CS-2072
| 中文名称 | CS-2072 |
|---|---|
| 中文同义词 | 化合物 T15377;化合物 RAVOXERTINIB HYDROCHLORIDE;RAVOXERTINIB HYDROCHLORIDE |CAS 2070009-58-2 |
| 英文名称 | GDC-0994 (hydrochloride) |
| 英文同义词 | GDC-0994 (hydrochloride);GDC-0994 HCl;CS-2072;Ravoxertinib hydrochloride;RAVOXERTINIB HYDROCHLORIDE (GDC-0994 HYDROCHLORIDE);Ravoxertinib hydrochloride (GDC-0994 |
| CAS号 | 2070009-58-2 |
| 分子式 | C21H19Cl2FN6O2 |
| 分子量 | 477.32 |
| EINECS号 | |
| 相关类别 | |
| Mol文件 | 2070009-58-2.mol |
| 结构式 | ![]() |
CS-2072 性质
| 储存条件 | Store at -20°C |
|---|---|
| 溶解度 | 二甲基亚砜:100 mg/mL(209.50 mM) |
| 形态 | 固体 |
| 颜色 | 浅黄至黄色 |
|
ERK2 3.1 nM (IC 50 ) |
ERK1 6.1 nM (IC 50 ) |
p-RSK 12 nM (IC 50 ) |
Ravoxertinib also inhibits p90RSK with IC
50
of 12 nM.
Ravoxertinib is highly selective for ERK1 and ERK2, with biochemical potency of 1.1 nM and 0.3 nM, respectively.
Ravoxertinib (GDC0994; 50 nM, 0.5 µM, and 5 µM; 48 hours) decreases the viability of lung adenocarcinoma cell lines (A549, HCC827, HCC4006).
In CD-1 mice, a 10 mg/kg oral dose of Ravoxertinib is sufficient to achieve the desired target coverage for at least 8 h. Daily, oral dosing of Ravoxertinib results in significant single-agent activity in multiple in vivo cancer models, including KRAS-mutant and BRAF-mutant human xenograft tumors in mice.
安全信息
| 海关编码 | 2924297099 |
|---|
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2026/06/05 | HY-15947A | CS-2072 Ravoxertinib hydrochloride | 2070009-58-2 | 2mg | 1000元 |
| 2026/06/05 | HY-15947A | CS-2072 Ravoxertinib hydrochloride | 2070009-58-2 | 5mg | 1500元 |
