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Catalog Number:
32554
CAS Number:
1926163-07-6
Fmoc-Lis(Boc)-Cys(Psi(Dmp,H)pro)-OH
Purity:
≥ 99 % (HPLC, TLC)
Synonym(s):
["["Hasta(1, 1-Dimetiletil)azodicarboxilato, "Bajo la dirección"]
Antibiotic
Documents
$66.80 /100 mg
Tamaño
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Información del producto

Fmoc-Lys(Boc)-Cys(Psi(Dmp,H)pro)-OH is a sophisticated amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique structure that combines the protective Fmoc and Boc groups, making it an ideal choice for researchers focused on solid-phase peptide synthesis. Its thiolane ring enhances stability and reactivity, which is particularly beneficial in the formation of disulfide bonds in peptides, a key factor in the development of biologically active molecules.

This compound is especially valuable in the pharmaceutical industry for the design of peptide-based therapeutics, where precise control over amino acid sequences is essential. Its application extends to the synthesis of complex peptides that can be utilized in vaccine development, targeted drug delivery systems, and as research tools in molecular biology. The unique properties of Fmoc-Lys(Boc)-Cys(Psi(Dmp,H)pro)-OH not only streamline the synthesis process but also improve the yield and purity of the final products, making it a preferred choice among professionals in the field.

Número CAS
1926163-07-6
Fórmula molecular
C38H45N3O9S
Peso molecular
719.86
Número MDL
MFCD28053689
Condiciones
Conservar a ≤ -10 °C
Información general
Número CAS
1926163-07-6
Fórmula molecular
C38H45N3O9S
Peso molecular
719.86
Número MDL
MFCD28053689
Condiciones
Conservar a ≤ -10 °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

Fmoc-Lys(Boc)-Cys(Psi(Dmp,H)pro)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its protective groups allow for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates that target specific biological pathways, particularly in cancer and autoimmune diseases, providing a platform for tailored therapies.
  • Bioconjugation: The compound is instrumental in bioconjugation processes, where it helps attach drugs or imaging agents to biomolecules, improving the specificity and effectiveness of treatments.
  • Research in Protein Engineering: It is valuable in protein engineering applications, allowing researchers to modify proteins for better stability or activity, which is crucial in developing enzyme-based therapies.
  • Diagnostics: This chemical is also applied in the development of diagnostic tools, where it aids in the creation of assays that detect specific biomolecules, enhancing the accuracy of medical diagnostics.

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