酪氨酸激酶抑制剂AG 490

AG-490 (Tyrphostin B42) (订货以英文为准)

编号:A126525
CAS号:133550-30-8
分子式:C17H14N2O3
分子量:294.30
货号 品牌 包装 目录价 您的价格 库存 数量 购买
A126525-250mg 阿拉丁 250mg ¥1598.90
A126525-20mg 阿拉丁 20mg ¥226.90
A126525-50mg 阿拉丁 50mg ¥378.90
A126525-1g 阿拉丁 1g ¥2772.90
产品名称 AG-490 (Tyrphostin B42)
中文名称 酪氨酸激酶抑制剂AG 490
CAS号 133550-30-8
分子式(M.F.) C17H14N2O3
分子量(M.W.) 294.30
储存条件 -20°C储存
熔点215°C
溶解性DMSO ≥57mg/mL Water <1.2mg/mL Ethanol ≥8mg/mL
存贮条件储存温度-20°C
应用Tyrphostin AG has been used to block IL-6 cytokine signaling to study its effects on glial cell reactivity. AG 490 has also been used as a JAK2 inhibitor in human umbilical vein endothelial cells
产品介绍AG-490 (Tyrphostin AG 490)是EGFR抑制剂,IC50为100nM,比对ErbB2的抑制性高135倍,对Lck,Lyn,Btk,Syk和Src无活性。
备注AG-490 (Tyrphostin B42) is an inhibitor of EGFR with IC50 of 0.1 μM, 135-fold more selective for EGFR versus ErbB2, also inhibits JAK2 with no activity to Lck, Lyn, Btk, Syk and Src.
生化机理AG-490 is a selective inhibitor of EGF receptor tyrosine kinase (IC50 values are 2 and 13.5 μM for EGFR and ErbB2 respectively). Inhibitor of JAK2, JAK3/STAT, JAK3/AP-1 and JAK3/MAPK pathways and potently inhibits cytokine-independent cell growth in vitro and tumor cell invasion in vivo.
别名酪氨酸激酶抑制剂AG 490;(E)-N-苯甲基-2-氰基-3-(3,4-二羟苯基)丙烯酰胺;AG 490;Tyrphostin AG 490;AG490; tyrphostin ag 490;ag 490; (E)-N-Benzyl-2-cyano-3-(3,4-dihydroxyphenyl)acrylamide;2-Cyano-3-(3,4-dihydroxyphenyl)-N-(benzyl)-2-propenamide; 2-Cyano-3-(3,4-dihydroxyphenyl)-N-(phenylmethyl)-2-propenamide
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