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Catalog Number:
21696
CAS Number:
620-30-4
DL-α-Methyltyrosine
Synonym(s):
α-Methyl-DL-p-tyrosine, (RS-α-Methyl-4-hydroxyphenylalanine
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Product Information

DL-a-Methyltyrosine is a versatile amino acid derivative known for its role as a competitive inhibitor of tyrosine hydroxylase, making it a valuable compound in both research and therapeutic applications. This compound, also recognized by its synonyms such as α-Methyltyrosine and 3-(4-Hydroxyphenyl)-2-methylalanine, is particularly significant in the study of catecholamine biosynthesis. Researchers utilize DL-a-Methyltyrosine to explore its effects on neurotransmitter levels, providing insights into conditions such as hypertension and certain neurodegenerative disorders.

In the pharmaceutical industry, DL-a-Methyltyrosine has been employed in the development of treatments for pheochromocytoma, a type of tumor that secretes excess catecholamines. Its ability to inhibit catecholamine synthesis makes it a crucial component in managing symptoms associated with this condition. Additionally, its applications extend to studies in metabolic pathways and the synthesis of other biologically active compounds, highlighting its importance in both academic and clinical settings. With its unique properties and practical uses, DL-a-Methyltyrosine stands out as a key compound for professionals in biochemistry and pharmacology.

Synonyms
α-Methyl-DL-p-tyrosine, (RS-α-Methyl-4-hydroxyphenylalanine
CAS Number
620-30-4
Molecular Formula
C10H13NO3
Molecular Weight
195.22
MDL Number
MFCD00004187
PubChem ID
3125
Conditions
Store at 0-8°C
General Information
Synonyms
α-Methyl-DL-p-tyrosine, (RS-α-Methyl-4-hydroxyphenylalanine
CAS Number
620-30-4
Molecular Formula
C10H13NO3
Molecular Weight
195.22
MDL Number
MFCD00004187
PubChem ID
3125
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

DL-a-Methyltyrosine is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders.
  • Biochemical Research: It is used in studies related to neurotransmitter synthesis, helping researchers understand the role of amino acids in brain function.
  • Metabolic Studies: The compound aids in investigating metabolic pathways, particularly in conditions like phenylketonuria, where amino acid metabolism is disrupted.
  • Animal Studies: Often employed in animal models to study the effects of altered neurotransmitter levels, providing insights into mental health treatments.
  • Dietary Supplements: It is explored as a potential ingredient in supplements aimed at enhancing cognitive function and mood regulation.

Citations