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Catalog Number:
11187
CAS Number:
159857-60-0
N α -Fmoc- N ε -4-méthoxyyltrityl-L-lysine
Purity:
≥ 98,5 % (HPLC)
Synonym(s):
Fmoc-L-Lys(Mmt)-OH, Fmoc-Lys(4-méthoxytrityl)-OH
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Informations sur le produit

Na-Fmoc-Ne-4-methoxyyltrityl-L-lysine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it an essential building block for researchers in the field of medicinal chemistry. Its unique trityl protection enhances stability and solubility, facilitating smoother reactions and higher yields in complex peptide sequences.

In practical applications, Na-Fmoc-Ne-4-methoxyyltrityl-L-lysine is particularly valuable in the synthesis of biologically active peptides and proteins, which are crucial for therapeutic development. Its ability to incorporate into various peptide chains allows for the exploration of novel drug candidates and the study of protein interactions. Researchers appreciate its compatibility with solid-phase peptide synthesis (SPPS) techniques, enabling efficient and streamlined workflows. This compound stands out for its reliability and effectiveness in producing high-purity peptides, making it a preferred choice among professionals in pharmaceutical and biotechnological industries.

Numéro CAS 
159857-60-0
Formule moléculaire
C41H40N2O5
Poids moléculaire 
640.8
Informations générales
Numéro CAS 
159857-60-0
Formule moléculaire
C41H40N2O5
Poids moléculaire 
640.8
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-Ne-4-methoxyyltrityl-L-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in enhancing the stability and bioavailability of drug candidates.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Cancer Therapy: Its application in developing peptide conjugates has shown promise in targeted cancer therapies, improving the efficacy of treatment while minimizing side effects.
  • Protein Engineering: Researchers utilize this compound to modify lysine residues in proteins, allowing for the study of protein interactions and functions in various biological systems.

Citations