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A benzo[b]thiophene-based selective type 4 S1P receptor agonist.

Authors :
Hur W
Rosen H
Gray NS
Source :
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2017 Jan 01; Vol. 27 (1), pp. 1-5. Date of Electronic Publication: 2016 Nov 18.
Publication Year :
2017

Abstract

S1P receptors (S1PR1-5) are a group of GPCRs activated by a high affinity binding with S1P that have important roles in the regulation of the immune system. A potent S1PR agonist FTY720 is an immunomodulator used to treat multiple sclerosis and several 'second generation' drugs are under clinical development. Subtype-selective agonists have been reported for each S1PR isotype, some of which are used as pharmacological tools for functional studies. Here we report the discovery and initial characterization of compound 5c, a benzo[b]thiophene amino carboxylate which exhibits potent and selective agonist activity for S1PR4. Compound 5c has an EC <subscript>50</subscript> =200nM as an agonist in GTPĪ³ <superscript>35</superscript> S binding assay for S1PR4 and exhibits no activity against S1PR1,2,3,5. We confirmed its potent activity and decent S1PR subtype selectivity using biochemical and cellular assays.<br /> (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1464-3405
Volume :
27
Issue :
1
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry letters
Publication Type :
Academic Journal
Accession number :
27894870
Full Text :
https://doi.org/10.1016/j.bmcl.2016.11.050