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Catalog Number:
02380
CAS Number:
157774-30-6
N α - Fmoc- N ω -(2,2,5,7,8-pentaméthylchroman-6-sulfonyl)-D-arginine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Arg(Pmc)-OH
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Informations sur le produit

Na-Fmoc-Nw-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-D-arginine is a specialized amino acid derivative that serves as a crucial building block in peptide synthesis and drug development. This compound is particularly valued in the field of medicinal chemistry for its unique sulfonyl group, which enhances the stability and solubility of peptides. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains while facilitating selective deprotection, making it an ideal choice for researchers focused on synthesizing complex peptides with high purity and yield.

In addition to its role in peptide synthesis, this compound has potential applications in the development of targeted therapeutics, particularly in the design of peptide-based drugs that require specific modifications for enhanced bioactivity. The incorporation of the pentamethylchroman moiety not only contributes to the compound's stability but also may improve its pharmacokinetic properties. Researchers and industry professionals can leverage the unique features of Na-Fmoc-Nw-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-D-arginine to advance their work in drug discovery and development, making it a valuable addition to any chemical toolkit.

Numéro CAS 
157774-30-6
Formule moléculaire
C 35 H 42 N 4 O 7 S
Poids moléculaire 
662.8
Rotation optique 
=+3,0º à +5,0º (c=1, DMF)
Informations générales
Numéro CAS 
157774-30-6
Formule moléculaire
C 35 H 42 N 4 O 7 S
Poids moléculaire 
662.8
Rotation optique 
=+3,0º à +5,0º (c=1, DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
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)-D-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in enhancing the stability and bioavailability of drug candidates.
  • Bioconjugation: The sulfonyl group facilitates the conjugation of peptides to various biomolecules, aiding in the development of targeted drug delivery systems.
  • Research in Neuroscience: This compound is used in studies related to neuropeptides, contributing to the understanding of neurological functions and potential treatments for neurodegenerative diseases.
  • Analytical Chemistry: It is employed in the development of analytical methods for the detection and quantification of peptides, improving the accuracy and efficiency of biochemical assays.

Citations