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Catalog Number:
02687
CAS Number:
142994-45-4
Fmoc-3-(3'-piridil)-D-alanina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Ala(3'-piridil)-OH, Fmoc-β-(3'-piridil)-D-Ala-OH, Ácido Fmoc-( R -2-amino-3-(3'-piridil)propanoico
Documents
$86.23 /1G
Tamaño
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Información del producto

Fmoc-3-(3'-pyridyl)-D-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the incorporation of a pyridine ring, enhances its reactivity and compatibility with various coupling reagents, making it an excellent choice for researchers focused on developing complex peptide sequences.

In the pharmaceutical industry, Fmoc-3-(3'-pyridyl)-D-alanine serves as a building block for bioactive peptides, which can be pivotal in therapeutic applications, including cancer treatment and antimicrobial agents. Its ability to facilitate the synthesis of peptides with specific biological activities positions it as a valuable tool for medicinal chemists and biochemists alike. The compound's stability and ease of use in solid-phase peptide synthesis further contribute to its appeal, allowing for efficient and reproducible results in laboratory settings.

Número CAS
142994-45-4
Fórmula molecular
C23H20N2O4
Peso molecular
388.4
Número MDL
MFCD00080267
Punto de fusión
164 - 169 °C
Rotación óptica
[a] 20 D = 11 ± 1 ° (C = 1,034 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
142994-45-4
Fórmula molecular
C23H20N2O4
Peso molecular
388.4
Número MDL
MFCD00080267
Punto de fusión
164 - 169 °C
Rotación óptica
[a] 20 D = 11 ± 1 ° (C = 1,034 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
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

Fmoc-3-(3'-pyridyl)-D-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific receptors or pathways involving pyridine derivatives.
  • Bioconjugation: Researchers use this compound to create bioconjugates, which can enhance the delivery of therapeutic agents, improving their efficacy and reducing side effects.
  • Research in Neuroscience: The pyridine moiety is significant in neuroscience research, where it can be utilized to study neuroactive compounds and their interactions with neuronal receptors.
  • Analytical Chemistry: It is employed in analytical methods to detect and quantify specific biomolecules, providing a reliable way to monitor biological processes in various samples.

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