U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C18H17I4NO4.ClH
Molecular Weight 855.411
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETIROXATE HYDROCHLORIDE

SMILES

Cl.CCOC(=O)C(C)(N)CC1=CC(I)=C(OC2=CC(I)=C(O)C(I)=C2)C(I)=C1

InChI

InChIKey=YKFOTONIBHUPOM-UHFFFAOYSA-N
InChI=1S/C18H17I4NO4.ClH/c1-3-26-17(25)18(2,23)8-9-4-13(21)16(14(22)5-9)27-10-6-11(19)15(24)12(20)7-10;/h4-7,24H,3,8,23H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula C18H17I4NO4
Molecular Weight 818.9498
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Etiroxate is a synthetic thyroxine derivative. It was used for the treatment of patients with hyperlipoproteinaemia. There were only slight side effects, such as gastric and autonomic nervous system symptoms. No statistically significant increase in anginal symptoms was found, even in patients with known coronary insufficiency. No negative effects on hepatic and renal function or the peripheral blood count were observed. Etiroxate caused a significant reduction in serum cholesterol, LDL-cholesterol, and serum apolipoprotein B. There was a significant decrease in HDL-cholesterol. Etiroxate might be used for the treatment and prevention of atherosclerotic disease.

Approval Year

Targets

Sample Use Guides

40 mg daily
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:47:16 GMT 2023
Edited
by admin
on Fri Dec 15 17:47:16 GMT 2023
Record UNII
ZY22G48A03
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETIROXATE HYDROCHLORIDE
MART.   MI   WHO-DD  
Common Name English
ETHYL DL-2-AMINO-3-(4-(4-HYDROXY-3,5-DI-IODOPHENOXY)-3,5-DI-IODOPHENYL)-2-METHYLPROPIONATE HYDROCHLORIDE
Common Name English
ETIROXATE HYDROCHLORIDE [MART.]
Common Name English
ETIROXATE HCL
Common Name English
Etiroxate hydrochloride [WHO-DD]
Common Name English
ETHYL O-(4-HYDROXY-3,5-DIIODOPHENYL)-3,5-DIIODO-.ALPHA.-METHYL-DL-TYROSINATE HYDROCHLORIDE
Systematic Name English
CG-635
Code English
ETIROXATE HYDROCHLORIDE [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m1142
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY Merck Index
SMS_ID
100000087497
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
EVMPD
SUB02043MIG
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
ECHA (EC/EINECS)
259-593-1
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
PUBCHEM
3085082
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
CAS
55327-22-5
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
FDA UNII
ZY22G48A03
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
EPA CompTox
DTXSID90970662
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
MESH
C010150
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY