Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T77734 |
ERK5-IN-5
|
ERK | MAPK |
ERK5-IN-5 是一种有效的细胞外信号调节激酶 5 (ERK5)抑制剂,有抗癌活性和潜在的抗惊厥活性,抑制 A549 细胞增殖。 | |||
T5535 |
ERK5-IN-2
|
ERK | MAPK |
ERK5-IN-2 是具有口服活性,亚微摩尔效力,选择性ERK5抑制剂,对ERK5和ERK5 MEF2D 的IC50s 分别是 0.82 和 3 μM。它抑制肿瘤异种移植生长和碱性成纤维细胞生长因子驱动的基质胶塞血管生成。 | |||
T5184 |
ERK5-IN-1
|
ERK | MAPK |
ERK5-IN-1 是 ERK5抑制剂,IC50为 87 nM。它也抑制 LRRK2[G2019S],IC50为 26 nM。 | |||
T1842 |
XMD17-109
XMD17 109,ERK5-IN-1 |
ERK | MAPK |
XMD17-109 (ERK5-IN-1) 是一种特异性的ERK-5抑制剂,在 HEK293 细胞系中的EC50为 4.2 μM。 | |||
T63268 |
ERK5-IN-3
|
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ERK5-IN-3 是选择性的、有效的 ERK5 (细胞外信号相关激酶 5) 抑制剂 (IC50: 6 nM)。ERK5-IN-3 对 Hela 细胞表现出抗增殖作用 (IC50: 31 nM)。 | |||
T61628 | ERK5-IN-4 | ||
ERK5-IN-4 (compound 34b) is a powerful and specific inhibitor of extracellular signal-related kinase 5 (ERK5) activity. It effectively inhibits both the full-length ERK5 and the truncated ERK5 (ERK5 ΔTAD) kinase activity in HEK293 cells with IC50 values of 77 nM and 300 nM, respectively [1]. | |||
T35536 |
Tpl2 Kinase Inhibitor (hydrochloride)
|
||
Tpl2 kinase inhibitor is an inhibitor of tumor progression locus 2 (Tpl2; IC50= 0.05 μM).1It is selective for Tpl2 over MEK, p38 MAPK, Src, MK2, and PKC (IC50s = >40, 180, >400, 110, and >400 μM, respectively). Tpl2 kinase inhibitor inhibits LPS-induced TNF-α production in isolated human monocytes and whole blood (IC50s = 0.7 and 8.5 μM, respectively). It enhances differentiation induced by calcitriol in HL-60 and U937 leukemia cells when used at a concentration of 5 μM.2Tpl2 kinase inhibitor (5... |