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Catalog Number:
29756
CAS Number:
159610-89-6
N a -Fmoc-N e -azida-L-Lisina
Purity:
≥ 99,7 % (HPLC quiral)
Synonym(s):
Fmoc-Lys( N3 )-OH, Fmoc-ε-azido-Nle-OH
Documents
$55.00 /100 mg
Tamaño
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Información del producto

Fmoc-Lys(N3)-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protective group, which is essential for the selective protection of amine functionalities during the synthesis of peptides. The azido group (N3) enhances its reactivity, making it an excellent candidate for click chemistry applications, particularly in the development of bioconjugates and targeted therapeutics. Researchers appreciate its stability under various conditions, allowing for streamlined synthesis processes in both academic and industrial settings.

In addition to its role in peptide synthesis, Fmoc-Lys(N3)-OH is also employed in the creation of novel biomaterials and drug delivery systems. Its unique properties facilitate the incorporation of bioactive molecules, enabling the design of targeted therapies with improved efficacy. The compound's ability to undergo selective reactions further expands its utility in medicinal chemistry, making it a valuable tool for researchers aiming to innovate in drug design and development.

Número CAS
159610-89-6
Fórmula molecular
C21H22N4O4
Peso molecular
394.43
Número MDL
MFCD13182319
Rotación óptica
[a] D 20 = -12,0 a -14,5 º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
159610-89-6
Fórmula molecular
C21H22N4O4
Peso molecular
394.43
Número MDL
MFCD13182319
Rotación óptica
[a] D 20 = -12,0 a -14,5 º (C=1 en DMF)
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-Lys(N3)-OH 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 incorporation of azide groups for further modifications.
  • Bioconjugation: Its azide functionality enables efficient bioconjugation reactions, such as click chemistry, facilitating the attachment of various biomolecules for drug development and diagnostic applications.
  • Drug Delivery Systems: Researchers leverage this compound in the design of advanced drug delivery systems, where its properties can enhance the stability and targeting of therapeutic agents.
  • Protein Engineering: Fmoc-Lys(N3)-OH is used in the modification of proteins, allowing scientists to introduce specific functionalities that can alter protein behavior for research and therapeutic purposes.
  • Fluorescent Labeling: The compound can be utilized in the development of fluorescently labeled peptides, which are essential for tracking and imaging in biological studies.

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