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

Details

Stereochemistry ABSOLUTE
Molecular Formula C9H9Br2NO3
Molecular Weight 338.981
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIBROMOTYROSINE

SMILES

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

InChI

InChIKey=COESHZUDRKCEPA-ZETCQYMHSA-N
InChI=1S/C9H9Br2NO3/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
Dibromotyrosine is a brominated derivative of a natural amino acid tyrosine. In the human body, dibromotyrosine is produced by eosinophil peroxidase secreted from activated eosinophils. Dibromotyrosine is naturally produced by marine sponges. Dibromotyrosine is used in medicine for the treatment of functional hyperthyroidisms. It acts by competing with iodination of tyrosines, thus reducing the active form of the thyroid hormones. Dibromotyrosine also appears to maintain the ability to control TSH production through negative feedback on the pituitary gland, reducing the biological activity of the thyroid. Dibromotyrosine is marketed in Italy under tradename Bromotiren.

Approval Year

Name Type Language
DIBROMOTYROSINE
MART.   WHO-DD  
Systematic Name English
DIBROMOTYROSINE [MART.]
Common Name English
3,5-DIBROMO-L-TYROSINE [MI]
Common Name English
NSC-210786
Code English
3,5-DIBROMO-L-TYROSINE
MI  
Systematic Name English
Dibromotyrosine [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC H03BX02
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
WHO-VATC QH03BX02
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID401015579
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
CAS
300-38-9
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
EVMPD
SUB13561MIG
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
CHEBI
28335
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
ChEMBL
CHEMBL1232132
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
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WIKIPEDIA
DIBROMOTYROSINE
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
NSC
210786
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
DRUG CENTRAL
4413
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
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DRUG BANK
DB07637
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
PUBCHEM
67532
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
MERCK INDEX
m4305
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY Merck Index
SMS_ID
100000079549
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
ECHA (EC/EINECS)
206-091-5
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
FDA UNII
QD49LEP46E
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY