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Catalog Number:
41755
CAS Number:
4332-95-0
Phénylthiohydantoïne-tyrosine
Purity:
≥ 98 % (HPLC)
Synonym(s):
5-(4-hydroxybenzyl)-3-phényl-2-thiohydantoïne, PTH-tyrosine
Documents
$49.67 /100 mg
Taille
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Informations sur le produit

Phenylthiohydantoin-tyrosine is a specialized compound that plays a significant role in biochemical research and applications. This compound, known for its unique structure, features a phenyl group and a thiohydantoin moiety, making it particularly useful in the study of protein interactions and modifications. Its ability to form stable derivatives with amino acids, especially tyrosine, allows researchers to explore various biochemical pathways and mechanisms. This property is especially valuable in the fields of proteomics and drug development, where understanding protein behavior is crucial.

In practical applications, Phenylthiohydantoin-tyrosine is utilized in peptide synthesis and as a reagent in the analysis of amino acids. Its effectiveness in labeling and detecting tyrosine residues in proteins enhances its utility in both academic and industrial laboratories. Additionally, its stability and reactivity make it a preferred choice for researchers looking to develop new methodologies in protein chemistry. By integrating this compound into their workflows, professionals can gain deeper insights into protein structure and function, ultimately driving innovation in therapeutic development and biochemistry.

Numéro CAS 
4332-95-0
Formule moléculaire
C16H14N2O2S
Poids moléculaire 
298.36
Point de fusion 
217 - 225 °C
Informations générales
Numéro CAS 
4332-95-0
Formule moléculaire
C16H14N2O2S
Poids moléculaire 
298.36
Point de fusion 
217 - 225 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Phenylthiohydantoin-tyrosine is widely utilized in research focused on:

  • Protein Sequencing: This compound is used in the Edman degradation method, a technique for sequencing amino acids in proteins. It allows researchers to determine the sequence of tyrosine residues in proteins, which is crucial for understanding protein structure and function.
  • Biochemical Analysis: It serves as a valuable reagent in biochemical assays, helping to identify and quantify tyrosine in various biological samples. This application is essential in fields like biochemistry and molecular biology.
  • Drug Development: The compound plays a role in the synthesis of pharmaceuticals targeting tyrosine-related pathways. Its unique properties can enhance the efficacy of drug candidates in treating conditions such as cancer, where tyrosine metabolism is often altered.
  • Diagnostic Tools: It is utilized in the development of diagnostic tests for diseases associated with tyrosine metabolism disorders. This application is vital for early detection and management of metabolic diseases.
  • Research on Neurotransmitters: The compound aids in studying the role of tyrosine in neurotransmitter synthesis, particularly dopamine. This research is important for understanding neurological disorders and developing potential treatments.

Citations