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Catalog Number:
47697
CAS Number:
159610-92-1
6-Azido-L-lysine
Purity:
≥ 99 % (HPLC)
Synonym(s):
H-Lys( N3 )-OH, 6-Azido-L-norleucine
Documents
$65.00 /25 mg
Taille
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Product Information

H-Lys(N3)-OH est incorporé dans des protéines qui peuvent être modifiées de manière sélective à l'aide de la ligature de Staudinger ou de la chimie Click.

Synonyms
H-Lys( N3 )-OH, 6-Azido-L-norleucine
CAS Number
159610-92-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H12N4O2
Molecular Weight
172.2
Appearance
Poudre blanche
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
H-Lys( N3 )-OH, 6-Azido-L-norleucine
CAS Number
159610-92-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H12N4O2
Molecular Weight
172.2
Appearance
Poudre blanche
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

6-Azido-L-lysine is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile building block for bioconjugation, allowing researchers to attach biomolecules like proteins or antibodies to surfaces or other molecules, enhancing drug delivery systems.
  • Click Chemistry: It plays a crucial role in click chemistry reactions, which are used to create complex molecular structures quickly and efficiently, making it valuable in drug discovery and development.
  • Protein Labeling: The azido group enables specific labeling of proteins in biological studies, aiding in the visualization and tracking of protein interactions within cells.
  • Peptide Synthesis: As a modified amino acid, it is used in peptide synthesis to create novel peptides with unique properties, which can be used in therapeutic applications.
  • Research in Neuroscience: It is being explored for its potential in neuroscience research, particularly in studying neuronal signaling and the development of neuroprotective agents.

Citations