1. Academic Validation
  2. YM-50001: a novel, potent and selective dopamine D4 receptor antagonist

YM-50001: a novel, potent and selective dopamine D4 receptor antagonist

  • Neuroreport. 1996 Nov 4;7(15-17):2543-6.
K Hidaka 1 S Tada M Matsumoto J Ohmori K Maeno T Yamaguchi
Affiliations

Affiliation

  • 1 Pharmacology Laboratories, Institute for Drug Discovery Research, Yamanouchi Pharmaceutical Co., Ltd., Ibaraki, Japan.
PMID: 8981420
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.

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