1. Signaling Pathways
  2. Apoptosis
  3. RIP kinase
  4. RIP kinase Isoform

RIP kinase

 

RIP kinase Related Products (87):

Cat. No. Product Name Effect Purity
  • HY-155151
    RIPK2/3-IN-1
    Inhibitor
    RIPK2/3-IN-1 is a potent dual RIPK2/3 kinases inhibitor with IC50 values of 3 nM and 117 nM, respectively. RIPK2/3-IN-1 is against RIPK2 with IC50 value 14 nM in 14-TriLAN-Gly/NOD1 THP-1 cell-based NF-κB reporter assay.
  • HY-156368
    RIPK3-IN-4
    Inhibitor
    RIPK3-IN-4 (Compound 42) is a RIPK3 inhibitor. RIPK3-IN-4 inhibits HK-2 cell damage, necroptosis and inflammatory responses. RIPK3-IN-4 reduces Cisplatin (HY-17394)- and I/R-induced kidney damage, inflammatory response and necroptosis in acute kidney injury.
  • HY-RS11994
    Ripk1 Rat Pre-designed siRNA Set A
    Inhibitor

    Ripk1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Ripk1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

  • HY-153436
    RIP1 kinase inhibitor 6
    Inhibitor
    RIP1 kinase inhibitor 6 is a potent and selective RIP1 kinase inhibitor with an IC50 of < 100 nM in human R1P1 kinase assay. RIP1 kinase inhibitor 6 is extracted from patent WO2020103884, example 80.
  • HY-157751
    RIPK1-IN-21
    Inhibitor
    RIPK1-IN-21 (Compound I-5) is an inhibitor of RIPK1 with an EC50 value of 14.8 nM. RIPK1-IN-21 can be used in the research of neurodegenerative, autoimmune, and inflammatory diseases.
  • HY-163390
    RIP1 kinase inhibitor 9
    Inhibitor
    RIP1 kinase inhibitor 9 (compound SY-1) is a selective RIP kinase inhibitor. RIP1 kinase inhibitor 9 effectively suppresses the central inflammatory response induced by epilepsy. RIP1 kinase inhibitor 9 inhibits Z-VAD-FMK (HY-16658B)-induced necroptosis in HT-29 cells with an EC50 of 7.04 nM.
  • HY-168640
    RIP3 activator 1
    Activator
    RIP3 activator 1 (compound C8) is a potent RIP3 activator. RIP3 activator 1 inhibits cell growth. RIP3 activator 1 induces necroptosis through the RIP3/p62/Keap1 signaling pathway. RIP3 activator 1 increases the protein expression of p-MLKL. RIP3 activator 1 induces autophagy. RIP3 activator 1 increases accumulation of LC3-II and p62 protein expression.
  • HY-168974
    Fosizensertib
    Inhibitor
    Fosizensertib is the inhibitor for RIP-1 kinase and can be used in researchs of ulcerative colitis.
  • HY-146694
    RIPK2-IN-1
    Inhibitor
    RIPK2-IN-1 (compound 18f) is a potent RIPK2 inhibitor with an IC50 of 51 nM. RIPK2-IN-1 inhibits ALK2 with an IC50 of 5 nM. RIPK2-IN-1 has an IC50 of 390 nM on RIPK2/NOD2 in cell assay.
  • HY-143480
    RIPK1-IN-15
    Inhibitor
    RIPK1-IN-15 (Compound 2.5) is a potent inhibitor of RIPK1. RIPK1-IN-15 has the potential for the research neurodegenerative, autoimmune, and inflammatory diseases.
  • HY-168116
    RIPK1-IN-27
    Inhibitor
    RIPK1-IN-27 (compund 19) is a RIPK1 inhibitor.
  • HY-160216A
    RIPK1-IN-18 sulfate hydrate
    Inhibitor
    RIPK1-IN-18 sulfate hydrate is a potent RIPK1 inhibitor that can be used in autoimmune diseases research (NZ748385A; compound i).
  • HY-157309
    RIPK2-IN-4
    Inhibitor
    RIPK2-IN-4 is a potent and specific RIPK2 inhibitor with an IC50 value of 5 nM.
  • HY-RS11999
    Ripk3 Mouse Pre-designed siRNA Set A
    Inhibitor

    Ripk3 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Ripk3 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

  • HY-162928
    RIPK1-IN-26
    Inhibitor
    RIPK1-IN-26 (Compound 8a) is a potent receptor-interacting serine/threonine-protein kinase 1 (RIPK1) inhibitor with cell anti-necroptosis potency. RIPK1-IN-26 demonstrats good metabolic stability and good binding specificity in mice. RIPK1-IN-26 is promising for research of PET imaging probe development and neurodegenerative disorders.
  • HY-120600
    Sibiriline
    Inhibitor
    Sibiriline is a specific competitive inhibitor of RIPK1 that targets the RIPK1 ATP-binding site and locks it in an inactive conformation. Sibiriline inhibits TNF-induced RIPK1-dependent necroptosis and RIPK1-dependent apoptosis, but does not protect cells from caspase-dependent apoptosis. Sibiriline protects mice from concanavalin A-induced hepatitis and has the potential to inhibit immune-dependent hepatitis..
  • HY-161843
    Necroptosis-IN-4
    Inhibitor
    Necroptosis-IN-4, a potent necroptosis inhibitor, is a RIP kinase 1 (RIPK1) inhibitor. Necroptosis-IN-4 has no inhibitory activity against RIPK3 and weak inhibitory activity against VEGFR1/2 and PDGFR-α.
  • HY-148253
    TP-030-1
    Inhibitor
    TP-030-1, a chemical probe, is an inhibitor of RIPK1. TP-030-1 inhibits hRIPK1 with a Ki value of 3.9 nM and inhibits mRIPK1 with an IC50 value of 4.2 μM. TP-030-1 can be used for the research of inflammatory diseases and neurodegenerative diseases.
  • HY-168567
    RIPK2-IN-6
    Inhibitor
    RIPK2-IN-6 (Compound 15a) is an inhibitor for RIPK, that inhibits the phosphorylation of RIPK2, and thus inhibits the NF-κB and MAPK signaling pathways. RIPK2-IN-6 exhibits anti-inflammatory and anti-fibrotic activities in Dextran sodium sulfate (HY-116282C)-induced mice colitis models.
  • HY-173075
    Anticancer agent 267
    Activator
    Anticancer agent 267 (Compound 5q) is the activator for RIPK3 and MLKL. Anticancer agent 267 inhibits the proliferation in a variety of cancer cell lines (IC50 for MDA-MB-231, MDA-MB-486 and MCF-7 is 9.79, 10.77 and 5.94 μM, respectively), arrests cell cycle at subG1 phase, and induces necroptosis in cell MDA-MB-231. Anticancer agent 267 exhibits antitumor activity in mouse xenograft models.