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7-Chlorokynurenic acid (7-chloro-4-hydroxy-2-carboxyquinoline) is an effecitve and selective antagonist of NMDA receptor with IC50 of 0.56 μM for the glycine B coagonist site. 7-Chlorokynurenic acid inhibits the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM and shows antinociceptive actions after neuraxial delivery.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
5 mg | $38 | In Stock | |
10 mg | $61 | In Stock | |
25 mg | $128 | In Stock | |
50 mg | $245 | In Stock | |
100 mg | $473 | In Stock | |
500 mg | $987 | In Stock | |
1 mL x 10 mM (in DMSO) | $67 | In Stock |
Description | 7-Chlorokynurenic acid (7-chloro-4-hydroxy-2-carboxyquinoline) is an effecitve and selective antagonist of NMDA receptor with IC50 of 0.56 μM for the glycine B coagonist site. 7-Chlorokynurenic acid inhibits the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM and shows antinociceptive actions after neuraxial delivery. |
Targets&IC50 | Glycine B coagonist site of NMDA receptor:0.56 μM(ki), Reuptake of glutamate:(ki)0.59 μM |
In vivo | In male Sprague-Dawley rats, 7-Chlorokynurenic acid (10 nM) retardates the development of both the electroencephalographic and motor (17.7 daily stimulations) components of the seizure response[3]. |
Alias | 7-CKA, 7-chloro-4-hydroxy-2-carboxyquinoline |
Molecular Weight | 223.61 |
Formula | C10H6ClNO3 |
Cas No. | 18000-24-3 |
Smiles | OC(=O)c1cc(O)c2ccc(Cl)cc2n1 |
Relative Density. | 1.549 g/cm3 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||
Solubility Information | DMSO: 15 mg/mL (67.1 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
DMSO
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