Chemical Name: 5-[[4-[(2,3-Dimethyl-2H-indazol-6-yl)methylamino]-2-pyrimidinyl]amino]-2-methylbenzenesulfonamide. Alternate Names: GSK-VEG10003, GW786034B
Multi-receptor tyrosine kinase inhibitor
Molekulargewicht:
437.52
Reinheit:
>98% by HPLC NMR (Conforms)
Formulierung:
White to off-white solid
CAS Nummer:
[444731-52-6]
Formel:
C21H23N7O2S
Anwendungsbeschreibung:
Inhibits multiple receptor tyrosine kinases including VEGFR1,2 and 3 (IC50s=10, 30, 47 nM respectively) and PDGFRalpha, beta and c-Kit (IC50s=71, 84, 74 nM respectively) and others such as FGFR.1 The drug targets both the tumor and endothelial cells in a mouse xenograft model of human multiple myeloma.2 It reduces joint pain and inhibits cartilage degeneration in rodent osteoarthritis models.3 VEGF inhibitors such as pazopanib have potential for treatment of neovascular age-related macular degeneration.4 In clinical use for renal cell carcinoma.5
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