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             Images    (RS)-MCPG product vial image | Hello Bio
 
      (RS)-MCPG product vial image | Hello Bio   Biological Data   Biological description   Non-selective group I and II mGluR antagonist.
Also competitive antagonist of ACPD sensitive receptors.
Shows no effect on locomotor activity.
Water soluble (R,S)-MCPG sodium salt  and (S)-MCPG sodium salt  also available. (S)-MCPG  also available.
  
Solubility & Handling   Solubility overview   Soluble in 0.1M NaOH (100mM)  
 Storage instructions   Room temperature  
 Storage of solutions   Prepare and use solutions on the same day if possible. Store solutions at -20°C for up to one month if storage is required. Equilibrate to RT and ensure the solution is precipitate free before use.  
 Shipping Conditions   Stable for ambient temperature  shipping. Follow storage instructions on receipt.  
 Important   This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.  
Chemical Data    Chemical name   (RS )-α-Methyl-4-carboxyphenylglycine  
 Chemical structure       
 Molecular Formula   C10 H11 NO4   
 SMILES   CC(C1=CC=C(C=C1)C(=O)O)(C(=O)O)N  
 InChi   InChI=1S/C10H11NO4/c1-10(11,9(14)15)7-4-2-6(3-5-7)8(12)13/h2-5H,11H2,1H3,(H,12,13)(H,14,15)  
 InChiKey   DNCAZYRLRMTVSF-UHFFFAOYSA-N  
References for (RS)-MCPG References are publications that support the biological activity of the product
   The metabotropic glutamate receptor antagonist (RS)-MCPG produces hyperlocomotion in amphetamine pre-exposed rats. Kim JH et al  (1998) Neuropharmacology 37(2) : 189-97.       MCPG antagonizes metabotropic glutamate receptors but not long-term potentiation in the hippocampus. Manzoni OJ et al  (1994) Eur J Neurosci 6(6) : 1050-4.       Competitive antagonism at metabotropic glutamate receptors by (S)-4-carboxyphenylglycine and (RS)-alpha-methyl-4-carboxyphenylglycine. Eaton SA et al  (1993) Eur J Pharmacol  244(2) : 195-7.           
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          Non-selective group I and II mGluR antagonist