B2753
Butyrylcholine chloride
≥98%
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About This Item
Fórmula lineal:
C9H20NO2Cl
Número de CAS:
Peso molecular:
209.71
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
Quality Level
assay
≥98%
form
powder
storage temp.
−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
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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
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].
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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
The substrate specificity of the cholinesterase activity of the brain of the sea Pacific herring (Cluippea pallasi Val) from different populations.
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