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    cgp-52432-gabab-antagonist-ab120330.pdf

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Neuroscience Neurotransmitter Amino Acids GABA
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CGP 52432, GABAB antagonist (ab120330)

  • Datasheet
  • COA
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Chemical Structure - CGP 52432, GABA<sub>B</sub> antagonist (ab120330)

    Key features and details

    • Potent GABAB antagonist
    • CAS Number: 139667-74-6
    • Soluble in water to 10 mM
    • Form / State: Solid
    • Source: Synthetic

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    Overview

    • Product name

      CGP 52432, GABAB antagonist
    • Description

      Potent GABAB antagonist
    • Biological description

      Potent, selective GABAB antagonist (IC50 = 85 nM).

      Also available in simple stock solutions (ab146709) - add 1 ml of water to get an exact, ready-to-use concentration.

    • CAS Number

      139667-74-6
    • Chemical structure

      Chemical Structure

    Properties

    • Chemical name

      3-[[(3,4-Dichlorophenyl)methyl]amino]propyl(diethoxymethyl)phosphinic acid
    • Molecular weight

      384.24
    • Molecular formula

      C15H24Cl2NO4P
    • PubChem identifier

      132252
    • Storage instructions

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

      Soluble in water to 10 mM
    • 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

      Clc1ccc(CNCCCP(=O)(O)C(OCC)OCC)cc1Cl
    • Source

      Synthetic

    • Research areas

      • Neuroscience
      • Neurotransmitter
      • Amino Acids
      • GABA
      • Biochemicals
      • Product Range
      • Just Add Water
      • Biochemicals
      • Chemical Type
      • Amino Acid
      • Biochemicals
      • Chemical Type
      • Biochemicals
      • Biochemicals
      • Pharmacology
      • Receptors & Transporters
      • GABA
      • GABAB
      • Biochemicals
      • Pharmacology
      • Receptors & Transporters
      • GABA
      • GABAB
      • Antagonists
      • Biochemicals
      • Research Area
      • Pain & inflammation
      • GABA
      • GABAB
      • Biochemicals
      • Research Area
      • Pain & inflammation
      • GABA
      • GABAB
      • Antagonists
      • Biochemicals
      • Research Area
      • Schizophrenia
      • GABA
      • GABAB
      • Biochemicals
      • Research Area
      • Schizophrenia
      • GABA
      • GABAB
      • Antagonists
      • Biochemicals
      • Research Area
      • Stress / Anxiety
      • GABA
      • GABAB
      • Biochemicals
      • Research Area
      • Stress / Anxiety
      • GABA
      • GABAB
      • Antagonists

    Images

    • Chemical Structure - CGP 52432, GABA<sub>B</sub> antagonist (ab120330)
      Chemical Structure - CGP 52432, GABAB antagonist (ab120330)
      2D chemical structure image of ab120330, CGP 52432, GABAB antagonist

    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 ab120330? Please let us know so that we can cite the reference in this datasheet.

    ab120330 has been referenced in 10 publications.

    • Dorgans K  et al. Short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing. Elife 8:N/A (2019). PubMed: 31081751
    • Kim S  et al. Dendritic spikes in hippocampal granule cells are necessary for long-term potentiation at the perforant path synapse. Elife 7:N/A (2018). PubMed: 29578411
    • Minge D  et al. Heparan Sulfates Support Pyramidal Cell Excitability, Synaptic Plasticity, and Context Discrimination. Cereb Cortex 27:903-918 (2017). PubMed: 28119345
    • Schauer C  et al. Hypothalamic gonadotropin-releasing hormone (GnRH) receptor neurons fire in synchrony with the female reproductive cycle. J Neurophysiol 114:1008-21 (2015). PubMed: 26063780
    • Hernández VM  et al. Parvalbumin+ Neurons and Npas1+ Neurons Are Distinct Neuron Classes in the Mouse External Globus Pallidus. J Neurosci 35:11830-47 (2015). PubMed: 26311767
    • Hedrick T & Waters J Acetylcholine excites neocortical pyramidal neurons via nicotinic receptors. J Neurophysiol 113:2195-209 (2015). PubMed: 25589590
    • Russo G  et al. Dynamics of action potential firing in electrically connected striatal fast-spiking interneurons. Front Cell Neurosci 7:209 (2013). PubMed: 24294191
    • Valera AM  et al. Adaptation of granule cell to Purkinje cell synapses to high-frequency transmission. J Neurosci 32:3267-80 (2012). PubMed: 22378898
    • Min R & Nevian T Astrocyte signaling controls spike timing-dependent depression at neocortical synapses. Nat Neurosci 15:746-53 (2012). PubMed: 22446881
    • Brager DH  et al. Impaired dendritic expression and plasticity of h-channels in the fmr1(-/y) mouse model of fragile X syndrome. Cell Rep 1:225-33 (2012). PubMed: 22662315

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