2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
生物活性
Description
In Vivo
In Vitro
化合物的使用
Kinase Assay
Cell Assay
Animal Administration
参考文献
Description of Zosuquidar: Zosuquidar is a potent P-glycoprotein inhibitor, which binds with high affinity to P-glycoprotein and inhibits P-glycoprotein-mediated multidrug resistance (MDR). P-glycoprotein, encoded by the MDR-1 gene, is a member of the ATP-binding cassette superfamily of transmembrane transporters and prevents the intracellular accumulation of many natural product-derived cytotoxic agents. Check For active clinical trials or closed clinical trials using this agent. (NCI Thesaurus).
For the detailed information about the solubility of LY335979 (Zosuquidar 3HCl) in water, the solubility of LY335979 (Zosuquidar 3HCl) in DMSO, the solubility of LY335979 (Zosuquidar 3HCl) in PBS buffer, the animal experiment（test） of LY335979 (Zosuquidar 3HCl),the in vivo,in vitro and clinical trial test of LY335979 (Zosuquidar 3HCl),the cell experiment（test） of LY335979 (Zosuquidar 3HCl),the IC50, EC50 and Affinity of LY335979 (Zosuquidar 3HCl), please contact DC Chemicals.
