18000-24-3

7-Chlorokynurenic acid Chemical Structure
18000-24-3

Chemical Structure

7-Chlorokynurenic acid

Synonym(s): 7-CKA

  • CAS No.: 18000-24-3
  • Formula:C10H6ClNO3
  • Molecular Weight:223.61

IUPAC Name: 7-chloro-4-hydroxyquinoline-2-carboxylic acid

InChIKey: UAWVRVFHMOSAPU-UHFFFAOYSA-N

SMILES: O=C(C1=NC2=CC(Cl)=CC=C2C(O)=C1)O

Biological Activity: 7-Chlorokynurenic acid (7-CKA) is a potent and selective antagonist of the glycine B coagonist site of the N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 7-Chlorokynurenic acid is also a potent inhibitor of the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM. 7-Chlorokynurenic acid has potent antinociceptive actions after neuraxial delivery[1][2].

Cat. No. Product Name Purity Description Pricing
HY-100811
7-Chlorokynurenic acid 99.86% 7-Chlorokynurenic acid (7-CKA) is a potent and selective antagonist of the glycine B coagonist site of the N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 7-Chlorokynurenic acid is also a potent inhibitor of the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM. 7-Chlorokynurenic acid has potent antinociceptive actions after neuraxial delivery.
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HY-100811R
7-Chlorokynurenic acid (Standard) ≥98% 7-Chlorokynurenic acid (Standard) is the analytical standard of 7-Chlorokynurenic acid. This product is intended for research and analytical applications. 7-Chlorokynurenic acid (7-CKA) is a potent and selective antagonist of the glycine B coagonist site of the N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 7-Chlorokynurenic acid is also a potent inhibitor of the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM. 7-Chlorokynurenic acid has potent antinociceptive actions after neuraxial delivery.
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References