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YM-50001
- Source :
- NeuroReport. 7:2543-2546
- Publication Year :
- 1996
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 1996.
-
Abstract
- We investigated some in vitro pharmacological properties of a novel human dopamine D2-like receptor antagonist, YM-50001 [(R)-5-chloro-4-cyclopropylacarbonylamino-2-methoxy-N-[1-(3-methox ybenzyl)- 3-pyrrolidinyl]benzamide monooxalate]. Receptor binding studies revealed that YM-50001 had a potent affinity for human D4 receptors (Ki = 5.62 nM). YM-50001 displayed weak or negligible affinity for other neurotransmitter receptors including human D2 and D3 receptors. YM-50001 shifted the dopamine response curve on each human D2-like receptor subtype-mediated low-Km GTPase activity to the right. YM-50001 also exhibited good D4 selectivity with respect to D2-like receptor antagonism in the functional assay. These results indicate that YM-50001 is a novel, potent and selective D4 receptor antagonist.
- Subjects :
- Dose-Response Relationship, Drug
medicine.drug_class
Chemistry
Dopamine
General Neuroscience
Pharmacology
Receptor antagonist
Binding, Competitive
Dopamine receptor D1
Competitive antagonist
Neurotransmitter receptor
Dopamine receptor
Dopamine receptor D2
Benzamides
medicine
Enzyme-linked receptor
Dopamine Antagonists
Haloperidol
Humans
Receptor
Subjects
Details
- ISSN :
- 09594965
- Volume :
- 7
- Database :
- OpenAIRE
- Journal :
- NeuroReport
- Accession number :
- edsair.doi.dedup.....d76b120cd2e7dd97e925ddcd0cd6f782
- Full Text :
- https://doi.org/10.1097/00001756-199611040-00028