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线性分子式:
HO2CCH2CH(NHCOCH3)CO2H
化学文摘社编号:
分子量:
175.14
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
1726198
产品名称
N-乙酰基-L-天冬氨酸, ≥99.0% (T)
InChI
1S/C6H9NO5/c1-3(8)7-4(6(11)12)2-5(9)10/h4H,2H2,1H3,(H,7,8)(H,9,10)(H,11,12)/t4-/m0/s1
SMILES string
CC(=O)N[C@@H](CC(O)=O)C(O)=O
InChI key
OTCCIMWXFLJLIA-BYPYZUCNSA-N
assay
≥99.0% (T)
form
powder
optical activity
[α]20/D +12±1°, c = 2% in 6 M HCl
reaction suitability
reaction type: solution phase peptide synthesis
color
colorless to white
mp
137-140 °C (lit.)
141-146 °C
application(s)
peptide synthesis
Quality Level
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Other Notes
综述;大脑中乙酰胆碱合成时的乙酰基供体。
Application
N-乙酰基-L-天门冬氨酸可用作合成以下物质的反应物:
- 通过选择性还原和酸催化环化反应形成受保护的高丝氨酸γ-内酯。
- 通过环缩合形成外消旋氨基取代琥珀酰亚胺衍生物。
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)
Malgorzata Marjańska et al.
Movement disorders : official journal of the Movement Disorder Society, 28(2), 201-209 (2012-12-15)
Measurements of the concentrations of γ-aminobutyric acid (GABA) and glutamate in the motor cortices and lentiform nuclei of dystonic patients using single-voxel (1)H magnetic resonance spectroscopy (MRS) have yielded conflicting results so far. This study aimed to investigate dynamic changes
Studies on the metabolic pathway of the acetyl group for acetylcholine synthesis.
G E Gibson et al.
Biochemical pharmacology, 29(2), 167-174 (1980-02-01)
Paola Leone et al.
Science translational medicine, 4(165), 165ra163-165ra163 (2012-12-21)
Canavan disease is a hereditary leukodystrophy caused by mutations in the aspartoacylase gene (ASPA), leading to loss of enzyme activity and increased concentrations of the substrate N-acetyl-aspartate (NAA) in the brain. Accumulation of NAA results in spongiform degeneration of white
E A Kvittingen et al.
Clinica chimica acta; international journal of clinical chemistry, 158(3), 217-227 (1986-08-15)
Excessive excretion of N-acetylaspartic acid in urine is reported in a 6-yr-old child with extensive and progressive cerebral atrophy. The concentration in urine was 947-1,433 mumol/mmol creatinine (controls, n = 10, 5-21 mumol/mmol creatinine) and the daily excretion approximately 3-4
R. Bakhash et al.
Bios (Madison, N.J.), 49, 13-13 (1978)
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