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Tariquidar
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。
Tariquidar图片
CAS NO:206873-63-4
规格:98%
分子量:646.73
包装与价格:
包装价格(元)
10mg电议
50mg电议

产品介绍
P-glycoprotein inhibitor,potent and non-competitive
CAS:206873-63-4
分子式:C38H38N4O6
分子量:646.73
纯度:98%
存储:Store at -20°C

Background:

Tariquidar is a potent inhibitor of P-glycoprotein (Pgp), a 170-kDa transmembrane protein acting as a drug efflux pump to actively transport structurally unrelated compounds out of cells, that noncompetitively inhibits the basal the activity of ATPase associated with Pgp. Tariquidar contains a tertiary amine, dimethoxyphenyl group and amide group in its chemical structure, which contribute to its inhibition against Pgp. Results of in vitro assays of three different models have shown that Tariquidar inhibits Pgp with 50% inhibition concentration IC50values ranging from 15 to 223 nM. However, the inhibition by tariquidar is Pgp-specific and attenuated in tumor cell lines, where multidrug resistance is mediated by multidrug resistance-associated protein.


Reference


[1].Fox E, Bates SE. Tariquidar (XR9576): a P-glycoprotein drug efflux pump inhibitor. Expert Rev Anticancer Ther. 2007 Apr;7(4):447-59.
[2].Bankstahl JP, Bankstahl M, R?mermann K, Wanek T, Stanek J, Windhorst AD, Fedrowitz M, Erker T, Müller M, L?scher W, Langer O, Kuntner C. Tariquidar and elacridar are dose-dependently transported by P-glycoprotein and Bcrp at the blood-brain barrier: a small-animal positron emission tomography and in vitro study. Drug Metab Dispos. 2013 Apr;41(4):754-62. doi: 10.1124/dmd.112.049148. Epub 2013 Jan 10.