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Catalog Number:
12620
CAS Number:
1198321-33-3
N α -Fmoc- N δ -(4,4-dimetil-2,6-dioxociclohex-1-ilideno)-3-metilbutil-L-ornitina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Orn(ivDde)-OH
Documents
$72.31 /250 mg
Tamaño
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Información del producto

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.

Número CAS
1198321-33-3
Fórmula molecular
C33H40N2O6
Peso molecular
560.6
Número MDL
MFCD03788161
Punto de fusión
> 57 °C
Rotación óptica
[α] D 20 = +33 ± 5º (C=1 en CHCl 3 )
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
1198321-33-3
Fórmula molecular
C33H40N2O6
Peso molecular
560.6
Número MDL
MFCD03788161
Punto de fusión
> 57 °C
Rotación óptica
[α] D 20 = +33 ± 5º (C=1 en CHCl 3 )
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

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.

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