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ChemicalBook--->CAS DataBase List--->151937-76-7

151937-76-7

151937-76-7 Structure

151937-76-7 Structure
IdentificationBack Directory
[Name]

Penehyclidine HCl (Mixture of IsoMers)
[CAS]

151937-76-7
[Synonyms]

Penehyclidine HCl
Penehyclidine HCl (Mixture of IsoMers)
2-(1-azabicyclo[2.2.2]octan-3-yloxy)-1-cyclopentyl-1-phenylethanol,hydrochloride
2-(1-azabicyclo[2.2.2]oct-3-yloxy)-1-cyclopentyl-1-phenylethanol hydrochloride (1:1)
[Molecular Formula]

C20H30ClNO2
[MDL Number]

MFCD32709946
[MOL File]

151937-76-7.mol
[Molecular Weight]

351.92
Chemical PropertiesBack Directory
[storage temp. ]

-20°C, away from moisture
[form ]

Liquid
[color ]

Colorless to light yellow
[Water Solubility ]

H2O: 2mg/mL, clear
Hazard InformationBack Directory
[Uses]

Penehyclidine (Penequinine) hydrochloride, a anticholinergic agent, is a selective antagonist of M1 and M3 receptors. Penehyclidine hydrochloride activates NF-kβ in lung tissue and inhibits the release of inflammatory factors. Penehyclidine hydrochloride can alleviate the pulmonary inflammatory response in rats with chronic obstructive pulmonary disease (COPD) undergoing mechanical ventilation[1].
[Biological Activity]

Penehyclidine hydrochloride is a brain penetrant anticholinergic drug th at exhibits both antimuscarinic and antinicotinic activity. Penehyclidine hydrochloride does not induce muscarinic 2 receptor-associated cardiovascular side effects. Penehyclidine hydrochloride is effective in experimental models of heartlung and brain ischemia reperfusion injury.
[in vivo]

Penehyclidine (0.3-3 mg/kg, ip, single dose) exhibits protective activity in rats ALI models[2].
Penehyclidine (1 mg/kg, ip, single dose) enhances the expression of BDNF and phosphorylation of ERK1/2 in the hippocampus, exhibits antidepressant-like effects in mouse CUMS model[4].

Animal Model:rats ALI models[2]
Dosage:0.3-3 mg/kg
Administration:ip, single dose
Result:Alleviated LPS-induced lung injury in rats.
Animal Model:Mouse chronic unpredictable mild stress (CUMS) model[4]
Dosage:1 mg/kg
Administration:ip, single dose
Result:Reduced the immobility time in the forced swimming test (FST) and tail suspension test (TST).
[IC 50]

mAChR1; mAChR3; NF-κB
[storage]

-20°C, away from moisture
[References]

[1] Zhi-Yuan Chen, et al. The Mechanism of Penehyclidine Hydrochloride and Its Effect on the Inflammatory Response of Lung Tissue in Rats with Chronic Obstructive Pulmonary Disease During Mechanical Ventilation. Int J Chron Obstruct Pulmon Dis. 2021 Mar 31;16:877-885. DOI:10.2147/COPD.S295329
[2] Wang X, et al., Penehyclidine hydrochloride alleviates lipopolysaccharide?induced acute respiratory distress syndrome in cells via regulating autophagy?related pathway. Mol Med Rep. 2021 Feb;23(2):100. DOI:10.3892/mmr.2020.11739
[3] Zi C, et al., Penehyclidine hydrochloride protects against anoxia/reoxygenation injury in cardiomyocytes through ATP-sensitive potassium channels, and the Akt/GSK-3β and Akt/mTOR signaling pathways. Cell Biol Int. 2020 Jun;44(6):1353-1362. DOI:10.1002/cbin.11329
[4] Sun X, et al., A Selective M1 and M3 Receptor Antagonist, Penehyclidine Hydrochloride, Exerts Antidepressant-Like Effect in Mice. Neurochem Res. 2019 Dec;44(12):2723-2732. DOI:10.1007/s11064-019-02891-5
Spectrum DetailBack Directory
[Spectrum Detail]

Penehyclidine HCl (Mixture of IsoMers)(151937-76-7)1HNMR
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