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
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
Molecular Formula | C9H9Br2NO3 |
Molecular Weight | 338.981 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
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
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:14:33 GMT 2023
by
admin
on
Fri Dec 15 19:14:33 GMT 2023
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Record UNII |
QD49LEP46E
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Record Status |
Validated (UNII)
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Record Version |
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WHO-ATC |
H03BX02
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WHO-VATC |
QH03BX02
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DTXSID401015579
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300-38-9
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SUB13561MIG
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28335
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CHEMBL1232132
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DIBROMOTYROSINE
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210786
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4413
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DB07637
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67532
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m4305
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100000079549
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206-091-5
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QD49LEP46E
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