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Description
Overview
A selective positive allosteric modulator for mGlu receptor subtype 2 (EC50 = 33.2 nM in CHO cells expressing human mGlu2). No effect on other mGlu receptor subtypes. Exhibits antipsychotic and anxiolytic properties in mice.
Catalogue Number
504463
Brand Family
Calbiochem®
Synonyms
Biphenyl-indanone A
References
References
Bonnefous, C., et al. 2005. Bioorg. Med. Chem. Lett.15, 4354. Galici, R., et al. 2006. J. Pharmacol. Exp. Ther.318, 173. Benneyworth, M., et al. 2007. Mol. Pharmacol.72, 477. Sheffler, D., et al. 2011. ACS Chem. Neurosci.2, 382.
Bonnefous, C., et al. 2005. Bioorg. Med. Chem. Lett.15, 4354. Galici, R., et al. 2006. J. Pharmacol. Exp. Ther.318, 173. Benneyworth, M., et al. 2007. Mol. Pharmacol.72, 477. Sheffler, D., et al. 2011. ACS Chem. Neurosci.2, 382.
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
28-June-2013 JSW
Synonyms
Biphenyl-indanone A
Description
A selective positive allosteric modulator for mGlu receptor subtype 2 (EC50 = 33.2 nM in CHO cells expressing human mGlu2). No effect on other mGlu receptor subtypes. Exhibits antipsychotic and anxiolytic properties in mice.
Form
White powder
CAS number
866823-73-6
Chemical formula
C₃₀H₃₀O₄
Structure formula
Purity
≥98% by HPLC
Solubility
DMSO (18 mg/ml)
Storage
Protect from light
+2°C to +8°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity
Standard Handling
References
Bonnefous, C., et al. 2005. Bioorg. Med. Chem. Lett.15, 4354. Galici, R., et al. 2006. J. Pharmacol. Exp. Ther.318, 173. Benneyworth, M., et al. 2007. Mol. Pharmacol.72, 477. Sheffler, D., et al. 2011. ACS Chem. Neurosci.2, 382.