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Catalog Number:
02379
CAS Number:
119831-72-0
N α - Fmoc- N ω -(2,2,5,7,8-pentaméthylchroman-6-sulfonyl)-L-arginine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Arg(Pmc)-OH
Documents
$29.34 /1G
Taille
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Informations sur le produit

Na-Fmoc-Nw-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-arginine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the field of medicinal chemistry for its ability to enhance the solubility and stability of peptides, making it an ideal choice for researchers focused on developing therapeutic agents. Its unique structure, featuring a pentamethylchroman sulfonyl group, provides significant advantages in terms of bioactivity and selectivity, which can be pivotal in designing targeted therapies.

This compound is widely utilized in the synthesis of complex peptides and proteins, especially in the development of peptide-based drugs and bioconjugates. Its application extends to various fields, including pharmaceuticals, biotechnology, and academic research, where it aids in the exploration of new therapeutic pathways. Researchers appreciate its compatibility with solid-phase peptide synthesis, enabling efficient and high-yield production of peptides. By incorporating Na-Fmoc-Nw-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-arginine into their workflows, scientists can achieve greater precision and effectiveness in their projects, ultimately leading to innovative solutions in drug discovery and development.

Numéro CAS 
119831-72-0
Formule moléculaire
C 35 H 42 N 4 O 7 S
Poids moléculaire 
662.8
Rotation optique 
-2°±2°(c=1% FMS)
Informations générales
Numéro CAS 
119831-72-0
Formule moléculaire
C 35 H 42 N 4 O 7 S
Poids moléculaire 
662.8
Rotation optique 
-2°±2°(c=1% FMS)
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 
-
Applications

Na-Fmoc-Nw-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it aids in the design of novel therapeutic agents, particularly those targeting specific biological pathways, enhancing drug efficacy and specificity.
  • Bioconjugation: The compound is instrumental in bioconjugation processes, where it helps link biomolecules to drugs or imaging agents, improving the delivery and effectiveness of treatments.
  • Research in Cancer Therapy: Its unique structure allows researchers to explore new avenues in cancer treatment, potentially leading to more effective and targeted therapies.
  • Protein Engineering: This chemical is used in modifying proteins to study their functions and interactions, providing insights that can lead to advancements in biotechnology and medicine.

Citations