Cy3-UTP 抑制剂 BMPO Leukotriene D4 荧光染料 DMAPP 定制合成
双链RNA激活蛋白激酶(PKR)抑制剂,PKR-IN-C16 是特异性蛋白激酶 (PKR) 抑制剂。PKR-IN-C16 能够抑制 PKR 的自磷酸化,PKR 在原代神经元细胞培养中诱导的翻译阻断可被 PKR-IN-C16 解除。
Rp-8-pCPT-Cyclic GMPS is a stable, cell-permeable cGMP analog that competitively inhibits cGMP-dependent protein kinases (cGKs), including cGK Iα and cGK II (IC50s = 18.3 and 0.16 µM, respectively). The pCPT (p-chlorophenylthio) group at the 8-position of the purine increases both enzyme affinity and membrane permeability over related compounds. At 10 µM, it blocks the relaxation of rat tail arteries induced by the nitric oxide donor SIN-1.
Staurosporine 是一种有效,非选择性蛋白激酶抑制剂,抑制 PKC,PKA,c-Fgr,和 Phosphorylase kinase 的 IC50 分别为 6 nM,15 nM,2 nM,6 nM。
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