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Catalog Number:
32902
CAS Number:
660846-99-1
Sel de trifluoroacétate d'Ac-Arg-Gly-Lys-AMC
Synonym(s):
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
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$221.63 /5 mg
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Product Information

Ac-Arg-Gly-Lys-AMC trifluoroacetate salt is a specialized peptide compound that plays a crucial role in biochemical research and pharmaceutical applications. This compound is particularly valued for its ability to serve as a substrate in protease assays, enabling researchers to study enzyme activity and kinetics with precision. Its unique structure, featuring a combination of arginine, glycine, and lysine, enhances its interaction with various biological systems, making it an essential tool for scientists investigating cellular processes and protein interactions.

In addition to its utility in enzyme assays, Ac-Arg-Gly-Lys-AMC trifluoroacetate salt is also employed in drug development and therapeutic research, particularly in the design of peptide-based drugs. Its trifluoroacetate form ensures stability and solubility, which are critical for effective application in biological studies. Researchers and industry professionals can leverage this compound to gain insights into proteolytic pathways and develop innovative solutions in biochemistry and molecular biology.

Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
660846-99-1
Molecular Formula
C26H38N8O6 · C2HF3O2
Molecular Weight
672.66
MDL Number
MFCD18782522
PubChem ID
168005996
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
660846-99-1
Molecular Formula
C26H38N8O6 · C2HF3O2
Molecular Weight
672.66
MDL Number
MFCD18782522
PubChem ID
168005996
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ac-Arg-Gly-Lys-AMC trifluoroacetate salt is widely utilized in research focused on:

  • Protease Activity Measurement: This compound serves as a substrate for various proteases, allowing researchers to measure enzyme activity in biochemical assays. Its specificity helps in distinguishing between different protease types.
  • Cellular Uptake Studies: It can be used to study the cellular uptake mechanisms of peptides and proteins, providing insights into how these molecules interact with cell membranes, which is crucial for drug delivery research.
  • Fluorescent Labeling: The compound can be conjugated with fluorescent tags for imaging applications in live-cell microscopy, enabling scientists to visualize protein interactions in real-time.
  • Drug Development: It plays a role in the development of peptide-based therapeutics, particularly in targeting specific cellular pathways, enhancing the efficacy of drug candidates.
  • Biomarker Discovery: Researchers utilize this compound in the identification of biomarkers for diseases, aiding in the early detection and monitoring of various health conditions.

Citations