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Apoptosis

Apoptosis

Los inhibidores de la apoptosis son compuestos que previenen o retrasan el proceso de muerte celular programada, conocido como apoptosis. Estos inhibidores son vitales para estudiar los mecanismos de supervivencia celular y se utilizan para investigar enfermedades donde la apoptosis está desregulada, como el cáncer, los trastornos neurodegenerativos y las enfermedades autoinmunes. Al modular la apoptosis, estos inhibidores pueden ayudar en el desarrollo de terapias dirigidas a controlar la muerte celular. En CymitQuimica, ofrecemos una amplia selección de inhibidores de la apoptosis de alta calidad para apoyar su investigación en biología celular, oncología y campos relacionados.

Subcategorías de "Apoptosis"

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Se han encontrado 5903 productos de "Apoptosis"

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  • RTX-002


    RTX-002 is a human monoclonal antibody (mAb) targeting PDCD1/PD-1/CD279. This compound is applicable in the research of autoimmune diseases such as systemic lupus erythematosus and multiple sclerosis.
    Forma y color:Odour Liquid
  • AZD5582 dihydrochloride

    CAS:
    <p>Dimeric Smac mimetic inhibits XIAP, cIAP1/2 (IC50: 15/15/21 nM); binds BIR3 domain; degrades cIAPs; induces apoptosis in cancer cells; shrinks tumors in mice.</p>
    Fórmula:C58H80Cl2N8O8
    Forma y color:Solid
    Peso molecular:1088.23
  • OPBP-1


    <p>OPBP-1 is a D-peptide developed through phage display screening, molecular docking, and molecular dynamics simulations. It exhibits high stability, strong antitumor activity, and oral bioavailability. OPBP-1 selectively binds to the PD-L1 protein, significantly blocking the interaction between PD-1 and PD-L1, which helps restore and enhance T lymphocyte function while reducing the proportion of myeloid-derived suppressor cells (MDSCs), counteracting tumor-induced immune evasion. OPBP-1 is applicable for research in cancer immunotherapy.</p>
    Fórmula:C64H92N20O19S
    Peso molecular:1476.65683
  • Antitumor agent-41


    Antitumor Agent-41 (Compound N-12) exhibits potent antitumor properties, demonstrating significant antimigration and anti-invasion activities.
    Fórmula:C64H109IN2O21
    Forma y color:Solid
    Peso molecular:1369.46
  • ATPase-IN-3

    CAS:
    ATPase-IN-3 is an ATPase (ATPase) inhibitor that can be used in the study of metabolism-related diseases.
    Fórmula:C10H6N2O3S2
    Pureza:97.76%
    Forma y color:Soild
    Peso molecular:266.3
  • Verproside

    CAS:
    Verproside is a useful organic compound for research related to life sciences. The catalog number is T124745 and the CAS number is 50932-20-2.
    Fórmula:C22H26O13
    Forma y color:Solid
    Peso molecular:498.437
  • Golimumab

    CAS:
    Golimumab (CNTO-148), an anti-TNFα IgG1κ monoclonal antibody with anti-inflammatory and anti-cancer activity, can be used to prevent inflammation and cartilage.
    Forma y color:Liquid
    Peso molecular:146.93 kDa
  • RIP1-IN-1


    <p>RIP1-IN-1 is an orally bioavailable RIP1 inhibitor with a high binding affinity (Kd: 110 nM). This compound exhibits significant activity against necroptosis and effectively suppresses necrosome formation by inhibiting the phosphorylation of RIP1, RIP3, and MLKL pathways. RIP1-IN-1 can inhibit necroptosis and is applicable in research on acute liver injury.</p>
    Forma y color:Odour Solid
  • Mcl1-IN-12

    CAS:
    <p>Mcl1-IN-12 has anti-tumor activity.It is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.29 and 3.1 μM, respectively.</p>
    Fórmula:C45H46N4O6S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:803
  • Topoisomerase I/II inhibitor 6


    TopoisomeraseI/II inhibitor 6 (compound 3i) acts as an effective inhibitor of topoisomerase I and II, with IC50 values of 4.77 µM and 15 µM, respectively. Additionally, it exhibits antiproliferative activity against the human melanoma cell line LOX IMVI, demonstrating IC50 values of 26.7 µM and 25.4 µM.
    Fórmula:C31H28F2N4O6S
    Forma y color:Solid
    Peso molecular:622.64
  • Vonlerolizumab

    CAS:
    <p>Vonlerolizumab (MOXR 0916) is a humanized IgG OX40 agonist monoclonal antibody with potential in cancer and immune disease research.</p>
    Pureza:SDS-PAGE:97.3%;SEC-HPLC:99.4%
    Forma y color:Liquid
    Peso molecular:145.25 kDa
  • MG-277


    MG-277 is a molecular glue compound transformed from PROTAC degradation agent, MG-277 potently inhibits tumor cell growth in a p53-independent manner.
    Fórmula:C41H42Cl2FN5O5
    Pureza:98%
    Forma y color:Solid
    Peso molecular:774.71
  • ARI-1


    ARI-1 is a receptor tyrosine kinase-like orphan receptor 1 (ROR1) inhibitor that binds to ROR1's extracellular Frizzled domain, effectively inhibiting aberrant
    Forma y color:Odour Solid
  • Ferroptosis-IN-14


    Ferroptosis-IN-14 (compund 36) exhibits the most potent anti-ferroptotic activity with an EC50 value of 0.58 ± 0.02 μM, demonstrating excellent anti-ferroptotic efficacy, as well as stability in microsomes and plasma.
    Forma y color:Odour Solid
  • MDM2 ligand 4


    <p>MDM2ligand 4 is a ligand of MDM2 and can be used in the synthesis of the PROTAC degrader [KT-253].</p>
    Fórmula:C31H33Cl2FN2O4
    Forma y color:Solid
    Peso molecular:587.509
  • PERK-IN-4

    CAS:
    PERK-IN-4 is a potent and selective PERK inhibitor with an IC50 value of 0.3 nM.PERK-IN-4 can be used in the study of cancer and neurological disorders.
    Fórmula:C24H19F4N5O
    Pureza:99.44% - 99.49%
    Forma y color:Solid
    Peso molecular:469.43
  • PD-1-IN-20


    PD-1-IN-20 is the less active enantiomer of PD-1-IN-1.
    Fórmula:C12H20N6O7
    Pureza:98%
    Forma y color:Solid
    Peso molecular:360.32
  • Ianalumab

    CAS:
    <p>Ianalumab (VAY-736) is a decarboxylated humanized antibody against BAFF-R.</p>
    Pureza:100% (SEC-HPLC) - > 95%
    Forma y color:Liquid
    Peso molecular:146.44 kDa
  • TNF-α-IN-11


    <p>TNF-α-IN-11 (Compound 10) is a TNF-α inhibitor exhibiting a dissociation constant (K D) of 12.06 μM.</p>
    Fórmula:C24H26N2O5
    Forma y color:Solid
    Peso molecular:422.47
  • LL-K9-3

    CAS:
    LL-K9-3, a selective hydrophobic tagging technology (HyT)-based degrader, specifically targets the CDK9-cyclin T1 complex, displaying DC50 values of 589 nM for
    Fórmula:C31H49N5O6S3
    Forma y color:Solid
    Peso molecular:683.94