1. Signaling Pathways
  2. Apoptosis
  3. RIP kinase

RIP kinase (受体相互作用蛋白激酶)

Receptor-interacting protein kinases; RIPK

Receptor-interacting protein (RIP) kinases are a group of threonine/serine protein kinases with a relatively conserved kinase domain but distinct non-kinase regions. There are seven members of the RIPK family, RIPK1-7, some of which have emerged as critical effectors of immunity to infection with a diverse array of bacterial, viral, and protozoal pathogens.

RIP kinases are cellular signaling molecules that are critical for homeostatic signaling in both communicable and non-communicable disease processes. RIPK1, RIPK2, RIPK3 and RIPK7 have emerged as key mediators of intracellular signal transduction including inflammation, autophagy and programmed cell death, and are thus essential for the early control of many diverse pathogenic organisms.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-144276
    RIPK1-IN-11 Inhibitor
    RIPK1-IN-11是一种口服有效的RIPK1抑制剂 (Kd=9.2 nM; IC50=67 nM),可抑制人和小鼠细胞坏死。具有抗炎活性。
    RIPK1-IN-11
  • HY-158334
    NDs-IN-1 Inhibitor
    (神经退行性疾病) NDs-IN-1 (Compound 3g) 抑制 hBACE-1hAChEhMAO-B 等关键酶的活性。NDs-IN-1 是一种新型的非共价多靶点抑制剂。NDs-IN-1 主要用于研究神经退行性疾病。
    NDs-IN-1
  • HY-136010
    RIP2 Kinase Inhibitor 4 Inhibitor
    RIP2 Kinase Inhibitor 4,一种有效且选择性的 RIPK2 PROTAC,可有效降解 RIPK2 (pIC50 of 8) 并抑制相关 TNF-α 的释放。
    RIP2 Kinase Inhibitor 4
  • HY-160216A
    RIPK1-IN-18 sulfate hydrate Inhibitor
    RIPK1-IN-18 sulfate hydrate 是一种有效的 RIPK1 抑制剂,可用于自身免疫性疾病研究 (NZ748385A; compound i)。
    RIPK1-IN-18 sulfate hydrate
  • HY-160216
    RIPK1-IN-18 Inhibitor
    RIPK1-IN-18 (compound i) 是 RIPK1 的有效抑制剂。RIPK1-IN-18 可用于自身免疫性疾病研究。
    RIPK1-IN-18
  • HY-148297
    Ocadusertib Inhibitor
    Ocadusertib 是一种有效的丝氨酸/苏氨酸激酶受体相互作用蛋白激酶 1 (RIPK1) 抑制剂。
    Ocadusertib
  • HY-146758
    RIPK1-IN-14 Inhibitor
    RIPK1-IN-14 (Compound 41) 是一种有效的 RIPK1 抑制剂,IC50 值为 92 nM。RIPK1-IN-14 在 U937 细胞的坏死性凋亡模型中显示出显着的抗坏死性凋亡作用。
    RIPK1-IN-14
  • HY-155151
    RIPK2/3-IN-1 Inhibitor
    RIPK2/3-IN-1 是一种有效的双 RIPK2/3 kinases 激酶抑制剂,其 IC50 值分别为 3 nM 和 117 nM。在 C14-TriLAN-Gly/NOD1 THP-1 细胞的 NF-κB 报告细胞实验中 RIPK2/3-IN-1 对 RIPK2 具有抑制作用,IC50 值 14±4 nM。
    RIPK2/3-IN-1
  • HY-148253
    TP-030-1 Inhibitor
    TP-030-1 是 RIPK1 的抑制剂。TP-030-1 抑制 hRIPK1 的 Ki 值为 3.9 nM,抑制 mRIPK1 的 IC50 值为 4.2 μM。TP-030-1 可用于炎症性疾病和神经退行性疾病的研究。
    TP-030-1
  • HY-141453
    Desmethyl-WEHI-345 analog Inhibitor
    Desmethyl-WEHI-345 analog 是一种蛋白激酶抑制剂,可用于结肠癌的研究。详细信息请参考专利文献 WO2012003544A1 中的化合物 12。
    Desmethyl-WEHI-345 analog
  • HY-151542
    MLKL-IN-4 Inhibitor
    MLKL-IN-4 (compound 56) 是一种有效的 MLKL (混合谱系激酶结构域样蛋白)抑制剂。MLKL-IN-4 可抑制 HT-29 细胞的坏死 (necroptosis),作用于 MLKL 磷酸化的下游,其 EC50 为 82 nM。
    MLKL-IN-4
  • HY-125466
    cRIPGBM
    cRIPGBM 是RIPGBM 的促凋亡衍生物,是通过与受体相互作用蛋白激酶2 (RIPK2)结合,诱导 GBM 肿瘤干细胞 凋亡的选择性诱导剂,对 GBM-1 细胞的 EC50 值为 68 nM。
    cRIPGBM
  • HY-18900
    Nec-4 Inhibitor
    Nec-4, 一个三环衍生物,是受体相互作用蛋白 1 (RIP1) 的一个有效抑制剂,其 IC50 值为 2.6 μM,Ki 值为 0.46 μM。
    Nec-4
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