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Catalog Number:
32555
CAS Number:
1926163-08-7
Fmoc-Val-Cys(Psi(Dmp,H)pro)-OH
Purity:
≥ 99 % (HPLC, CCM)
Synonym(s):
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
Antibiotic
Documents
$66.80 /100 mg
Taille
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Informations sur le produit

Fmoc-Val-Cys(Psi(Dmp,H)pro)-OH is a sophisticated compound widely utilized in peptide synthesis and drug development. This derivative of cysteine features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure, characterized by the presence of a thiolane ring and a dimethoxyphenyl group, enhances its stability and reactivity, making it an excellent choice for researchers focused on developing novel peptides and therapeutic agents.

This compound is particularly valuable in the field of medicinal chemistry, where it can be employed in the design of peptide-based drugs, including those targeting specific biological pathways. Its ability to facilitate the formation of disulfide bonds in peptides allows for the creation of more complex and biologically active molecules. Additionally, the incorporation of the Psi(Dmp,H)pro modification can improve the pharmacokinetic properties of the resulting peptides, making them more effective in therapeutic applications. Researchers and industry professionals will find Fmoc-Val-Cys(Psi(Dmp,H)pro)-OH to be a versatile tool in their synthetic arsenal, enabling the advancement of peptide chemistry and drug discovery.

Numéro CAS 
1926163-08-7
Formule moléculaire
C32H34N2O7S
Poids moléculaire 
590.7
Informations générales
Numéro CAS 
1926163-08-7
Formule moléculaire
C32H34N2O7S
Poids moléculaire 
590.7
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

Fmoc-Val-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 solid-phase peptide synthesis. Its protective Fmoc group allows for selective deprotection, facilitating the assembly of complex peptide chains.
  • Drug Development: Researchers in pharmaceutical industries leverage this compound to develop novel therapeutics. Its unique structure can enhance the bioactivity of peptide-based drugs, making it valuable in creating targeted treatments.
  • Bioconjugation: The compound's reactive thiol group is useful for bioconjugation applications, enabling the attachment of peptides to other biomolecules. This is crucial in creating targeted drug delivery systems and diagnostic agents.
  • Research in Cancer Therapeutics: Its application in developing peptide-based inhibitors has shown promise in cancer research, where it can be used to design molecules that selectively target cancer cells, minimizing side effects.
  • Protein Engineering: In the field of protein engineering, this compound aids in the design of modified proteins with enhanced stability and activity, which is essential for various biotechnological applications.

Citations