Chemical Name: 6-Methoxy-N-(4-methoxyphenyl)-4-quinazolinamine hydrochloride
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Selective mGlu1 receptor antagonist (IC50 values are 143 nM and > 10 μM for mGlu1 and mGlu5 receptors respectively). Reduces hyperalgesic behavior induced by formalin in both mouse and rat with ED50 values of 28 and 16.3 mg/kg respectively.
Compound Libraries
LY 456236 hydrochloride is also offered as part of the
Tocriscreen Plus. Find out more about compound libraries available from Tocris.
Technical Data
M. Wt
317.77
Formula
C16H15N3O2.HCl
Storage
Desiccate at RT
Purity
≥99% (HPLC)
CAS Number
338736-46-2
PubChem ID
9926998
InChI Key
AVKFOWUSTVWZQN-UHFFFAOYSA-N
Smiles
Cl.COC1=CC=C(NC2=C3C=C(OC)C=CC3=NC=N2)C=C1
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
6.36
20
Preparing Stock Solutions
The following data is based on the product molecular weight 317.77. 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
3.15 mL
15.73 mL
31.47 mL
5 mM
0.63 mL
3.15 mL
6.29 mL
10 mM
0.31 mL
1.57 mL
3.15 mL
50 mM
0.06 mL
0.31 mL
0.63 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.
Shannonet al (2005) Anticonvulsant effects of LY456236, a selective mGlu1 receptor antagonist. Neuropharmacology 49 188 PMID: 16011839
Bertorelliet al (2005) Selective blockade of metabotropic glutamate subtype mGluR1 receptors induce anti-nociceptive effects. Neuropharmacology 49 231 PMID: