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Details

Stereochemistry RACEMIC
Molecular Formula C18H17I4NO4
Molecular Weight 818.9498
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETIROXATE

SMILES

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

InChI

InChIKey=LWZCMKGGFONJPB-UHFFFAOYSA-N
InChI=1S/C18H17I4NO4/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

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 ( + / - )

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 Mon Mar 31 18:25:27 GMT 2025
Edited
by admin
on Mon Mar 31 18:25:27 GMT 2025
Record UNII
0S3LDN5P7H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETIROXATE
INN   MI   WHO-DD  
INN  
Official Name English
ETIROXATE [MI]
Preferred Name English
Etiroxate [WHO-DD]
Common Name English
etiroxate [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1553
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
Code System Code Type Description
SMS_ID
100000082098
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
PUBCHEM
65683
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
MESH
C010150
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104225
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
MERCK INDEX
m1142
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY Merck Index
NCI_THESAURUS
C65580
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
FDA UNII
0S3LDN5P7H
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
EPA CompTox
DTXSID30864773
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
EVMPD
SUB07309MIG
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
DRUG CENTRAL
3210
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
CAS
17365-01-4
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
INN
3603
Created by admin on Mon Mar 31 18:25:27 GMT 2025 , Edited by admin on Mon Mar 31 18:25:27 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY