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Catalog Number:
03723
CAS Number:
333973-51-6
N α -Fmoc- N ε -1-(4,4-dimetil-2,6-dioxociclohex-1-ilideno)etil-D-lisina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Lis(Dde)-OH
Documents
$50.00 /250 mg
Tamaño
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Información del producto

Na-Fmoc-Ne-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-D-lysine is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure, characterized by the presence of a cyclohexenylidene moiety, enhances its reactivity and stability, making it an ideal candidate for researchers focused on developing complex peptide-based therapeutics.

In practical applications, Na-Fmoc-Ne-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-D-lysine is particularly valuable in the fields of medicinal chemistry and biochemistry, where it facilitates the synthesis of bioactive peptides with improved pharmacological properties. The compound's ability to streamline the synthesis process while maintaining high yields and purity levels positions it as a preferred choice for professionals aiming to innovate in peptide design and development. Its notable advantages over similar compounds include enhanced stability and reactivity, which can lead to more efficient synthesis pathways.

Número CAS
333973-51-6
Fórmula molecular
C31H36N2O6
Peso molecular
532.58
Número MDL
MFCD01862894
Rotación óptica
[a] D 20 = 5 ± 1 ° (C = 1,2 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
333973-51-6
Fórmula molecular
C31H36N2O6
Peso molecular
532.58
Número MDL
MFCD01862894
Rotación óptica
[a] D 20 = 5 ± 1 ° (C = 1,2 en DMF)
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-Ne-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-D-lysine 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. Its stability under various reaction conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: In pharmaceutical research, it aids in the design of novel peptides and proteins, which can lead to the development of new therapeutics. Its unique structure can enhance the bioactivity of drug candidates.
  • Bioconjugation: The compound can be used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, facilitating the creation of targeted drug delivery systems or diagnostic tools.
  • Protein Engineering: It is valuable in the field of protein engineering, where it helps in modifying proteins to improve their stability and functionality, which is crucial for industrial applications.
  • Research in Cancer Therapy: The compound's ability to modify peptides can be leveraged in cancer research, where tailored peptides are designed to target specific cancer cells, potentially leading to more effective treatments.

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