Radiosynthesis of a selective dopamine D-1 receptor antagonist: R(+)-7-chloro-8-hydroxy-3-[11C]methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine ([11C]SCH 23390)
Open Access
- 1 January 1987
- journal article
- research article
- Published by Elsevier in International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes
- Vol. 38 (4) , 305-306
- https://doi.org/10.1016/0883-2889(87)90045-1
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Some atypical neuroleptics inhibit [3H]SCH 23390 binding in vivoEuropean Journal of Pharmacology, 1986
- An improved synthesis of (3-N-[11C]methyl)spiperoneInternational Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1986
- A comparison between dopamine-stimulated adenylate cyclase and 3H-SCH 23390 binding in rat striatumLife Sciences, 1985
- Two dopamine receptors: Biochemistry, physiology and pharmacologyLife Sciences, 1984
- Characterization of the binding of 3H-SCH 23390, a selective D-1 receptor antagonist ligand, in rat striatumLife Sciences, 1984
- Pharmacological effects of a specific dopamine D-1 antagonist SCH 23390 in comparison with neurolepticsLife Sciences, 1984
- 77Br-p-bromospiperone: A ligand for in vivo labelling of dopamine receptorsLife Sciences, 1983
- SCH 23390—The first selective dopamine D-1 antagonistEuropean Journal of Pharmacology, 1983
- Multiple receptors for dopamineNature, 1979
- Spiperone: A ligand of choice for neuroleptic receptorsBiochemical Pharmacology, 1978