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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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  • DWP-05195

    CAS:
    <p>DWP-05195 is a TRPV1 antagonist capable of inhibiting pain signal transduction. Additionally, it induces ER stress-dependent apoptosis in human ovarian cancer cells via the ROS-p38-CHOP pathway.</p>
    Fórmula:C18H10BrF3N4
    Forma y color:Solid
    Peso molecular:419.2
  • MDK-3345

    CAS:
    MDK-3345 is a reversible covalent inhibitor for Mcl-1.
    Fórmula:C36H34BN3O7
    Pureza:98%
    Forma y color:Solid
    Peso molecular:631.48
  • JAK2/FLT3-IN-1 TFA


    JAK2/FLT3-IN-1 (TFA), an oral JAK2/FLT3 inhibitor, shows anticancer properties; IC50: JAK2 (0.7 nM), FLT3 (4 nM), JAK1 (26 nM), JAK3 (39 nM).
    Fórmula:C27H35F4N7O3
    Forma y color:Solid
    Peso molecular:581.61
  • Tubulin inhibitor 14


    Tubulin inhibitor 14 blocks NQO2 and microtubule formation, disrupts blood vessels, and may target tumors; IC50 of 1.0 μM.
    Fórmula:C15H9F2NO
    Forma y color:Solid
    Peso molecular:257.23
  • Flizasertib

    CAS:
    Flizasertib is a serine/threonine kinase inhibitor that acts by inhibiting RIPK1, which has anti-inflammatory and therapeutic effects on immune disorders.
    Fórmula:C15H14FN3O
    Pureza:99.39% - 99.57%
    Forma y color:Solid
    Peso molecular:271.29
  • NCAO

    CAS:
    <p>N-ω-chloroacetyl-L-ornithine (NCAO) serves as a powerful reversible competitive inhibitor of ornithine decarboxylase (ODC), displaying cytotoxic and antiproliferative properties against various tumor cell lines, with EC50 values spanning from 1 to 50.6 µM. In vitro studies reveal that NCAO promotes Apoptosis and restricts tumor cell migration. Additionally, it demonstrates significant antitumor efficacy in a mouse model, targeting both solid and ascitic tumors using the myeloma (Ag8) cell line. NCAO holds promise in the development of antitumor agents.</p>
    Fórmula:C7H13ClN2O3
    Forma y color:Solid
    Peso molecular:208.64
  • 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%
    Forma y color:Solid
    Peso molecular:447.49
  • PF-07328948

    CAS:
    <p>PF-07328948 is a branched-chain keto-acid dehydrogenase kinase (BDK) inhibitor, useful for studying CVD metabolic disorders.</p>
    Fórmula:C16H8F4O3S
    Pureza:98.42%
    Forma y color:Solid
    Peso molecular:356.29
  • Darizmetinib

    CAS:
    Darizmetinib (HRX215) is an MKK4 inhibitor.
    Fórmula:C21H17F2N5O3S
    Pureza:98.03% - 99.57%
    Forma y color:Solid
    Peso molecular:457.45
  • 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%
    Forma y color:Solid
    Peso molecular:487.55
  • HC-5404

    CAS:
    HC-5404 is a potent and selective PERK inhibitor, blocking the activation of the PERK pathway, anti-tumor effects, advanced solid tumors and renal cell Cancer.
    Fórmula:C24H24F2N4O3
    Pureza:99.33%
    Forma y color:Solid
    Peso molecular:454.47
  • Vatalanib hydrochloride

    CAS:
    <p>Vatalanib hydrochloride (PTK787 hydrochloride) is an orally available and highly potent tyrosine kinase (VEGF) inhibitor that reduces the number and size of Aβ plaques in the cortex of 5xFAD mice, which may be useful in the study of Alzheimer's disease and cancer.</p>
    Fórmula:C20H16Cl2N4
    Pureza:99.7%
    Forma y color:Solid
    Peso molecular:383.27
  • Tuvusertib

    CAS:
    Tuvusertib (M1774), an oral ATR inhibitor (Ki<1µM), selectively blocks CHK1 phosphorylation, disrupts DNA repair, and induces tumor cell apoptosis.
    Fórmula:C16H12F2N8O
    Pureza:98.44% - 99.66%
    Forma y color:Solid
    Peso molecular:370.32
  • Lometrexol

    CAS:
    <p>Lometrexol (LY 264618) is an antifolate that inhibits GARFT, blocks purine synthesis, induces apoptosis, and has anticancer properties.</p>
    Fórmula:C21H25N5O6
    Pureza:97.76% - 99.56%
    Forma y color:Solid
    Peso molecular:443.45
  • BCL6-IN-3

    CAS:
    BCL6-IN-3: potent BCL6 inhibitor, 70 nM GI50 in SU-DHL4, affects cell functions, antitumor.
    Fórmula:C24H31ClF2N6O2
    Pureza:98.17%
    Forma y color:Solid
    Peso molecular:508.99
  • SY-5609

    CAS:
    SY-5609 (CDK7-IN-3) is a selective non-covalent CDK7 inhibitor, with weak inhibitory activity against CDK2, CDK9 and CDK12.Cost-effective and quality-assured.
    Fórmula:C23H26F3N6OP
    Pureza:99.34% - >99.99%
    Forma y color:Solid
    Peso molecular:490.46
  • 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%
    Forma y color:Solid
    Peso molecular:618.53
  • UH15-38

    CAS:
    <p>UH15-38 is a potent and selective RIPK3 inhibitor that blocks necroptosis in alveolar epithelial cells triggered by IAV, useful for studying lung inflammation.</p>
    Fórmula:C26H27N5O2
    Pureza:99.85%
    Forma y color:Solid
    Peso molecular:441.53
  • JAK2-IN-7

    CAS:
    JAK2-IN-7 selectively inhibits JAK2 (IC50: 3 nM), shows 14-fold selectivity over JAK1/3, FLT3, induces G0/G1 arrest, apoptosis, and has antitumor effects.
    Fórmula:C26H33N7O
    Pureza:99.54%
    Forma y color:Solid
    Peso molecular:459.59
  • Gemcitabine elaidate hydrochloride

    CAS:
    <p>CP-4126, a lipophilic pro-drug of Gemcitabine, converts to active form by esterases, allowing oral administration with dose-dependent effects.</p>
    Fórmula:C27H44ClF2N3O5
    Pureza:98.50% - 99.6%
    Forma y color:Solid
    Peso molecular:564.11