Protein Kinase C (PKC)

Protein kinase C (PKC) inhibitors and activators act on a family of lipid-regulated serine/threonine kinases. Conventional PKC isoforms require calcium and diacylglycerol, novel isoforms need only diacylglycerol, and atypical isoforms respond to neither. Tumor-promoting phorbol esters mimic diacylglycerol and were shown in 1982 to activate PKC directly. 12-O-tetradecanoyl phorbol-13-acetate (TPA) is the standard activator of this kind, and ingenol mebutate also activates several isoforms. Staurosporine was first described as a PKC inhibitor but blocks a wide range of protein kinases. Enzastaurin is selective for PKCβ, while GO6983 and Ro 31-8220 mesylate inhibit multiple conventional and novel isoforms.

Items 201-212 of 212

  • LY 170198
    Cat. No.
    A46262

    LY 170198

    LY 170198 is a potent protein kinase C inhibitor and LTD4 antagonist. This compound exhibits significant biological activity relevant to studies on tumor promotion, oncogene activation, and protein phosphorylation. Additionally, it is valuable for investigating feedback mechanisms in signal transduction pathways and cellular responses to growth factors, making it a useful tool for cancer research and related fields.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • Go 7874
    Cat. No.
    A46263

    Go 7874

    Go 7874 is a protein kinase C (PKC) inhibitor that exhibits neuroprotective effects in models of immune-mediated neurotoxicity. This compound mitigates LPS/IFNg-induced neuronal cell death not through conventional PKC inhibition, but by suppressing the expression of inducible nitric oxide synthase (iNOS), leading to decreased nitric oxide (NO) production. Its unique mechanism makes Go 7874 a valuable tool for studying neuroprotective strategies in inflammatory conditions.

    25 mg
    $1,655.00
    50 mg
    $2,115.00
    All 3 sizes
  • (±)-1,2-Diolein-CC3
    Cat. No.
    A46264

    (±)-1,2-Diolein-CC3

    Synonyms: 1,2-Dioleoyl-rac-glycerol-CC3

    (±)-1,2-Diolein-CC3 is a stable isotope-labeled derivative of (±)-1,2-Diolein, also known as 1,2-Dioleoyl-rac-glycerol-13C3. This compound acts as an activator of protein kinase C (PKC) and is known to enhance calcium ion influx in myotubes. It is particularly useful in research applications studying lipid signaling pathways, cell proliferation, and muscle physiology.

    Out of stock

    All 3 sizes
  • Bisindolylmaleimide IV
    Cat. No.
    A50661

    Bisindolylmaleimide IV

    Synonyms: Arcyriarubin A

    Bisindolylmaleimide IV is a selective inhibitor of protein kinase C (PKC), exhibiting IC50 values between 0.1 and 0.55 μM. It also demonstrates inhibition of protein kinase A (PKA) with IC50 ranging from 3.1 to 11.8 μM. In addition to its kinase inhibitory properties, Bisindolylmaleimide IV effectively inhibits human cytomegalovirus (HCMV) replication in cell culture, displaying an IC50 of 0.2 μM. This reagent is valuable for research applications focused on signal transduction and viral pathogenesis.

    2 mg
    $30.00
    5 mg
    $45.00
    All 7 sizes
  • 1,2-Dimyristoyl-sn-glycerol
    Cat. No.
    A52270

    1,2-Dimyristoyl-sn-glycerol

    1,2-Dimyristoyl-sn-glycerol is a saturated diacylglycerol that acts as a weak second messenger for the activation of Protein Kinase C (PKC). This compound is utilized in research applications to study PKC signaling pathways, which are crucial in various cellular processes including growth, differentiation, and apoptosis. As a PKC activator, it can help elucidate the role of PKC in different biological contexts and disease models.

    50 mg
    $25.00
    100 mg
    $40.00
    All 4 sizes
  • Ilmofosine
    Cat. No.
    A53084

    Ilmofosine

    Synonyms: BM41440

    Ilmofosine is a selective inhibitor of protein kinase C, exhibiting potent activity in modulating cellular signaling pathways. This compound induces cell cycle arrest at the G2 phase, highlighting its potential for cancer research. Additionally, Ilmofosine serves as an effective anti-leishmanial agent, making it valuable for studies related to parasitic infections and therapeutic interventions.

    Out of stock

    All 3 sizes
  • DL-erythro-Dihydrosphingosine
    Cat. No.
    A53665

    DL-erythro-Dihydrosphingosine

    DL-erythro-Dihydrosphingosine is a sphingosine-derived protein kinase C (PKC) inhibitor that functions by directly inhibiting phospholipase A2 (PLA2) activity. This compound also attenuates the function of Bcl-2, a protein that plays a crucial role in regulating apoptosis. Additionally, DL-erythro-Dihydrosphingosine inhibits matrix metalloproteinases (MMPs), which are involved in various cellular processes. Its unique biological activity makes it valuable for research in cancer and inflammatory disease models.

    5 mg
    $180.00
    All 1 sizes
  • Desmethylglycitein
    Cat. No.
    A54176

    Desmethylglycitein

    Synonyms: 4',6,7-Trihydroxyisoflavone

    Desmethylglycitein (4',6,7-Trihydroxyisoflavone) is an inhibitor of protein kinase C (PKC)α, demonstrating significant anti-cancer and antioxidant activities. It directly binds to CDK1 and CDK2, leading to the suppression of their activity. Additionally, Desmethylglycitein inhibits PI3K in an ATP-competitive manner, affecting downstream signaling pathways and reducing adipogenesis in 3T3-L1 preadipocytes. Its mechanisms make it a valuable tool for research in cancer biology and metabolic disorders.

    5 mg
    $25.00
    10 mg
    $35.00
    All 6 sizes
  • Bisindolylmaleimide X
    Cat. No.
    A54431

    Bisindolylmaleimide X

    Synonyms: BIM-X; Ro31-8425

    Bisindolylmaleimide X is a potent protein kinase C (PKC) inhibitor that exhibits cell-penetrating properties. It effectively inhibits the proliferation of CD4 T cells in vitro and shows antagonistic activity against cyclin-dependent kinase 2 (CDK2) with an IC50 of 200 nM. Additionally, Bisindolylmaleimide X suppresses eNOS-Ser1177 phosphorylation in human embryonic vein endothelial cells. This compound is valuable for studying mechanisms in the immune system and cardiovascular diseases.

    Out of stock

    All 3 sizes
  • Sangivamycin
    Cat. No.
    A55098

    Sangivamycin

    Synonyms: NSC 65346; BA-90912

    Sangivamycin is a nucleoside analog that serves as a potent inhibitor of protein kinase C (PKC) with a Ki value of 10 μM. This compound exhibits significant antiproliferative activity against a diverse range of human cancers, making it a valuable tool for cancer research and therapeutic studies focused on PKC modulation. Its targeted mechanism of action positions Sangivamycin as a promising candidate for further exploration in cancer treatment.

    1 mg
    $100.00
    5 mg
    $235.00
    All 6 sizes
  • PKC-iota inhibitor 1
    Cat. No.
    A57634

    PKC-iota inhibitor 1

    PKC-iota inhibitor 1 is an inhibitor of protein kinase C-iota (PKC-ι) with an IC50 value of 0.34 μM. This compound demonstrates significant biological activity relevant to cancer research, making it a valuable tool for investigating the role of PKC-ι in tumorigenesis and signal transduction pathways. It is suitable for studies focused on cancer biology and therapeutic interventions targeting PKC-ι.

    1 mg
    $90.00
    2 mg
    $135.00
    All 8 sizes
  • PKCζ/ι pseudosubstrate inhibitor
    Cat. No.
    A77421

    PKCζ/ι pseudosubstrate inhibitor

    PKCζ/ι Pseudosubstrate Inhibitor serves as a specific inhibitor of protein kinase C (PKC) isoforms ζ and ι. This compound exhibits broad-spectrum inhibitory effects on the PKC enzyme family, making it valuable for studies investigating the role of PKC in cell signaling and neurobiology. Additionally, it has been shown to induce memory impairment, which may be relevant for research on cognitive function and associated disorders.

    0.5 mg
    $280.00
    1 mg
    $445.00
    All 3 sizes

Items 201-212 of 212

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