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1177279-49-0

1177279-49-0 Structure

1177279-49-0 Structure
IdentificationBack Directory
[Name]

4-(aminomethyl)-1-benzylpyrrolidin-2-one hydrochloride
[CAS]

1177279-49-0
[Synonyms]

Nebracetam hydrochloride
WEB 1881 FU hydrochloride
4-(aminomethyl)-1-benzylpyrrolidin-2-one hydrochloride
[Molecular Formula]

C12H17ClN2O
[MDL Number]

MFCD09743242
[MOL File]

1177279-49-0.mol
[Molecular Weight]

240.729
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C, protect from light, sealed storage, away from moisture
[solubility ]

Soluble in DMSO
[form ]

Solid
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302-H315
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Hazard InformationBack Directory
[Uses]

Nebracetam hydrochloride, a nootropic M1-muscarinic agonist, induces a rise of intracellular Ca2+ concentration. Nebracetam hydrochloride exhibits an EC50 of 1.59 mM for elevating [Ca2+]i[1].
[in vivo]

Nebracetam (10 mg/kg, p.o.) involves not only cholinergic mechanisms but also involves lymbic and hippocampal noradrenergic mechanisms[2].

Animal Model:Male Wistar rats weighing 200-250 g[2].
Dosage:10, 20 mg/kg.
Administration:P.O. (single dose).
Result:Able to correct this scopolamine-induced disruption of spatial cognition.
[References]

[1] Kitamura Y, et al. Effects of nebracetam (WEB 1881 FU), a novel nootropic, as a M1-muscarinic agonist. Jpn J Pharmacol. 1991 Jan;55(1):177-80. DOI:10.1254/jjp.55.177
[2] Iwasaki K, et al. Effect of nebracetam on the disruption of spatial cognition in rats. Jpn J Pharmacol. 1992 Feb;58(2):117-26. DOI:10.1254/jjp.58.117
Spectrum DetailBack Directory
[Spectrum Detail]

4-(aminomethyl)-1-benzylpyrrolidin-2-one hydrochloride(1177279-49-0)1HNMR
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