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Catalog Number:
48171
CAS Number:
1197025-85-6
Na-Fmoc-Nim-méthyl-D-histidine
Purity:
≥ 95 % (HPLC)
Synonym(s):
Fmoc-D-His(1-Me)-OH
Documents
$80.00 /25 mg
Taille
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Informations sur le produit

Na-Fmoc-Nim-methyl-D-histidine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which facilitates the selective modification of amino acids during solid-phase peptide synthesis. Its unique structure, characterized by the incorporation of a methylated imidazole side chain, enhances the stability and bioactivity of peptides, making it an essential building block for researchers in medicinal chemistry and biochemistry.

In practical applications, Na-Fmoc-Nim-methyl-D-histidine is particularly valuable in the design of peptide-based therapeutics and in the study of protein interactions. Its ability to mimic natural histidine residues allows for the exploration of enzyme mechanisms and the development of inhibitors. Furthermore, the compound's favorable solubility and compatibility with various coupling reagents make it an ideal choice for researchers aiming to synthesize complex peptides efficiently. With its robust profile, Na-Fmoc-Nim-methyl-D-histidine stands out as a crucial tool for advancing peptide research and development.

Numéro CAS 
1197025-85-6
Formule moléculaire
C22H21N3O4
Poids moléculaire 
391.42
Point de fusion 
135 - 167 °C
Rotation optique 
[a] D 20 = 9,1 ± 5 ° (C = 1 dans HCl 2N)
Informations générales
Numéro CAS 
1197025-85-6
Formule moléculaire
C22H21N3O4
Poids moléculaire 
391.42
Point de fusion 
135 - 167 °C
Rotation optique 
[a] D 20 = 9,1 ± 5 ° (C = 1 dans HCl 2N)
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

Na-Fmoc-Nim-methyl-D-histidine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, especially in the production of modified peptides that can enhance biological activity.
  • Drug Development: It is used in the development of pharmaceuticals, particularly in creating compounds that target specific biological pathways, offering potential advantages in efficacy and specificity.
  • Bioconjugation: The chemical is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic applications.
  • Protein Engineering: It plays a significant role in protein engineering, where modifications can lead to improved stability and functionality of proteins, benefiting various biotechnological applications.
  • Research in Neuroscience: The compound is relevant in neuroscience research, particularly in studying receptor interactions and signaling pathways, which can lead to advancements in understanding neurological disorders.

Citations