唑喹达三盐酸盐
唑喹达三盐酸盐 性质
| 熔点 | 172-176°C |
|---|---|
| 储存条件 | Inert atmosphere,Room Temperature |
| 溶解度 | 可溶于甲醇(轻微)、水(轻微、超声处理) |
| 形态 | 固体 |
| 颜色 | 淡黄色至浅黄色 |
| InChIKey | VQJFFWJUYDGTQZ-NMTXSAMUNA-N |
| SMILES | FC1([C@H]2C3C=CC=CC=3[C@H](N3CCN(C[C@@H](O)COC4C=CC=C5N=CC=CC=45)CC3)C3C=CC=CC=3[C@@H]12)F.Cl |&1:2,9,15,37,r| |
唑喹达三盐酸盐 用途与合成方法
| Target | Value |
|
P-gp
(Cell-free assay) | 60 nM(Ki) |
LY335979 竞争性抑制[LY335979作用于表达P-gp的白血病细胞系,包括K562/HHT40, K562/HHT90, K562/DOX 和 HL60/DNR,显著恢复药物敏感性,且作用于携带活性P-gp的原发性AML细胞,增强蒽环类药物(Daunorubicin, Idarubicin, Mitoxantrone)和gemtuzumab ozogamicin 的毒性。 最新文献说明LY335979作用于ABCB1转导的细胞,完全抑制(Z)-endoxifen在顶端调控的运输。
Zosuquidar trihydrochloride is only moderately active as an inhibitor of P-gp at the blood-brain. An oral dose of 25 mg/kg of zosuquidar trihydrochloride increases the brain concentrations by about 2.5-fold at 1 h and 5-fold at 24 h after paclitaxel administrationbarrier. Zosuquidar enhances the brain uptake of nelfinavir in a dose-dependent manner. Brain tissue/plasma nelfinavir concentration ratios increase from 0.06±0.03 in the absence of zosuquidar administration and 0.09±0.02 between 2 and 6 h after a 2 mg/kg intravenous dose of zosuquidar to 0.85±0.19 after 6h and 1.58±0.67 after 20 mg/kg zosuquidar.
唑喹达三盐酸盐 价格(试剂级)
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2026-07-06 | S1481 | 唑喹达三盐酸盐 | 167465-36-3 | 5mg | 1398.44 |
| 2026-07-06 | S1481 | 唑喹达三盐酸盐 | 167465-36-3 | 10mM(1mL in DMSO) | 1970 |