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Details

Stereochemistry ACHIRAL
Molecular Formula C14H9I3O4
Molecular Weight 621.9323
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TIRATRICOL

SMILES

OC(=O)CC1=CC(I)=C(OC2=CC=C(O)C(I)=C2)C(I)=C1

InChI

InChIKey=UOWZUVNAGUAEQC-UHFFFAOYSA-N
InChI=1S/C14H9I3O4/c15-9-6-8(1-2-12(9)18)21-14-10(16)3-7(4-11(14)17)5-13(19)20/h1-4,6,18H,5H2,(H,19,20)

HIDE SMILES / InChI
Molecular Formula C14H9I3O4
Molecular Weight 621.9323
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:09:23 UTC 2023
Edited
by admin
on Fri Dec 15 15:09:23 UTC 2023
Record UNII
29OQ9EU4R1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TIRATRICOL
INN   MART.   MI   WHO-DD  
INN  
Official Name English
tiratricol [INN]
Common Name English
LEVOTHYROXINE SODIUM IMPURITY C [EP IMPURITY]
Common Name English
TRIIODOTHYROACETIC ACID
Common Name English
3,3',5-TRIIODOTHYROACETIC ACID
Systematic Name English
TIRATRICOL [MI]
Common Name English
TIRACANA
Brand Name English
T3-ACETIC ACID
Common Name English
NSC-759294
Code English
3,5,3'-TRIIODOTHYROACETATE
Common Name English
TRIIODOTHYROACETIC ACID [USP IMPURITY]
Common Name English
TIRATRICOL [WHO-DD]
Common Name English
LIOTHYRONINE SODIUM IMPURITY C [EP IMPURITY]
Common Name English
BENZENEACETIC ACID, 4-(4-HYDROXY-3-IODOPHENOXY)-3,5-DIIODO-
Systematic Name English
LEVOTHYROXINE SODIUM IMPURITY [USP IMPURITY]
Common Name English
T3-ACETIC ACID [USP IMPURITY]
Common Name English
TIRATRICOL [MART.]
Common Name English
(4-(4-HYDROXY-3-IODOPHENOXY)-3,5-DIIODOPHENYL)ACETIC ACID
Systematic Name English
Classification Tree Code System Code
WHO-VATC QD11AX08
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
FDA ORPHAN DRUG 137200
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
FDA ORPHAN DRUG 666618
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
FDA ORPHAN DRUG 862421
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
WHO-ATC D11AX08
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
WHO-ATC H03AA04
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
WHO-VATC QH03AA04
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
NCI_THESAURUS C1553
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
EU-Orphan Drug EU/3/17/1945
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
FDA ORPHAN DRUG 46890
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
Code System Code Type Description
FDA UNII
29OQ9EU4R1
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
DRUG BANK
DB03604
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-086-1
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
PUBCHEM
5803
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
MESH
C010642
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
ChEMBL
CHEMBL41632
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
EVMPD
SUB11116MIG
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
EPA CompTox
DTXSID2045232
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
SMS_ID
100000077266
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
DRUG CENTRAL
3611
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
RXCUI
13982
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY RxNorm
NCI_THESAURUS
C66605
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
WIKIPEDIA
TIRATRICOL
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
MERCK INDEX
m10888
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY Merck Index
CAS
51-24-1
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
INN
4368
Created by admin on Fri Dec 15 15:09:24 UTC 2023 , Edited by admin on Fri Dec 15 15:09:24 UTC 2023
PRIMARY
Related Record Type Details
Structure of TIRATRICOL SODIUM
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of LIOTHYRONINE SODIUM
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of LEVOTHYROXINE SODIUM
PARENT -> IMPURITY
UNSPECIFIED
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of LEVOTHYROXINE SODIUM
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
Structure of TIRATRICOL
ACTIVE MOIETY
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