Merck
CN

B2753

Sigma-Aldrich

氯化丁酰胆碱

≥98%

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线性分子式:
C9H20NO2Cl
CAS号:
分子量:
209.71
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

≥98%

形式

powder

储存温度

−20°C

SMILES string

O.[Cl-].CCCC(=O)OCC[N+](C)(C)C

InChI

1S/C9H20NO2.ClH/c1-5-6-9(11)12-8-7-10(2,3)4;/h5-8H2,1-4H3;1H/q+1;/p-1

InChI key

VCOBYGVZILHVOO-UHFFFAOYSA-M

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Samreen Begum et al.
Computational biology and chemistry, 74, 212-217 (2018-04-14)
Amide derivatives of N-phthaloylglycine were synthesized under Schotten Baumann reaction condition. The structures of synthesized compounds (4a-d) were characterized by using FTIR, 1HNMR and EI-MS. The compounds were evaluated for their in-vitro Butyrylcholinesterase inhibition and all of them exhibited good
The substrate specificity of the cholinesterase activity of the brain of the sea Pacific herring (Cluippea pallasi Val) from different populations.
N N Kovalev et al.
Doklady. Biochemistry and biophysics, 392, 256-259 (2004-07-17)
Sultan Darvesh et al.
Experimental neurology, 188(2), 461-470 (2004-07-13)
Cholinesterase inhibitors used to treat the symptoms of Alzheimer's disease (AD) inhibit both acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE), albeit to different degrees. Because central and peripheral neurons, including intrinsic cardiac neurons located on the surface of the mammalian heart, express
[Treatment of Alzheimer's disease: status quo and future considerations].
Shun Shimohama
Nihon yakurigaku zasshi. Folia pharmacologica Japonica, 131(5), 351-356 (2008-05-16)
G Petroianu et al.
Journal of toxicology. Clinical toxicology, 39(1), 27-31 (2001-05-01)
Intoxications with organophosphorous compounds, especially paraoxon, are frequent. Organophosphorous compounds inhibit serine hydrolases such as acetylcholine, butyrilcholine, and carboxyl esterases although acetylcholine and butyrylcholine are too sensitive to paraoxon to be useful markers of severity. They cannot show a dose-dependent

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