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Catalog Number:
48172
CAS Number:
2002499-17-2
Fmoc-D-His(3-Me)-OH
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-3-méthyl-D-histidine, Fmoc-D-His(p-Me)-OH
Documents
$50.00 /25 mg
Taille
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Informations sur le produit

Fmoc-D-His(3-Me)-OH is a versatile 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 solid-phase peptide synthesis. Its unique structure, incorporating a 3-methylimidazole side chain, enhances its compatibility with various coupling reagents, making it an ideal choice for researchers focused on synthesizing complex peptides and proteins.

In addition to its role in peptide synthesis, Fmoc-D-His(3-Me)-OH is also valuable in the development of pharmaceuticals and bioconjugates, where its imidazole functionality can participate in metal coordination and enzyme catalysis. This compound's stability and ease of handling further contribute to its appeal in laboratory settings, allowing for efficient synthesis processes. Researchers and industry professionals can leverage Fmoc-D-His(3-Me)-OH to create innovative solutions in drug discovery and development, making it a crucial tool in modern biochemical research.

Numéro CAS 
2002499-17-2
Formule moléculaire
C22H21N3O4
Poids moléculaire 
391.42
Point de fusion 
165 - 168 °C
Rotation optique 
[a] D 20 = 5,2 ± 3 °C (C = 1 dans HCl 1N)
Informations générales
Numéro CAS 
2002499-17-2
Formule moléculaire
C22H21N3O4
Poids moléculaire 
391.42
Point de fusion 
165 - 168 °C
Rotation optique 
[a] D 20 = 5,2 ± 3 °C (C = 1 dans HCl 1N)
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

Fmoc-D-His(3-Me)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for researchers in biochemistry.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in targeting specific biological pathways. This can enhance the efficacy of drug candidates in the pharmaceutical industry.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and targeted drug delivery systems.
  • Research in Cancer Therapy: Its application in the synthesis of histidine-containing peptides is significant in cancer research, where these peptides can be used to develop targeted therapies that improve treatment outcomes.
  • Protein Engineering: Fmoc-D-His(3-Me)-OH is instrumental in protein engineering, allowing scientists to create modified proteins with enhanced properties for various applications, including enzyme design and therapeutic proteins.

Citations