N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride

N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride Basic information
Product Name:N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride
Synonyms:N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride;LORCAINIDE HYDROCHLORIDE;Isocainide hydrochloride;4'-Chloro-N-(1-isopropyl-4-piperidyl)-2-phenylacetanilide monohydrochloride;Benzeneacetamide, N-(4-chlorophenyl)-N-[1-(1-methylethyl)-4-piperidinyl]-, monohydrochloride;Nsc310411;N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride USP/EP/BP;Lorcainide HCl
CAS:58934-46-6
MF:C22H28Cl2N2O
MW:407.37652
EINECS:261-504-6
Product Categories:
Mol File:58934-46-6.mol
N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride Structure
N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride Chemical Properties
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
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 Information
MSDS Information
N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride Usage And Synthesis
DescriptionLorcainide 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
UsesCardiac depressant (anti-arrhythmic).
References1) 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
N-(4-chlorophenyl)-N-(1-isopropyl-4-piperidyl)phenylacetamide monohydrochloride Preparation Products And Raw materials
N,N-DIETHYL-N',N'-DIMETHYL-1,3-PROPANDIAMINE N,N-Dimethylpiperidin-4-amine 1,3-Propanediamine,N3,N3-diethyl-1-phenyl- N-ETHYL-N-ISOPROPYLANILINE N-PHENYLPIPERIDIN-4-AMINE DIHYDROCHLORIDE 4-ACETAMIDOPIPERIDINE N,N-DIMETHYL-2-PHENYLACETAMIDE N-METHYL-N-4-PIPERIDINYL-BENZENEACETAMIDE N,N,N',N'-TETRAMETHYL-1,3-BUTANEDIAMINE N-METHYL-N-4-PIPERIDINYLACETAMIDE N-phenylpiperidin-4-amine 1,3-DIAMINOPROPANE DIHYDROCHLORIDE 1-ETHYL-PIPERIDIN-4-YLAMINE 4-Aminopiperidine dihydrochloride 4-(dimethylammonio)piperidinium dichloride N-(4-CHLOROPHENYL)-N-ETHYLFORMAMIDE 2,N-DIPHENYLACETAMIDE 4-CHLORO-N-METHYLFORMANILIDE

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