Chemical Name: 4-Ethyl-6,7-dimethoxy-9H-pyrido[3,4-b]indole-3-carboxylic acid methyl ester hydrochloride
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Benzodiazepine inverse agonist that displays anxiogenic and potent convulsant activity.
Technical Data
M. Wt
350.8
Formula
C17H18N2O4.HCl
Storage
Desiccate at RT
Purity
≥98% (HPLC)
CAS Number
1215833-62-7
PubChem ID
45261899
InChI Key
FHCRBVQGMZUJKY-UHFFFAOYSA-N
Smiles
CCC1=C(C(OC)=O)N=CC3=C1C2=CC(OC)=C(OC)C=C2N3.Cl
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
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
DMSO
17.54
50
water
31.43
100
Preparing Stock Solutions
The following data is based on the product molecular weight 350.8. 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
2.85 mL
14.25 mL
28.51 mL
5 mM
0.57 mL
2.85 mL
5.7 mL
10 mM
0.29 mL
1.43 mL
2.85 mL
50 mM
0.06 mL
0.29 mL
0.57 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.
Contoet al (2005) Behavioral differences between subgroups of rats with high and low threshold to clonic convulsions induced by DMCM, a benzodiazepine inverse agonist. Pharmacol.Biochem.Behav. 82 417 PMID: 16297441
Sieveet al (2001) Pain and negative affect: evidence the inverse benzodiazepine agonist DMCM inhibits pain and learning in rats. Psychopharmacol. 153 180 PMID: