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Informacje o tej pozycji
Wzór liniowy:
CH3CONH(CH2)4CH(NH2)CO2H
Numer CAS:
Masa cząsteczkowa:
188.22
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
211-725-9
MDL number:
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Pomoc techniczna
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Pozwól nam pomócNazwa produktu
Nε-Acetyl-L-lysine,
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
SMILES string
CC(=O)NCCCC[C@H](N)C(O)=O
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
InChI key
DTERQYGMUDWYAZ-ZETCQYMHSA-N
1 of 4
Ta pozycja | |||
|---|---|---|---|
| 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.
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Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
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
S L Hazen et al.
The Journal of biological chemistry, 272(27), 16990-16998 (1997-07-04)
Activated human phagocytes employ the myeloperoxidase-H2O2-Cl- system to convert L-tyrosine to p-hydroxyphenylacetaldehyde (pHA). We have explored the possibility that pHA covalently reacts with proteins to form Schiff base adducts, which may play a role in modifying targets at sites of
C Crane-Robinson et al.
Methods (San Diego, Calif.), 12(1), 48-56 (1997-05-01)
Acetylation of specific lysine residues in the N-terminal domains of core histones is a biochemical marker of active genes. To determine the spatial and temporal distribution of this reversible posttranslational modification, affinity-purified polyclonal antibodies recognizing the epitope epsilon-acetyllysine have been
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
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| A4021-1G | 04061826055427 |
| A4021-5G | 04061833368404 |
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