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Merck
CN

C7041

McN-A-343

≥98% (TLC)

别名:

(4-羟基-2-丁炔基)-1-三甲基铵-3-氯苯基­氨基甲酸酯氯化物, 4-[N-(3-氯苯基)氨基甲酰氧]-2-丁炔基­三甲基氯化铵

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关于此项目

经验公式(希尔记法):
C14H18Cl2N2O2
化学文摘社编号:
分子量:
317.21
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352106
MDL number:
Assay:
≥98% (TLC)
Form:
powder
Quality level:
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Quality Level

assay

≥98% (TLC)

form

powder

color

off-white

solubility

H2O: soluble, ethanol: soluble

SMILES string

[Cl-].C[N+](C)(C)CC#CCOC(=O)Nc1cccc(Cl)c1

InChI

1S/C14H17ClN2O2.ClH/c1-17(2,3)9-4-5-10-19-14(18)16-13-8-6-7-12(15)11-13;/h6-8,11H,9-10H2,1-3H3;1H

InChI key

CXFZFEJJLNLOTA-UHFFFAOYSA-N

Biochem/physiol Actions

M1 毒蕈碱型乙酰胆碱受体激动剂。

Preparation Note

Solutions may be stored for several days at 4 °C.


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)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Laura Oliveira et al.
Neuro-Signals, 14(5), 262-272 (2005-11-23)
At the rat motor endplate, pre-synaptic facilitatory adenosine A2A and muscarinic M1 receptors are mutually exclusive. We investigated whether these receptors share a common intracellular signalling pathway. Suppression of McN-A-343-induced M1 facilitation of [3H]ACh release was partially recovered when CGS21680C
Hinako Suga et al.
Molecular pharmacology, 78(4), 745-755 (2010-07-21)
Investigating how a test drug alters the reaction of a site-directed electrophile with a receptor is a powerful method for determining whether the drug acts competitively or allosterically, provided that the binding site of the electrophile is known. In this
Frederick J Mitchelson
Pharmacology & therapeutics, 135(2), 216-245 (2012-05-31)
The unusual pharmacology of McN-A-343 was first described by Roszowski in 1961. The agonist appeared to be a selective stimulant of muscarinic receptors in sympathetic ganglia, now known to be the muscarinic M₁ receptor subtype. However, subsequent research demonstrated that



全球贸易项目编号

货号GTIN
C7041-25MG04061833511862
C7041-100MG04061833511855