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PI3K

PI3K

PI3K inhibitors are compounds that block the activity of Phosphoinositide 3-Kinases (PI3Ks), a family of enzymes involved in a wide range of cellular processes, including growth, proliferation, survival, and metabolism. The PI3K/Akt/mTOR pathway is often dysregulated in cancer, making PI3K a key target for cancer therapy. PI3K inhibitors are critical tools for studying signal transduction, cancer biology, and the development of targeted therapies. At CymitQuimica, we provide a variety of PI3K inhibitors to support your research in cell signaling, oncology, and therapeutic development.

Found 238 products for "PI3K".

products per page.
  • IHMT-PI3K-315


    IHMT-PI3K-315 (20e) serves as a potent, selective inhibitor of PI3Kγ/δ, exhibiting IC 50 values of 4.0 nM for PI3Kγ and 9.1 nM for PI3Kδ. Additionally, it demonstrates antitumor activity.
    Formula:C22H20F2N6O4
    Color and Shape:Solid
    Molecular weight:470.43

    Ref: TM-T200165

    10mg
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    50mg
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  • GSK251

    CAS:
    GSK251 is a novel, orally bioavailable inhibitor of PI3Kδ, exhibiting high potency and selectivity, with a unique binding mode.
    Formula:C29H37FN6O4S
    Purity:99.8%
    Color and Shape:White Solid
    Molecular weight:584.71

    Ref: TM-T39573

    10mg
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    25mg
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    1mg
    155.00€
    5mg
    375.00€
  • D-106669

    CAS:
    D-106669 (comppun 150) is a potent inhibitor of PI3Kα, with an IC50 value of 0.129 μM, and plays a significant role in cancer research.
    Formula:C17H18N6O
    Color and Shape:Solid
    Molecular weight:322.36

    Ref: TM-T203326

    10mg
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    50mg
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  • IHMT-PI3Kδ-372 S-isomer

    CAS:
    IHMT-PI3Kδ-372 S-isomer is a potent and selective PI3Kδ inhibitor with an IC50 of 14 nM.
    Formula:C26H23F2N7O2
    Purity:99.97%
    Color and Shape:White Solid
    Molecular weight:503.5

    Ref: TM-T60196

    1mg
    109.00€
    2mg
    163.00€
    5mg
    241.00€
    1mL*10mM (DMSO)
    294.00€
    10mg
    354.00€
    25mg
    532.00€
    50mg
    745.00€
    100mg
    1,018.00€
  • PI3Kδ-IN-22


    PI3Kδ-IN-22 (Compound 26) is a selective inhibitor of PI3Kδ with a pKi value of 9.3. It effectively inhibits the PI3Kδ-AKT signaling pathway in THP-1 cells, demonstrating a pIC50 of 9.4. Additionally, PI3Kδ-IN-22 exhibits favorable pharmacokinetic properties in rats.
    Formula:C27H35FN8O4S
    Molecular weight:586.2486

    Ref: TM-T210218

    10mg
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    50mg
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  • 740 Y-P acetate


    740 Y-P acetate (740YPDGFR acetate) is a potent and cell-permeable PI3K activator.740 Y-P acetate tends to bind to GST fusion proteins containing the N- and C-
    Formula:C143H226N43O41PS3
    Purity:99.92%
    Color and Shape:Soild
    Molecular weight:3330.79

    Ref: TM-TQ0003L1

    1mg
    93.00€
    2mg
    130.00€
    5mg
    239.00€
    10mg
    354.00€
    25mg
    592.00€
    50mg
    843.00€
  • (3S)-GSK-F1

    CAS:
    (3S)-GSK-F1 is a selective small molecule inhibitor of Type III Phosphatidylinositol 4‑Kinase Alpha (PI4KIIIα), pIC50=8.3.
    Formula:C27H18F5N5O4S
    Purity:99.04%
    Color and Shape:Solid
    Molecular weight:603.52

    Ref: TM-T67837

    100mg
    To inquire
    1mg
    70.00€
    5mg
    133.00€
    1mL*10mM (DMSO)
    182.00€
    10mg
    210.00€
    25mg
    371.00€
    50mg
    532.00€
  • PROTAC PI3K/110β degrader-1

    CAS:
    PROTACPI3K/110β degrader-1 (J-9) acts as a PROTAC degrader specifically targeting PI3K/110β.
    Formula:C51H65N9O9S
    Color and Shape:Solid
    Molecular weight:980.18

    Ref: TM-T207401

    10mg
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    50mg
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  • ARUK2001607

    CAS:
    ARUK2001607 selectively inhibits PI5P4Kγ (Kd=7.1 nM) with high selectivity over 150+ kinases.
    Formula:C14H13N3O2S2
    Purity:99.75%
    Color and Shape:Solid
    Molecular weight:319.40

    Ref: TM-T67845

    10mg
    34.00€
    1mL*10mM (DMSO)
    34.00€
    25mg
    49.00€
    50mg
    71.00€
  • VVD-699

    CAS:
    VVD-699 is a covalent inhibitor of RAS-PI3K. It forms a covalent bond with cysteine at position 242 within the RAS-binding domain of PI3Kp110α, thereby obstructing the ability of RAS to activate PI3K. VVD-699 is capable of inhibiting the growth of tumors with RAS mutations and HER2 overexpression. It is applicable in research related to RAS mutation-associated cancers, such as those involving H358 lung cancer cells, A549 cells, and FaDu cells.
    Formula:C25H30ClFN2O6S2
    Color and Shape:Solid
    Molecular weight:573.097

    Ref: TM-T206721

    10mg
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    50mg
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  • PI3K-IN-57


    PI3K-IN-57 (Compound 4a) is a PI3K inhibitor that shows strong inhibitory effects on the proliferation of HeLa tumor ectopic xenografts in vivo. It holds promise for anticancer agent research.
    Color and Shape:Odour Solid

    Ref: TM-T206765

    10mg
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    50mg
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  • FDA-Approved Kinase Inhibitor Library


    A unique collection of xnum kinase inhibitors/regulators for specific targeting of kinases, ready for high-throughput screening and high-content screening.
    Color and Shape:Liquid

    Ref: TM-L1610

    1mg
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    10μL*10mM (DMSO)
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    30μL*10mM (DMSO)
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    50μL*10mM (DMSO)
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    100μL*10mM (DMSO)
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  • Kinase Inhibitor Library


    A unique collection of xnum kinase inhibitors/regulators for high throughput screening and high content screening for drug discovery in kinase related diseases;
    Color and Shape:Odour Solid

    Ref: TM-L1600

    1mg
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    10μL*10mM (DMSO)
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    30μL*10mM (DMSO)
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    50μL*10mM (DMSO)
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    100μL*10mM (DMSO)
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  • PI3K-AKT-mTOR Compound Library


    A unique collection of xnum compounds targeting PI3K/Akt/mTOR signaling for research in PI3K/Akt/mTOR signaling, and drug discovery in diseases involved with PI3K/Akt/mTOR signaling;
    Color and Shape:Odour Solid

    Ref: TM-L1300

    1mg
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    10μL*10mM (DMSO)
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    20μL*10mM (DMSO)
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    30μL*10mM (DMSO)
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    50μL*10mM (DMSO)
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    100μL*10mM (DMSO)
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    250μL*10mM (DMSO)
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  • Umbralisib R-enantiomer

    CAS:
    Umbralisib R-enantiomer (RP5264 R-enantiomer) is a delta inhibitor of PI3K and a less active enantiomer of TGR-1202.
    Formula:C31H24F3N5O3
    Purity:97.34%
    Color and Shape:Solid
    Molecular weight:571.55

    Ref: TM-T13140

    1mg
    177.00€
    5mg
    432.00€
    1mL*10mM (DMSO)
    532.00€
    10mg
    620.00€
    25mg
    1,108.00€
    50mg
    1,431.00€
    100mg
    1,783.00€
  • BAY1082439

    CAS:
    BAY1082439, an orally bioavailable, selective inhibitor of PI3Kα/β/δ, demonstrates high efficacy in inhibiting the growth of Pten-null prostate cancer [1][2].
    Formula:C25H30N6O5
    Purity:98%
    Color and Shape:White Solid
    Molecular weight:494.54

    Ref: TM-T14511

    1mg
    34.00€
    2mg
    49.00€
    5mg
    74.00€
    10mg
    113.00€
    25mg
    178.00€
    50mg
    333.00€
    100mg
    495.00€
  • PI3Kα-IN-25


    PI3Kα-IN-25 (Compound Djh1) is a selective inhibitor of PI3Kα, suitable for research in triple-negative breast cancer.
    Formula:C21H19ClN4O4
    Color and Shape:Solid
    Molecular weight:426.853

    Ref: TM-T205675

    25mg
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    50mg
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    100mg
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  • Penetratin-PI3Kγ(126-150)


    Penetratin-PI3Kγ(126-150) is a peptide inhibitor of PI3Kγ that plays a significant role in respiratory diseases.
    Formula:C229H362N76O57S
    Color and Shape:Solid
    Molecular weight:5120.74849

    Ref: TM-TP3313

    10mg
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    50mg
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  • GSK2292767 FA


    GSK2292767 FA: potent PI3Kδ inhibitor, pIC50=10.1, 500x selectivity, for respiratory research.
    Formula:C25H30N6O7S
    Purity:99.52%
    Color and Shape:Solid
    Molecular weight:558.61

    Ref: TM-T6850L

    50mg
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    25mg
    2,610.00€
  • PI3Kδ-IN-12


    PI3Kδ-IN-12 (compound 13), a PI3Kδ inhibitor with a pIC50 of 5.8, exhibits differential binding affinities with pKi values of 8.0 for PI3Kδ, 6.5 for PI3Kγ, 6.4
    Formula:C20H15Cl2N5O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:444.27

    Ref: TM-T78691

    5mg
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    50mg
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