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|  | Motesanib DiphosphateDescription of:Motesanib DiphosphateMotesanib Diphosphate potently inhibited VEGF-induced but not bFGF-induced proliferation of HUVECs with IC...
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|  | RAF265(CHIR-265)Description of:RAF265(CHIR-265)RAF is a key component of the RAS/RAF/MEK/ERK signal-transduction pathway, which controls cell proliferation, d...
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|  | Sunitinib Malate(SU 11248)Description of:Sunitinib Malate(SU 11248)Sunitinib dose-dependently inhibited stem cell factor (SCF)-induced phosphotyrosine levels on KIT (IC...
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|  | PD173074Description of:PD173074PD173074 is a potent ATP-competitive, reversible FGFR and VEGFR inhibitor with IC50 of 5, 21.5 and ~100 nM for FGFR3, F...
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|  | Regorafenib(瑞格非尼)Description of:Regorafenib(瑞格非尼)BAY 73-4506 is an orally bioavailable multikinase inhibitor targeting both the tumor and its vasculature.
 
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|  | Brivanib(BMS-540215)Description of:Brivanib(BMS-540215)Brivanib (BMS-540215) is a VEGFR -2 inhibitor with an IC50 of 25 nM and Ki of 26 nM.
 Theoret...
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|  | SU-5402Description of:SU-5402SU 5402 inhibits tyrosine phosphorylation of VEGFR2 and PDGFR in NIH 3T3 cells with IC50 values of 0.4 and 60.9 μM, r...
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|  | SU-6668(TSU-68)Description of:SU-6668(TSU-68)TSU-68 (SU6668)is a novel multiple receptor tyrosine kinase inhibitor with IC50 of 2.1 µM, 8 nM and 1.2 &m...
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|  | AV-951(Tivozanib)Description of:AV-951(Tivozanib)AV-951 (Tivozanib) is a novel quinoline-urea derivative and now developed by AVEO. AV-951 also inhibits phosph...
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|  | Lenvatinib(E7080)Description of:Lenvatinib(E7080)Lenvatinib(E7080) has been evaluated in vitro (pre-clinical) for anti-cancer effects. E7080 suppresses lymph n...
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