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Vanoxerine dihydrochloride
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Vanoxerine dihydrochloride图片
CAS NO:67469-78-7
规格:98%
分子量:523.49
包装与价格:
包装价格(元)
10mg电议
25mg电议
50mg电议

产品介绍
potent and selective DRI (Dopamine reuptake inhibitor)
CAS:67469-78-7
分子式:C28H34Cl2F2N2O
分子量:523.49
纯度:98%
存储:Store at -20°C

Background:

Vanoxerine is an antagonist of dopamine transporter (DAT1) with Ki value of 16.9nM [1].


As an antagonist of DAT, vanoxerine is developed for treatment of Parkinson's disease and depression but has no effect on these diseases. Vanoxerine is also found to have desirable cardiac antiarrhythmic properties. It is a blocker of cardiac hERG (hKv11.1) with IC50 value of 0.84nM. It also blocks the ICa,L and hNav1.5 channel with IC50 values of 320nM and 830nM, respectively. Vanoxerine does not significantly prolong Purkinje fiber APD60 and APD90 and has no significant effect on QT or TDR. Further, the clinical trial demonstrates that the effective concentrations of vanoxerine are well tolerated and safe in man [2].


参考文献:
[1] Giros B, el Mestikawy S, Godinot N, Zheng K, Han H, Yang-Feng T, Caron MG. Cloning, pharmacological characterization, and chromosome assignment of the human dopamine transporter. Mol Pharmacol. 1992 Sep;42(3):383-90.
[2] Lacerda AE, Kuryshev YA, Yan GX, Waldo AL, Brown AM. Vanoxerine: cellular mechanism of a new antiarrhythmic. J Cardiovasc Electrophysiol. 2010 Mar;21(3):301-10.