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CAS No. : 15966-93-5
MCE 站:SU5408
产品活性:SU5408 (VEGFR2 Kinase Inhibitor I) 是有效的,可渗透细胞的 VEGFR2 激酶抑制剂,IC50 值为 70 nM。
研究领域:Protein Tyrosine Kinase/RTK
作用靶点:VEGFR
In Vitro: 3-Substituted indolin-2-ones have been designed and synthesized as a novel class of tyrosine kinase inhibitors which exhibit selectivity toward different receptor tyrosine kinases (RTKs). These compounds have been evaluated for their relative inhibitory properties against a panel of RTKs in intact cells. SU5408 (VEGFR2 Kinase Inhibitor I) is found to be the most potent and selective VEGFR2 inhibitor among the compounds. SU5408 (VEGFR2 Kinase Inhibitor I) shows little or no effect against receptors for platelet-derived growth factor, epidermal growth factor, or insulin-like growth factor (IC50>100 ?M).
相关产品:Bioactive Compound Library Plus | Kinase Inhibitor Library | Protein Tyrosine Kinase Compound Library | Differentiation Inducing Compound Library | Reprogramming Compound Library | Anti-Cardiovascular Disease Compound Library | Anti-Breast Cancer Compound Library | Anti-Pancreatic Cancer Compound Library | Anti-Blood Cancer Compound Library | Bevacizumab | Sunitinib | Semaxinib | SU 5402 | PD173074 | 5Z-7-Oxozeaenol | Cediranib | SAR131675 | Gandotinib | GW806742X | Tanshinone IIA | PF-03814735 | Vatalanib dihydrochloride | CP-547632 | AST 487 | Tyrphostin A9 | Ki20227 | Motesanib | SU14813 | Ramucirumab | SU1498 | MAZ51 | PP121 | Ki8751 | ZM 306416 | ZM323881 hydrochloride
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更新时间:2024/1/2 10:17:29
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