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Catalog Number:
02571
CAS Number:
19883-77-3
3-Fluoro-L-fenilalanina
Purity:
≥ 98% (HPLC, HPLC quiral)
Synonym(s):
L-Fe(3-F)-OH, m -Fluoro-L-fenilalanina, H-Fe(3-F)-OH
Documents
$29.34 /1G
Tamaño
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Información del producto

3-Fluoro-L-phenylalanine is a fluorinated amino acid that has garnered attention in the fields of medicinal chemistry and biochemistry. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders and cancer therapies. Its unique fluorine substitution enhances lipophilicity and metabolic stability, making it an attractive candidate for drug development. Researchers have utilized 3-Fluoro-L-phenylalanine in the design of novel peptides and proteins, allowing for the exploration of new therapeutic pathways and mechanisms of action.

In addition to its applications in drug synthesis, 3-Fluoro-L-phenylalanine is also instrumental in studying protein structure and function. Its incorporation into peptides can help elucidate the effects of fluorination on biological activity, providing insights that are crucial for the development of more effective therapeutic agents. With its potential to improve drug efficacy and specificity, 3-Fluoro-L-phenylalanine stands out as a key compound for researchers and industry professionals focused on advancing pharmaceutical innovations.

Número CAS
19883-77-3
Fórmula molecular
C9H10FNO2
Peso molecular
183.2
Número MDL
MFCD00066450
Punto de fusión
198,0-200,5 °C (descenso)
Condiciones
Tienda en RT
Información general
Número CAS
19883-77-3
Fórmula molecular
C9H10FNO2
Peso molecular
183.2
Número MDL
MFCD00066450
Punto de fusión
198,0-200,5 °C (descenso)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

3-Fluoro-L-phenylalanine is widely utilized in research focused on:

  • Drug Development: This compound serves as a valuable building block in the synthesis of novel pharmaceuticals, particularly in the development of targeted therapies for cancer and neurological disorders.
  • Protein Engineering: It is employed in the modification of proteins to study structure-function relationships, enabling researchers to create proteins with enhanced stability or altered activity.
  • Biochemical Research: The compound is used in studies investigating metabolic pathways and enzyme mechanisms, providing insights into biochemical processes that could lead to new therapeutic strategies.
  • Fluorinated Amino Acids: Its unique fluorine atom allows for improved imaging techniques in molecular biology, aiding in the visualization of protein interactions and cellular processes.
  • Pharmaceutical Formulations: As a chiral building block, it plays a role in the formulation of drugs that require specific stereochemistry, enhancing efficacy and reducing side effects compared to non-fluorinated counterparts.

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