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ChemicalBook--->CAS DataBase List--->58934-46-6

58934-46-6

58934-46-6 Structure

58934-46-6 Structure
IdentificationBack Directory
[Name]

N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride
[CAS]

58934-46-6
[Synonyms]

Nsc310411
Lorcainide HCl
EINECS 261-504-6
LORCAINIDE HYDROCHLORIDE
Isocainide hydrochloride
4'-Chloro-N-(1-isopropyl-4-piperidyl)-2-phenylacetanilide monohydrochloride
N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride
N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride USP/EP/BP
Benzeneacetamide, N-(4-chlorophenyl)-N-[1-(1-methylethyl)-4-piperidinyl]-, monohydrochloride
[EINECS(EC#)]

261-504-6
[Molecular Formula]

C22H28Cl2N2O
[MOL File]

58934-46-6.mol
[Molecular Weight]

407.377
Chemical PropertiesBack Directory
[Melting point ]

263°
[storage temp. ]

-20°C
[solubility ]

Soluble in DMSO (up to 20 mg/ml), in Water (up to 20 mg/ml), or in Ethanol (up to 20 mg/ml).
[form ]

White solid.
[color ]

Powder
[Water Solubility ]

H2O: 10mg/mL, clear
[Stability:]

Stable for 1 year from date of purchase as supplied. Solutions in DMSO, distilled water or ethanol may be stored at -20°C for up to 1 month
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312a-P330-P501a
Hazard InformationBack Directory
[Description]

Lorcainide hydrochloride (58934-46-6) is a voltage-gated Na+?channel blocker.1?Protects murine cultured cortical neurons from injury induced by oxygen-glucose deprivation.2?Acts at the ouabain binding site of guinea pig cardiac Na+/K+?ATPase and inhibits the enzyme (IC50?= 34 μM).3
[Uses]

Cardiac depressant (anti-arrhythmic).
[References]

1) Sheldon?et al.?(1989),?Antiarrhythmic drugs and the cardiac sodium channel: current models; Clin. Chem.,?35?748 2) Lynch?et al.?(1995),?Sodium channel clockers reduce oxygen-glucose deprivation-induced cortical neuronal injury when combined with glutamate receptor antagonists; J. Pharmacol. Exp. Ther.,?273?554 3) Almotrefi?et al. (1999),?Class I antiarrhythmic drug effects on ouabain binding to guinea pig cardiac Na+ -K+ ATPase; Can. J. Physiol. Pharmacol.,?77?866
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