Chemical Property of Acetyllysine
Chemical Property:
- Appearance/Colour:white crystalline powder
- Vapor Pressure:4.76E-09mmHg at 25°C
- Melting Point:250 °C
- Refractive Index:1.49
- Boiling Point:442 °C at 760 mmHg
- PKA:2.53±0.24(Predicted)
- Flash Point:221.1 °C
- PSA:92.42000
- Density:1.139 g/cm3
- LogP:0.79590
- Storage Temp.:−20°C
- Sensitive.:Hygroscopic
- Solubility.:Aqueous Base (Slightly), Water (Slightly)
- Water Solubility.:Soluble in water (miscible), and 80% acetic acid (50 mg/ml).
- XLogP3:-2.3
- Hydrogen Bond Donor Count:2
- Hydrogen Bond Acceptor Count:3
- Rotatable Bond Count:5
- Exact Mass:188.11609238
- Heavy Atom Count:13
- Complexity:177
- Purity/Quality:
-
97% *data from raw suppliers
Nepsilon-Acetyl-L-lysine *data from reagent suppliers
Safty Information:
- Pictogram(s):
Xi
- Hazard Codes:Xi
- Statements:
36/37/38
- Safety Statements:
24/25-36-26
- MSDS Files:
-
Total 1 MSDS from other Authors
Useful:
- Canonical SMILES:CC(=O)NCCCCC(C(=O)[O-])[NH3+]
- Isomeric SMILES:CC(=O)NCCCC[C@@H](C(=O)[O-])[NH3+]
-
Description
Acetyllysine (or acetylated lysine) is an acetyl-derivative of the amino acid lysine. There are multiple forms of acetyllysine - this article refers to N-ε-acetyl-L-lysine. The other form is N-α-acetyl-Llysine. In proteins, the acetylation of lysine residues is an important mechanism of epigenetics. It functions by regulating the binding of histones to DNA in nucleosomes and thereby controlling the expression of genes on that DNA. Non-histone proteins are acetylated as well. Unlike the functionally similar methyllysine, acetyllysine does not carry a positive charge on its side chain. Histone acetyltransferases (HATs) catalyze the addition of acetyl groups from acetyl-CoA onto certain lysine residues of histones and non-histone proteins. Histone deacetylases (HDACs) catalyze the removal of acetyl groups from acetylated lysines. Acetyllysine can be synthesized from lysine by the selective acetylation of the terminal amine group.
-
Uses
N-Epsilon-acetyl-l-lysine is used in the metabolomics study on the combined effect of cocaine and ethanol via liquid chromatography-mass spectrometry metabolomics approach.