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Catalog Number:
02063
CAS Number:
201531-77-3
Fmoc- S -acétamidométhyl-D-pénicillamine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Pen(Acm)-OH, Fmoc- S -acétamidométhyl-β,β-diméthyl-D-Cys-OH
Documents
$96.34 /250 mg
Taille
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Informations sur le produit

Fmoc-S-acetamidomethyl-D-penicillamine is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its acetamidomethyl and D-penicillamine components enhance its reactivity and stability, making it an ideal choice for researchers focused on developing novel peptides and therapeutic agents.

In the pharmaceutical industry, Fmoc-S-acetamidomethyl-D-penicillamine is particularly valuable for its role in the synthesis of bioactive peptides, which can be used in various applications, including drug delivery systems and targeted therapies. Its ability to facilitate the incorporation of sulfur-containing amino acids into peptides allows for the development of compounds with improved biological activity and specificity. Researchers appreciate its ease of use and compatibility with standard peptide synthesis protocols, making it a preferred choice for both academic and industrial applications.

Numéro CAS 
201531-77-3
Formule moléculaire
C23H26N2O5S
Poids moléculaire 
442.5
Point de fusion 
189 - 191°C
Rotation optique 
[a] D 20 = + 13 ± 2° (C=1 dans le méthanol)
Informations générales
Numéro CAS 
201531-77-3
Formule moléculaire
C23H26N2O5S
Poids moléculaire 
442.5
Point de fusion 
189 - 191°C
Rotation optique 
[a] D 20 = + 13 ± 2° (C=1 dans le méthanol)
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

Fmoc-S-acetamidomethyl-D-penicillamine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interference from other functional groups.
  • Drug Development: It plays a crucial role in the development of novel pharmaceuticals, particularly in designing compounds that target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Analytical Chemistry: It is applied in analytical methods to improve the detection and quantification of various substances, providing more accurate results in research.
  • Research in Biochemistry: The compound is valuable in studying protein interactions and modifications, contributing to a deeper understanding of biochemical processes.

Citations