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Details

Stereochemistry RACEMIC
Molecular Formula C23H29N3O3
Molecular Weight 395.4947
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EPROXINDINE

SMILES

CCN(CC)CC(O)CNC(=O)C1=C(OC)C2=C(C=CC=C2)N1C3=CC=CC=C3

InChI

InChIKey=JZQYAVBXJCQSOK-UHFFFAOYSA-N
InChI=1S/C23H29N3O3/c1-4-25(5-2)16-18(27)15-24-23(28)21-22(29-3)19-13-9-10-14-20(19)26(21)17-11-7-6-8-12-17/h6-14,18,27H,4-5,15-16H2,1-3H3,(H,24,28)

HIDE SMILES / InChI

Molecular Formula C23H29N3O3
Molecular Weight 395.4947
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Eproxindine (KC 3791) is an antiarrythmic. It is able to inactivate voltage-dependent sodium channels. Eproxindine also proved to be capable of blocking open potassium channels at outwardly directed potassium currents

Approval Year

PubMed

PubMed

TitleDatePubMed
The role of inactivation in the cumulative blockage of voltage-dependent sodium channels by local anesthetics and antiarrythmics.
1984 Dec
Use-dependent blockade of sodium channels by local anaesthetics and antiarrhythmic drugs. Effects of chloramine-T and calcium ions.
1986
Effects of KC 3791 on sodium and potassium channels in frog node of Ranvier.
1986 Dec
Determination of eproxindine hydrochloride in human plasma by capillary gas chromatography.
1988 May 13
Patents

Patents

Sample Use Guides

Eproxindine (KC 3791) When applied externally to the node of Ranvier, KC 3791 (KC) at concentrations of 10-100 uM produced both tonic and cumulative (use-dependent) inhibition of sodium currents.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:39:52 GMT 2023
Edited
by admin
on Fri Dec 15 17:39:52 GMT 2023
Record UNII
E229K2HE7F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EPROXINDINE
INN   MART.   WHO-DD  
INN  
Official Name English
Eproxindine [WHO-DD]
Common Name English
EPROXINDINE [MART.]
Common Name English
eproxindine [INN]
Common Name English
(±)-N-(3-(DIETHYLAMINO)-2-HYDROXYPROPYL)-3-METHOXY-1-PHENYLINDOLE-2-CARBOXAMIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C47793
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL254194
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
FDA UNII
E229K2HE7F
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
NCI_THESAURUS
C81429
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
PUBCHEM
54965
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
EPA CompTox
DTXSID50868697
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
MESH
C044002
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
EVMPD
SUB06588MIG
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
CAS
83200-08-2
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
INN
5310
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
SMS_ID
100000084575
Created by admin on Fri Dec 15 17:39:52 GMT 2023 , Edited by admin on Fri Dec 15 17:39:52 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY