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Catalog Number:
14855
CAS Number:
386213-32-7
N α -Fmoc- N ε -7-méthoxycoumarine-4-acétyl-L-lysine
Purity:
≥ 95 % (HPLC)
Synonym(s):
Fmoc-L-Lys(Mca)-OH
Documents
$154.43 /100 mg
Taille
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Informations sur le produit

Na-Fmoc-Ne-7-methoxycoumarin-4-acetyl-L-lysine is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This compound features a unique structure that combines the protective Fmoc group with a methoxycoumarin moiety, making it particularly valuable for researchers in the fields of medicinal chemistry and biochemistry. Its ability to facilitate the selective labeling of peptides allows for enhanced tracking and analysis in various biological studies, including drug delivery systems and cellular imaging.

The incorporation of the methoxycoumarin group not only aids in fluorescence but also provides a means for studying protein interactions and dynamics in live cells. Additionally, Na-Fmoc-Ne-7-methoxycoumarin-4-acetyl-L-lysine can be employed in the development of novel therapeutics, where its unique properties can be leveraged to create targeted delivery systems. This compound stands out due to its dual functionality, enabling researchers to explore new avenues in drug design and molecular biology with greater precision and efficiency.

Numéro CAS 
386213-32-7
Formule moléculaire
C33H32N2O8
Poids moléculaire 
584.63
Point de fusion 
181 - 196 ?C
Rotation optique 
[a] 20 D = -10 ± 1 ° (C=1 dans DMF)
Informations générales
Numéro CAS 
386213-32-7
Formule moléculaire
C33H32N2O8
Poids moléculaire 
584.63
Point de fusion 
181 - 196 ?C
Rotation optique 
[a] 20 D = -10 ± 1 ° (C=1 dans DMF)
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-7-methoxycoumarin-4-acetyl-L-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions and facilitating the formation of complex structures.
  • Fluorescent Probes: Its unique structure enables it to act as a fluorescent probe, making it valuable in biological imaging and tracking cellular processes in real-time.
  • Drug Development: The compound is used in the development of new pharmaceuticals, particularly in designing targeted therapies that require precise molecular interactions.
  • Bioconjugation: It allows for the conjugation of biomolecules, enhancing the stability and functionality of therapeutic agents, which is crucial in the field of biomedicine.
  • Research in Cancer Biology: The compound's properties make it a useful tool in cancer research, aiding in the study of tumor behavior and the development of novel treatment strategies.

Citations