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Penehyclidine hydrochloride

Cat. No. M28563
Penehyclidine hydrochloride Structure
Synonym:

Penequinine hydrochloride

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Quality Control & Documentation
Biological Activity

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.

Chemical Information
Molecular Weight 351.91
Formula C20H30ClNO2
CAS Number 151937-76-7
Form Liquid
Storage -20°C, dry, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Qiang Yang, et al. Bioimpacts. Penehyclidine hydrochloride ameliorates renal ischemia reperfusion-stimulated lung injury in mice by activating Nrf2 signaling

[2] Shao-Hua Zheng, et al. Mol Pain. Penehyclidine hydrochloride suppressed peripheral nerve injury-induced neuropathic pain by inhibiting microglial MAPK/p-p38/IL-1 β pathway activation

[3] Yaguang Wang, et al. Drug Des Devel Ther. Pleiotropic effects and pharmacological properties of penehyclidine hydrochloride

[4] Fei Zheng, et al. Inflammation. Penehyclidine Hydrochloride Decreases Pulmonary Microvascular Endothelial Inflammatory Injury Through a Beta-Arrestin-1-Dependent Mechanism

[5] Hong-Tao Xiao, et al. Drug Des Devel Ther. Penehyclidine hydrochloride: a potential drug for treating COPD by attenuating Toll-like receptors

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