H-L-Lys(4-N3-Z)-OH hydrochloride

For research use only. Not for therapeutic Use.

  • CAT Number: I042584
  • CAS Number: 2084913-49-3
  • Molecular Formula: C14H20ClN5O4
  • Molecular Weight: 357.79
  • Purity: ≥95%
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H-L-Lys(4-N3-Z)-OH hydrochloride is a click chemistry reagent containing an azide group. H-L-Lys(4-N3-Z)-OH hydrochloride contains a lysine-modified azide moiety and as a bioorthogonal ligation handle. H-L-Lys(4-N3-Z)-OH hydrochloride is an infrared probe and a photo-affinity reagent[1][2].


Catalog Number I042584
CAS Number 2084913-49-3
Synonyms

(2S)-2-amino-6-[(4-azidophenyl)methoxycarbonylamino]hexanoic acid;hydrochloride

Molecular Formula C14H20ClN5O4
Purity ≥95%
InChI InChI=1S/C14H19N5O4.ClH/c15-12(13(20)21)3-1-2-8-17-14(22)23-9-10-4-6-11(7-5-10)18-19-16;/h4-7,12H,1-3,8-9,15H2,(H,17,22)(H,20,21);1H/t12-;/m0./s1
InChIKey AQUASNYNCOKBBC-YDALLXLXSA-N
SMILES C1=CC(=CC=C1COC(=O)NCCCCC(C(=O)O)N)N=[N+]=[N-].Cl
Reference

[1]. Ge Y, et, al. A genetically encoded multifunctional unnatural amino acid for versatile protein manipulations in living cells. Chem Sci. 2016 Dec 1;7(12):7055-7060.
 [Content Brief]

[2]. Wesalo JS, et, al. Phosphine-Activated Lysine Analogues for Fast Chemical Control of Protein Subcellular Localization and Protein SUMOylation. Chembiochem. 2020 Jan 15;21(1-2):141-148.
 [Content Brief]

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