01310
N-乙酰基-L-蛋氨酸
≥98.5% (T)
别名:
N-acetyl-L-lysine
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关于此项目
线性分子式:
CH3SCH2CH2CH(NHCOCH3)CO2H
化学文摘社编号:
分子量:
191.25
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-617-7
Beilstein/REAXYS Number:
1725552
MDL number:
产品名称
N-乙酰基-L-蛋氨酸, ≥98.5% (T)
InChI key
XUYPXLNMDZIRQH-LURJTMIESA-N
InChI
1S/C7H13NO3S/c1-5(9)8-6(7(10)11)3-4-12-2/h6H,3-4H2,1-2H3,(H,8,9)(H,10,11)/t6-/m0/s1
SMILES string
CSCC[C@H](NC(C)=O)C(O)=O
assay
≥98.5% (T)
≥98.5% (TLC)
form
powder or crystals
optical activity
[α]20/D -21.0±1.0°, c = 1% in H2O
reaction suitability
reaction type: solution phase peptide synthesis
mp
103-106 °C (lit.)
solubility
methanol: 50 mg/mL, clear to very slightly hazy, colorless
application(s)
peptide synthesis
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Agnieszka Kołodziejczak-Radzimska et al.
Biotechnology progress, 34(3), 767-777 (2018-01-10)
Acylase I from Aspergillus melleus was immobilized on supports consisting of unmodified and modified silica. Modification was performed using 3-aminopropyltriethoxysilane (APTES) and glutaraldehyde (GA). The effectiveness of immobilization was investigated using the standard Bradford method in addition to a number
Mie R Rasmussen et al.
Journal of proteome research, 15(12), 4591-4600 (2016-11-05)
Loss-of-function mutations in the transmembrane ABCC6 transport protein cause pseudoxanthoma elasticum (PXE), an ectopic, metabolic mineralization disorder that affects the skin, eye, and vessels. ABCC6 is assumed to mediate efflux of one or several small molecule compounds from the liver
James B Thoden et al.
Biochemistry, 43(19), 5716-5727 (2004-05-12)
Divergent evolution of enzyme function is commonly explained by a gene duplication event followed by mutational changes that allow the protein encoded by the copy to acquire a new function. An alternate hypothesis is that this process is facilitated when
M J Wick et al.
Biochemical pharmacology, 37(7), 1225-1231 (1988-04-01)
Both N-hydroxy-2-acetamidofluorene (N-OH-AAF) and the heterocyclic analogue, 2-(N-hydroxyacetamido)carbazole (N-OH-AAC), were shown to be mechanism-based irreversible inhibitors (suicide inhibitors) of partially purified rat hepatic N-acetyltransferase (NAT) activity. Although N-OH-AAC exhibited an apparent first-order inactivation rate constant (ki) that was 7-fold lower
Wen-Fang Ji et al.
The journal of physical chemistry. B, 111(2), 485-489 (2007-01-12)
The amino acid oxidation mechanism has been a research focus in recent years. Although various experimental techniques have been employed to address the problem, it is still a great challenge to identify the oxidation intermediates of amino acids. To explore
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