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Details

Stereochemistry ACHIRAL
Molecular Formula C28H42N2O5.ClH
Molecular Weight 523.104
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENOXEDIL HYDROCHLORIDE

SMILES

Cl.CCCCOC1=CC=C(OCC(=O)N(CCN(CC)CC)C2=C(OCC)C=CC(OCC)=C2)C=C1

InChI

InChIKey=UFFFQSODDRXNMI-UHFFFAOYSA-N
InChI=1S/C28H42N2O5.ClH/c1-6-11-20-34-23-12-14-24(15-13-23)35-22-28(31)30(19-18-29(7-2)8-3)26-21-25(32-9-4)16-17-27(26)33-10-5;/h12-17,21H,6-11,18-20,22H2,1-5H3;1H

HIDE SMILES / InChI
Fenoxedil is a quinidine-like agent that has a very strong class I antiarrhythmic effect, to the point that it is now almost abandoned after having given toxicity accidents.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Treatment of atrial fibrillation with fenoxedil hydrochloride. Apropos of 112 cases].
1984-01
Patents
Name Type Language
FENOXEDIL HYDROCHLORIDE
MI  
Common Name English
SUPLEXEDIL
Preferred Name English
2-(P-BUTOXYPHENYL)-N-(2-(DIETHYLAMINO)ETHYL)-2',5'-DIETHOXYACETANILIDE HYDROCHLORIDE
Common Name English
FENOXEDIL HYDROCHLORIDE [MI]
Common Name English
ACETAMIDE, 2-(4-BUTOXYPHENOXY)-N-(2,5-DIETHOXYPHENYL)-N-(2-(DIETHYLAMINO)ETHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
FDA UNII
1056JI5L58
Created by admin on Mon Mar 31 21:20:07 GMT 2025 , Edited by admin on Mon Mar 31 21:20:07 GMT 2025
PRIMARY
ECHA (EC/EINECS)
248-478-1
Created by admin on Mon Mar 31 21:20:07 GMT 2025 , Edited by admin on Mon Mar 31 21:20:07 GMT 2025
PRIMARY
SMS_ID
100000128531
Created by admin on Mon Mar 31 21:20:07 GMT 2025 , Edited by admin on Mon Mar 31 21:20:07 GMT 2025
PRIMARY
EVMPD
SUB35639
Created by admin on Mon Mar 31 21:20:07 GMT 2025 , Edited by admin on Mon Mar 31 21:20:07 GMT 2025
PRIMARY
MERCK INDEX
m1159
Created by admin on Mon Mar 31 21:20:07 GMT 2025 , Edited by admin on Mon Mar 31 21:20:07 GMT 2025
PRIMARY Merck Index
CAS
27471-60-9
Created by admin on Mon Mar 31 21:20:07 GMT 2025 , Edited by admin on Mon Mar 31 21:20:07 GMT 2025
PRIMARY
PUBCHEM
119645
Created by admin on Mon Mar 31 21:20:07 GMT 2025 , Edited by admin on Mon Mar 31 21:20:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID30181896
Created by admin on Mon Mar 31 21:20:07 GMT 2025 , Edited by admin on Mon Mar 31 21:20:07 GMT 2025
PRIMARY