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Catalog Number:
11607
CAS Number:
233691-67-3
N-Boc-N-acetyl-L-lysine 7-amido-4-methylcoumarin
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-Lys(Ac)-AMC
Documents
$127.79 /25MG
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Product Information

Na-Boc-Ne-acetyl-L-lysine 7-amido-4-methylcoumarin is a versatile compound that plays a significant role in biochemical research and pharmaceutical applications. This compound is recognized for its unique structure, which combines a protective tert-butyl group with an acetamido-L-lysine moiety and a 4-methylcoumarin fluorophore. Its properties make it an excellent choice for use in peptide synthesis and as a fluorescent probe in biological assays. Researchers utilize this compound to study enzyme activity, protein interactions, and cellular processes, providing valuable insights into various biological mechanisms.

The incorporation of the 4-methylcoumarin group enhances its utility as a fluorescent marker, allowing for easy visualization in live-cell imaging and other analytical techniques. This compound stands out due to its stability and compatibility with a range of biological systems, making it a preferred choice for scientists looking to explore complex biochemical pathways. Its applications extend to drug development, where it aids in the design of novel therapeutics targeting specific biological functions.

Synonyms
Boc-L-Lys(Ac)-AMC
CAS Number
233691-67-3
Purity
≥ 99% (HPLC)
Molecular Formula
C23H31N3O6
Molecular Weight
445.52
MDL Number
MFCD02683946
PubChem ID
4003
Appearance
White to yellow powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Lys(Ac)-AMC
CAS Number
233691-67-3
Purity
≥ 99% (HPLC)
Molecular Formula
C23H31N3O6
Molecular Weight
445.52
MDL Number
MFCD02683946
PubChem ID
4003
Appearance
White to yellow powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Boc-Ne-acetyl-L-lysine 7-amido-4-methylcoumarin is widely utilized in research focused on:

  • Fluorescent Labeling: This compound is often used in bioconjugation techniques to label proteins and peptides, enabling researchers to track biological processes in real-time.
  • Drug Development: It serves as a key intermediate in synthesizing novel pharmaceuticals, particularly in developing targeted therapies for various diseases.
  • Biochemical Assays: The compound is employed in assays to study enzyme activity and protein interactions, providing insights into cellular mechanisms.
  • Peptide Synthesis: It is used in the solid-phase synthesis of peptides, enhancing the efficiency and yield of complex peptide sequences.
  • Research in Cancer Therapeutics: Its unique structure allows for the exploration of new cancer treatment options, particularly in targeting specific cancer cell types.

Citations