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Catalog Number:
48166
CAS Number:
1094617-45-4
Fmoc-Arg(Z) 2 -OH (asimétrico)
Purity:
≥ 95%
Synonym(s):
Na-Fmoc-Nw,w'-bis-benciloxicarbonil-arginina (asimétrica)
Documents
$156.00 /1G
Tamaño
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Información del producto

Fmoc-Arg(Z)2-OH (asymmetric) is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. The Z (benzyloxycarbonyl) group further enhances its stability and compatibility with various coupling reactions, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

Its unique structure allows for efficient coupling reactions, enabling the formation of complex peptide sequences with high purity and yield. Fmoc-Arg(Z)2-OH is particularly valuable in the synthesis of bioactive peptides, which can serve as potential therapeutics or research tools in understanding protein interactions and functions. The compound's ability to facilitate the synthesis of peptides with specific sequences positions it as a critical component in the development of novel drugs and therapeutic agents.

Número CAS
1094617-45-4
Fórmula molecular
C37H36N4O8
Peso molecular
664.72
Número MDL
MFCD05663439
Condiciones
Conservar a ≤ -10 °C
Información general
Número CAS
1094617-45-4
Fórmula molecular
C37H36N4O8
Peso molecular
664.72
Número MDL
MFCD05663439
Condiciones
Conservar a ≤ -10 °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-Arg(Z)2-OH (asymmetric) is widely utilized in research focused on:

  • Peptide Synthesis: This compound is commonly used as a building block in solid-phase peptide synthesis, allowing researchers to create complex peptides for various applications in biochemistry and pharmacology.
  • Drug Development: Its role in modifying peptide structures makes it valuable in drug discovery, particularly for developing peptide-based therapeutics that can target specific biological pathways.
  • Bioconjugation: The chemical is employed in bioconjugation techniques, where it helps attach peptides to other molecules, enhancing the functionality of drugs or diagnostic agents.
  • Protein Engineering: By incorporating this compound into proteins, researchers can study protein folding, stability, and interactions, which are crucial for understanding biological processes.
  • Research in Cancer Therapeutics: Its application in synthesizing peptide analogs is particularly relevant in cancer research, where modified peptides can be designed to inhibit tumor growth or enhance immune responses.

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