Alternative Names: Normethylclozapine, Norclozapine
Chemical Name: 8-Chloro-11-(1-piperazinyl)-5H-dibenzo[b,e][1,4]diazepine
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
A major metabolite of clozapine; a potent and selective 5-HT2C serotonin receptor antagonist.
Technical Data
M. Wt
312.8
Formula
C17H17ClN4
Storage
Store at RT
Purity
≥99% (HPLC)
CAS Number
6104-71-8
PubChem ID
210172
InChI Key
NIBOMXUDFLRHRV-UHFFFAOYSA-N
Smiles
ClC1=CC=C2NC3=C(C=CC=C3)C(=NC2=C1)N1CCNCC1
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
31.28
100
ethanol
31.28
100
Preparing Stock Solutions
The following data is based on the product molecular weight 312.8. 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
3.2 mL
15.98 mL
31.97 mL
5 mM
0.64 mL
3.2 mL
6.39 mL
10 mM
0.32 mL
1.6 mL
3.2 mL
50 mM
0.06 mL
0.32 mL
0.64 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.
Fox and Brotchie
(1996) Normethylclozapine potentiates the action of quinpirole in the 6-hydroxydopamine lesioned rat. Eur.J.Pharmacol. 301 27 PMID: 8773443
Kuoppamäkiet al (1993) Clozapine and methylclozapine are potent 5-HT1C receptor antagonists. Eur.J.Pharmacol. 245 179 PMID: 8387927
Wonget al (1996) Effects of clozapine metabolites and chronic clozapine treatment on rat brain GABAA receptors. Eur.J.Pharmacol. 314 319 PMID: 8957253