1. Signaling Pathways
  2. Epigenetics
    TGF-beta/Smad
  3. PKC

PKC

Protein kinase C

PKC (Protein kinase C) is a family of protein kinase enzymes that are involved in controlling the function of otherproteins through the phosphorylation of hydroxyl groups of serine and threonine amino acid residues on these proteins. PKC enzymes in turn are activated by signals such as increases in the concentration of diacylglycerol (DAG) or calcium ions (Ca2+). Hence PKC enzymes play important roles in several signal transduction cascades. The PKC family consists of 15 isozymes in humans: PKC-α (PRKCA), PKC-β1 (PRKCB), PKC-β2 (PRKCB), PKC-γ (PRKCG), PKC-δ (PRKCD), PKC-δ1 (PRKD1), PKC-δ2 (PRKD2), PKC-δ3 (PRKD3), PKC-ε (PRKCE), PKC-η (PRKCH), PKC-θ (PRKCQ), PKC-ι (PRKCI), PKC-ζ (PRKCZ), PK-N1 (PKN1), PK-N2 (PKN2), PK-N3 (PKN3). PKC is involved in receptor desensitization, in modulating membrane structure events, in regulating transcription, in mediating immune responses, in regulating cell growth, and in learning and memory. These functions are achieved by PKC-mediated phosphorylation of other proteins.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-N6734
    K-252b
    Inhibitor
    K-252b, an indolocarbazole isolated from the actinomycete Nocardiopsis, is a PKC inhibitor. K-252b can be used to inhibit extracellular kinases of cells in culture because it can’t pass through cell membrane freely .
    K-252b
  • HY-12880
    HA-100 dihydrochloride
    Inhibitor
    HA-100 dihydrochloride is a potent protein kinase inhibitor, with IC50s of 4 μM, 8 μM, 12 μM and 240 μM for cGMP-dependent protein kinase (PKG), cAMP-dependent protein kinase (PKA), protein kinase C (PKC) and MLC-kinase, respectively. HA-100 dihydrochloride also used as a ROCK inhibitor.
    HA-100 dihydrochloride
  • HY-108136
    Bisindolylmaleimide X
    Inhibitor
    Bisindolylmaleimide X (Ro 31-8425, BIM-X) is a cell-penetrating PKC inhibitor. Bisindolylmaleimide X is a potent cyclin-dependent kinase 2 (CDK2) antagonist with an IC50 of 200 nM. Bisindolylmaleimide X inhibits the proliferation of CD4 T cells in vitro. Bisindolylmaleimide X inhibits eNOS-Ser1177 phosphorylation in human embryonic vein endothelial cells. Bisindolylmaleimide X can be used for research on the immune system and cardiovascular diseases.
    Bisindolylmaleimide X
  • HY-P1286A
    PKC β pseudosubstrate TFA
    Inhibitor
    PKC β pseudosubstrate TFA is a selective cell-permeable inhibitor of PKC.
    PKC β pseudosubstrate TFA
  • HY-P1399
    Pep2m, myristoylated
    Inhibitor
    Pep2m, myristoylated (Myr-Pep2m) is a cell-permeable peptide. Pep2m, myristoylated can disrupt the protein kinase ζ (PKMζ) downstream targets, N-ethylmaleimide-sensitive factor/glutamate receptor subunit 2 (NSF/GluR2) interactions. PKMζ is an autonomously active isozyme of protein kinase C (PKC).
    Pep2m, myristoylated
  • HY-P1289C
    [Ala113]MBP(104-118) TFA
    Inhibitor
    [Ala113]MBP(104-118) TFA is an noncompetitive peptide inhibitors of protein kinase C (PKC), with IC50s ranging from 28-62 μM.
    [Ala113]MBP(104-118) TFA
  • HY-114554
    KS 619-1
    Inhibitor
    KS 619-1 is a Ca2+/calmodulin-dependent cyclic nucleotide phosphodiesterase inhibitor. KS 619-1 exhibits strong inhibitory activity against this enzyme derived from bovine brain and heart, but shows weak inhibitory effects on calmodulin-independent phosphodiesterase and protein kinase C. KS 619-1 displays weak antibacterial activity against Staphylococcus aureus.
    KS 619-1
  • HY-P3083
    N-Myristoyl-Lys-Arg-Thr-Leu-Arg
    Inhibitor
    N-Myristoyl-Lys-Arg-Thr-Leu-Arg is a protein kinase C (PKC) inhibitor with an IC50 value of 75 μM. N-Myristoyl-Lys-Arg-Thr-Leu-Arg inhibits IL-2 receptor induction and IL-2 production in the human leukemic cell line Jurkat.
    N-Myristoyl-Lys-Arg-Thr-Leu-Arg
  • HY-RS11146
    Prkd1 Rat Pre-designed siRNA Set A
    Inhibitor

    Prkd1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Prkd1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Prkd1 Rat Pre-designed siRNA Set A
  • HY-112681B
    PKC-theta inhibitor 2 hydrochloride
    Inhibitor
    PKC-theta inhibitor 2 hydrochloride is a potent and selective PKC-θ inhibitor with an IC50 value of 18 nM.
    PKC-theta inhibitor 2 hydrochloride
  • HY-RS11122
    PRKCD Human Pre-designed siRNA Set A
    Inhibitor

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

    PRKCD Human Pre-designed siRNA Set A
  • HY-RS11121
    Prkcb Rat Pre-designed siRNA Set A
    Inhibitor

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

    Prkcb Rat Pre-designed siRNA Set A
  • HY-155619
    Protein kinase inhibitor 7
    Inhibitor
    Protein kinase inhibitor 7 is an inhibitor for protein kinase A and protein kinase C. Protein kinase inhibitor 7 affects autocrine motility factor (AMF) signaling pathway, without affecting the cell motility.
    Protein kinase inhibitor 7
  • HY-W782599
    Senkyunolide B
    Inhibitor
    Senkyunolide B is a phthalide found in Angelica sinensis. Senkyunolide B has broad antifungal activities. Senkyunolide B affects the spore germination and hyphae growth of Aspergillus fumigatus via down-regulating phosphatidylinositol-PKC-calcineurin axis and the expression of ENG genes.
    Senkyunolide B
  • HY-13502S
    Mitoxantrone-d8
    Inhibitor
    Mitoxantrone-d8 (mitozantrone-d8) is the deuterium labeled Mitoxantrone. Mitoxantrone is a topoisomerase II inhibitor and also inhibits protein kinase C (PKC) activity with an IC50 of 8.5 μM.
    Mitoxantrone-d<sub>8</sub>
  • HY-RS11129
    Prkcg Mouse Pre-designed siRNA Set A
    Inhibitor

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

    Prkcg Mouse Pre-designed siRNA Set A
  • HY-RS11130
    Prkcg Rat Pre-designed siRNA Set A
    Inhibitor

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

    Prkcg Rat Pre-designed siRNA Set A
  • HY-N12466
    3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine
    Inhibitor
    3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine (Compound 7) is an inhibitor of protein kinases, with IC50s of 0.092, 0.26, 0.77 μM for PKC-α, ROCK, ASK1. 3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine shows potent cytotoxicity against PC-3 cancer cells with an IC50 value of 0.16 μM.
    3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine
  • HY-N0281R
    Daphnetin (Standard)
    Inhibitor
    Daphnetin (Standard) is the analytical standard of Daphnetin. This product is intended for research and analytical applications. Daphnetin (7,8-dihydroxycoumarin), one coumarin derivative can be found in plants of the Genus Daphne, is a potent, oral active protein kinase inhibitor, with IC50s of 7.67 μM, 9.33 μM and 25.01 μM for EGFR, PKA and PKC in vitro, respectively. Daphnetin triggers ROS-induced cell apoptosis and induces cytoprotective autophagy by modulating the AMPK/Akt/mTOR pathway. Daphnetin has anti-inflammation activitity and inhibits TNF-α, IL-1 , ROS, and MDA production. Daphnetin has schizontocidal activity against malaria parasites. Daphnetin can be used for rheumatoid arthritis , cancer and anti-malarian research.
    Daphnetin (Standard)
  • HY-RS11118
    Prkca Rat Pre-designed siRNA Set A
    Inhibitor

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

    Prkca Rat Pre-designed siRNA Set A
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