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Description
Overview
An agonist selective for muscarinic acetylcholine receptor (mAChR) subtype M1 (EC50 = 0.3, 5, 42, 52 and 92.5 nM at M1, M3, M5, M4 and M2 receptors respectively). An antipsychotic agent. Used in improving cognitive deficits and behavioral disturbances in Alzheimer's disease and schizophrenia.
Wang, D., et al., 2011. Biochem. Biophys. Res. Commun.410, 229. Si, W., et al., 2010. Neurosci. Lett.473, 115. Stanhope, et al., 2001. J. Exp. Pharmacol. Ther.299, 782.
Wang, D., et al., 2011. Biochem. Biophys. Res. Commun.410, 229. Si, W., et al., 2010. Neurosci. Lett.473, 115. Stanhope, et al., 2001. J. Exp. Pharmacol. Ther.299, 782.
Data Sheet
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.
An agonist selective for muscarinic acetylcholine receptor (mAChR) subtype M1 (EC50 = 0.3, 5, 42, 52 and 92.5 nM at M1, M3, M5, M4 and M2 receptors respectively). An antipsychotic agent. Used in improving cognitive deficits and behavioral disturbances in Alzheimer′s disease and schizophrenia.
Form
Off-white solid
CAS number
141064-23-5
Chemical formula
C₁₄H₂₃N₃OS•C₂H₂O₄
Structure formula
Purity
≥99% by HPLC
Solubility
DMSO (10 mM) or Ethanol (25 mM)
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
Wang, D., et al., 2011. Biochem. Biophys. Res. Commun.410, 229. Si, W., et al., 2010. Neurosci. Lett.473, 115. Stanhope, et al., 2001. J. Exp. Pharmacol. Ther.299, 782.