1215204-46-8

N-ε-propargyloxycarbonyl-L-lysine Chemical Structure
1215204-46-8

Chemical Structure

N-ε-propargyloxycarbonyl-L-lysine

Synonym(s): H-​L-​Lys(Poc)​-​OH

  • CAS No.: 1215204-46-8
  • Formula:C10H16N2O4
  • Molecular Weight:228.25

IUPAC Name: N6-((prop-2-yn-1-yloxy)carbonyl)-L-lysine

InChIKey: KRFMMSZGIQEBIJ-QMMMGPOBSA-N

SMILES: N[C@@H](CCCCNC(OCC#C)=O)C(O)=O

Biological Activity: N-ε-propargyloxycarbonyl-L-lysine (H-L-Lys(Poc)-OH) is a lysine-based unnatural amino acid (UAA). N-ε-propargyloxycarbonyl-L-lysine is widely used for bio-conjugation of fluorescent probes in diverse organisms from E. coli to mammalian cells even in animals[1][2]. N-ε-propargyloxycarbonyl-L-lysine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

Cat. No. Product Name Purity Description Pricing
HY-139014
N-ε-propargyloxycarbonyl-L-lysine 98.05% N-ε-propargyloxycarbonyl-L-lysine (H-L-Lys(Poc)-OH) is a lysine-based unnatural amino acid (UAA). N-ε-propargyloxycarbonyl-L-lysine is widely used for bio-conjugation of fluorescent probes in diverse organisms from E. coli to mammalian cells even in animals. N-ε-propargyloxycarbonyl-L-lysine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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