| 常用名 | JAK3抑制剂VII,AD412 | CAS号 | 796041-65-1 |
|---|---|---|---|
| 价格 | ¥1354.0/25mg ¥需询单/1g ¥需询单/1g ¥需询单/1g | 纯度 | 98.0% |
| 备货期 | 1天 | 库存 | 现货 |
| 产品网页 | http://www.aladdin-e.com/zh_cn/J339443.html | ||
| 产品详情(用途,包装等)
用途: JAK3抑制剂VII,AD412是一种细胞可渗透的吲哚-3-丙酰胺免疫抑制剂,与JAK2的活性(分别为29%和0)相比,选择性抑制JAK3激酶活性(分别在90和30μM时分别抑制81%和36%)。分别在90和30μM时产生%),并降低IL-2刺激的CTL-L2细胞中Akt,STAT5a / b和Erk1 / 2的JAK1和JAK3依赖性磷酸化,但不降低INF中JAK1 / 2依赖性STAT1磷酸化-γ刺激的U266培养物。据报道,JAK3抑制剂VII,AD412在体外抑制ConA刺激的鼠脾细胞和PHA刺激 JAK3 Inhibitor VII, AD412 is a cell-permeable indole-3-propanamide immunosuppressant that is shown to selectively inhibit JAK3 kinase activity (by 81% and 36% at 90 and 30 μM, respectively) over that of JAK2 (by 29% and 0% at 90 and 30 μM, respectively) and reduce JAK1 and JAK3-dependent phosphorylations of Akt, STAT5a/b, and Erk1/2 in IL-2-stimulated CTL-L2 cells, but not JAK1/2-dependent STAT1 phosphorylation in INF-γ-stimulated U266 cultures. JAK3 Inhibitor VII, AD412 is reported to inhibit ConA-stimulated murine splenocytes and PHA-stimulated human PBL proliferation (IC|50|= 17 and 25 μM, respectively)|in vitro|. 物理化学性质: CAS号:796041-65-1 常用中文名:JAK3抑制剂VII,AD412 常用英文名:JAK3 Inhibitor VII, AD412 分子式:C23H20ClN3O 分子量:389.88 密度:1.2±0.1 g/cm3 沸点:669.0±55.0 °C at 760 mmHg 熔点:N/A 闪点:358.4±31.5 °C 储存条件:2-8°C储存 |