ChemicalBook--->CAS DataBase List--->195615-83-9

195615-83-9

195615-83-9 Structure

195615-83-9 Structure
IdentificationBack Directory
[Name]

AVex-73
[CAS]

195615-83-9
[Synonyms]

AE38
AE37
CS-2603
AVex-73
Blarcamesine (Anavex-2-73)
1-(2,2-diphenyloxolan-3-yl)-N,N-dimethylmethanamine
3-Furanmethanamine, tetrahydro-N,N-dimethyl-2,2-diphenyl-
[Molecular Formula]

C19H23NO
[MDL Number]

MFCD28502178
[MOL File]

195615-83-9.mol
[Molecular Weight]

281.39
Chemical PropertiesBack Directory
[solubility ]

DMF: 30 mg/ml
DMSO: Slightly soluble
Ethanol: 30 mg/ml
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

Blarcamesine is an orally bioavailable Sigma-1 receptor agonist and muscarinic receptor modulator, with anticonvulsant, anti-amnesic, neuroprotective and antidepressant properties. Blarcamesine ameliorates neurologic impairments in a mouse model of Rett syndrome[1].
[in vivo]

Blarcamesine (10 mg/kg, 30 mg/kg; p.o.; daily; for 6.5 weeks) ameliorates motor deficits in Mecp2 HET mice with chronic administration[1].
Blarcamesine ameliorates acoustic startle deficit in Mecp2 HET mice[1].
Blarcamesine reverses deficits in visual acuity in older Mecp2 HET mice using the optokinetic response[1].
Blarcamesine produces minimal effects on body weight gain in Mecp2 HET mice[1].

Animal Model:Female Mecp2tm1.1Bird/J HET (C57 background) mice[1]
Dosage:10 mg/kg, 30 mg/kg
Administration:Oral administration, daily, for 6.5 weeks
Result:Reverse the deficits observed in the HET animals.
[IC 50]

Sigma 1 Receptor
[References]

[1] Walter E Kaufmann, et al. ANAVEX?2-73 (Blarcamesine), a Sigma-1 Receptor Agonist, Ameliorates Neurologic Impairments in a Mouse Model of Rett Syndrome. Pharmacol Biochem Behav . 2019 Dec;187:172796. DOI:10.1016/j.pbb.2019.172796
Spectrum DetailBack Directory
[Spectrum Detail]

AVex-73(195615-83-9)1HNMR
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