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Apoptosis

Apoptosis

Apoptosis inhibitors are compounds that prevent or delay the process of programmed cell death, known as apoptosis. These inhibitors are vital in studying cell survival mechanisms and are used to investigate diseases where apoptosis is dysregulated, such as cancer, neurodegenerative disorders, and autoimmune diseases. By modulating apoptosis, these inhibitors can help in the development of therapies aimed at controlling cell death. At CymitQuimica, we provide a comprehensive selection of high-quality apoptosis inhibitors to support your research in cell biology, oncology, and related fields.

Subcategories of "Apoptosis"

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Found 6063 products of "Apoptosis"

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  • VEGFR-2-IN-19
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    VEGFR-2-IN-19

    CAS:
    VEGFR-2-IN-19 (15b) effectively inhibits VEGFR2, induces apoptosis, and increases oxidative stress, showing potential as an anticancer drug.
    Formula:C21H19N3O2
    Color and Shape:Solid
    Molecular weight:345.39

    Ref: TM-T61137

  • Filanesib
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    Filanesib

    CAS:
    <p>Filanesib (ARRY 520) is a selective inhibitor of kinesin spindle protein (KSP, IC50 = 6 nM) with potent anti-proliferative activity.</p>
    Formula:C20H22F2N4O2S
    Purity:99.8%
    Color and Shape:Solid
    Molecular weight:420.48

    Ref: TM-TQ0318

  • Anticancer agent 57
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    Anticancer agent 57

    CAS:
    Anticancer agent 57 blocks TNBC cell growth with IC50: 6.43-8 μM, induces apoptosis, and shrinks tumors in mice.
    Formula:C20H21Cl2NO2
    Color and Shape:Solid
    Molecular weight:378.29

    Ref: TM-T61582

  • BPTQ
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    BPTQ

    CAS:
    BPTQ: DNA intercalator, halts cancer cell growth by blocking S/G2/M phases.
    Formula:C17H16N4S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:308.4

    Ref: TM-T23817

  • SMI-6860766
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    SMI-6860766

    CAS:
    SMI-6860766 is a CD40-Traf6 interactions blocker that acts by ameliorating the complications of diet-induced obesity in mice.
    Formula:C15H11BrClNO
    Purity:98%
    Color and Shape:Solid
    Molecular weight:336.61

    Ref: TM-T24808

  • Merck-22-6
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    Merck-22-6

    CAS:
    Merck-22-6 is an allosteric dual inhibitor of Akt1, Akt2.
    Formula:C40H43N7O2
    Color and Shape:Solid
    Molecular weight:653.82

    Ref: TM-T25791

  • HS56
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    HS56

    CAS:
    HS56: ATP-competitive Pim/DAPK3 inhibitor, Ki: DAPK3 (0.26μM), Pim-3 (0.208μM), Pim-1 (2.94μM), Pim-2 (>100μM), reduces hypertension in mice.
    Formula:C13H8ClN5OS
    Color and Shape:Solid
    Molecular weight:317.75

    Ref: TM-T68341

  • Antitumor agent-70
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    Antitumor agent-70

    CAS:
    Antitumor agent-70, a potent c-Kit kinase inhibitor, induces apoptosis with an IC50 of 0.12 μM, showing promise as a cancer therapy.
    Formula:C21H18N4O2
    Color and Shape:Solid
    Molecular weight:358.39

    Ref: TM-T61313

  • Nimustine
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    Nimustine

    CAS:
    Nimustine: treats brain tumors, used with other drugs or radiotherapy for neoplasms.
    Formula:C9H13ClN6O2
    Color and Shape:Solid
    Molecular weight:272.69

    Ref: TM-T21310

  • OT-82
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    OT-82

    CAS:
    OT-82 is a NAMPT inhibitor with anticancer activity and cytotoxicity and is used in the study of leukemias.
    Formula:C26H21FN4O
    Purity:98.91% - 99.315%
    Color and Shape:Solid
    Molecular weight:424.47

    Ref: TM-T12330

  • IV-23
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    IV-23

    CAS:
    IV-23 hinders cell growth, blocks M phase, induces apoptosis, and shows promise as an anticancer agent.
    Formula:C18H18BrNO4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:392.24

    Ref: TM-T11691

  • BMS-200
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    BMS-200

    CAS:
    BMS-200 is a potent PD-1/PD-L1 interaction inhibitor with IC50 of 80 nM.
    Formula:C27H27F2NO6
    Color and Shape:Solid
    Molecular weight:499.5

    Ref: TM-T70285

  • BMS-1166 hydrochloride
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    BMS-1166 hydrochloride

    CAS:
    "Motixafortide blocks CXCR4 with 1 nM potency. BMS-1166 hinders PD-1/PD-L1, boosting T cell activation, IC50: 1.4 nM."
    Formula:C36H34Cl2N2O7
    Purity:98%
    Color and Shape:Solid
    Molecular weight:677.57

    Ref: TM-T14670

  • 3-ATA
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    3-ATA

    CAS:
    <p>3-ATA is a selective cyclin-dependent kinase 4 (Cdk4) inhibitor, attenuating kainic acid-induced apoptosis in neurons.</p>
    Formula:C13H10N2S
    Color and Shape:Solid
    Molecular weight:226.3

    Ref: TM-T71030

  • HDAC-IN-39
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    HDAC-IN-39

    CAS:
    <p>HDAC-IN-39 inhibits HDAC1-3 (IC50: 1.07-2.27 μM), arrests G2/M phase, hinders microtubule polymerization, and is effective against drug-resistant cancers.</p>
    Formula:C27H26N4O4S
    Color and Shape:Solid
    Molecular weight:502.58

    Ref: TM-T63416

  • Flupenthixol
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    Flupenthixol

    CAS:
    Flupentixol is a typical antipsychotic drug of the thioxanthene class. Flupentixol is also used in low doses as an antidepressant.
    Formula:C23H25F3N2OS
    Purity:98%
    Color and Shape:Solid
    Molecular weight:434.52

    Ref: TM-T21401

  • FL3
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    FL3

    CAS:
    FL3 is a novel potent eIF4F inhibitor, it induces the death of cancer cells by an original mechanism that involves the apoptosis-inducing factor and caspase 12.
    Formula:C25H23BrO5
    Color and Shape:Solid
    Molecular weight:483.35

    Ref: TM-T27330

  • Norartocarpetin
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    Norartocarpetin

    CAS:
    Norartocarpetin inhibits tyrosinase (IC50 0.47μM), prevents browning in food, and fights lung cancer (IC50 22μM) by disrupting cell mechanisms.
    Formula:C15H10O6
    Color and Shape:Solid
    Molecular weight:286.24

    Ref: TM-T72803

  • RETRA
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    RETRA

    CAS:
    RETRA is an agent of anticancer that acts by exerting anticancer activity in Ewing's sarcoma cells independent of their TP53 status.
    Formula:C11H12BrNO3S2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:350.25

    Ref: TM-T24709

  • hGGPPS-IN-2
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    hGGPPS-IN-2

    CAS:
    hGGPPS-IN-2, a C2-ThP-BP analogue, inhibits hGGPPS, targets MM cells, induces apoptosis, and has anti-myeloma effects.
    Formula:C20H18FN5O7P2S
    Color and Shape:Solid
    Molecular weight:553.4

    Ref: TM-T63906