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Merck

A4021

Nε-Acetyl-L-lysine

≥98% (TLC)

Nε-Acetyl-L-lysine

Sinónimos:

N6-acetyl-L-lysine

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1 G

US$ 151,00

5 G

US$ 455,00

US$ 151,00

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Fórmula lineal:
CH3CONH(CH2)4CH(NH2)CO2H
Número CAS:
692-04-6
Peso molecular:
188.22
NACRES:
NA.26
PubChem Substance ID:
24890737
UNSPSC Code:
12352209
EC Number:
211-725-9
MDL number:
MFCD00002639

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Nombre del producto

Nε-Acetyl-L-lysine,

InChI key

DTERQYGMUDWYAZ-ZETCQYMHSA-N

InChI

1S/C8H16N2O3/c1-6(11)10-5-3-2-4-7(9)8(12)13/h7H,2-5,9H2,1H3,(H,10,11)(H,12,13)/t7-/m0/s1

SMILES string

CC(=O)NCCCC[C@H](N)C(O)=O

assay

≥98% (TLC)

form

powder

concentration

50 mg/mL in 80% acetic acid

color

colorless to white

mp

250 °C (dec.) (lit.)

storage temp.

−20°C

Quality Level

200

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1 of 4

Este artículo
A2010P4510A3626
Nε-Acetyl-L-lysine

Sigma-Aldrich

A4021

Nε-Acetyl-L-lysine

Nα-Acetyl-L-lysine

Sigma-Aldrich

A2010

Nα-Acetyl-L-lysine

Poly-ε-Cbz-L-lysine mol wt 500-4,000

Sigma-Aldrich

P4510

Poly-ε-Cbz-L-lysine

Nα-Acetyl-L-ornithine

Sigma-Aldrich

A3626

Nα-Acetyl-L-ornithine

form

powder

form

powder

form

powder

form

powder

assay

≥98% (TLC)

assay

≥98% (TLC)

assay

-

assay

≥98% (TLC)

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

color

colorless to white

color

colorless to white

color

white

color

colorless to white

mp

250 °C (dec.) (lit.)

mp

256-258 °C (dec.) (lit.)

mp

-

mp

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

Application


  • Nε-Acetyl L-α Lysine Improves Activity and Stability of α-Amylase at Acidic Conditions: A Comparative Study with other Osmolytes. This study highlights the use of Nε-Acetyl-ʟ-lysine in enhancing the functional stability and activity of α-amylase under acidic conditions, demonstrating its potential as a valuable additive in industrial enzyme applications (Joghee et al., 2020).

Biochem/physiol Actions

Nε-Acetyl-L-lysine (L-AcK) is an R-chain N-acetylated α amino acid used together with other lysine analogues to differentiate and characterized various aminoacylases and regulator 2 (Sir2) enzymes/sirtuins.

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificados de análisis (COA)

Lot/Batch Number
BCCM7176
BCCL9812
BCCK2331
BCCJ0164
BCCF1097

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Morten B Trelle et al.
Analytical chemistry, 80(9), 3422-3430 (2008-03-15)
Tandem mass spectrometry (MS/MS) is a powerful tool for characterization of post-translationally modified proteins, including epsilon-N-acetyllysine-containing species. Previous reports indicate that epsilon-N-acetyllysine immonium ions are useful marker ions for peptides containing epsilon-N-acetyllysine, but the specificity and sensitivity of these ions
Ying Huang et al.
Molecular bioSystems, 6(4), 683-686 (2010-03-20)
By overexpressing the C-terminal domain of the ribosomal protein L11 to decrease release factor 1-mediated termination of protein translation, enhanced amber suppression is achieved in E. coli. This enhanced amber suppression efficiency allows the genetic incorporation of three N(epsilon)-acetyl-l-lysines into
K Hoffmann et al.
Die Pharmazie, 55(8), 601-606 (2000-09-16)
Inhibitors of histone deacetylase (HD) are of great potential as new drugs due to their ability to influence transcriptional regulation and to induce apoptosis or differentiation in cancer cells. So far only radioactive enzyme activity assays or in-vivo assays with
A Pähler et al.
Chemical research in toxicology, 11(9), 995-1004 (1998-10-07)
Antibodies directed against chemical specific protein modifications are valuable tools to detect and comparatively quantify protein modifications. Both Nepsilon-(dichloroacetyl)-L-lysine and Nepsilon-(trichloroacety)l-L-lysine have been detected as modified amino acids in liver and kidneys of rats treated with perchloroethene (PER) after proteolysis.
Heinz Neumann et al.
Nature chemical biology, 4(4), 232-234 (2008-02-19)
N(epsilon)-acetylation of lysine (1) is a reversible post-translational modification with a regulatory role that rivals that of phosphorylation in eukaryotes. No general methods exist to synthesize proteins containing N(epsilon)-acetyllysine (2) at defined sites. Here we demonstrate the site-specific incorporation of
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