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 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

Detrothyronine is the (R)-(D)-form of triiodothyronine and has antihyperlipidaemic actions with beneficial effects upon coronary disease and hypertension. Detrothyronine has been tried in the treatment of hypercholesterolemia but its toxic effects outweigh any therapeutic advantage.

Approval Year

Sample Use Guides

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
Related Record Type Details
RACEMATE -> ENANTIOMER
Related Record Type Details
ACTIVE MOIETY