Chemical Name: 7-Chloro-3-(cyclopropylcarbonyl)-4-hydroxy-2(1H)-quinolinone
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
An antagonist at the glycine-NMDA site (IC50 = 420 nM). Also a potent systemic anticonvulsant.
Licensing Information
Sold with the permission of Merck Sharp and Dohme Ltd.
Technical Data
M. Wt
263.68
Formula
C13H10ClNO3
Storage
Desiccate at +4°C
Purity
≥99% (HPLC)
CAS Number
151057-13-5
PubChem ID
54687453
InChI Key
MXEFWCFPCLDOOG-UHFFFAOYSA-N
Smiles
OC1=C(C(=O)C2CC2)C(=O)NC2=C1C=CC(Cl)=C2
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solubility
Soluble to 50 mM in DMSO
Preparing Stock Solutions
The following data is based on the product molecular weight 263.68. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
3.79 mL
18.96 mL
37.92 mL
5 mM
0.76 mL
3.79 mL
7.58 mL
10 mM
0.38 mL
1.9 mL
3.79 mL
50 mM
0.08 mL
0.38 mL
0.76 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Rowleyet al (1993) 3-Acyl-4-hydroxyquinolin-2(1H)-ones. Systemically active anticonvulsants acting by antagonism at the glycine site of the NMDA receptor complex. J.Med.Chem. 36 3386 PMID: 8230129
Stone
(2000) Development and therapeutic potential of kynurenic acid and kynurenine derivatives for neuroprotection. TiPS 21 149 PMID: 10740291