1. Signaling Pathways
  2. MAPK/ERK Pathway
  3. MAP3K

MAP3K 

MAP3Ks (Mitogen-activated protein kinase kinase kinases), the top components of MAPK cascades, provide specificity for stimulus-dependent activation of MAP2K-MAPK pathways through unique protein-protein interactions and phosphorylation of signaling effectors. The MAP3Ks are highly divergent in gene numbers and structure, including TAK1, ASK1, A-Raf and C-Raf.

MAPK system is a three-step sequential phosphorylation cascade which is composed of MAPK, MAP2K, and MAP3K. ERK, p38 MAPK, and JNK, which are known to be activated by mechanical stimuli, belong to the MAPK family. MAP3Ks function as “platforms to integrate MAPK signaling, and activation of multiple MAP3Ks provides the spatiotemporal regulation of the MAPK pathways, which induces a wide range of physiological responses required for determining cell fate, such as cytokine production, survival, differentiation and apoptosis”.

MAP3K 亚型特异性产品:

  • MAP3K5/ASK1

  • MAP3K7/TAK1

  • MAP3K8

MAP3K 相关产品 (6):

目录号 产品名 作用方式 纯度
  • HY-12686
    5Z-7-Oxozeaenol Inhibitor ≥99.0%
    5Z-7-Oxozeaneol 是一种天然的抗原生动物化合物,为有效的,不可逆的,选择性的 TAK1VEGF-R2 抑制剂,IC50 值分别为 8 nM 和 52 nM。
  • HY-32018
    Cot inhibitor-2 Inhibitor 99.22%
    Cot inhibitor-2 是一种有效的,选择性的,具有口服活性的 cot (Tpl2/MAP3K8) 抑制剂,IC50 为 1.6 nM。Cot inhibitor-2 抑制 LPS 刺激的人全血中 TNF-α 的产生,IC50 为 0.3 μM。
  • HY-12358
    Tpl2 Kinase Inhibitor 1 Inhibitor ≥99.0%
    Tpl2 Kinase Inhibitor 1 (Compound 1) 是一种有效的选择性 Tpl2 (COT 激酶,MAP3K8) 抑制剂,可用于炎症反应和某些癌症的研究。
  • HY-32015
    Cot inhibitor-1 Inhibitor 98.13%
    Cot inhibitor-1 (compound 28) 是一种选择性的Tpl2 kinase抑制剂,IC50 为 28 nM。Cot inhibitor-1 对人全血中 TNF-alpha 的产生具有抑制作用,IC50 为 5.7 nM。
  • HY-103258
    TC ASK 10 Inhibitor ≥99.0%
    TC ASK 10 (Compound 10) 是一种有效的,选择性的,口服活性的细胞凋亡信号调节激酶 1 (ASK1) 抑制剂,IC50 为 14 nM。TC ASK 10 对其他代表性激酶的抑制活性低于 50%,ASK2 除外 (IC50 为 0.51 μM)。
  • HY-136848
    SM1-71 Inhibitor
    SM1-71 是一种有效的 TAK1 抑制剂,Ki 值为 160 nM,同时可以共价抑制 MKNK2MAP2K1/2/3/4/6/7GAKAAK1BMP2KMAP3K7MAPKAPK5GSK3A/BMAPK1/3SRCYES1FGFR1ZAK (MLTK)MAP3K1LIMK1RSK2。SM1-71 在体外抑制多种癌细胞系的增殖。
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