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Details

Stereochemistry ACHIRAL
Molecular Formula C15H9I3O5
Molecular Weight 649.9424
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACETIROMATE

SMILES

CC(=O)OC1=CC=C(OC2=C(I)C=C(C=C2I)C(O)=O)C=C1I

InChI

InChIKey=AXVCIZJRCOHMQX-UHFFFAOYSA-N
InChI=1S/C15H9I3O5/c1-7(19)22-13-3-2-9(6-10(13)16)23-14-11(17)4-8(15(20)21)5-12(14)18/h2-6H,1H3,(H,20,21)

HIDE SMILES / InChI

Molecular Formula C15H9I3O5
Molecular Weight 649.9424
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Acetiromate was studied to treat patients with hyperlipidemia.

Approval Year

PubMed

PubMed

TitleDatePubMed
Long-term administration of 3,5-diodo-4(3'-iodo4'-acetoxyphenoxy) benzoic acid (acetiromate) in hyperlipidemic patients.
1974 Aug
[Therapeutic of acetiromate on hyperlipidemia--comparison with clofibrate using a double-blind method].
1974 Jul 10

Sample Use Guides

A daily dose of 20-50 mg of 3, 5-diiodo-4 (3'-iodo-4'-acetoxyphenoxy) benzoic acid (acetiromate) was given to four hyperlipidemic patients for a long period ranging from 2 years and 8 months to 5 years and 6 months.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:38:26 GMT 2023
Edited
by admin
on Fri Dec 15 16:38:26 GMT 2023
Record UNII
8Q5153W1NW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACETIROMATE
INN   MART.  
INN  
Official Name English
ACETIROMATE [MART.]
Common Name English
acetiromate [INN]
Common Name English
4-(4-HYDROXY-3-IODOPHENOXY)-3,5-DIIODOBENZOIC ACID ACETATE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29703
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
Code System Code Type Description
SMS_ID
100000087920
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
MESH
C002002
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
WIKIPEDIA
Acetiromate
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
CAS
2260-08-4
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
INN
3434
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
EVMPD
SUB05222MIG
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105921
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
FDA UNII
8Q5153W1NW
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
NCI_THESAURUS
C72981
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
PUBCHEM
16748
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
EPA CompTox
DTXSID60177121
Created by admin on Fri Dec 15 16:38:26 GMT 2023 , Edited by admin on Fri Dec 15 16:38:26 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY