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

Details

Stereochemistry ABSOLUTE
Molecular Formula C15H12I3NO4
Molecular Weight 650.9735
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LIOTHYRONINE

SMILES

N[C@@H](CC1=CC(I)=C(OC2=CC=C(O)C(I)=C2)C(I)=C1)C(O)=O

InChI

InChIKey=AUYYCJSJGJYCDS-LBPRGKRZSA-N
InChI=1S/C15H12I3NO4/c16-9-6-8(1-2-13(9)20)23-14-10(17)3-7(4-11(14)18)5-12(19)15(21)22/h1-4,6,12,20H,5,19H2,(H,21,22)/t12-/m0/s1

HIDE SMILES / InChI

Molecular Formula C15H12I3NO4
Molecular Weight 650.9735
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:34:01 UTC 2023
Edited
by admin
on Fri Dec 15 15:34:01 UTC 2023
Record UNII
06LU7C9H1V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LIOTHYRONINE
HSDB   INN   MI   USP-RS   VANDF   WHO-DD  
INN  
Official Name English
LIOTHYRONINE [MI]
Common Name English
LEVOTHYROXINE SODIUM RELATED COMPOUND LIOTHYRONINE [USP IMPURITY]
Common Name English
CYRONINE
Brand Name English
T3
Common Name English
NSC-80203
Code English
LIOTHYRONINE [USP IMPURITY]
Common Name English
3,5,3'-TRIIODOTHYRONINE, L-
Common Name English
LEVOTHYROXINE SODIUM IMPURITY A [EP IMPURITY]
Common Name English
Liothyronine [WHO-DD]
Common Name English
LIOTHYRONINE [VANDF]
Common Name English
O-(4-HYDROXY-3-IODOPHENYL)-3,5-DIIODO-L-TYROSINE
Systematic Name English
3,3',5-TRIIODO-L-THYRONINE
Systematic Name English
L-TYROSINE, O-(4-HYDROXY-3-IODOPHENYL)-3,5-DIIODO-
Systematic Name English
3,5,3'-TRIIODOTHYRONINE
Systematic Name English
RATHYRONINE, (S)-
Common Name English
ALANINE, 3-(4-(4-HYDROXY-3-IODOPHENOXY)-3,5-DIIODOPHENYL)-, L-
Systematic Name English
T-3
Common Name English
TRIIODOTHYRONINE
Systematic Name English
THYRONINE, 3,3',5-TRIIODO-, L-
Systematic Name English
(2S)-2-AMINO-3-(4-(4-HYDROXY-3-IODOPHENOXY)-3,5-DIIODOPHENYL)PROPANOIC ACID
Systematic Name English
liothyronine [INN]
Common Name English
LIOTHYRONINE [HSDB]
Common Name English
LIOTHYRONINE [USP-RS]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 862.1715
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LOINC 83124-8
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LOINC 26879-7
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LOINC 83125-5
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
FDA ORPHAN DRUG 539116
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
NCI_THESAURUS C1553
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
WHO-VATC QH03AA03
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
NDF-RT N0000006165
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
CFR 21 CFR 862.1710
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
CFR 21 CFR 520.1284
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LOINC 3053-6
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LOINC 14930-2
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
WHO-ATC H03AA03
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LOINC 3055-1
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
NDF-RT N0000175946
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
NCI_THESAURUS C886
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LIVERTOX 1000
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LOINC 70152-4
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
NDF-RT N0000006165
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LOINC 35231-0
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
LOINC 57899-7
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
Code System Code Type Description
DAILYMED
06LU7C9H1V
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
RS_ITEM_NUM
1368008
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
CAS
57164-27-9
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
SUPERSEDED
DRUG CENTRAL
1585
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
EVMPD
SUB08527MIG
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
EPA CompTox
DTXSID8023216
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
ECHA (EC/EINECS)
229-999-3
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
RXCUI
10814
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY RxNorm
SMS_ID
100000082541
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
NSC
80203
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
DRUG BANK
DB00279
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
MERCK INDEX
m6835
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY Merck Index
HSDB
3110
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
NCI_THESAURUS
C907
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
INN
653
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
FDA UNII
06LU7C9H1V
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
CHEBI
18258
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
LACTMED
Liothyronine
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
CAS
6893-02-3
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
WIKIPEDIA
LIOTHYRONINE
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
ChEMBL
CHEMBL1544
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
IUPHAR
2634
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
MESH
D014284
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
CHEBI
533015
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
CAS
7013-53-8
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
SUPERSEDED
PUBCHEM
5920
Created by admin on Fri Dec 15 15:34:01 UTC 2023 , Edited by admin on Fri Dec 15 15:34:01 UTC 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
SALT/SOLVATE -> PARENT
LABELED -> NON-LABELED
TRANSPORTER -> SUBSTRATE
LABELED -> NON-LABELED
TRANSPORTER -> SUBSTRATE
SALT/SOLVATE -> PARENT
Related Record Type Details
PARENT -> METABOLITE ACTIVE
MAJOR
PRODRUG -> METABOLITE ACTIVE
Related Record Type Details
PARENT -> IMPURITY
The relative response factor is 1.00
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY