PI3K
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 20633 | STX-478 | 2883540-92-7 | ≧98.0% |  |
| STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。 | ||||
| 711401 | Eganelisib ( IPI-549 ) | 1693758-51-8 | ≧98.0% | _1693758-51-8.png) |
| Eganelisib (IPI-549) 是一种首创、口服、高选择性 PI3Kγ 抑制剂，单独 | ||||
| 51603 | AZD6482 | 1173900-33-8 | ≧98.0% |  |
| AZD6482 is aPI3Kinhibitor withIC50of 10 nM, 8-, 87- and 109-fold more selective to PI | ||||
| 52026 | AMG-319 | 1608125-21-8 | 98% |  |
| AMG 319 is an investigational, highly selective, small molecule inhibitor of PI3K tha | ||||
| 611902 | PF-04979064 | 1220699-06-8 | ≧98.0% |  |
| PF-04979064 is a potent and selective PI3K/mTOR dual kinase inhibitor with an IC(50) | ||||
| 20618 | Pirtobrutinib | 2101700-15-4 | 98% Min. |  |