Bulk Products
| CATALOG NO | PRODUCT NAME | CAS | PURITY | STRUCTURE |
|---|---|---|---|---|
| 51703 | Luminespib ( NVP-AUY922 ; VER-52296 ) | 747412-49-3 | 98% | _747412-49-3.png) |
| NVP-AUY922 is an experimental drug candidate for the treatment of cancer. It was disc | ||||
| 51902 | AT13148 | 1056901-62-2 | ≧98% |  |
| AT13148, a first-in-class multi-AGC kinase inhibitor, against gastric cancer cells. A | ||||
| 51702 | AZD1208 | 1204144-28-4 | 98% |  |
| AZD1208 is a potent, highly selective, and orally available Pim kinase inhibitor that | ||||
| 51603 | AZD6482 | 1173900-33-8 | ≧98.0% |  |
| AZD6482 is aPI3Kinhibitor withIC50of 10 nM, 8-, 87- and 109-fold more selective to PI | ||||
| 51802 | TIC10 ( ONC201 ) | 1616632-77-9 | 99.85% |  |
| ONC201 / TIC10是人类TRAIL基因的新型小分子诱导剂，可改善重组TRAIL的 | ||||
| 52003 | Zosuquidar trihydrochloride | 167465-36-3 | 99% |  |
| zosuquidar trihydrochloride is adifluorocyclopropyl quinoline. Zosuquidar trihydrochl | ||||
| 51614 | AMG-925 | 1401033-86-0 | 98% |  |
| AMG-925 is a potent and orally bioavailable dual inhibitor of CDK4 and FLT3, includin | ||||
| 102703 | AZD-8835 | 1620576-64-8 | ≧98.0% |  |
| AZD8835 is a potent and selective inhibitor ofPI3KαandPI3KδwithIC50s of 6.2 and 5.7 | ||||
| 111013 | MGCD-265-analog | 875337-44-3 | ≧98.0% |  |
| MGCD-265-analogis a tyrosine kinase inhibitor that selectively targets MET and Axl.MG | ||||
| 112101 | AV-412 | 451492-95-8 | 99.38% |  |
| AV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth fact | ||||
| 122805 | Balipodect ( TAK-063 ) | 1238697-26-1 | 98% | _1238697-26-1.png) |
| Balipodect (TAK 063 )is a novel PDE10A inhibitor. It has shown high inhibitory activi | ||||
| 122919 | Tenapanor | 1234423-95-0 | 98% |  |
| Tenapanoris an inhibitor of the sodium-proton exchanger NHE3. Thisantiporter protein | ||||