Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
42546
CAS Number:
38739-13-8
3-Bromo-L-tyrosine
Purity:
≥ 98% (HPLC)
Synonym(s):
(S)-2-Amino-3-(3-bromo-4-hydroxyphenyl)propanoic acid
Documents
$55.00 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

3-Bromo-L-tyrosine is a valuable derivative of the amino acid tyrosine, distinguished by its bromine substitution at the 3-position of the aromatic ring. This compound is recognized for its potential applications in biochemical research, particularly in the study of neurotransmitter synthesis and function. As a brominated analog of L-tyrosine, it serves as a useful tool in the investigation of various physiological processes, including the modulation of dopamine and norepinephrine pathways. Researchers often utilize 3-Bromo-L-tyrosine in studies related to neuropharmacology and the development of therapeutic agents targeting neurological disorders.

Additionally, 3-Bromo-L-tyrosine's unique structure allows it to act as a precursor in the synthesis of novel compounds, making it a valuable asset in medicinal chemistry. Its ability to influence protein interactions and enzyme activities further enhances its relevance in drug discovery and development. With its specific properties and applications, 3-Bromo-L-tyrosine stands out as an essential compound for professionals in the fields of biochemistry, pharmacology, and medicinal research.

Synonyms
(S)-2-Amino-3-(3-bromo-4-hydroxyphenyl)propanoic acid
CAS Number
38739-13-8
Purity
≥ 98% (HPLC)
Molecular Formula
C9H10BrNO3
Molecular Weight
260.1
MDL Number
MFCD09836116
PubChem ID
148708
Appearance
Off-white to light yellow solid
Conditions
Store at 0-8 °C
General Information
Synonyms
(S)-2-Amino-3-(3-bromo-4-hydroxyphenyl)propanoic acid
CAS Number
38739-13-8
Purity
≥ 98% (HPLC)
Molecular Formula
C9H10BrNO3
Molecular Weight
260.1
MDL Number
MFCD09836116
PubChem ID
148708
Appearance
Off-white to light yellow solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Bromo-L-tyrosine is widely utilized in research focused on:

  • Neuroscience Research: This compound serves as a valuable tool for studying neurotransmitter systems, particularly in understanding the role of tyrosine derivatives in dopamine synthesis.
  • Drug Development: It is explored as a potential lead compound for developing new pharmaceuticals targeting neurological disorders, offering insights into structure-activity relationships.
  • Biochemical Assays: Researchers use it in assays to measure enzyme activity related to tyrosine metabolism, aiding in the investigation of metabolic disorders.
  • Protein Engineering: It is employed in the modification of proteins to enhance their stability and activity, particularly in therapeutic applications.
  • Antioxidant Studies: The compound is investigated for its antioxidant properties, contributing to research on oxidative stress and its implications in various diseases.

Citations