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Neuroscience Neurotransmitter Transporters Glutamate

Kynurenic acid, endogenous ionotropic / nicotinic antagonist (ab120064)

Price and availability

103 862 ₸

Availability

Order now and get it on Friday March 05, 2021

Kynurenic acid, endogenous ionotropic / nicotinic antagonist (ab120064)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Endogenous ionotropic / nicotinic antagonist
  • CAS Number: 492-27-3
  • Purity: > 99%
  • Soluble in 1 eq. NaOH to 100 mM and in DMSO to 50 mM
  • Form / State: Solid
  • Source: Synthetic

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Overview

  • Product name

    Kynurenic acid, endogenous ionotropic / nicotinic antagonist
  • Description

    Endogenous ionotropic / nicotinic antagonist
  • Biological description

    Endogenous antagonist at ionotropic, glycine β and α7 nicotinic receptors. Neuroprotective in vivo. Water-soluble form available - please see Kynurenic acid sodium salt (ab120256)

  • Purity

    > 99%
  • CAS Number

    492-27-3
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    4-Hydroxyquinoline-2-carboxylic acid
  • Molecular weight

    189.17
  • Molecular formula

    C10H7NO3
  • PubChem identifier

    3845
  • Storage instructions

    Store at Room Temperature. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in 1 eq. NaOH to 100 mM and in DMSO to 50 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

    O=C(O)c1cc(O)c2ccccc2n1
  • Source

    Synthetic

  • Research areas

    • Neuroscience
    • Neurotransmitter
    • Amino Acids
    • Glutamate
    • Neuroscience
    • Neurotransmission
    • Receptors / Channels
    • GPCR
    • Glutamate Receptors
    • Neuroscience
    • Neurotransmission
    • Receptors / Channels
    • GPCR
    • More GPCR
    • Neuroscience
    • Neurotransmission
    • Receptors / Channels
    • Ligand-Gated Ion Channels
    • NMDA Receptors
    • Neuroscience
    • Neurotransmission
    • Receptors / Channels
    • Ligand-Gated Ion Channels
    • nAch Receptors
    • Epigenetics and Nuclear Signaling
    • Transcription
    • Domain Families
    • HLH / Leucine Zipper
    • Helix-Turn-Helix
    • Signal Transduction
    • Signaling Pathway
    • G Protein Signaling
    • GPCR
    • Neuroscience
    • Sensory System
    • Somatosensory system
    • Nociception
    • Neuroscience
    • Neurology process
    • Neurodegenerative disease
    • Other
    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Nicotinic
    • α7
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Glutamate
    • Broad spectrum / non-selective
    • Antagonists
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Nicotinic
    • α7
    • Antagonists
    • Biochemicals
    • Research Area
    • Addiction
    • Glutamate
    • Broad spectrum / non-selective
    • Antagonists
    • Biochemicals
    • Research Area
    • Addiction
    • Nicotinic
    • α7
    • Biochemicals
    • Research Area
    • Addiction
    • Nicotinic
    • α7
    • Antagonists
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Glutamate
    • Broad spectrum / non-selective
    • Antagonists
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Nicotinic
    • α7
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Nicotinic
    • α7
    • Antagonists
    • Biochemicals
    • Research Area
    • Depression
    • Glutamate
    • Broad spectrum / non-selective
    • Antagonists
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Glutamate
    • Broad spectrum / non-selective
    • Antagonists
    • Biochemicals
    • Research Area
    • Parkinson's Disease
    • Glutamate
    • Broad spectrum / non-selective
    • Antagonists
    • Biochemicals
    • Research Area
    • Parkinson's Disease
    • Nicotinic
    • α7
    • Biochemicals
    • Research Area
    • Parkinson's Disease
    • Nicotinic
    • α7
    • Antagonists
    • Biochemicals
    • Research Area
    • Schizophrenia
    • Glutamate
    • Broad spectrum / non-selective
    • Antagonists
    • Biochemicals
    • Research Area
    • Schizophrenia
    • Nicotinic
    • α7
    • Biochemicals
    • Research Area
    • Schizophrenia
    • Nicotinic
    • α7
    • Antagonists
    • Biochemicals
    • Research Area
    • Stroke
    • Glutamate
    • Broad spectrum / non-selective
    • Antagonists

Images

  • Functional Studies - Kynurenic acid, endogenous ionotropic / nicotinic antagonist (ab120064)
    Functional Studies - Kynurenic acid, endogenous ionotropic / nicotinic antagonist (ab120064) Image from Rudolph S et al., Neuron. 2011;70(5):991-1004. Fig 3.; doi: 10.1016/j.neuron.2011.03.029 with permission from Elsevier.
    C1 and C2 - Inhibition of climbing fiber to Purkinje cell EPSCs in (control; black) by 1 mM Kynurenic acid (red, ab120064) or 100 nM NBQX (green, ab120045) recorded in 2.5 mM external Ca2+ at 0.05 Hz (C1) and 2 Hz (C2) stimulation frequency. D - Summary of inhibition of EPSCs by 1 mM Kynurenic acid (red, ab120064) and 100 nM NBQX (green, ab120045) in 2.5 mM external Ca2+.

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