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CAS 159190-45-1

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N6-(1-Iminoethyl)-L-lysine hydrochloride (1:2)

Description:
N6-(1-Iminoethyl)-L-lysine hydrochloride (1:2) is a synthetic derivative of the amino acid L-lysine, characterized by the presence of an iminoethyl group at the N6 position of the lysine side chain. This modification enhances its biological activity and potential applications in biochemical research and pharmaceutical development. The compound is typically encountered as a hydrochloride salt, which improves its solubility in aqueous solutions, making it suitable for various experimental conditions. It is often utilized in studies related to protein synthesis, enzyme inhibition, and as a building block in peptide synthesis. The molecular structure includes a primary amine group, a secondary amine, and a carboxylic acid functional group, contributing to its basicity and reactivity. As with many amino acid derivatives, it may exhibit specific interactions with biological macromolecules, influencing its pharmacological properties. Safety and handling precautions should be observed, as with any chemical substance, to mitigate potential hazards during laboratory use.
Formula:C8H17N3O2·2ClH
InChI:InChI=1S/C8H17N3O2.2ClH/c1-6(9)11-5-3-2-4-7(10)8(12)13;;/h7H,2-5,10H2,1H3,(H2,9,11)(H,12,13);2*1H/t7-;;/m0../s1
InChI key:InChIKey=OQIBCXRAFAHXMM-KLXURFKVSA-N
SMILES:C([C@@H](C(O)=O)N)CCCNC(C)=N.Cl
Synonyms:
  • <span class="text-smallcaps">L</span>-Lysine, N<sup>6</sup>-(1-iminoethyl)-, dihydrochloride
  • <span class="text-smallcaps">L</span>-Lysine, N<sup>6</sup>-(1-iminoethyl)-, hydrochloride (1:2)
  • N6-(1-Iminoethyl)-L-Lysine Dihydrochloride
  • N<sup>6</sup>-(1-Iminoethyl)-<span class="text-smallcaps">L</span>-lysine hydrochloride (1:2)
  • L-Lysine, N6-(1-iminoethyl)-, dihydrochloride
  • L-Lysine, N6-(1-iminoethyl)-, hydrochloride (1:2)
  • N6-(1-Iminoethyl)-L-lysine hydrochloride (1:2)
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