产品名称
氯化丁酰胆碱, ≥98%
InChI key
VCOBYGVZILHVOO-UHFFFAOYSA-M
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
SMILES string
O.[Cl-].CCCC(=O)OCC[N+](C)(C)C
assay
≥98%
form
powder
storage temp.
−20°C
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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
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
S Darvesh et al.
Journal of the autonomic nervous system, 71(2-3), 75-84 (1998-10-06)
Cholinergic neurotransmission plays a significant role in intrinsic cardiac ganglia with the action of acetylcholine being terminated by acetylcholinesterase (AChE, EC 3.1.1.7). Anatomical studies were performed to characterize neurons associated with AChE and a closely related enzyme, butyrylcholinesterase (BuChE, EC
[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)
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)
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