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Details

Stereochemistry RACEMIC
Molecular Formula C15H12I3NO4
Molecular Weight 650.9735
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RATHYRONINE

SMILES

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

InChI

InChIKey=AUYYCJSJGJYCDS-UHFFFAOYSA-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)

HIDE SMILES / InChI

Molecular Formula C15H12I3NO4
Molecular Weight 650.9735
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:09:15 UTC 2023
Edited
by admin
on Fri Dec 15 16:09:15 UTC 2023
Record UNII
O48UO55HR0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RATHYRONINE
INN  
INN  
Official Name English
3,3',5-TRIIODO-DL-THYRONINE
Systematic Name English
ALANINE, 3-(4-(4-HYDROXY-3-IODOPHENOXY)-3,5-DIIODOPHENYL)-, DL-
Systematic Name English
DL-TRIIODOTHYRONINE
Common Name English
LIOTHYRONINE, DL-
Common Name English
TYROSINE, O-(4-HYDROXY-3-IODOPHENYL)-3,5-DIIODO-
Systematic Name English
DL-3-(4-(4-HYDROXY-3-IODOPHENOXY)-3,5-DIIODOPHENYL)ALANINE
Common Name English
DL-TYROSINE, O-(4-HYDROXY-3-IODOPHENYL)-3,5-DIIODO-
Systematic Name English
rathyronine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1553
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
Code System Code Type Description
CAS
3130-96-9
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
SMS_ID
100000080318
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
ECHA (EC/EINECS)
221-522-7
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
CAS
327-86-6
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
SUPERSEDED
NCI_THESAURUS
C61710
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
EPA CompTox
DTXSID30858995
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
PUBCHEM
861
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
CAS
51-25-2
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
SUPERSEDED
CAS
137-56-4
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
SUPERSEDED
ChEMBL
CHEMBL789
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
INN
3213
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
FDA UNII
O48UO55HR0
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
EVMPD
SUB10262MIG
Created by admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY