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Apoptose

Apoptose

Os inibidores da apoptose são compostos que previnem ou retardam o processo de morte celular programada, conhecido como apoptose. Esses inibidores são vitais no estudo dos mecanismos de sobrevivência celular e são usados para investigar doenças onde a apoptose é desregulada, como câncer, distúrbios neurodegenerativos e doenças autoimunes. Ao modular a apoptose, esses inibidores podem ajudar no desenvolvimento de terapias destinadas a controlar a morte celular. Na CymitQuimica, oferecemos uma ampla seleção de inibidores da apoptose de alta qualidade para apoiar sua pesquisa em biologia celular, oncologia e áreas relacionadas.

Subcategorias de "Apoptose"

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Foram encontrados 6114 produtos de "Apoptose"

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  • RIP3 activator 1

    CAS:
    RIP3 Activator 1 (compound C8) is an effective RIP3 activator that inhibits cell growth and induces necroptotic cell death (necroptosis) and autophagy through the RIP3/p62/Keap1 signaling pathway. Additionally, this compound enhances the expression of p-MLKL and promotes the accumulation of LC3-II and p62 proteins.
    Fórmula:C26H50N4O3
    Cor e Forma:Solid
    Peso molecular:466.7

    Ref: TM-T201677

    10mg
    A consultar
    50mg
    A consultar
  • Neral

    CAS:
    Neral, a monoterpenoid compound, exhibits anti-inflammatory and anticancer activities. It inhibits TNF-α and IL-6, along with inflammatory mediators such as pro-IL-1β, iNOS, COX-2, and NLRP-3.
    Fórmula:C10H16O
    Cor e Forma:Solid
    Peso molecular:152.23

    Ref: TM-T201808

    10mg
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    50mg
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  • CRI9


    CRI9 effectively inhibits the c-MET/PI3K/Akt/mTOR axis, suppressing the proliferation of hepatocellular carcinoma (HCC) cells. This compound exhibits potent cytotoxicity against HCC cells and induces apoptosis.
    Fórmula:C26H18N6O4
    Cor e Forma:Solid
    Peso molecular:478.46

    Ref: TM-T201493

    10mg
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    50mg
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  • Hdm2 E3 ligase inhibitor 1

    CAS:
    Hdm2 E3ligaseinhibitor 1 (Compound 1) is a reversible inhibitor of Hdm2-mediated p53 protein ubiquitination, with an IC50 of 12.7 μM. It binds to Hdm2, blocking the transfer of ubiquitin catalyzed by Hdm2 from pre-linked Ub-Ubc4 to p53, thereby inhibiting p53 ubiquitination, stabilizing p53 protein in tumor cells, and exerting antitumor activity.
    Fórmula:C10H8F6N2O3S
    Peso molecular:350.24

    Ref: TM-T210014

    10mg
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    50mg
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  • Anticancer agent 44


    Anticancer agent 44 induces apoptosis, is selective, cytotoxic to cancer cells, and minimally toxic to human lymphocytes.
    Fórmula:C22H13Cl2N3O5S2
    Cor e Forma:Solid
    Peso molecular:534.39

    Ref: TM-T63759

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • Anticancer agent 17


    Anticancer agent 17 was effective against HeLa cells (IC50: 0.19 μM) and A2780 cells (IC50: 0.09 μM).
    Fórmula:C27H34BrN3O
    Cor e Forma:Solid
    Peso molecular:496.48

    Ref: TM-T63354

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • Minnelide free acid

    CAS:
    Minnelide treats pancreatic cancer, hinders androgen-related prostate growth, shrinks tumors, and improves survival.
    Fórmula:C21H27O10P
    Cor e Forma:Solid
    Peso molecular:470.41

    Ref: TM-T71113

    25mg
    2.988,00€
    50mg
    3.943,00€
    100mg
    5.490,00€
  • Kahweol Acetate

    CAS:
    Kahweol Acetate, a semi-synthetic coffee bean derivative, inhibits osteoclasts, cancer cells, DNA damage, and oxidative stress.
    Fórmula:C22H28O4
    Cor e Forma:Solid
    Peso molecular:356.46

    Ref: TM-T68641

    25mg
    4.204,00€
    50mg
    5.563,00€
    100mg
    7.920,00€
  • BRD1991

    CAS:
    BRD1991 is a chemical compound that specifically disrupts the interaction between Beclin 1 and Bcl-2, thereby inducing autophagy.
    Fórmula:C33H35Cl2N3O4
    Cor e Forma:Solid
    Peso molecular:608.55

    Ref: TM-T69752

    25mg
    2.442,00€
    50mg
    3.212,00€
    100mg
    4.370,00€
  • ASCT2-IN-1

    CAS:
    ASCT2-IN-1 (compound 20k) is an inhibitor of ASCT2, demonstrating IC50 values of 5.6 μM in A549 cells and 3.5 μM in HEK293 cells. It induces apoptosis and inhibits tumor growth.
    Fórmula:C36H32Cl2N2O4
    Peso molecular:627.56

    Ref: TM-T209188

    10mg
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    50mg
    A consultar
  • HDAC6/HSP90-IN-2


    HDAC6/HSP90-IN-2, a cancer research chemical, inhibits HDAC6 & Hsp90 with IC50s of 105.7 & 61 nM.
    Fórmula:C19H22N2O5
    Cor e Forma:Solid
    Peso molecular:358.39

    Ref: TM-T61315

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • UR-AK49

    CAS:
    UR-AK49 (compound 11) is an agonist for the human histamine H1 and H2 receptors. It exhibits an EC50 of 23 nM in the GTPase assay involving hH2R-Gsalpha fusion protein expressed in Sf9 insect cells. UR-AK49 is applicable in neurologically related research.
    Fórmula:C16H27N5O
    Cor e Forma:Solid
    Peso molecular:305.42

    Ref: TM-T201412

    10mg
    A consultar
    50mg
    A consultar
  • Apoptosis inducer 42

    CAS:
    Apoptosis inducer42 is an apoptosis inducer that triggers late-stage apoptosis and inhibits the secretion of IL-6. It exhibits high cytotoxicity toward cancer cells and is applicable in cancer research, including studies on colon cancer.
    Fórmula:C11H13OPS
    Cor e Forma:Solid
    Peso molecular:224.26

    Ref: TM-T212363

    10mg
    A consultar
    50mg
    A consultar
  • CDK4/6-IN-10


    CDK4/6-IN-10: Oral CDK4 (IC50: 22 nM) & CDK6 (IC50: 10 nM) inhibitor with anti-cancer potential for MM research.
    Cor e Forma:Solid

    Ref: TM-T64244

    25mg
    1.444,00€
    50mg
    1.882,00€
    100mg
    2.375,00€
  • PD-1/PD-L1-IN-30

    CAS:
    PD-1/PD-L1-IN-30: Cancer research inhibitor with 0.018 μM IC50.
    Fórmula:C29H28F3NO5
    Cor e Forma:Solid
    Peso molecular:527.53

    Ref: TM-T72724

    25mg
    2.097,00€
    50mg
    2.935,00€
    100mg
    4.085,00€
  • LLW-018

    CAS:
    LLW-018 is a potent PD-1/PD-L1 inhibitor with an IC50 value of 2.61 nM. It can disrupt the PD-1/PD-L1 interaction, with a cell-based PD-1/PD-L1 blocking bioassay IC50 value of 0.88 μM. LLW-018 holds potential for research in immune-related diseases.
    Fórmula:C35H38Cl2N4O5S
    Peso molecular:697.67

    Ref: TM-T210223

    10mg
    A consultar
    50mg
    A consultar
  • Zharp1-211

    CAS:
    Zharp1-211 is a RIPK3 inhibitor,reduces JAK/ stat1-mediated chemokines and MHC class II molecules in IECs, (GVHD) for gastrointestinal inflammation.
    Fórmula:C24H25N5O4
    Pureza:99.71%
    Cor e Forma:Solid
    Peso molecular:447.49

    Ref: TM-T87664

    1mg
    87,00€
    5mg
    183,00€
    10mg
    283,00€
    25mg
    562,00€
    50mg
    873,00€
    100mg
    1.311,00€
    200mg
    1.768,00€
    1mL*10mM (DMSO)
    202,00€
  • Zotatifin

    CAS:
    Zotatifin (eFT226) is a selective eIF4A inhibitor with antiviral and antitumor properties, inhibiting Sox4 translation and inducing apoptosis.
    Fórmula:C28H29N3O5
    Pureza:98.85%
    Cor e Forma:Solid
    Peso molecular:487.55

    Ref: TM-T17296

    1mg
    1.035,00€
    5mg
    2.992,00€
    10mg
    4.684,00€
    25mg
    7.115,00€
  • Darizmetinib

    CAS:
    Darizmetinib (HRX215) is an MKK4 inhibitor.
    Fórmula:C21H17F2N5O3S
    Pureza:98.03% - 99.57%
    Cor e Forma:Solid
    Peso molecular:457.45

    Ref: TM-T72956

    1mg
    69,00€
    2mg
    89,00€
    5mg
    147,00€
    10mg
    224,00€
    25mg
    324,00€
    50mg
    400,00€
    100mg
    587,00€
    1mL*10mM (DMSO)
    148,00€
  • Milademetan

    CAS:
    Milademetan (DS-3032), an MDM2 inhibitor, exhibits antitumor activity, induces G1 cell cycle arrest and apoptosis, and can be used to study solid tumors.
    Fórmula:C30H34Cl2FN5O4
    Pureza:>99.99%
    Cor e Forma:Solid
    Peso molecular:618.53

    Ref: TM-T12040

    1mg
    87,00€
    5mg
    170,00€
    10mg
    274,00€
    25mg
    518,00€
    50mg
    847,00€
    100mg
    1.454,00€
    1mL*10mM (DMSO)
    234,00€