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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 6041 products of "Apoptosis"

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  • TV 3279

    CAS:

    TV 3279 is a ChE-MAI inhibitor with neuroprotection via anti-apoptotic protein induction and blocks pro-apoptotic enzymes in cells.

    Formula:C16H20N2O2
    Purity:97%
    Color and Shape:Soild
    Molecular weight:272.34

    Ref: TM-T77332

    1mg
    89.00€
    5mg
    173.00€
    10mg
    259.00€
    25mg
    393.00€
    50mg
    562.00€
    100mg
    778.00€
    200mg
    1,035.00€
  • Antitumor photosensitizer-3


    Antitumor Photosensitizer-3 (Compound I), a chlorin derivative, effectively induces apoptosis and necrosis in tumor cells upon exposure to 650 nm laser
    Formula:C48H34N4O4
    Color and Shape:Solid
    Molecular weight:730.81

    Ref: TM-T74601

    5mg
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    50mg
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  • N-Stearoyltyrosine

    CAS:
    N-Stearoyltyrosine (N-(1-Oxooctadecyl)-L-tyrosine) is an analog of Anandamide. It exhibits neuroprotective effects by safeguarding the CA1 region of the hippocampus in a gerbil ischemia-reperfusion model. Additionally, N-Stearoyltyrosine inhibits free radical generation, enhances antioxidant capacity, and reduces IR-induced apoptosis (cell apoptosis).
    Formula:C27H45NO4
    Color and Shape:Solid
    Molecular weight:447.65

    Ref: TM-T203491

    10mg
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    50mg
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  • c-JUN peptide

    CAS:

    Peptide from c-Jun (33-57) blocks JNK binding, inhibits phosphorylation, upregulates p21, and induces HeLa cell apoptosis.

    Formula:C121H210N36O34S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:2743.55

    Ref: TM-TP2134

    1mg
    1,008.00€
  • Antitumor agent-36


    Antitumor agent-36: potent anti-cancer; causes DNA damage, triggers apoptosis, enhances immune response by upregulating T cells.
    Formula:C32H30Cl2N2O6Pt
    Color and Shape:Solid
    Molecular weight:804.58

    Ref: TM-T74393

    5mg
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    50mg
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  • Bursehernin

    CAS:
    Bursehernin is a useful organic compound for research related to life sciences and the catalog number is T124894.
    Formula:C21H22O6
    Color and Shape:Solid
    Molecular weight:370.401

    Ref: TM-T124894

    1mg
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    5mg
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  • (Rac)-AMXT-1501 4HCl

    CAS:
    AMXT-1501 tetrahydrochloride is an inhibitor of polyamine transport.
    Formula:C32H72Cl4N6O2
    Purity:98.31%
    Color and Shape:Solid
    Molecular weight:714.77

    Ref: TM-T10313

    1mg
    170.00€
    2mg
    243.00€
    5mg
    410.00€
    10mg
    627.00€
    25mg
    1,378.00€
    50mg
    2,125.00€
  • Asparanin A

    CAS:
    Asparanin A, an apoptosis inducer with anticancer properties, arrests the cell cycle in the G0/G1 phase via the mitochondria and PI3K/AKT signaling pathways.
    Formula:C39H64O13
    Purity:98%
    Color and Shape:Solid
    Molecular weight:740.92

    Ref: TM-T79971

    5mg
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    50mg
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  • Caerin 1.1 TFA


    Caerin 1.1 TFA, a host defense peptide derived from the Australian tree frog Litoria's glandular secretions, exhibits anti-proliferative effects on HeLa cells
    Purity:98%
    Color and Shape:Odour Solid

    Ref: TM-T82793

    5mg
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    50mg
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  • Ara-SH


    Ara-SH, a derivative of Cytarabine with a mercaptopropionic acid substitution, serves as the initiator for the self-assembly of a smart, co-loaded Cytarabine
    Formula:C12H17N3O6S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:331.34

    Ref: TM-T79224

    5mg
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    50mg
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  • 2'-epi-2'-O-Acetylthevetin B

    CAS:
    2'-Epi-2'-O-Acetylthevetin B (GHSC-74), a cardiac glycoside extractable from Cerbera manghas L.
    Formula:C44H68O19
    Purity:98%
    Color and Shape:Solid
    Molecular weight:901

    Ref: TM-T79982

    5mg
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    50mg
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  • PDL1 degrader-2


    PD-L1degrader-2 (Compound B3) is an orally effective AUTAC degrader that degrades PD-L1 via the autophagy-lysosome pathway with a DC50 of 0.5 μM. It inhibits the interaction between PD-1 and PD-L1, with an IC50 of 22.8 nM. PD-L1degrader-2 upregulates the expression of Atg9b, Lamp1, and Mitf, activating the autophagy-lysosome system. It exhibits antitumor activity in the CT26 mouse model.
    Formula:C45H48N8O5
    Color and Shape:Solid
    Molecular weight:780.91

    Ref: TM-T201649

    10mg
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    50mg
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  • CDK-IN-14


    CDK-IN-14 (B34) is a CDK2 inhibitor (IC50=0.097 μM) that exhibits anti-hepatocellular carcinoma activity. It inhibits the cell cycle in HepG-2 cancer cells and induces apoptosis (apoptosis) through a caspase-mediated mechanism.
    Color and Shape:Odour Solid

    Ref: TM-T200436

    10mg
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    50mg
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  • Estradiol (cypionate)

    CAS:
    Estradiol cypionate (Depofemin), the 17 β-cyclopentylpropinate ester of estradiol, inhibits ET-1 synthesis via estrogen receptor.
    Formula:C26H36O3
    Purity:99.53% - >99.99%
    Color and Shape:White Or Off-White Crystalline Powder
    Molecular weight:396.56

    Ref: TM-T0168

    1g
    87.00€
    200mg
    37.00€
    500mg
    50.00€
    1mL*10mM (DMSO)
    56.00€
  • DL-Sulforaphane N-acetyl-L-cysteine

    CAS:
    DL-Sulforaphane N-acetyl-L-cysteine (SFN-NAC), induces apoptosis through α-microtubulin and phosphorylation of ERK1/2-mediated Stathmin-1, and Hsp70 (NSCLC).
    Formula:C11H20N2O4S3
    Purity:99%
    Color and Shape:Solid
    Molecular weight:340.48

    Ref: TM-T36614

    1mg
    194.00€
  • NLRP3-IN-60


    NLRP3-IN-60 (Compound 39) is an orally bioavailable inhibitor of NLRP3. It effectively suppresses pyroptosis in THP-1 cells with an IC50 of 13 nM and inhibits IL-1β release in human whole blood, exhibiting an IC50 of 225 nM.

    Formula:C23H24F2N4O4S
    Color and Shape:Solid
    Molecular weight:490.523

    Ref: TM-T204143

    10mg
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    50mg
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  • XIAP BIR2/BIR2-3 inhibitor-3

    CAS:
    XIAP BIR2/BIR2-3 Inhibitor-3 functions as a dual inhibitor targeting both BIR2 and BIR2-3 domains, exhibiting potent activity with IC50 values below 1 nM. This compound is utilized in cancer research [1].
    Formula:C86H106N18O16S2
    Color and Shape:Solid
    Molecular weight:1712

    Ref: TM-T87642

    10mg
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    50mg
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  • RD-23

    CAS:
    RD-23 is an orally active and selective RET PROTAC degrader. It facilitates the ubiquitination and degradation of the RETG810C mutant with a DC50 value of 11.7 nM. Additionally, RD-23 inhibits the activation of downstream Shc signaling and induces apoptosis (Apoptosis). It is useful for studying RET-related cancers.
    Formula:C52H56N12O4
    Color and Shape:Solid
    Molecular weight:913.079

    Ref: TM-T204442

    10mg
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    50mg
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  • Anticancer agent 132


    Compound Rh1 (Anticancer agent 132) acts as an inducer of apoptosis and autophagy, exhibiting both antitumor and antimetastatic activities.
    Formula:C24H16Cl3F3N5ORh
    Purity:98%
    Color and Shape:Solid
    Molecular weight:656.68

    Ref: TM-T78742

    5mg
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    50mg
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  • HPCR

    CAS:
    HPCR exhibits antiproliferative activity against various cancer cells and is involved in apoptosis (apoptosis).
    Formula:C52H40O12
    Color and Shape:Solid
    Molecular weight:856.867

    Ref: TM-T204176

    10mg
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    50mg
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