Synthesis and pharmacological validation of a novel radioligand for the orphan GPR88 receptor

1Citations
Citations of this article
3Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

GPR88 is an orphan G protein-coupled receptor which has been implicated in a number of striatal-associated disorders. Herein we describe the synthesis and pharmacological characterization of the first GPR88 radioligand, [3H]RTI-33, derived from a synthetic agonist RTI-13951-33. [3H]RTI-33 has a specific activity of 83.4 Ci/mmol and showed one-site, saturable binding (KD of 85 nM) in membranes prepared from stable PPLS-HA-hGPR88-CHO cells. A competition binding assay was developed to determine binding affinities of several known GPR88 agonists. This radioligand represents a powerful tool for future mechanistic and cell-based ligand-receptor interaction studies of GPR88.

Author supplied keywords

Cite

CITATION STYLE

APA

Decker, A. M., Rahman, M. T., Kormos, C. M., Hesk, D., Darcq, E., Kieffer, B. L., & Jin, C. (2023). Synthesis and pharmacological validation of a novel radioligand for the orphan GPR88 receptor. Bioorganic and Medicinal Chemistry Letters, 80. https://doi.org/10.1016/j.bmcl.2022.129120

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free