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Catalog Number:
33407
Fmoc-D-Aph(L-Hor)-OH
Purity:
≥ 99 % (HPLC)
Synonym(s):
( R -2-((((Fmoc)amino)-3-(4-(( S -2,6-dioxohexahidropirimidina-4-carboxamido)fenil)ácido propanoico
Documents
$82.02 /100 mg
Tamaño
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Product Information

Fmoc-D-Aph(L-Hor)-OH is a valuable amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethyloxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing complex peptide sequences. The incorporation of D-Aphenylalanine and L-Homophenylalanine enhances the compound's stability and bioactivity, making it suitable for applications in medicinal chemistry and biochemistry.

Researchers and industry professionals can leverage Fmoc-D-Aph(L-Hor)-OH in various applications, including the design of peptide-based therapeutics, drug delivery systems, and the development of novel biomaterials. Its ability to facilitate the synthesis of peptides with specific structural and functional properties positions it as a crucial tool in the pharmaceutical and biotechnology sectors. With its advantageous features, this compound stands out in the crowded field of amino acid derivatives, offering significant benefits in efficiency and effectiveness for peptide synthesis.

Synonyms
( R -2-((((Fmoc)amino)-3-(4-(( S -2,6-dioxohexahidropirimidina-4-carboxamido)fenil)ácido propanoico
Purity
≥ 99 % (HPLC)
Molecular Formula
C29H26N4O7
Molecular Weight
542.4
MDL Number
MFCD31555213
Appearance
Polvo rosa claro
Conditions
Tienda en RT
General Information
Synonyms
( R -2-((((Fmoc)amino)-3-(4-(( S -2,6-dioxohexahidropirimidina-4-carboxamido)fenil)ácido propanoico
Purity
≥ 99 % (HPLC)
Molecular Formula
C29H26N4O7
Molecular Weight
542.4
MDL Number
MFCD31555213
Appearance
Polvo rosa claro
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-D-Aph(L-Hor)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, especially in solid-phase peptide synthesis, allowing for the creation of complex structures with high purity.
  • Drug Development: It plays a crucial role in the development of peptide-based therapeutics, which are increasingly important in treating various diseases, including cancer and metabolic disorders.
  • Protein Engineering: Researchers use it to modify proteins, enhancing their stability and functionality, which is vital for applications in biotechnology and pharmaceuticals.
  • Bioconjugation: The compound is employed in bioconjugation techniques, linking peptides to other biomolecules, which is essential for creating targeted drug delivery systems.
  • Research in Neuroscience: It is utilized in studies related to neuropeptides, helping scientists understand their role in neurological functions and potential therapeutic targets.