Back to Search Start Over

YM-50001

Authors :
Shoko Tada
Junya Ohmori
Kyoichi Maeno
Mitsuyuki Matsumoto
Kazuyuki Hidaka
Tokio Yamaguchi
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.

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