Chir-258
WebJun 20, 2006 · Methods: CHIR-258 was administered once daily in a dose-escalating phase 1 study to patients with relapsed/refractory MM. Drug tolerability and safety, pharmacokinetics (PK) and pharmacodynamics ... WebJun 23, 2011 · This is a prospective, multi-center, open-label, single-arm, non-randomized, Phase II study to evaluate the efficacy and safety of TKI258 as second-line therapy in patients with either FGFR2 mutated or wild-type advanced and/or metastatic endometrial cancer. Study Design Go to Arms and Interventions Go to Outcome Measures Primary …
Chir-258
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WebJan 14, 2024 · Dovitinib is a multi-targeted tyrosine kinase inhibitor with IC50s of 1, 2, 8/9, 10/13/8, 27/210 nM for FLT3, c-Kit, FGFR1/3, VEGFR1/2/3 and PDGFRα/β, respectively. Dovitinib potently inhibits the FGF-stimulated growth of WT and F384L-FGFR3-expressing B9 cells with IC50 values of 25 nM. WebNov 16, 2004 · Dovitinib (TKI258; formerly CHIR-258) is an orally bioavailable inhibitor of a number of RTKs [5]. It targets several members of the class III, IV and V RTK family, including vascular endothelial ...
WebJul 20, 2005 · CHIR-258 has ≤10 nmol/L activity against VEGF1/2/3 kinases, and our data clearly showed that CHIR-258 can inhibit autocrine VEGF levels in MV4;11 in vitro …
WebJun 1, 2005 · Background: CHIR-258 is an orally active small molecule that exhibits potent inhibitory activity against multiple RTKs involved in tumor growth and angiogenesis (IC … WebIn addition, CHIR-258 potently inhibited class IV (FGFR1 and 3) and class V (VEGFR1-4) RTKs with IC50 values of 0.008 to 0.013 mM. For insulin receptor, EGFR, c-Met, EphrinA2, Tie2, IGFR1, and HER2 significant inhibition was observed only at more than 10-fold higher concentrations. These studies demonstrated that CHIR-258 is a selective but ...
Dovitinib(TKI-258) is a highly potent, novel multitargeted growth factor receptor kinase inhibitor with IC50 of 1, 2, 5, 10, 8, 27, 36 nM for FLT3, c-KIT, FGFR, VEGFR1/2/3, PDGFRß and CSF-1R, respectively. Find all the information about Dovitinib(TKI-258) for cell signaling research.
WebMay 15, 2005 · CHIR-258 exhibits properties that make it a promising candidate for clinical develop … These studies provide evidence that biological activity of CHIR-258 in tumors correlates with efficacy and aids in the identification of potential biomarkers of this multitargeted receptor tyrosine kinase inhibitor. daily mercury personal classifiedsWebJun 20, 2006 · 17502. Background: CHIR-258 is an orally active small molecule receptor tyrosine kinase (RTK) inhibitor which has potent activity against multiple RTKs involved in tumor growth and angiogenesis (IC50 ≤13 nM for FGFR, VEGFR, PDGFR, C-KIT, and FLT3). Approximately 15% of newly diagnosed MM patients harbor a t(4;14) … biological procedures online版面费WebDovitinib (CHIR-258) is a multi-targeted tyrosine kinase inhibitor with IC50 s of 1, 2, 8/9, 10/13/8, 27/210 nM for FLT3, c-Kit, FGFR1/FGFR3, VEGFR1/VEGFR2/VEGFR3 and PDGFRα/PDGFRβ, respectively. For research use only. We do not sell to patients. Dovitinib-d8 Chemical Structure CAS No. : 1246819-84-0 * Please select Quantity before … daily mercury editorWebCHIR-258, a novel, multitargeted tyrosine kinase inhibitor for the potential treatment of t(4;14) multiple myeloma. Blood. 2005 Apr 1;105(7):2941-8. Epub 2004 Dec 14. PubMed ID biological principles the way life worksWebApr 1, 2005 · CHIR-258 potently inhibits FGFR3 with an inhibitory concentration of 50% (IC50) of 5 nM in in vitro kinase assays and selectively inhibited the growth of B9 cells … daily messenger canandaigua ny obituariesWebAug 16, 2006 · CHIR-258 is a small-molecule inhibitor that targets multiple receptor tyrosine kinases, including VEGF receptor 2 and platelet-derived growth factor receptor (IC 50 … biological problems in the worldWebJ. De-Bono 3043 Background: CHIR-258 is a potent small molecule inhibitor of VEGF, FGF, PDGF and c-KIT RTKs with IC 50 ≤10nM that demonstrates activity in a variety of angiogenesis, tumour and... biological problems and solutions