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Details

Stereochemistry RACEMIC
Molecular Formula C27H31NO3
Molecular Weight 417.5399
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ASOCAINOL

SMILES

COC1=CC2=C(CCN(C)C(CCC3=CC=CC=C3)CC4=CC=C(OC)C(O)=C24)C=C1

InChI

InChIKey=IORHSKBXWWSQME-UHFFFAOYSA-N
InChI=1S/C27H31NO3/c1-28-16-15-20-10-13-23(30-2)18-24(20)26-21(11-14-25(31-3)27(26)29)17-22(28)12-9-19-7-5-4-6-8-19/h4-8,10-11,13-14,18,22,29H,9,12,15-17H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C27H31NO3
Molecular Weight 417.5399
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Asocainol is a rather efficient antiarrhythmic agent that has the effects of both class Ia and class IV antiarrhythmic drugs. Asocainol interfere with the sodium channel and lengthens the action potential. Besides that, Asocainol decreases conduction through the AV node, and shorten phase two (the plateau) of the cardiac action potential. Asocainol reduce the contractility of the heart, so may be inappropriate in heart failure. Asocainol is an effective antiarrhythmic agent in a variety of animal arrhythmia models and species.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:57:23 GMT 2023
Edited
by admin
on Fri Dec 15 16:57:23 GMT 2023
Record UNII
J40338OKKT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ASOCAINOL
INN  
INN  
Official Name English
asocainol [INN]
Common Name English
(±)-6,7,8,9-TETRAHYDRO-2,12-DIMETHOXY-7-METHYL-6-PHENETHYL-5H-DIBENZ(D,F)AZONIN-1-OL
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C47793
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
Code System Code Type Description
INN
5092
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
EVMPD
SUB05583MIG
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
MESH
C042287
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
NCI_THESAURUS
C72574
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104050
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
WIKIPEDIA
ASOCAINOL
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
FDA UNII
J40338OKKT
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
CAS
77400-65-8
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
PUBCHEM
71161
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
SMS_ID
100000086608
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
EPA CompTox
DTXSID90868434
Created by admin on Fri Dec 15 16:57:23 GMT 2023 , Edited by admin on Fri Dec 15 16:57:23 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY