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195615-84-0

195615-84-0 structure
195615-84-0 structure
  • Name: AN2/AVex-73 hydrochloride salt
  • Chemical Name: 1-(2,2-Diphenyltetrahydro-3-furanyl)-N,N-dimethylmethanamine hydrochloride (1:1)
  • CAS Number: 195615-84-0
  • Molecular Formula: C19H24ClNO
  • Molecular Weight: 317.853
  • Catalog: Signaling Pathways GPCR/G Protein Sigma Receptor
  • Create Date: 2018-04-18 12:16:44
  • Modify Date: 2024-01-09 23:06:54
  • AVex-73 hydrochloride is a Sigma-1 Receptor agonist with an IC50 of 860 nM.

Name 1-(2,2-Diphenyltetrahydro-3-furanyl)-N,N-dimethylmethanamine hydrochloride (1:1)
Synonyms 1-(2,2-Diphenyltetrahydro-3-furanyl)-N,N-dimethylmethanaminhydrochlorid (1:1)
3-Furanmethanamine, tetrahydro-N,N-dimethyl-2,2-diphenyl-, hydrochloride (1:1)
1-(2,2-Diphényltétrahydro-3-furanyl)-N,N-diméthylméthanamine, chlorhydrate (1:1)
1-(2,2-Diphenyltetrahydro-3-furanyl)-N,N-dimethylmethanamine hydrochloride (1:1)
Anavex 2-73
AVex-73 hydrochloride
Description AVex-73 hydrochloride is a Sigma-1 Receptor agonist with an IC50 of 860 nM.
Related Catalog
Target

IC50: 860 nM (Sigma-1 Receptor)[1]

In Vivo The pre-administration of AVex-73 hydrochloride (ANAVEX2-73) leads to a dose-dependent attenuation of the scopolamine induced alternation deficit, significant at 1 and 3 mg/kg. The pre-treatment with AVex-73 hydrochloride attenuates the impairments of step-through latency, dose dependently and significantly at doses higher than 0.3 mg/kg[1]. The AVex-73 hydrochloride treatment dose-dependently blocks the recognition memory deficit, with a significant effect measured at 1 mg/kg. One day after injections, the significant Aβ25-35-induced decrease in Akt phosphorylation is significantly attenuated by AVex-73 hydrochloride at 0.1 and 1 mg/kg dose. Seven days after injections,AVex-73 hydrochloride attenuates the decrease in Ser9 phosphorylation induced by the peptide at 0.3 and 1 mg/kg. The AVex-73 hydrochloride treatment dose-dependently prevents the Aβ25-35-induced increase in Aβ1-42 content, with a significant effect at the highest dose tested[2].
Animal Admin Male mice aged 7-9 weeks and weighing 32±2 g are used. Drugs (including AVex-73 hydrochloride) are brought up to each dose by dilution and injected in a volume of 100 μL/20 g body weight. Animals are used between days 1 and 9 after i.c.v. injections for behavioral testing or killed before biochemical measures[2].
References

[1]. Villard V, et al. Anti-amnesic and neuroprotective potentials of the mixed muscarinic receptor/sigma 1 (σ1) ligand ANAVEX2-73, a novel aminotetrahydrofuran derivative. J Psychopharmacol. 2011 Aug;25(8):1101-17.

[2]. Valentine Lahmy, et al. Blockade of Tau Hyperphosphorylation and Aβ1-42 Generation by the Aminotetrahydrofuran Derivative ANAVEX2-73, a Mixed Muscarinic andσ1 Receptor Agonist, in a Nontransgenic Mouse Model of Alzheimer's Disease. Neuropsychopharmacology. 2013 Aug; 38(9): 1706-1723.

Molecular Formula C19H24ClNO
Molecular Weight 317.853
Exact Mass 317.154633
Storage condition -20℃