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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 /100MG
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Product Information

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.

Synonyms
Na-Fmoc-L-prolyl-D-alanine
CAS Number
144574-97-0
Purity
≥ 98% (HPLC)
Molecular Formula
C23H24N2O5
Molecular Weight
408.45
Appearance
White to off-white powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Na-Fmoc-L-prolyl-D-alanine
CAS Number
144574-97-0
Purity
≥ 98% (HPLC)
Molecular Formula
C23H24N2O5
Molecular Weight
408.45
Appearance
White to off-white powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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