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Catalog Number:
21460
CAS Number:
60115-45-9
S-2-Nitrophényl-L-cystéine
Purity:
≥ 98 % (HPLC)
Synonym(s):
H-Cys(Sonp)-OH
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Informations sur le produit

S-2-Nitrophenyl-L-cysteine is a versatile compound recognized for its unique properties and applications in various fields, particularly in biochemical research and pharmaceutical development. This amino acid derivative features a nitrophenyl group, which enhances its reactivity and makes it a valuable tool for studying protein interactions and enzyme mechanisms. Researchers utilize S-2-Nitrophenyl-L-cysteine in the synthesis of peptide-based probes and as a building block in the development of novel therapeutics. Its ability to participate in nucleophilic substitution reactions allows for the modification of biomolecules, facilitating the exploration of cellular processes and drug design.

In addition to its applications in research, S-2-Nitrophenyl-L-cysteine has potential uses in the development of targeted therapies, particularly in cancer treatment, where it can be employed to create compounds that selectively interact with tumor cells. The compound's unique structure and reactivity provide a significant advantage over similar compounds, making it an essential addition to any laboratory focused on innovative biochemical research.

Numéro CAS 
60115-45-9
Formule moléculaire
C9H10N2O4S
Poids moléculaire 
242.25
Informations générales
Numéro CAS 
60115-45-9
Formule moléculaire
C9H10N2O4S
Poids moléculaire 
242.25
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

S-2-Nitrophenyl-L-cysteine is widely utilized in research focused on:

  • Biochemical Research: This compound serves as a valuable tool in studying protein interactions and enzyme activity, particularly in the context of redox reactions.
  • Drug Development: It is used in the synthesis of novel pharmaceutical compounds, providing a framework for developing drugs that target specific biological pathways.
  • Analytical Chemistry: The compound acts as a reagent in various analytical techniques, helping to detect and quantify thiol-containing compounds in biological samples.
  • Antioxidant Studies: Researchers utilize it to investigate the antioxidant properties of different compounds, contributing to the understanding of oxidative stress in cells.
  • Bioconjugation Applications: It is employed in bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in developing biosensors and targeted drug delivery systems.

Citations