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Catalog Number:
11176
CAS Number:
268564-10-9(net)
Chlorhydrate de N a -Fmoc-N w,w -diméthyl-L-arginine (asymétrique)
Purity:
≥ 98 % (HPLC)
Synonym(s):
Chlorhydrate de Fmoc-L-Arg(Me)2-OH (asymétrique)
Documents
$159.84 /100 mg
Taille
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Informations sur le produit

Na-Fmoc-Nw,w-dimethyl-L-arginine (asymmetrical) hydrochloride is a versatile and valuable compound widely used in peptide synthesis and drug development. This derivative of L-arginine features a fluorenylmethyloxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique asymmetrical structure allows for the introduction of specific functional groups, making it an ideal choice for researchers aiming to create complex peptide sequences with precision.

In the pharmaceutical industry, this compound plays a crucial role in the development of novel therapeutics, particularly in the field of cardiovascular and metabolic research. Its ability to modulate nitric oxide production makes it a candidate for studies related to vasodilation and blood flow regulation. Additionally, Na-Fmoc-Nw,w-dimethyl-L-arginine (asymmetrical) hydrochloride is utilized in academic research to explore the biochemical pathways involving arginine derivatives, providing insights into their physiological roles. With its reliable performance and adaptability, this compound is a must-have for professionals engaged in peptide chemistry and related fields.

Numéro CAS 
268564-10-9(net)
Formule moléculaire
C23H28N4O4 · HCl
Poids moléculaire 
461.0
Informations générales
Numéro CAS 
268564-10-9(net)
Formule moléculaire
C23H28N4O4 · HCl
Poids moléculaire 
461.0
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Na-Fmoc-Nw,w -dimethyl-L-arginine (asymmetrical) hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing researchers to selectively modify amino acids without affecting others. Its use can streamline the process and improve yields in peptide production.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, particularly in creating compounds that target specific biological pathways. This can lead to more effective treatments with fewer side effects.
  • Biochemical Research: Researchers use this compound to study the function of nitric oxide synthase, which is important for understanding cardiovascular health and related diseases.
  • Diagnostics: It can be utilized in the development of diagnostic tools for various conditions, enhancing the ability to detect and monitor diseases through targeted biochemical interactions.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential benefits in skin care products, particularly those aimed at improving skin elasticity and hydration.

Citations