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Catalog Number:
48160
CAS Number:
144574-97-0
Fmoc-Pro-D-Ala-OH
Purity:
≥ 98 % (HPLC)
Synonym(s):
Na-Fmoc-L-prolyl-D-alanine
Documents
$60.00 /100 mg
Taille
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Informations sur le produit

Fmoc-Pro-D-Ala-OH is a valuable compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protective group, which is essential for the selective protection of amine functionalities during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers looking to create complex peptide sequences with precision.

In the pharmaceutical industry, Fmoc-Pro-D-Ala-OH plays a crucial role in the development of peptide-based therapeutics, particularly in the design of inhibitors and modulators for various biological pathways. Its stability and compatibility with standard coupling reagents enhance its utility in solid-phase peptide synthesis (SPPS), enabling the production of high-purity peptides for research and clinical applications. Researchers appreciate its ease of use and the high yields it provides, making it a preferred choice for both academic and industrial laboratories focused on peptide chemistry.

Numéro CAS 
144574-97-0
Formule moléculaire
C23H24N2O5
Poids moléculaire 
408.45
Informations générales
Numéro CAS 
144574-97-0
Formule moléculaire
C23H24N2O5
Poids moléculaire 
408.45
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-Pro-D-Ala-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 (SPPS), allowing researchers to create complex peptide chains efficiently.
  • Drug Development: It plays a significant role in the development of peptide-based drugs, offering a way to modify peptide structures for enhanced stability and bioactivity, which is crucial in pharmaceutical research.
  • Bioconjugation: The compound is used in bioconjugation processes to attach peptides to other biomolecules, facilitating the creation of targeted drug delivery systems, which can improve therapeutic efficacy.
  • Protein Engineering: Researchers utilize it in the design of modified proteins, enabling the exploration of structure-function relationships and the development of novel proteins with desired characteristics.
  • Research in Neuroscience: It is applied in studies related to neuropeptides, helping scientists understand their role in neurological functions and potential therapeutic targets for neurological disorders.

Citations