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Details

Stereochemistry ACHIRAL
Molecular Formula C22H27N3O3S
Molecular Weight 413.533
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHACIZINE

SMILES

CCOC(=O)NC1=CC2=C(SC3=CC=CC=C3N2C(=O)CCN(CC)CC)C=C1

InChI

InChIKey=PQXGNJKJMFUPPM-UHFFFAOYSA-N
InChI=1S/C22H27N3O3S/c1-4-24(5-2)14-13-21(26)25-17-9-7-8-10-19(17)29-20-12-11-16(15-18(20)25)23-22(27)28-6-3/h7-12,15H,4-6,13-14H2,1-3H3,(H,23,27)

HIDE SMILES / InChI

Molecular Formula C22H27N3O3S
Molecular Weight 413.533
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Ethacizine (ethacyzine) is a class Ic antiarrhythmic agent, related to moracizine. It is used in Russia and some other Commonwealth of Independent States countries for the treatment of severe and/or refractory ventricular and supraventricular arrhythmias, especially those accompanied by organic heart disease. It is also indicated as a treatment of refractory tachycardia associated with Wolff–Parkinson–White syndrome.

Originator

Sources: Farmakologiya i Toksikologiya (Moscow) (1971), 34, (2), 163-7.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Ethacyzin

Approved Use

Unknown
Primary
Ethacyzin

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Ethacizin metabolism in humans.
1989 Jul
Patents

Patents

Sample Use Guides

In Vivo Use Guide
The initial dose is 50 mg (1 table) 2-3 times a day. In case of insufficient clinical effect, the dose is increased (under compulsory ECG monitoring) to 50 mg 4 times a day (200 mg) or 100 mg 3 times daily (300 mg).
Route of Administration: Oral
In Vitro Use Guide
Ethacizine applied in the concentration range between 1 X 10(-7) and 1 X 10(-5) g/ml decreased the rate of action potential growth (Vmax) of the mammal myocardium. Inhibition of the Vmax was accompanied by the diminution of the force of contraction which involved two phases. Ethacizine also decreased the overshoot of slow response action potential with the time constant similar to that in the first rapid phase of force reduction.
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:32:55 GMT 2023
Edited
by admin
on Fri Dec 15 18:32:55 GMT 2023
Record UNII
FE5SPV1Z6G
Record Status Validated (UNII)
Record Version
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Name Type Language
ETHACIZINE
MART.   WHO-DD  
Common Name English
ETMOZINE DAA
Brand Name English
ETHACIZIN
Common Name English
ETHACIZINE [MART.]
Common Name English
NSC-621878
Code English
ETHACYZIN
Common Name English
Ethacizine [WHO-DD]
Common Name English
EZ-55
Code English
ETHYL 10-(3-(DIETHYLAMINO)PROPIONYL)PHENOTHIAZINE-2-CARBAMATE
Common Name English
ETACIZIN
Common Name English
NIK-244
Code English
Classification Tree Code System Code
WHO-VATC QC01BC09
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
WHO-ATC C01BC09
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
Code System Code Type Description
NSC
621878
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
PUBCHEM
107841
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
DRUG CENTRAL
4835
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
SMS_ID
100000126035
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
CAS
33414-33-4
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
FDA UNII
FE5SPV1Z6G
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
WIKIPEDIA
Ethacizine
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
EVMPD
SUB32872
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
MESH
C046818
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
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EPA CompTox
DTXSID50187057
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
ChEMBL
CHEMBL1997663
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
DRUG BANK
DB13645
Created by admin on Fri Dec 15 18:32:55 GMT 2023 , Edited by admin on Fri Dec 15 18:32:55 GMT 2023
PRIMARY
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SALT/SOLVATE -> PARENT