CINPA1 is a CAR inhibitor capable of reducing CAR-mediated transcription with an IC50 of ∼70 nM.
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描述 | CINPA1 is a selective CAR (Constitutive androstane receptor) with IC50 value of ~70nM for inhibition of CAR-mediated gene expression in primary human hepatocytes. It showed no activity on PXR and did not alter the protein levels or subcellular localization of CAR. CINPA1 attenuated CAR-mediated gene expression, including CYP2B6 and CYP3A4 at concentration of 1μM or 5μM at different cells expressing CAR post 24h or 48h. |
作用机制 | CINPA1 could reside in the ligand-binding pocket to stabilize the CAR-LBD (ligand-binding domain) in a more rigid, less fluid state and disrupt CAR binding to the DNA response elements at promoter regions of target gene.[1][2] |
Dose | Mice: 1 mg/kg - 50 mg/kg[3] (i.p.) |
Administration | i.p. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.53mL 0.51mL 0.25mL |
12.64mL 2.53mL 1.26mL |
25.28mL 5.06mL 2.53mL |
CAS号 | 102636-74-8 |
分子式 | C23H29N3O3 |
分子量 | 395.495 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,2-8°C |
溶解度 |
DMSO: 250 mg/mL(632.12 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |