Tyrphostin AG 879 酪氨酸激酶的抑制剂

Tyrphostin AG 879 (订货以英文为准)

编号:T129799
CAS号:148741-30-4
分子式:C18H24N2OS
分子量:316.46
货号 品牌 包装 目录价 您的价格 库存 数量 购买
T129799-5mg 阿拉丁 5mg ¥514.90
T129799-100mg 阿拉丁 100mg ¥3307.90
T129799-25mg 阿拉丁 25mg ¥1853.90
产品名称 Tyrphostin AG 879
中文名称 Tyrphostin AG 879 酪氨酸激酶的抑制剂
CAS号 148741-30-4
MDL编码 MFCD00236450
分子式(M.F.) C18H24N2OS
分子量(M.W.) 316.46
储存条件 -20°C储存
沸点~443.81° C at 760 mmHg
熔点219-220° C
折光率1.61
溶解性DMSO 36 mg/mL Water <1 mg/mL Ethanol 3 mg/mL
存贮条件储存温度-20°C
应用A protein tyrosine kinase inhibitor with potent effects on TrkA
产品介绍AG879是酪氨酸激酶的抑制剂,能够抑制TrKA的磷酸化,但不能抑制TrKB 和TrKC,也是高选择性的ErbB2激酶抑制剂。
备注Tyrphostin AG 879 potently inhibits HER2/ErbB2 with IC50 of 1 μM, 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR.
生化机理Tyrphostin AG 879 is a protein tyrosine kinase inhibitor with potent effects on TrkA. This product reportedly inhibits NGF-induced PLC-γ 1 phosphorylation and phosphatidylinositol-3 kinase activation. Has been shown in lab studies to disrupt Sertoli cell aggregation and stop androgen-induced cell proliferation. AG 879 also displays anti-cancer effects by inhibiting the expression of RAF-1 gene encoding MAP kinase activity necessary for human breast cancer cell proliferation. Shown to inhibit Neu (HER-2 or ERBB2) expression and reduced tumor sizes in mice leukemia cells. Tyrphostin AG 879 is an inhibitor of Flk-1.
别名AG 879;AG-879;AG879;AG 879;AG-879;AG879; α-Cyano-(3,5-di-t-butyl-4-hydroxy)thiocinnamide; (E)-3-[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]-2-cyano-2-propenethioamide
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