MDL | MFCD00674924 |
---|---|
Molecular Weight | 223.61 |
Molecular Formula | C10H6ClNO3 |
SMILES | O=C(C1=NC2=CC(Cl)=CC=C2C(O)=C1)O |
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 ( IC 50 =0.56 μM). 7-Chlorokynurenic acid is also a potent inhibitor of the reuptake of glutamate into synaptic vesicles with a K i of 0.59 μM. 7-Chlorokynurenic acid has potent antinociceptive actions after neuraxial delivery [1] [2] .
Male 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 [3] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : 16.67 mg/mL ( 74.55 mM ; Need ultrasonic)
H 2 O : 1 mg/mL ( 4.47 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 4.4721 mL | 22.3604 mL | 44.7207 mL |
5 mM | 0.8944 mL | 4.4721 mL | 8.9441 mL |
10 mM | 0.4472 mL | 2.2360 mL | 4.4721 mL |