[3H]SCH 23390 Binding to Human Putamen D-1 Dopamine Receptors: Stereochemical and Structure-Affinity Relationships Among l-Phenyl-1H-3-Benzazepine Derivatives as a Guide to D-l Receptor Topography-Reference-Cited by-同舟云学术

[3H]SCH 23390 Binding to Human Putamen D-1 Dopamine Receptors: Stereochemical and Structure-Affinity Relationships Among l-Phenyl-1H-3-Benzazepine Derivatives as a Guide to D-l Receptor Topography

Published:1987-04 Issue:4 Volume:48 Page:1039-1042
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J Neurochem

Author:

O'Boyle Kathy M.,Waddington John L.

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-4159.1987.tb05623.x/fullpdf

Reference21 articles.

1. A comparison between dopamine-stimulated adenylate cyclase and 3H-SCH 23390 binding in rat striatum

2. Characterization of the binding of 3H-SCH 23390, a selective D-1 receptor antagonist ligand, in rat striatum

3. Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction

4. Pharmacological effects of a specific dopamine D-1 antagonist SCH 23390 in comparison with neuroleptics

5. SCH 23390—The first selective dopamine D-1 antagonist

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