L-701,324
Cat. No.: DC8159
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Chemical Structure
142326-59-8
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Field of application
L-701,324 is a selective antagonist at the glycine site of the NMDA receptor, counteracts haloperidol-induced muscle rigidity in rats.
Cas No.: |
142326-59-8 |
Chemical Name: |
2(1H)-Quinolinone,7-chloro-4-hydroxy-3-(3-phenoxyphenyl)- |
Synonyms: |
2(1H)-Quinolinone,7-chloro-4-hydroxy-3-(3-phenoxyphenyl)-;7-Chloro-1-(4-hydroxy-3-phenoxyphenyl)-quinolin-2(1H)-one;7-Chloro-4-hydroxy-3-(3-phenoxy)phenyl-2(1H)-quinolinone;7-chloro-4-hydroxy-3-(3-phenoxyphenyl)-1H-quinolin-2-one;L-701,324;Sulprostone;7-Chloro-4-hydroxy-3-(3-phenoxy)phenylquinolin-2[1H]-one;L 701324;L-701324 |
SMILES: |
O=C1NC2=C(C=CC(Cl)=C2)C(O)=C1C3=CC=CC(OC4=CC=CC=C4)=C3 |
Formula: |
C21H14NO3Cl |
M.Wt: |
363.79376 |
Purity: |
>98% |
Sotrage: |
2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: |
L-701324 is an orally active and long acting anticonvulsant with high affinity and selectivity for the glycine site on the NMDA receptor.Target: NMDA ReceptorL-701324 is a potent, active anticonvulsant with a reduced propensity to activate mesolimbic dopaminergic systems in rodents. L-701324 exhibits a beneficial action in the animal model of parkinsonian rigidity, but not that of parkinsonian akinesia. L-701324 (2.5-40 mg/kg, i.p.) dose-dependently decreased the muscle tone enhanced by haloperidol (1-5 mg/kg, i.p.). |
References: |
[1]. Piotr Wlaz, et al. Differential effects of glycine on the anticonvulsant activity of D-cycloserine and L-701,324 in mice. Pharmacological Reports 2011,63,1231-1234 |
MSDS
COA
LOT NO. |
DOWNLOAD |
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2018-0101 |
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2018-0101 |
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