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Catalog Number:
46591
CAS Number:
2108145-17-9
Fmoc-Arg(Pbf)-Ser(Psi(Me,Me)pro)-OH
Purity:
≥ 97% (HPLC)
Documents
$80.00 /25MG
Pack Size Availability Price
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Product Information

Fmoc-Arg(Pbf)-Ser(Psi(Me,Me)pro)-OH is a sophisticated amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the field of biochemistry and pharmaceutical research for its ability to enhance the stability and solubility of peptides. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group is widely recognized for its effectiveness in solid-phase peptide synthesis, allowing for the selective deprotection of amino acids. The inclusion of the Pbf (2,2,4,6,7-pentamethyl-3H-1-benzofuran-5-sulfonyl) group further enhances the compound's utility by providing additional protection against unwanted side reactions during synthesis.

Researchers and industry professionals utilize Fmoc-Arg(Pbf)-Ser(Psi(Me,Me)pro)-OH in the development of therapeutic peptides, particularly those targeting specific biological pathways. Its unique structure allows for the incorporation of non-standard amino acids, which can lead to the creation of peptides with improved pharmacological properties. This compound is essential for advancing drug discovery and development, making it a valuable asset in laboratories focused on innovative therapeutic solutions.

CAS Number
2108145-17-9
Purity
≥ 97% (HPLC)
Molecular Formula
C40H49N5O9S
Molecular Weight
775.92
Appearance
White to off-white powder
Conditions
Store at 2 - 8 °C
General Information
CAS Number
2108145-17-9
Purity
≥ 97% (HPLC)
Molecular Formula
C40H49N5O9S
Molecular Weight
775.92
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-Arg(Pbf)-Ser(Psi(Me,Me)pro) is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing researchers to create complex peptides with high purity and yield.
  • Drug Development: Its unique structure makes it valuable in the design of peptide-based therapeutics, especially for targeting specific biological pathways, enhancing drug efficacy and specificity.
  • Bioconjugation: The compound can be used to attach peptides to various biomolecules, facilitating the development of targeted delivery systems in drug formulation, improving therapeutic outcomes.
  • Research in Protein Engineering: It plays a significant role in the modification of proteins, helping scientists to study protein interactions and functions, which is crucial in understanding diseases.
  • Diagnostics: The compound's properties can be leveraged in the development of diagnostic tools, particularly in assays that require specific peptide interactions, enhancing sensitivity and specificity in detection methods.

Citations