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Description: TG 100572 HCl, the hydrochloride salt of TG 100572, is a novel, potent and selective multi-targeted kinase inhibitor which inhibits receptor tyrosine kinases and Src kinases with IC50s of 2, 7, 2, 16, 13, 5, 0.5, 6, 0.1, 0.4, 1, 0.2 nM for VEGFR1, VEGFR2, FGFR1, FGFR2, PDGFRbeta, Fgr, Fyn, Hck, Lck, Lyn, Src, Yes, respectively. By inhibiting Src kinases and selected receptor tyrosine kinases, TG100572 induced apoptosis of proliferating endothelial cells in vitro. TG100572 inhibits downstream molecules involved in the vascular endothelial growth factor (VEGF) signaling pathway resulted in markedly diminished levels of HSV-induced angiogenesis and significantly reduced the severity of SK lesions..
References: J Med Chem. 2008 Mar 27; 51(6):1546-59.; J Cell Physiol. 2008 Jul; 216(1):29-37.
Related CAS #: 867331-64-4 (HCl); 867334-05-2 (free base)
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