates dopamine-induced relaxation of opossum lower esophageal sphincter in vitro.
    Gastroenterology, 1986, Volume: 91, Issue:3

    Topics: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; Animals; Apomorphine; Aporphines; Benzazepines; Deoxyepinephrine; Domperidone; Dopamine; Dose-Response Relationship, Drug; Esophagogastric Junction; Female; In Vitro Techniques; Male; Metoclopramide; Muscle Contraction; Muscle Relaxation; Muscle, Smooth; Opossums; Receptors, Dopamine

1986
The enantiomers of SK&F 83566, a new selective D-1 dopamine antagonist, stereospecifically block stereotyped behaviour induced by apomorphine and by the selective D-2 agonist RU 24213.
    European journal of pharmacology, 1985, Oct-08, Volume: 116, Issue:1-2

    Topics: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; Animals; Apomorphine; Benzazepines; Male; Motor Activity; Phenethylamines; Rats; Rats, Inbred Strains; Receptors, Dopamine; Stereoisomerism; Stereotyped Behavior

1985