7-Chloro-4-hydroxyquinoline-2-carboxylic acid HCl

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Company Name: J & K SCIENTIFIC LTD.  
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7-Chloro-4-hydroxyquinoline-2-carboxylic acid HCl manufacturers

7-Chloro-4-hydroxyquinoline-2-carboxylic acid HCl Basic information
Target
Product Name:7-Chloro-4-hydroxyquinoline-2-carboxylic acid HCl
Synonyms:7-CHLOROKYNURENIC ACID HYDROCHLORIDE;7-CL-KYNA;7-Chloro-4-hydroxyquinoline-2-carboxylic acid, 7-Cl-KYNA;7-Chloro-4-hydroxy-2-quinolinecarboxylic acid;7-Chloroquinurenic acid;7-CKA;7-chloro-4-keto-1H-quinoline-2-carboxylic acid;7-chloro-4-oxo-1H-quinoline-2-carboxylic acid
CAS:18000-24-3
MF:C10H6ClNO3
MW:223.61
EINECS:241-913-6
Product Categories:pharmacetical;Glutamate;Glutamate receptor
Mol File:18000-24-3.mol
7-Chloro-4-hydroxyquinoline-2-carboxylic acid HCl Structure
7-Chloro-4-hydroxyquinoline-2-carboxylic acid HCl Chemical Properties
Melting point 277-278 °C (decomp)
Boiling point 461.5±45.0 °C(Predicted)
density 1.600±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility 0.1 M NaOH: 13.7 mg/mL
form solid
pka0.90±0.30(Predicted)
color tan
CAS DataBase Reference18000-24-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
7-Chloro-4-hydroxyquinoline-2-carboxylic acid HCl Usage And Synthesis
Target Ki: 0.59 μM (reuptake of glutamate)    IC50: 0.56 μM (Glycine B coagonist site of NMDA receptor)
UsesNMDA receptor antagonist at the glycine site
DefinitionChEBI: A quinolinemonocarboxylic acid that is quinaldic acid which is substituted by a hydroxy group at position 4 and by a chlorine at position 7. It is a potent NMDA glutamate receptor antagonist which antagonizes the strychnine-insensitive glycine site of the MDA receptor. It also prevents neurodegeneration produced by quinolinic acid.
Biological FunctionsGlycine B agonist site antagonist of N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 7-Chlorokynurenic acid is also a potent inhibitor of glutamate reuptake into synaptic vesicles with a Ki of 0.59 μM. 7-Chlorokynurenic acid has potent analgesic effects in neurotransmission.
Biological ActivityNMDA receptor antagonist acting at the glycine site. Potent competitive inhibitor of L-glutamate transport into synaptic vesicles. Also available as part of the NMDA Receptor - Glycine Site Tocriset™ .
in vivoMale Sprague-Dawley rats pretreated with 7-Chlorokynurenic acid (10 nM) shows a significant retardation of development of both the electroencephalographic and motor (17.7±2.9 daily stimulations) components of the seizure response.
storageRoom temperature
7-Chloro-4-hydroxyquinoline-2-carboxylic acid HCl Preparation Products And Raw materials
Tag:7-Chloro-4-hydroxyquinoline-2-carboxylic acid HCl(18000-24-3) Related Product Information
Trichloroisocyanuric acid Methyl 7-chloro-4-hydroxyquinoline-2-carboxylate 5,7-Dichloro-4-hydroxy-quinoline-2-carboxylic acid ethyl ester 5,7-Dichlorokynurenic acid 5-CHLORO-4-HYDROXYQUINOLINE-2-CARBOXYLIC ACID HCL 7-CHLORO-4-HYDROXYQUINOLINE-2-CARBOXYLIC ACID HCL DICHLOROKYNURENIC ACID, 5,7-[3-3H]-