FMK
FMK 是一种强效、高度特异性且不可逆的 p90 核糖体蛋白 S6 激酶 RSK1 和 RSK2 抑制剂;FMK 结合在 CTKD ATP 结合位点,并抑制 RSK 在 Ser386 的自磷酸化。FMK 在表达人类 FGFR3、t(4;14)阳性的多发性骨髓瘤细胞中诱导显著的凋亡。
Discription | FMK is potent, highly specific and irreversible inhibitor of p90 ribosomal protein S6 kinase RSK1 and RSK2; Fmk binds in the CTKD ATP-binding site and inhibits RSK autophosphorylation at Ser386. Fmk induces significant apoptosis in human FGFR3-expressing, t(4;14)-positive multiple myeloma cells. | |||||
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Cell Research |
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目录号 | A11423 |
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分子式 | C18H19FN4O2 |
分子量 | 342.37 |
CAS号 | 821794-92-7 |
SMILES | CC1=CC=C(C=C1)C2=C(N(C3=C2C(=NC=N3)N)CCCO)C(=O)CF |
储存条件 | Store lyophilized at -20ºC, keep desiccated. |
Calculate the dilution required to prepare a stock solution. This equation is commonly abbreviated as: C1V1 = C2V2