CAS NO: | 212141-54-3 |
规格: | ≥98% |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
250mg | 电议 |
500mg | 电议 |
1g | 电议 |
Vatalanib ((PTK787 or ZK 222584, cpg-79787) is a novel, potent and orally bioavailable inhibitor of VEGFR2/KDR with IC50 of 37 nM in a cell-free assay, it is less potent against VEGFR1/Flt-1, and is 18-fold against VEGFR3/Flt-4. It is an anilinophthalazine analog with potential antineoplastic activity. Vatalanib binds to and inhibits the protein kinase domain of VEGFR 1 and 2. This agent also binds to and inhibits related receptor tyrosine kinases, including PDGF receptor, c-Kit, and c-Fms.
纯度:≥98%
CAS:212141-54-3