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    products/biochemicals/s-mcpg-group-i--ii-mglu-antagonist-ab120059.pdf

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Neuroscience Neurotransmitter Amino Acids Glutamate
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(S)-MCPG, Group I / II mGlu antagonist (ab120059)

  • Datasheet
  • COA
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Chemical Structure - (S)-MCPG, Group I / II mGlu antagonist (ab120059)
  • Immunocytochemistry/ Immunofluorescence - (S)-MCPG, Group I / II mGlu antagonist (ab120059)

Key features and details

  • Group I / II mGlu antagonist
  • CAS Number: 150145-89-4
  • Soluble in 1.1eq. NaOH to 100mM
  • Form / State: Solid
  • Source: Synthetic

Overview

  • Product name

    (S)-MCPG, Group I / II mGlu antagonist
  • Description

    Group I / II mGlu antagonist
  • CAS Number

    150145-89-4
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    (S)-a-Methyl-4-carboxyphenylglycine
  • Molecular weight

    209.20
  • Molecular formula

    C10H11NO4
  • PubChem identifier

    446355
  • Storage instructions

    Store at +4°C. Store under desiccating conditions. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in 1.1eq. NaOH to 100mM
  • Handling

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    N[C@](C)(C(=O)O)c1ccc(cc1)C(=O)O
  • Source

    Synthetic

  • Research areas

    • Neuroscience
    • Neurotransmitter
    • Amino Acids
    • Glutamate
    • Neuroscience
    • Neurotransmission
    • Receptors / Channels
    • GPCR
    • Glutamate Receptors
    • Signal Transduction
    • Signaling Pathway
    • G Protein Signaling
    • GPCR
    • Biochemicals
    • Product Range
    • Just Add Water
    • Biochemicals
    • Chemical Type
    • Amino Acid
    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Glutamate
    • mGlu
    • Group I & II
    • Antagonists
    • Biochemicals
    • Research Area
    • Addiction
    • Glutamate
    • mGlu
    • Group I & II
    • Antagonists
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Glutamate
    • mGlu
    • Group I & II
    • Antagonists
    • Biochemicals
    • Research Area
    • Depression
    • Glutamate
    • mGlu
    • Group I & II
    • Antagonists
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Glutamate
    • mGlu
    • Group I & II
    • Antagonists
    • Biochemicals
    • Research Area
    • Parkinson's Disease
    • Glutamate
    • mGlu
    • Group I & II
    • Antagonists
    • Biochemicals
    • Research Area
    • Schizophrenia
    • Glutamate
    • mGlu
    • Group I & II
    • Antagonists
    • Biochemicals
    • Research Area
    • Stroke
    • Glutamate
    • mGlu
    • Group I & II
    • Antagonists

Associated products

  • Related Products

    • (R,S)-MCPG, Group I /II metabotropic glutamate antagonist (ab120033)

Applications

The Abpromise guarantee

Our Abpromise guarantee covers the use of ab120059 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
Functional Studies
Use at an assay dependent concentration.
Notes
Functional Studies
Use at an assay dependent concentration.

Images

  • Chemical Structure - (S)-MCPG, Group I / II mGlu antagonist (ab120059)
    Chemical Structure - (S)-MCPG, Group I / II mGlu antagonist (ab120059)
    2D chemical structure image of ab120059, (S)-MCPG, Group I / II mGlu antagonist
  • Immunocytochemistry/ Immunofluorescence - (S)-MCPG, Group I / II mGlu antagonist (ab120059)
    Immunocytochemistry/ Immunofluorescence - (S)-MCPG, Group I / II mGlu antagonist (ab120059)
    ab17722 staining FMRP in SK-N-SH cells treated with (S)-MCPG (ab120059), by ICC/IF. Decrease of FMRP expression correlates with increased concentration of (S)-MCPG, as described in literature.
    The cells were incubated at 37°C for 30 minutes in media containing different concentrations of ab120059 ((S)-MCPG) in DMSO, fixed with 4% formaldehyde for 10 minutes at room temperature and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab17722 (5 µg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight 488 anti-rabbit polyclonal antibody (ab96899) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.

Protocols

To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

Click here to view the general protocols

Datasheets and documents

  • Datasheet download

    Download
  • COA

References (10)

Publishing research using ab120059? Please let us know so that we can cite the reference in this datasheet.

ab120059 has been referenced in 10 publications.

  • Brandalise F & Gerber U Mossy fiber-evoked subthreshold responses induce timing-dependent plasticity at hippocampal CA3 recurrent synapses. Proc Natl Acad Sci U S A 111:4303-8 (2014). PubMed: 24550458
  • Ledonne A  et al. A continuous high frequency stimulation of the subthalamic nucleus determines a suppression of excitatory synaptic transmission in nigral dopaminergic neurons recorded in vitro. Exp Neurol 233:292-302 (2012). PubMed: 22056941
  • Platt NJ  et al. Striatal dopamine transmission is subtly modified in human A53Ta-synuclein overexpressing mice. PLoS One 7:e36397 (2012). PubMed: 22570709
  • Threlfell S  et al. Striatal dopamine release is triggered by synchronized activity in cholinergic interneurons. Neuron 75:58-64 (2012). PubMed: 22794260
  • Gan J  et al. Indirect modulation of neuronal excitability and synaptic transmission in the hippocampus by activation of proteinase-activated receptor-2. Br J Pharmacol 163:984-94 (2011). PubMed: 21366553
  • Hartung H  et al. Nitric oxide donors enhance the frequency dependence of dopamine release in nucleus accumbens. Neuropsychopharmacology 36:1811-22 (2011). PubMed: 21508928
  • Fan W  et al. Activation conditions for the induction of metabotropic glutamate receptor-dependent long-term depression in hippocampal CA1 pyramidal cells. J Neurosci 30:1471-5 (2010). PubMed: 20107074
  • Threlfell S  et al. Striatal muscarinic receptors promote activity dependence of dopamine transmission via distinct receptor subtypes on cholinergic interneurons in ventral versus dorsal striatum. J Neurosci 30:3398-408 (2010). PubMed: 20203199
  • Andrade AL & Rossi DJ Simulated ischaemia induces Ca2+-independent glutamatergic vesicle release through actin filament depolymerization in area CA1 of the hippocampus. J Physiol 588:1499-514 (2010). PubMed: 20211977
  • Robberechts Q  et al. Long-term depression at parallel fiber to Golgi cell synapses. J Neurophysiol 104:3413-23 (2010). PubMed: 20861429

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