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

Details

Stereochemistry ABSOLUTE
Molecular Formula C9H9I2NO3
Molecular Weight 432.9816
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIIODOTYROSINE

SMILES

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

InChI

InChIKey=NYPYHUZRZVSYKL-ZETCQYMHSA-N
InChI=1S/C9H9I2NO3/c10-5-1-4(2-6(11)8(5)13)3-7(12)9(14)15/h1-2,7,13H,3,12H2,(H,14,15)/t7-/m0/s1

HIDE SMILES / InChI

Molecular Formula C9H9I2NO3
Molecular Weight 432.9816
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 16:27:54 UTC 2023
Edited
by admin
on Fri Dec 15 16:27:54 UTC 2023
Record UNII
6L57Q44ZWW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIIODOTYROSINE
MART.  
Systematic Name English
NSC-4143
Code English
DIIODOTYROSINE [EP IMPURITY]
Common Name English
LIOTHYRONINE SODIUM IMPURITY B [EP IMPURITY]
Common Name English
3,5-DIIODOTYROSINE, L-
Common Name English
3,5-DIIODOTYROSINE L-FORM [MI]
Common Name English
(2S)-2-AMINO-3-(4-HYDROXY-3,5-DIIODOPHENYL)PROPANOIC ACID
Systematic Name English
L-DIIODOTYROSINE
Common Name English
L-TYROSINE, 3,5-DIIODO-
Systematic Name English
3,5-DIIODOTYROSINE L-FORM
MI  
Common Name English
TYROSINE, 3,5-DIIODO-, L-
Systematic Name English
DIIODOTYROSINE, L-
Common Name English
DIIODOTYROSINE [MART.]
Common Name English
3,5-DIIODO-L-TYROSINE
Systematic Name English
Classification Tree Code System Code
WHO-VATC QH03BX01
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
WHO-ATC H03BX01
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
DSLD 3527 (Number of products:4)
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
Code System Code Type Description
CAS
300-39-0
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
PUBCHEM
9305
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
CHEBI
57506
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
NSC
4143
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
ECHA (EC/EINECS)
206-092-0
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
FDA UNII
6L57Q44ZWW
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
SMS_ID
100000079224
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
DRUG CENTRAL
3146
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
WIKIPEDIA
DIIODOTYROSINE
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
CHEBI
15768
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
MERCK INDEX
m4480
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY Merck Index
EVMPD
SUB13599MIG
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
EPA CompTox
DTXSID0048680
Created by admin on Fri Dec 15 16:27:54 UTC 2023 , Edited by admin on Fri Dec 15 16:27:54 UTC 2023
PRIMARY
Related Record Type Details
LABELED -> NON-LABELED
TRANSPORTER -> INHIBITOR
Inhbiting gabapentin accumulation in the HEK-LAT1 cells
IC50
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP