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Catalog Number:
32840
CAS Number:
120928-02-1
H-Ala-Phe-Lys-AMC trifluoroacetate salt
Synonym(s):
H-Ala-Phe-Lys-AMC trifluoroacetate salt
Documents
$194.99 /5MG
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Product Information

H-Ala-Phe-Lys-AMC trifluoroacetate salt is a specialized peptide compound that plays a crucial role in biochemical research and drug development. This compound is particularly valued for its application in protease activity assays, where it serves as a substrate that can be cleaved by specific enzymes, allowing researchers to monitor enzymatic activity effectively. Its unique structure, featuring a trifluoroacetate salt, enhances its stability and solubility, making it an ideal choice for various laboratory settings.

In addition to its use in enzymatic assays, H-Ala-Phe-Lys-AMC trifluoroacetate salt is also utilized in the synthesis of peptide-based therapeutics and in the study of peptide interactions within biological systems. Researchers appreciate its ability to provide insights into protein function and enzyme kinetics, which are essential for advancing drug discovery and development. With its robust performance and versatility, this compound stands out as a valuable tool for professionals in biochemistry and molecular biology.

Synonyms
H-Ala-Phe-Lys-AMC trifluoroacetate salt
CAS Number
120928-02-1
Molecular Formula
C28H35N5O5·C2HF3O2
Molecular Weight
635.64
MDL Number
MFCD00038709
PubChem ID
45157632
Conditions
Store at 2-8 °C
General Information
Synonyms
H-Ala-Phe-Lys-AMC trifluoroacetate salt
CAS Number
120928-02-1
Molecular Formula
C28H35N5O5·C2HF3O2
Molecular Weight
635.64
MDL Number
MFCD00038709
PubChem ID
45157632
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

H-Ala-Phe-Lys-AMC trifluoroacetate salt is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in various enzyme assays, particularly in studies involving proteases. Its structure allows for the easy monitoring of enzyme activity, making it valuable for researchers in enzymology.
  • Drug Development: The compound is used in the synthesis of peptide-based drugs. Its unique amino acid sequence can be modified to enhance therapeutic efficacy, providing a foundation for developing new pharmaceuticals.
  • Fluorescent Labeling: H-Ala-Phe-Lys-AMC trifluoroacetate salt can be conjugated with fluorescent dyes, enabling visualization of biological processes in live cells. This application is crucial in cell biology and molecular imaging.
  • Protein Interaction Studies: Researchers utilize this compound to investigate protein-protein interactions. Its ability to mimic natural substrates helps in understanding complex biological pathways and mechanisms.
  • Diagnostic Tools: The compound is also explored in the development of diagnostic assays for diseases, leveraging its specificity to certain enzymes. This can lead to more accurate and efficient diagnostic methods in clinical settings.

Citations