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159997-94-1

中文名称 159997-94-1
英文名称 Biricodar
CAS 159997-94-1
分子式 C34H41N3O7
分子量 603.71
MOL 文件 159997-94-1.mol
更新日期 2025/09/25 11:02:49
159997-94-1 结构式 159997-94-1 结构式

基本信息

中文别名
比立考达
英文别名
Biricodar
VX-710(biricodar)
2-Piperidinecarboxylic acid, 1-[2-oxo-2-(3,4,5-trimethoxyphenyl)acetyl]-, 4-(3-pyridinyl)-1-[3-(3-pyridinyl)propyl]butyl ester, (2S)-

物理化学性质

沸点752.1±70.0 °C(Predicted)
密度1.195±0.06 g/cm3(Predicted)
储存条件-20°C储存
溶解度溶于二甲基亚砜
酸度系数(pKa)5.80±0.10(Predicted)
形态Oil
颜色Colorless to light yellow

常见问题列表

生物活性
Biricodar (VX-710) 是 P-glycoprotein 和 MRP-1 的调节剂; 在多药耐药细胞中显示出有效的化学敏化活性。
体外研究

Biricodar shows activity against both P-glycoprotein (Pgp) and MRP-1 and also has activity in increasing drug uptake and retention and reversing drug resistance mediated by wild-type BCRP (BCRPR 482 ). In 8226/Dox6 cells (Pgp), biricodar increases mitoxantrone and daunorubicin uptake by 55 and 100%, respectively, increases their retention by 100 and 60%, respectively, and increases their cytotoxicity 3.1- and 6.9-fold, respectively. Biricodar also increases the uptake, retention and cytotoxicity in HL60/Adr (MRP-1) and 8226/MR20 cells (BCRP(R482)), but has little effect in MCF7 AdVP3000 cells (BCRP(R482T)). VX-710 is a non-macrocyclic pipecolinate derivative which binds the FK506 receptor protein. VX-710 has been shown to restore sensitivity in a range of multidrug-resistant cells, including myeloma, melanoma, carcinoma and leukaemia. Biricodar effectively inhibits photoaffinity labeling of P-glycoprotein by [ 3 H]azidopine or [ 125 I]iodoaryl azido-prazosin with EC 50 values of 0.75 and 0.55 μM.

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