Description
An allosteric agonist of M1 mAChRs (EC50 = 158 nM in CHO-K1 cells expressing rat recombinant receptors); selective for M1 over M2-5 receptors at concentrations up to 10 μM; potentiates NMDA-evoked currents in CA1 pyramidal cells at 3 μM; increases production of the non-amyloidogenic APP cleavage products APPsα and CTFα in PC12 cells overexpressing the human M1 receptor and APP at 1 μM; decreases amphetamine-induced hyperlocomotion in in a rat model that is predictive of antipsychotic-like activity
Formal name: 1,3-dihydro-1-[1′-[(2-methylphenyl)methyl][1,4′-bipiperidin]-4-yl]-2H-benzimidazol-2-one
Synonyms:
Molecular weight: 404.6
CAS: 634616-95-8
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Ion Channel Modulation|Activators||Product Type|Biochemicals|Receptor Pharmacology|Agonists||Research Area|Neuroscience|Behavioral Neuroscience|Schizophrenia & Psychosis||Research Area|Neuroscience|Neurodegenerative Disorders|Alzheimer’s Disease