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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 DETROTHYRONINE

SMILES

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

InChI

InChIKey=AUYYCJSJGJYCDS-GFCCVEGCSA-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-/m1/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 Sat Dec 16 16:52:13 UTC 2023
Edited
by admin
on Sat Dec 16 16:52:13 UTC 2023
Record UNII
46XII7C16X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DETROTHYRONINE
INN   MART.  
INN  
Official Name English
D-3-(4-(4-HYDROXY-3-IODOPHENOXY)-3,5-DIIODOPHENYL)-ALANINE
Common Name English
ALANINE, 3-(4-(4-HYDROXY-3-IODOPHENOXY)-3,5-DIIODOPHENYL)-, D-
Systematic Name English
DETROTHYRONINE [MART.]
Common Name English
D-TYROSINE, O-(4-HYDROXY-3-IODOPHENYL)-3,5-DIIODO-
Systematic Name English
RATHYRONINE, (R)-
Common Name English
NSC-46046
Code English
(+)-TRIIODOTHYRONINE
Systematic Name English
detrothyronine [INN]
Common Name English
DT-3
Code English
3,3',5-TRIIODO-D-THYRONINE
Systematic Name English
DEXTROTHYRONINE
Common Name English
Code System Code Type Description
INN
1008
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
FDA UNII
46XII7C16X
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
ECHA (EC/EINECS)
227-203-9
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
NCI_THESAURUS
C166730
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
PUBCHEM
71212
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
ChEMBL
CHEMBL557
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
CAS
6138-48-3
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
SUPERSEDED
CAS
5714-08-9
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
NSC
46046
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
EVMPD
SUB07014MIG
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
SMS_ID
100000083197
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
EPA CompTox
DTXSID501016651
Created by admin on Sat Dec 16 16:52:13 UTC 2023 , Edited by admin on Sat Dec 16 16:52:13 UTC 2023
PRIMARY
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RACEMATE -> ENANTIOMER
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ACTIVE MOIETY