Description: Potent systemically active anticonvulsant. Racemate of (R)-3,4,-DCPG (Cat. No. 1395)
Chemical Name: (RS)-3,4-Dicarboxyphenylglycine
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Systemically active anticonvulsant that is 30-100-fold more potent in vivo than the separate enantiomers (S)-3,4-DCPG (Cat. No. 1302) or (R)-3,4,-DCPG (Cat. No. 1395).
Technical Data
M. Wt
239.18
Formula
C10H9NO6
Storage
Desiccate at RT
Purity
≥99% (HPLC)
CAS Number
176796-64-8
PubChem ID
3313698
InChI Key
IJVMOGKBEVRBPP-UHFFFAOYSA-N
Smiles
NC(C(O)=O)C1=CC=C(C(O)=O)C(=C1)C(O)=O
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 water
Preparing Stock Solutions
The following data is based on the product molecular weight 239.18. 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
4.18 mL
20.9 mL
41.81 mL
5 mM
0.84 mL
4.18 mL
8.36 mL
10 mM
0.42 mL
2.09 mL
4.18 mL
50 mM
0.08 mL
0.42 mL
0.84 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.
Moldrichet al (2001) Anticonvulsant activity of 3,4-dicarboxyphenylglycines in DBA/2 mice. Neuropharmacology 40 732 PMID: 11311902
Thomaset al (1997) Dicarboxyphenylglycines antagonize AMPA- but not kainate-induced depolarizations in neonatal rat motoneurones. Eur.J.Pharmacol. 338 111 PMID: 9455991
Thomaset al (1998) Pharmacological differentiation of kainate receptors on neonatal rat spinal motoneurones and dorsal roots. Neuropharmacology 37 1223 PMID: 9849660