PKC
Protein kinase C
PKC Isoform Specific Products
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PKC
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PKCα
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PKCβ
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PKCγ
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PKCδ
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PKCε
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PKCη
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PKCζ
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PKCθ
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PKCμ
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PKC-ι ℩
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PKCι
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PKC Related Products (504)
Related Products (504)
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Antibodies (21)
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PKC Isoform Comparison
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Bacopaside I (Standard)
0 ImagesCat. No.: HY-N4246RCAS No.: 382148-47-2Bacopaside I (Standard) is the analytical standard of Bacopaside I. This product is intended for research and analytical applications. Bacopaside I is an orally active aquaporin AQP1 inhibitor and PKC modulator with neuroprotective and anticancer activities. Bacopaside I specifically blocks the water channel and cGMP-gated ion channel activities of AQP1 without affecting AQP4, thereby inhibiting the migration of colon cancer cells expressing AQP1. Bacopaside I activates the Akt pathway by interacting with PI3K, specifically inhibits MAO-A, effectively alleviates neuron necrosis and apoptosis induced by oxygen-glucose deprivation, reduces oxidative stress, and regulates the surface expression of neuroreceptors. When combined with Bacopaside II (HY-N6016), Bacopaside I significantly reduces the viability, proliferation and invasion ability of breast cancer cells, and binds to the pregnane X receptor (PXR). Bacopaside I is applicable to the research of colon cancer, breast cancer, vascular dementia, cerebral ischemia and other related diseases. -
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PRKCZ Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS11141PRKCZ Human Pre-designed siRNA Set A contains three designed siRNAs for PRKCZ gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Mitoxantrone-d8 dihydrochloride
0 ImagesCat. No.: HY-13502ASSynonyms: Mitozantrone-d8dihydrochloride; NSC 301739-d8 dihydrochlorideMitoxantrone-d8 dihydrochloride is deuterated labeled Mitoxantrone dihydrochloride (HY-13502A). Mitoxantrone dihydrochloride is a potent topoisomerase II inhibitor. Mitoxantrone dihydrochloride also inhibits protein kinase C (PKC) activity with an IC50 of 8.5 μM. Mitoxantrone dihydrochloride induces apoptosis of B-CLL (B-chronic lymphocytic leukaemia) cells. Mitoxantrone dihydrochloride shows antitumor activity. Mitoxantrone dihydrochloride also has anti-orthopoxvirus activity with EC50s of 0.25 μM and and 0.8 μM for cowpox and monkeypox, respectively. -
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TX-1918
0 ImagesCat. No.: HY-112393CAS No.: 503473-32-3TX-1918 is an inhibitor for eukaryotic elongation factor 2 kinase (eEF2-K) and Src kinase with IC50 of 0.44 and 4.4 μM, respectively. TX-1918 exhibits cytotoxicity in cell HepG2 and HCT116, with IC50 of 2.07 and 230 μM, respectively. TX-1918 inhibits the C-terminal domain of HIV-1 CA (CA CTD)(IC50 =3.81 μM), and inhibits the viral replication (IC50 =15.16 μM). -
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FIM-1
0 ImagesCat. No.: HY-D1493CAS No.: 220518-50-3 -
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Lyso-monosialoganglioside GM2 ammonium
0 ImagesCat. No.: HY-172546Purity: 98%Synonyms: LysoGM2 ammoniumLyso-monosialoganglioside GM2 (LysoGM2) ammonium is a lysosphingolipid and protein kinase C inhibitor (IC50: 50 μM). Lyso-monosialoganglioside GM2 ammonium can inhibit the binding of protein kinase C to Phorbol 12,13-dibutyrate (HY-18985). Lyso-monosialoganglioside GM2 ammonium is a specific biomarker for GM2 gangliosidosis. Lyso-monosialoganglioside GM2 ammonium can be used in the research of sphingolipidoses. -
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- Protein Kinase C (19-31) TFA
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Sapintoxin A
0 ImagesCat. No.: HY-123487CAS No.: 79083-69-5Sapintoxin A is a phorbol ester that can be isolated from the unripe fruits of Sapium indicum. -
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- Z-Arg-SBzl TFA
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- Protein Kinase C (19-35) Peptide
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Hypocrellin A (Standard)
0 ImagesCat. No.: HY-N2575RCAS No.: 77029-83-5Hypocrellin A (Standard) is the analytical standard of Hypocrellin A. This product is intended for research and analytical applications. Hypocrellin A is a PKC inhibitor that exerts antidiabetic activity by reversing the effects of high glucose on endothelin (ET-1) expression. Hypocrellin A is also a photosensitizer for photodynamic therapy (PDT) with anticancer, antibacterial and antiviral activities, especially against human immunodeficiency virus (HIV). In addition, Hypocrellin-A also possesses anti-Leishmania activity (IC50=0.27 μg/ml)[1][2][3][4][5][6][7][8][9]. -
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- TAT-P4-(DATC5)2
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PF-04577806
0 ImagesCat. No.: HY-139467CAS No.: 1072100-81-2 -
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PKCδ Peptide Substrate
0 ImagesCat. No.: HY-P3818CAS No.: 813416-46-5PKCδ Peptide Substrate is a highly selective peptide substrate targeting PKCδ. PKCδ Peptide Substrate can only be efficiently catalyzed for phosphorylation modification by PKCδ, and Thr431 is the sole phosphorylation site. PKCδ Peptide Substrate binds to the catalytic pocket of PKC in a competitive manner, but exhibits no PKC agonistic or inhibitory activity. PKCδ Peptide Substrate is a dedicated biochemical probe for the quantitative detection of PKCδ in vitro, and can be used for studies on PKCδ-related pathways. -
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Kiss2 peptide
0 ImagesCat. No.: HY-P10256CAS No.: 1111070-93-9Kiss2 peptide is a positive regulator of reproduction. Kiss2 peptide binds with its cognate receptor Kiss2R (GPR54) in COS-7 cells, activates PKA and PKC signaling pathways through Gas and Gaq proteins, and thus enhances the activity of cAMP response element-dependent luciferase (CRE-luc) and serum response element-dependent luciferase (SRE-luc). -
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Aurothiomalate disodium
0 ImagesCat. No.: HY-W010270ACAS No.: 74916-57-7Aurothiomalate disodium acts as an inhibitor of PKCI and TrxR1. Aurothiomalate disodium disrupts the PKCI-Par6-Rac1 signaling pathway, and also inhibits TrxR1 activity, TNFα-induced NF-κB activation, and the expression of pro-inflammatory genes. Aurothiomalate disodium blocks Kras-mediated BASC expansion and lung tumor growth, inhibits anchorage-independent growth and tumorigenicity of lung cancer cells, and suppresses neutrophil chemotaxis, phagocytosis, and leukocyte extravasation. Aurothiomalate disodium can be used in research related to rheumatoid arthritis and non-small cell lung cancer. -
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aPKC-IN-1
0 ImagesCat. No.: HY-131220CAS No.: 15854-12-3aPKC-IN-1 (compound 1) is an atypical protein kinase C (aPKCζ) inhibitor. aPKC-IN-1 can be used for the study of a host of diseases involving increased vascular permeability and inflammation. -
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AS2521780
0 ImagesCat. No.: HY-12663CAS No.: 1214726-89-2AS2521780 is a novel PKCθ selective inhibitor with an IC50 of 0.48 nM. -
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- ZIP(Scrambled) TFA
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ICP-103
0 ImagesCat. No.: HY-175401CAS No.: 153997-72-9ICP-103 (Compound 3K) is a highly selective protein kinase C (PKC) inhibitor with an IC50 of 30 nM. ICP-103 is promising for research of cancers. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.