| Name | ZN-c3 |
|---|
| Description | ZN-c3 is an orally active, highly potent and selective Wee1 inhibitor (IC50=3.9 nM). ZN-c3 can be used for the research of cancer[1]. |
|---|---|
| Related Catalog | |
| Target |
IC50: 3.9 nM (Wee1)[1] |
| In Vitro | ZN-c3 IC50 is 103 nM in H23c cells[1]. |
| In Vivo | ZN-c3 (80 mg/kg; p.o.; 28 days) can effectively shrank tumors at 80 mg/kg as a single agent[1]. ZN-c3 shows excellent exposures and bioavailability in the dog PK study[1]. |
| References |
| Molecular Formula | C29H34N8O2 |
|---|---|
| Molecular Weight | 526.63 |
| Storage condition | -20°C |