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(2S)-2-amino-6-{[(prop-2-yn-1-yloxy)carbonyl]amino}hexanoic acid

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(2S)-2-amino-6-{[(prop-2-yn-1-yloxy)carbonyl]amino}hexanoic acid Basic information

Product Name:
(2S)-2-amino-6-{[(prop-2-yn-1-yloxy)carbonyl]amino}hexanoic acid
Synonyms:
  • (2S)-2-amino-6-{[(prop-2-yn-1-yloxy)carbonyl]amino}hexanoic acid
  • Click-Amino-Acid / PrK - HCl-salt
  • N6-((prop-2-yn-1-yloxy)carbonyl)-L-lysine
  • N-propargyloxycarbonyl-L-lysine
  • L-Lysine, N6-[(2-propyn-1-yloxy)carbonyl]-
  • N6-[(2-propynyloxy)carbonyl]-L-lysine HCl
  • N-Propargyl-lysine
CAS:
1215204-46-8
MF:
C10H16N2O4
MW:
228.24
Product Categories:
  • SiChem
Mol File:
1215204-46-8.mol
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(2S)-2-amino-6-{[(prop-2-yn-1-yloxy)carbonyl]amino}hexanoic acid Chemical Properties

storage temp. 
Store at -20°C
form 
Solid
color 
White to off-white
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(2S)-2-amino-6-{[(prop-2-yn-1-yloxy)carbonyl]amino}hexanoic acid Usage And Synthesis

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]. Labeling of N-ε-propargyloxycarbonyl-L-lysine (H-L-Lys(Poc)-OH)-carrying cellular proteins, such as Sec61β, Htt74Q and the histone H3 variant H3.3, with a sensitive Raman tag by click chemistry for molecular hyperspectral SRS imaging[1].

References

[1]. Kyung Jin Lee, et al. Site-Specific Labeling of Proteins Using Unnatural Amino Acids. Mol Cells. 2019 May 31;42(5):386-396. [2]. Enke HEIKE, et al. Modified microcystins and nodularins.WO2018206715A2

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(2S)-2-amino-6-{[(prop-2-yn-1-yloxy)carbonyl]amino}hexanoic acid(1215204-46-8)Related Product Information