Description
A BKCa channel activator; increases BKCa currents in X. laevis oocytes expressing human BKCa; decreases electrically induced pEPSPs in vitro in CA1 rat neurons and in anesthetized rats from 0.005-1 mg/kg; reduces infarct volume in an MCAO-induced rat model of ischemic stroke at 0.001 and 0.3 mg/kg; decreases edema in the ipsilateral hippocampus, thalamus, and adjacent cortex and time to find the platform in the Morris water maze in a rat model of fluid percussion-induced TBI; reverses cortical hyperexcitability and reduces hyperactivity and grooming behaviors in the FmrI-/- mouse model of Fragile X syndrome
Formal name: (3S)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-1,3-dihydro-6-(trifluoromethyl)-2H-indol-2-one
Synonyms: (+)-BMS 204352
Molecular weight: 359.7
CAS: 187523-35-9
Purity: ≥98%
Formulation: A crystalline solid