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CAS 6367-10-8

:

N-A-acetyl-L-lysine-N-methylamide*free base

Description:
N-Acetyl-L-lysine-N-methylamide, also known by its CAS number 6367-10-8, is a derivative of the amino acid lysine. This compound features an acetyl group and a methylamide group attached to the lysine backbone, which influences its solubility and reactivity. It is typically a white to off-white crystalline solid, soluble in polar solvents such as water and methanol, due to the presence of both hydrophilic acetyl and amide functional groups. The compound is of interest in biochemical research, particularly in studies related to protein modification and epigenetics, as acetylation plays a crucial role in regulating gene expression. Its structure allows it to participate in various biochemical pathways, potentially acting as a substrate or inhibitor in enzymatic reactions. Additionally, N-Acetyl-L-lysine-N-methylamide may exhibit biological activities, including effects on cellular metabolism and signaling pathways. As with many amino acid derivatives, it is important to handle this compound with care, following appropriate safety protocols in laboratory settings.
Formula:C9H19N3O2
InChI:InChI=1/C9H19N3O2/c1-7(13)12-8(9(14)11-2)5-3-4-6-10/h8H,3-6,10H2,1-2H3,(H,11,14)(H,12,13)/t8-/m0/s1
InChI key:InChIKey=FECUPDBTEVPIIE-QMMMGPOBSA-N
SMILES:CC(=N[C@@H](CCCCN)C(=NC)O)O
Synonyms:
  • (2S)-2-(Acetylamino)-6-amino-N-methylhexanamide
  • (2S)-2-Acetamido-6-amino-N-methylhexanamide
  • Ac-Lys-NHMe
  • Hexanamide, 2-(acetylamino)-6-amino-N-methyl-, (2S)-
  • Hexanamide, 2-(acetylamino)-6-amino-N-methyl-, (S)-
  • Hexanamide, 2-acetamido-6-amino-N-methyl-, <span class="text-smallcaps">L</span>-
  • N-Acetyl-<span class="text-smallcaps">L</span>-lysine methylamide
  • N-Acetyl-N′-methyllysylamide
  • N<sup>α</sup>-Acetyllysine methylamide
  • N~2~-acetyl-N-methyl-L-lysinamide
  • Nα-Acetyl-<span class="text-smallcaps">L</span>-lysine-N-methylamide
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