300-38-9

300-38-9 structure

Name: 3,5-Dibromo-L-tyrosine
Chemical Name: 3,5-dibromo-L-tyrosine
CAS Number: 300-38-9
Molecular Formula: C₉H₉Br₂NO₃
Molecular Weight: 338.981
Catalog: Biochemical Amino acids and their derivatives Tyrosine derivatives
Create Date: 2018-07-07 09:27:32
Modify Date: 2026-07-16 10:23:42
3,5-Dibromotyrosine is a product of protein oxidation by eosinophil peroxidase[1].

Name	3,5-dibromo-L-tyrosine
Synonyms	##DISCONTINUED# 3,5-Dibromo-L-tyrosine H-TYR(3,5-BR 2)-OH 2H2O 5,5'-Dibromo-2,2'-dihydroxybenzil β-(3,5-Dibromo-4-hydroxyphenyl)alanine EINECS 206-091-5 β-(3,5-DibroMo-4-hydroxyphenyl)alanine L-(3,5-DIBROMO)TYROSINE DIHYDRATE Dibromotyrosine L-Tyr(3',5'-Br2) (S)-2-Amino-3-(3,5-dibromo-4-hydroxyphenyl)propanoic acid H-Tyr(3,5-DiBr)-OH 3,5-Dibromo-L-Tyr-OH b-(3,5-Dibromo-4-hydroxyphenyl)alanine 3,5-Dibromotyrosine 3,5-Dibrom-L-tyrosin L-4-hydroxy-3,5-dibromo-phenylalanine (2S)-2-amino-3-(3,5-dibromo-4-hydroxyphenyl)propanoic acid Dibromotirina L-(3,5-DIBROMO, 4-HYDROXY)PHENYLALANINE DIHYDRATE L-Tyrosine,3,5-dibromo 3,5-Dibromo-L-tyrosi Biotiren H-PHE(3,5-BR2, 4-OH)-OH DIHYDRATE 3,5-Dibromo-L-tyrosine //BP Dibromo L MFCD08271759 H-PHE(3,5-BR2,4-OH)-OH DIHYDRATE 3,5-Dibromo-L-tyrosine > L-3,5-Dibromotyrosine (S)-3-(3,5-dibromo-4-hydroxyphenyl)alanine C03224

Description	3,5-Dibromotyrosine is a product of protein oxidation by eosinophil peroxidase[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. Wu W, et al. 3-Bromotyrosine and 3,5-dibromotyrosine are major products of protein oxidation by eosinophil peroxidase: potential markers for eosinophil-dependent tissue injury in vivo. Biochemistry. 1999;38(12):3538-3548.

Safety Phrases	S22-S24/25
WGK Germany	3

60-18-4

~94%

300-38-9

Literature: Gao, Hongfeng; Kelly, Michelle; Hamann, Mark T. Tetrahedron, 1999 , vol. 55, # 32 p. 9717 - 9726

60-18-4

~19%

300-38-9

38739-13-8

Literature: Chemical and Pharmaceutical Bulletin, , vol. 54, # 12 p. 1715 - 1719

7726-95-6

60-18-4

64-19-7

300-38-9

Literature: Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, , vol. 144, p. 277,280