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Serine/threonin kinase

Serine/threonin kinase

Serine/threonine kinase inhibitors are compounds that target enzymes responsible for phosphorylating serine and threonine residues on proteins, which play a pivotal role in regulating apoptosis and other cellular processes. These kinases are involved in signaling pathways that control cell growth, division, and programmed cell death. Inhibiting specific serine/threonine kinases can alter the balance between cell survival and apoptosis, making these inhibitors essential tools in cancer research and other areas of cell biology. At CymitQuimica, we provide a comprehensive selection of high-quality serine/threonine kinase inhibitors to support your research in apoptosis, signal transduction, and disease mechanisms.

Found 23 products for "Serine/threonin kinase".

products per page.
  • CRA-2059

    CAS:
    CRA-2059 is a selective and reversible inhibitor of human tryptase beta, exhibiting a Ki value of 620 pM against recombinant human tryptase beta (rHTβ).
    Formula:C34H46N12O8
    Purity:97.68% - 99.29%
    Color and Shape:White Solid
    Molecular weight:750.82
  • MARK4 inhibitor 3


    MARK4 inhibitor 3 is a selective MARK4 inhibitor (IC₅₀=1.01 μM) that suppresses cancer cell proliferation for cancer and neurodegeneration studies.
    Formula:C33H27FN4O3
    Purity:99.47%
    Color and Shape:Solid
    Molecular weight:546.59
  • MASTL-IN-2

    CAS:
    MASTL-IN-2 is a MASTL kinase inhibitor. MASTL-IN-2 inhibits MIA PaCa pancreatic cancer cell proliferation with an IC50 of 2.8 nM.
    Formula:C21H25N7O2
    Color and Shape:Odour Solid
    Molecular weight:407.47
  • 1,8-Diazanaphthalene

    CAS:
    1,8-Diazanaphthalene inhibits Protein Kinase B with a binding constant Ka=407 μM.
    Formula:C8H6N2
    Color and Shape:Solid
    Molecular weight:130.1466
  • Tilpisertib

    CAS:
    Tilpisertib is a serine/threonine kinase inhibitor (WO2017007689).
    Formula:C33H33ClN8O
    Purity:99.88%
    Color and Shape:Solid
    Molecular weight:593.121
  • SGC-GAK-1

    CAS:
    SGC-GAK-1 is a selective cyclin G-associated kinase (GAK) inhibitor (Ki: 3.1 nM).
    Formula:C18H17BrN2O3
    Purity:99.85%
    Color and Shape:Yellow Solid
    Molecular weight:389.243
  • PKD-IN-1

    CAS:
    CRT0066101 is an inhibitor of PKD.
    Formula:C18H19ClN4O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:342.82
  • kb NB 142-70

    CAS:
    kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28.3, 58.7 and 53.2 nM for PKD1, 2 and 3 respectively).
    Formula:C11H9NO2S2
    Purity:98.01% - ≥95%
    Color and Shape:Solid
    Molecular weight:251.32
  • CID755673

    CAS:
    CID755673 inhibits PKD (IC50: 182 nM), with selectivity over PLK1, AKT, CAMKIIα, CAK, PKC.
    Formula:C12H11NO3
    Purity:97.68% - 99.84%
    Color and Shape:Solid
    Molecular weight:217.2206
  • MLCK inhibitor peptide 18 acetate


    MLCK inhibitor peptide 18 acetate: Selective (IC50=50nM), 4000x more than CaM kinase II. Does not block PKA. Cell-permeable.
    Formula:C62H109N23O13
    Purity:99.90%
    Color and Shape:Solid
    Molecular weight:1384.67
  • SRPIN340

    CAS:
    SRPIN340 (SRPK inhibitor), a serine/arginine-rich protein kinase (SRPK)-specific inhibitor, is potent for SRPK1 (IC50 = 0.89 uM).
    Formula:C18H18F3N3O
    Purity:99.79% - 99.96%
    Color and Shape:White Solid
    Molecular weight:349.35
  • CID 2011756

    CAS:
    CID 2011756 is an ATP-competitive and specific PKD1 inhibitor.
    Formula:C22H21ClN2O3
    Purity:98.15% - ≥95%
    Color and Shape:Solid
    Molecular weight:396.867
  • SPHINX31

    CAS:
    SPHINX31 is a potent inhibitor of serine/arginine-rich protein kinase 1 (SRPK1; IC50: 5.9 nM).
    Formula:C27H24F3N5O2
    Purity:99.3% - 99.87%
    Color and Shape:Solid
    Molecular weight:507.507
  • GAK inhibitor 49

    CAS:
    GAK inhibitor 49 is a highly selective and ATP-competitive cyclin G associated kinase (GAK) inhibitor (IC50: 56 nM; Ki: 0.54 nM ).
    Formula:C20H22N2O5
    Purity:98.71%
    Color and Shape:Solid
    Molecular weight:370.3991
  • 1-Naphthyl PP1

    CAS:
    1-Naphthyl PP1 (1-NA-PP 1) is a selective src inhibitor(v-Src and c-Fyn, c-Abl, CDK2 and CAMK II with IC50s of 1.0, 0.6, 0.6, 18 and 22 μM, respectively)
    Formula:C19H19N5
    Purity:99.85%
    Color and Shape:Solid
    Molecular weight:317.39
  • TLK1-IN-1


    TLK1-IN-1 (Compound 5n) is a TLK1 inhibitor with an IC50 of 7.2 μM for TLK1B and a GI50 of 2.7 μM for LNCaP cells. It induces DNA damage and apoptosis (Apoptosis) in cancer cells and is applicable in prostate cancer research.
    Formula:C24H23BrClN5O3
    Color and Shape:Solid
    Molecular weight:544.83
  • SRPKIN-1

    CAS:
    SRPKIN-1 is a covalent and irreversible inhibitor of SRPK1/2 (IC50s: 35.6 and 98 nM, respectively).
    Formula:C27H21FN2O3S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:472.531
  • Ofirnoflastum

    CAS:
    Ofirnoflastum (Ofirnoflast) is a selective serine/threonine-protein kinase Nek7 inhibitor that exerts potent anti-inflammatory effects by suppressing Nek7-dependent NLRP3 inflammasome activation, reducing caspase-1 cleavage, IL-1β and IL-18 secretion, and pyroptotic cell death in vitro, while significantly attenuating cytokine production and tissue injury in animal models of acute and chronic inflammation, supporting its therapeutic potential in autoimmune and inflammatory diseases.
    Formula:C23H19F4N7O2
    Purity:99.81% - 99.87%
    Color and Shape:Solid
    Molecular weight:501.44
  • MKI-3

    CAS:
    MKI-3 is a highly selective MASTL inhibitor with a quinazoline scaffold (IC50 5.72 nM), can inhibit ENSA phosphorylation and activate PP2A, and exhibits antiproliferative and in vivo antitumor activity in breast cancer models.
    Formula:C21H19N7O
    Purity:97.02%
    Molecular weight:385.42
  • 3-IN-PP1

    CAS:
    3-IN-PP1 is a potent inhibitor of PKD1, PKD2, and PKD3 (IC50 = 108, 94, and 108 nM, respectively), acting as a broad-spectrum anticancer agent.
    Formula:C17H18N6
    Color and Shape:Solid
    Molecular weight:306.365