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About This Item
Empirical Formula (Hill Notation):
C10H16ClNO
CAS Number:
Molecular Weight:
201.69
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
204-138-4
MDL number:
SMILES string
[Cl-].CC[N+](C)(C)c1cccc(O)c1
InChI
1S/C10H15NO.ClH/c1-4-11(2,3)9-6-5-7-10(12)8-9;/h5-8H,4H2,1-3H3;1H
InChI key
BXKDSDJJOVIHMX-UHFFFAOYSA-N
Gene Information
human ... ACHE(43)
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Biochem/physiol Actions
Acetycholinesterase inhibitor
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Manuel Martin-Flores et al.
Journal of the American Animal Hospital Association, 47(4), 294-298 (2011-06-16)
A case of prolonged muscle relaxation after vecuronium in an anesthetized dog is presented. After using peripheral nerve stimulation to confirm partial recovery of neuromuscular transmission, administration of 0.5 mg/kg IV of intravenous edrophonium failed to complete the reversal process.
Ulrike Schara et al.
Neuropediatrics, 43(4), 184-193 (2012-08-23)
Congenital myasthenic syndromes (CMS) are rare genetically and clinically heterogeneous disorders characterized by an impaired neuromuscular transmission. Exact prevalence data are not available, approximately 2000 to 3000 patients worldwide have been diagnosed on a molecular level; mutations in 14 different
Leonardo Pisani et al.
ChemMedChem, 5(9), 1616-1630 (2010-08-03)
A large series of substituted coumarins linked through an appropriate spacer to 3-hydroxy-N,N-dimethylanilino or 3-hydroxy-N,N,N-trialkylbenzaminium moieties were synthesized and evaluated as acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitors. The highest AChE inhibitory potency in the 3-hydroxy-N,N-dimethylanilino series was observed with a
Hariprasad Korsapati et al.
Gastroenterology, 135(3), 796-802 (2008-08-05)
Patients with high-amplitude esophageal contractions (nutcracker esophagus [NCE]) show asynchrony of circular muscle (CM) and longitudinal muscle (LM) contraction during peristalsis. The goal of our study was to determine if this asynchrony is related to an increase in the cholinergic
Mathilde M Triquigneaux et al.
The Biochemical journal, 448(1), 83-91 (2012-08-15)
The principal role of AChE (acetylcholinesterase) is termination of impulse transmission at cholinergic synapses by rapid hydrolysis of the neurotransmitter acetylcholine. The active site of AChE is near the bottom of a long and narrow gorge lined with aromatic residues.
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