溶解性 | DMSO ≥8mg/mL Water <1.2mg/mL Ethanol <1.2mg/mL |
存贮条件 | 储存温度-20°C |
应用 | An ATP-competitive inhibitor of VEGFR (Flt and Flk) kinase |
产品介绍 | KRN-633是可渗透细胞的,可逆的。ATP竞争性VEGFR抑制剂,对VEGFR-1,VEGFR-2和VEGFR-3的IC50分别为170 nM,160 nM和125 nM。 |
备注 | KRN 633 is an ATP-competitive inhibitor of VEGFR1/2/3 with IC50 of 170 nM/160 nM/125 nM, weakly inhibits PDGFR-α/β and c-Kit, does not block the phosphorylation of FGFR-1, EGFR or c-Met in cell. |
生化机理 | KRN633 is a cell-permeable; reversible and ATP-competitive inhibitor of vascular endothelial growth factor receptor tyrosine kinase (VEGFR) with IC50 values of 170, 160, and 125 nM for VEGFR-1, -2, -3, respectively. Krn633 inhibits PDGFR-α and c-Kit only at higher concentrations (IC50 = 0.97 and 4.33 μM, respectively) and is inactive towards a panel of 17 other kinases (IC50 >/= 10 μM). |
别名 | KRN 633; KRN633; N-[2-氯-4-[(6,7-二甲氧基-4-喹唑啉基)氧基]苯基]-N'-丙基脲;KRN 633; KRN633; N-[2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl]-N′-propyl-urea |
KRN-633,VEGFR 抑制剂
KRN-633 (订货以英文为准)
编号:K125907
CAS号:286370-15-8
分子式:C20H21CLN4O4
分子量:416.86
产品名称 | KRN-633 |
中文名称 | KRN-633,VEGFR 抑制剂 |
CAS号 | 286370-15-8 |
分子式(M.F.) | C20H21CLN4O4 |
分子量(M.W.) | 416.86 |
储存条件 | -20°C储存 |
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