基本信息
文件名称:Diphenidol-d10-hydrochloride-Difenidol-hydrochloride-d-sub-10-sub-生命科学试剂-MCE.pdf
文件大小:661.48 KB
总页数:2 页
更新时间:2025-05-24
总字数:约3.76千字
文档摘要

Hotline:400-820-3792

Inhibitors?ScreeningLibraries?Proteins

www.MedChemE

Diphenidol-d10hydrochloride

Cat.No.:HY-A0082S

Synonyms:Difenidolhydrochloride-d10

分?式:C??H??D??ClNO

分?量:355.97

作?靶点:Isotope-LabeledCompounds;SodiumChannel;mAChR

作?通路:Others;MembraneTransporter/IonChannel;GPCR/GProtein;

NeuronalSignaling

储存?式:Pleasestoretheproductundertherecommendedconditionsin

theCertificateofAnalysis.

BIOLOGICALACTIVITY

?物活性Diphenidol-d10(hydrochloride)(Difenidolhydrochloride-d10)是氘代标记的Diphenidol(hydrochloride).

Diphenidolhydrochloride(Difenidolhydrochloride)是?种?选择性的毒蕈碱M1-M4受体(muscarinicM1-

M4receptor)拮抗剂,具有抗?律失常活性。Diphenidolhydrochloride也是神经细胞电压门控离?通道(

Na+,K+,Ca2+)的有效?特异性阻滞剂。Diphenidolhydrochloride可?于抗眩晕、?吐的研究。

体外研究Stableheavyisotopesofhydrogen,carbon,andotherelementshavebeenincorporatedintodrugmolecules,

largelyastracersforquantitationduringthedrugdevelopmentprocess.Deuterationhasgainedattention

becauseofitspotentialtoaffectthepharmacoki