Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
11334
CAS Number:
200871-52-9
Boc-D-His(1-Me)-OH
Purity:
≥ 99 % (CCM)
Synonym(s):
Boc-D-His( N im-Me)-OH
Documents
$156.00 /100 mg
Taille
Request Bulk Quote
Informations sur le produit

Boc-D-His(1-Me)-OH is a valuable compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an excellent choice for researchers in the fields of biochemistry and medicinal chemistry. Its unique structure, characterized by the presence of a 1-methylimidazole side chain, allows for specific interactions in biological systems, facilitating the design of novel therapeutics and biologically active peptides.

In practical applications, Boc-D-His(1-Me)-OH is particularly beneficial in the synthesis of histidine-containing peptides, which are essential for various biological functions, including enzyme catalysis and metal ion binding. The compound's ability to improve the yield and purity of peptide products makes it a preferred choice among professionals in pharmaceutical and biotechnology industries. Its versatility and effectiveness in enhancing peptide stability and functionality underscore its significance in advancing research and development efforts.

Numéro CAS 
200871-52-9
Formule moléculaire
C12H19N3O4
Poids moléculaire 
269.3
Point de fusion 
111-115 ºC
Informations générales
Numéro CAS 
200871-52-9
Formule moléculaire
C12H19N3O4
Poids moléculaire 
269.3
Point de fusion 
111-115 ºC
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Boc-D-His(1-Me)-OH is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require histidine residues. Its protective Boc group allows for selective reactions, making it easier to construct complex peptide chains.
  • Drug Development: In pharmaceutical research, Boc-D-His(1-Me)-OH is used to create drug candidates that target specific biological pathways. Its unique structure can enhance the efficacy of therapeutic agents, particularly in oncology and immunology.
  • Bioconjugation: This chemical is employed in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules. This is particularly useful in developing targeted drug delivery systems and diagnostic tools.
  • Protein Engineering: Researchers use Boc-D-His(1-Me)-OH to modify proteins, improving their stability and functionality. This application is crucial in creating enzymes with enhanced activity or specificity for industrial processes.
  • Research in Molecular Biology: The compound is valuable in studying protein interactions and functions due to its ability to mimic natural amino acids. This helps scientists understand complex biological systems and develop new therapeutic strategies.

Citations