ADX 10059 hydrochloride

ADX 10059 hydrochloride

Catalog Number:
FC01365832APE
Mfr. No.:
APE-B5586
Price:
$513
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      • Overview
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          Background

          ADX 10059 hydrochloride is a potent and selective negative allosteric modulator of mGlu5 receptor with IC50 value of 17.1 nM [1].Metabotropic glutamate receptor 5 (mGlu5 receptor) is a G protein-coupled receptor and is a receptor for glutamate, which is a primary neurotransmitter involved in signaling in the central nervous system [2].ADX 10059 hydrochloride is a potent and selective mGlu5 receptor negative allosteric modulator. In patients with migraine, ADX10059 caused pain-free response in 16.1% patients compared with placebo of 4.5% [1]. In patients with gastro-oesophageal reflux disease (GORD) underwent 24-h oesophageal pH-metry, ADX10059 (250 mg) significantly reduced the percentage of acid exposure time with pH < 4 from 7.2% to 3.6%. Also, ADX 10059 significantly decreased the duration and number of symptomatic reflux episodes and reduced oesophageal acid exposure [2].

          [1]. Marin JC, Goadsby PJ. Glutamatergic fine tuning with ADX-10059: a novel therapeutic approach for migraine Expert Opin Investig Drugs, 2010, 19(4): 555-561.
          [2]. Keywood C, Wakefield M, Tack J. A proof-of-concept study evaluating the effect of ADX10059, a metabotropic glutamate receptor-5 negative allosteric modulator, on acid exposure and symptoms in gastro-oesophageal reflux disease. Gut, 2009, 58(9): 1192-1199.

      • Properties
        • Categories
          Negative allosteric modulator at mGlu5
          Alternative Name
          2-((3-fluorophenyl)ethynyl)-4,6-dimethylpyridin-3-amine hydrochloride
          CAS Number
          757949-98-7
          Molecular Formula
          C15H13FN2·HCl
          Molecular Weight
          276.74
          Appearance
          Yellow solid
          Purity
          98.00%
          Solubility
          <6.92mg/ml in H2O; <27.67mg/ml in DMSO
          Storage
          Desiccate at RT
          SMILES
          CC1=CC(C)=NC(C#CC2=CC(F)=CC=C2)=C1N.Cl

          * For Research Use Only

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