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Details

Stereochemistry RACEMIC
Molecular Formula C22H28N2O3
Molecular Weight 368.4693
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MODECAINIDE

SMILES

COC1=CC(=CC=C1O)C(=O)NC2=C(CCC3CCCCN3C)C=CC=C2

InChI

InChIKey=LBYXPDAENJSHDD-UHFFFAOYSA-N
InChI=1S/C22H28N2O3/c1-24-14-6-5-8-18(24)12-10-16-7-3-4-9-19(16)23-22(26)17-11-13-20(25)21(15-17)27-2/h3-4,7,9,11,13,15,18,25H,5-6,8,10,12,14H2,1-2H3,(H,23,26)

HIDE SMILES / InChI

Molecular Formula C22H28N2O3
Molecular Weight 368.4693
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Modecainide is a benzanilide derivative patented by American pharmaceutical company Bristol-Myers Co. as type Ic antiarrhythmic agent. Modecainide is a major metabolite of Encainide, a class Ic antiarrhythmic, with comparable antiarrhythmic activity. Modecainide is never marketed because of its frequent proarrhythmic side effects.

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative antiarrhythmic actions of encainide and its major metabolites.
1986 Jun
Patents

Patents

Sample Use Guides

50 mg, every 6 hours
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:17:42 GMT 2023
Edited
by admin
on Fri Dec 15 15:17:42 GMT 2023
Record UNII
JU27887FWK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MODECAINIDE
INN   USAN  
USAN   INN  
Official Name English
BENZAMIDE, 4-HYDROXY-3-METHOXY-N-(2-(2-(1-METHYL-2-PIPERIDINYL)ETHYL)PHENYL)-, (±)-
Systematic Name English
BENZAMIDE, 4-HYDROXY-3-METHOXY-N-(2-(2-(1-METHYL-2-PIPERIDINYL)ETHYL)PHENYL)-
Systematic Name English
modecainide [INN]
Common Name English
BMY-40327
Code English
MJ-14030
Code English
(±)-2'-(2-(1-METHYL-2-PIPERIDYL)ETHYL)VANILLANILIDE
Systematic Name English
3-METHOXY-O-DESMETHYLENCAINIDE
Common Name English
MODECAINIDE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47793
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
Code System Code Type Description
USAN
BB-52
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106770
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
PRIMARY
CAS
81329-71-7
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
PRIMARY
NCI_THESAURUS
C90665
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
PRIMARY
PUBCHEM
54737
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
PRIMARY
SMS_ID
100000080330
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
PRIMARY
FDA UNII
JU27887FWK
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
PRIMARY
EVMPD
SUB09028MIG
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
PRIMARY
INN
6634
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
PRIMARY
CAS
82522-70-1
Created by admin on Fri Dec 15 15:17:42 GMT 2023 , Edited by admin on Fri Dec 15 15:17:42 GMT 2023
SUPERSEDED
Related Record Type Details
ACTIVE MOIETY