Literature DB >> 24900835

Development of [(3)H]2-Carboxy-4,6-dichloro-1H-indole-3-propionic Acid ([(3)H]PSB-12150): A Useful Tool for Studying GPR17.

Meryem Köse1, Kirsten Ritter1, Katharina Thiemke1, Michel Gillard2, Evi Kostenis3, Christa E Müller1.   

Abstract

The recently described synthetic GPR17 agonist 2-carboxy-4,6-dichloro-1H-indole-3-propionic acid (1) was prepared in tritium-labeled form by catalytic hydrogenation of the corresponding propenoic acid derivative 8 with tritium gas. The radioligand [(3)H]PSB-12150 (9) was obtained with a specific activity of 17 Ci/mmol (629 GBq/mmol). It showed specific and saturable binding to a single binding site in membrane preparations from Chinese hamster ovary cells recombinantly expressing the human GPR17. A competition assay procedure was established, which allows the determination of ligand binding affinities.

Entities:  

Keywords:  MDL29,951; montelukast; multiple sclerosis; nucleotide; orphan GPCR; pranlukast; radioligand

Year:  2014        PMID: 24900835      PMCID: PMC4027623          DOI: 10.1021/ml400399f

Source DB:  PubMed          Journal:  ACS Med Chem Lett        ISSN: 1948-5875            Impact factor:   4.345


  26 in total

1.  1-alkyl-8-(piperazine-1-sulfonyl)phenylxanthines: development and characterization of adenosine A2B receptor antagonists and a new radioligand with subnanomolar affinity and subtype specificity.

Authors:  Thomas Borrmann; Sonja Hinz; Daniela C G Bertarelli; Wenjin Li; Nicole C Florin; Anja B Scheiff; Christa E Müller
Journal:  J Med Chem       Date:  2009-07-09       Impact factor: 7.446

Review 2.  Ligand binding assays at equilibrium: validation and interpretation.

Authors:  Edward C Hulme; Mike A Trevethick
Journal:  Br J Pharmacol       Date:  2010-11       Impact factor: 8.739

3.  Innovative functional cAMP assay for studying G protein-coupled receptors: application to the pharmacological characterization of GPR17.

Authors:  Michela Buccioni; Gabriella Marucci; Diego Dal Ben; Dania Giacobbe; Catia Lambertucci; Laura Soverchia; Ajiroghene Thomas; Rosaria Volpini; Gloria Cristalli
Journal:  Purinergic Signal       Date:  2011-07-20       Impact factor: 3.765

4.  UDP-glucose enhances outward K(+) currents necessary for cell differentiation and stimulates cell migration by activating the GPR17 receptor in oligodendrocyte precursors.

Authors:  Elisabetta Coppi; Giovanna Maraula; Marta Fumagalli; Paola Failli; Lucrezia Cellai; Elisabetta Bonfanti; Luca Mazzoni; Raffaele Coppini; Maria P Abbracchio; Felicita Pedata; Anna Maria Pugliese
Journal:  Glia       Date:  2013-05-02       Impact factor: 7.452

5.  6-Bromo-8-(4-[(3)H]methoxybenzamido)-4-oxo-4H-chromene-2-carboxylic Acid: a powerful tool for studying orphan G protein-coupled receptor GPR35.

Authors:  Dominik Thimm; Mario Funke; Anne Meyer; Christa E Müller
Journal:  J Med Chem       Date:  2013-08-15       Impact factor: 7.446

6.  Agonist-induced desensitization/resensitization of human G protein-coupled receptor 17: a functional cross-talk between purinergic and cysteinyl-leukotriene ligands.

Authors:  S Daniele; M L Trincavelli; P Gabelloni; D Lecca; P Rosa; M P Abbracchio; C Martini
Journal:  J Pharmacol Exp Ther       Date:  2011-04-29       Impact factor: 4.030

7.  Substituted indole-2-carboxylates as in vivo potent antagonists acting as the strychnine-insensitive glycine binding site.

Authors:  R Di Fabio; A M Capelli; N Conti; A Cugola; D Donati; A Feriani; P Gastaldi; G Gaviraghi; C T Hewkin; F Micheli; A Missio; M Mugnaini; A Pecunioso; A M Quaglia; E Ratti; L Rossi; G Tedesco; D G Trist; A Reggiani
Journal:  J Med Chem       Date:  1997-03-14       Impact factor: 7.446

8.  Forced unbinding of GPR17 ligands from wild type and R255I mutant receptor models through a computational approach.

Authors:  Chiara Parravicini; Maria P Abbracchio; Piercarlo Fantucci; Graziella Ranghino
Journal:  BMC Struct Biol       Date:  2010-03-16

9.  3-(2-Carboxyindol-3-yl)propionic acid-based antagonists of the N-methyl-D-aspartic acid receptor associated glycine binding site.

Authors:  F G Salituro; B L Harrison; B M Baron; P L Nyce; K T Stewart; J H Kehne; H S White; I A McDonald
Journal:  J Med Chem       Date:  1992-05-15       Impact factor: 7.446

10.  The recently identified P2Y-like receptor GPR17 is a sensor of brain damage and a new target for brain repair.

Authors:  Davide Lecca; Maria Letizia Trincavelli; Paolo Gelosa; Luigi Sironi; Paolo Ciana; Marta Fumagalli; Giovanni Villa; Claudia Verderio; Carlotta Grumelli; Uliano Guerrini; Elena Tremoli; Patrizia Rosa; Serena Cuboni; Claudia Martini; Annalisa Buffo; Mauro Cimino; Maria P Abbracchio
Journal:  PLoS One       Date:  2008-10-31       Impact factor: 3.240

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  3 in total

1.  Discovery of 3-Substituted 1H-Indole-2-carboxylic Acid Derivatives as a Novel Class of CysLT1 Selective Antagonists.

Authors:  Huayan Chen; Hui Yang; Zhilong Wang; Xin Xie; Fajun Nan
Journal:  ACS Med Chem Lett       Date:  2016-01-22       Impact factor: 4.345

2.  Involvement of GPR17 in Neuronal Fibre Outgrowth.

Authors:  Max Braune; Nico Scherf; Claudia Heine; Katja Sygnecka; Thanigaimalai Pillaiyar; Chiara Parravicini; Bernd Heimrich; Maria P Abbracchio; Christa E Müller; Heike Franke
Journal:  Int J Mol Sci       Date:  2021-10-28       Impact factor: 5.923

3.  Abnormal Upregulation of GPR17 Receptor Contributes to Oligodendrocyte Dysfunction in SOD1 G93A Mice.

Authors:  Elisabetta Bonfanti; Tiziana Bonifacino; Stefano Raffaele; Marco Milanese; Erica Morgante; Giambattista Bonanno; Maria P Abbracchio; Marta Fumagalli
Journal:  Int J Mol Sci       Date:  2020-03-31       Impact factor: 5.923

  3 in total

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