EPICAINIDE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C21H26N2O2
Molecular Weight	338.4433
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of EPICAINIDE

Structure Search

SMILES

CCN1CCCC1CNC(=O)C(O)(C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=LMXFPUVUUSHCMM-UHFFFAOYSA-N

InChI=1S/C21H26N2O2/c1-2-23-15-9-14-19(23)16-22-20(24)21(25,17-10-5-3-6-11-17)18-12-7-4-8-13-18/h3-8,10-13,19,25H,2,9,14-16H2,1H3,(H,22,24)

HIDE SMILES / InChI

Molecular Formula	C21H26N2O2
Molecular Weight	338.4433
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2756714

There is no information about pharmacological and biological properties of epicainide. It is known, that drug was a potent antiarrhythmic agent.

Approval Year

Conditions

Conditions

Condition	Modality	Targets	Highest Phase	Product
Unknown 2596

PubMed

PubMed

Title	Date	PubMed
Differences in the metabolism of epicainide in rats and man.	1989-01	2756714

Patents

Patents

Sample Use Guides

In Vivo Use Guide

Unknown

Route of Administration: Unknown

In Vitro Use Guide

Unknown

Substance Class	Chemical Created by `admin` on `Wed Apr 02 08:49:30 GMT 2025` Edited by `admin` on `Wed Apr 02 08:49:30 GMT 2025`
Record UNII	DZY7AR1B0U
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

epicainide [INN]

Preferred Name

English

EPICAINIDE

Official Name

English

N-((1-ETHYL-2-PYRROLIDINYL)METHYL)BENZILAMIDE

Systematic Name

English

Classification Tree Code System Code

NCI_THESAURUS

C47793

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

Code System Code Type Description

MESH

C060578

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

PRIMARY

PUBCHEM

68862

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

PRIMARY

INN

4531

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

PRIMARY

ChEMBL

CHEMBL2107538

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

PRIMARY

EVMPD

SUB06562MIG

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

PRIMARY

FDA UNII

DZY7AR1B0U

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

PRIMARY

EPA CompTox

DTXSID1057799

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

PRIMARY

SMS_ID

100000080450

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

PRIMARY

NCI_THESAURUS

C72580

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

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CAS

66304-03-8

Created by admin on Wed Apr 02 08:49:30 GMT 2025 , Edited by admin on Wed Apr 02 08:49:30 GMT 2025

PRIMARY

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					DZY7AR1B0U

ACTIVE MOIETY