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Catalog Number:
12620
CAS Number:
1198321-33-3
N α -Fmoc- N δ -(4,4-diméthyl-2,6-dioxocyclohex-1-ylidène)-3-méthylbutyl-L-ornithine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Orn(ivDde)-OH
Documents
$72.31 /250 mg
Taille
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Informations sur le produit

Na-Fmoc-Nd-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-ornithine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the field of medicinal chemistry for its ability to enhance the stability and bioavailability of peptides. Its unique structure, featuring the Fmoc (9-fluorenylmethoxycarbonyl) protecting group, allows for selective deprotection during synthesis, making it an ideal choice for researchers focused on developing complex peptide-based therapeutics.

In addition to its applications in peptide synthesis, this compound can be utilized in the design of novel drug candidates targeting various biological pathways. Its distinctive cyclohexenylidene moiety contributes to its potential as a building block in the creation of bioactive molecules. Researchers can leverage Na-Fmoc-Nd-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-ornithine for innovative applications in drug discovery, particularly in the development of targeted therapies and biologically active compounds.

Numéro CAS 
1198321-33-3
Formule moléculaire
C33H40N2O6
Poids moléculaire 
560.6
Point de fusion 
> 57 °C
Rotation optique 
[α] D 20 = +33 ± 5º (C=1 dans CHCl 3 )
Informations générales
Numéro CAS 
1198321-33-3
Formule moléculaire
C33H40N2O6
Poids moléculaire 
560.6
Point de fusion 
> 57 °C
Rotation optique 
[α] D 20 = +33 ± 5º (C=1 dans CHCl 3 )
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Na-Fmoc-Nd-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-ornithine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups, enhancing the efficiency of creating complex peptides.
  • Drug Development: It plays a crucial role in the development of peptide-based therapeutics, particularly in designing drugs that target specific biological pathways, which is essential in treating various diseases.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the efficacy of diagnostic tools and drug delivery systems.
  • Research in Cancer Therapy: It is being explored in cancer research for its potential to develop targeted therapies that can selectively attack cancer cells while sparing healthy tissue, thereby reducing side effects.
  • Material Science: This chemical is also applied in the development of novel materials, such as hydrogels, which have applications in tissue engineering and regenerative medicine, providing scaffolding for cell growth.

Citations