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Apoptosi

Apoptosi

Gli inibitori dell'apoptosi sono composti che prevengono o ritardano il processo di morte cellulare programmata, noto come apoptosi. Questi inibitori sono fondamentali per lo studio dei meccanismi di sopravvivenza cellulare e vengono utilizzati per indagare sulle malattie in cui l'apoptosi è disregolata, come il cancro, i disturbi neurodegenerativi e le malattie autoimmuni. Modulando l'apoptosi, questi inibitori possono aiutare nello sviluppo di terapie mirate a controllare la morte cellulare. Presso CymitQuimica, offriamo una vasta selezione di inibitori dell'apoptosi di alta qualità per supportare le tue ricerche in biologia cellulare, oncologia e campi correlati.

Sottocategorie di "Apoptosi"

Mostrare 6 più sottocategorie

Trovati 5599 prodotti di "Apoptosi"

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  • BCL6-IN-8c
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    BCL6-IN-8c

    CAS:
    <p>BCL6-IN-8c is an orally active and potent inhibitor of B-cell lymphoma 6 (BCL6)-corepressor interaction(IC50 of 0.10 μM in cell-free enzyme-linked immunosorbent</p>
    Formula:C20H20ClN3O5
    Colore e forma:Solid
    Peso molecolare:417.84

    Ref: TM-T14515

  • Ivaltinostat
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    Ivaltinostat

    CAS:
    <p>CG-200745 is a potent inhibitor of HDAC. CG200745 induces apoptosis and also inhibits the deacetylation of histone H3 and tubulin.</p>
    Formula:C24H33N3O4
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:427.54

    Ref: TM-T14936

  • Metoprolol fumarate
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    Metoprolol fumarate

    CAS:
    <p>Metoprolol fumarate (CGP 2175C): selective β1-blocker with anti-inflammatory, antitumor, anti-angiogenic effects.</p>
    Formula:C34H54N2O10
    Colore e forma:Solid
    Peso molecolare:650.8

    Ref: TM-T71752

  • MSN-50
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    MSN-50

    CAS:
    <p>MSN-50, an inhibitor of Bax and Bak oligomerization, inhibits liposome permeabilization, prevents genotoxic cell death and promotes neuroprotection.</p>
    Formula:C36H38BrN3O6
    Colore e forma:Solid
    Peso molecolare:688.61

    Ref: TM-T28117

  • Tubulin polymerization-IN-17
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    Tubulin polymerization-IN-17

    CAS:
    <p>Compound 23g, a potent inhibitor of tubulin aggregation, induces apoptosis, and inhibits cell migration; promising for cancer research.</p>
    Formula:C26H23NO5
    Colore e forma:Solid
    Peso molecolare:429.46

    Ref: TM-T62369

  • Shield-2
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    Shield-2

    CAS:
    <p>Shield-2 is a potent FKBP-derived destabilizing domain stabilizing ligand.</p>
    Formula:C35H51N3O7
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:625.8

    Ref: TM-T24788

  • Anticancer agent 77
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    Anticancer agent 77

    CAS:
    <p>Anticancer agent 77 exhibits anticancer effects and can be used extensively in synthetic and medicinal chemistry studies.</p>
    Formula:C25H30BrN7
    Colore e forma:Solid
    Peso molecolare:508.46

    Ref: TM-T63489

  • Ludartin
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    Ludartin

    CAS:
    <p>Ludartin activates TRPA1, induces DNA damage, and lowers mitochondrial potential, yielding anticancer effects.</p>
    Formula:C15H18O3
    Colore e forma:Solid
    Peso molecolare:246.3

    Ref: TM-T69359

  • EGFR-IN-57
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    EGFR-IN-57

    CAS:
    <p>EGFR-IN-57: potent EGFR-TK blocker, IC50 0.054 μM, oral. Halts VEGFR-2, CK2α, topo IIβ, tubulin. Causes G2/M, pre-G1 arrest, cancer cell death.</p>
    Formula:C22H15N3O2S
    Colore e forma:Solid
    Peso molecolare:385.44

    Ref: TM-T61696

  • DRAK2-IN-1
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    DRAK2-IN-1

    CAS:
    <p>Drak2-in-1: ATP-competitive DRAK2 inhibitor; IC50 = 3 nM, KI = 0.26 nM; affects DRAK1 (IC50 = 51 nM).</p>
    Formula:C21H20N4O3
    Colore e forma:Solid
    Peso molecolare:376.41

    Ref: TM-T11094

  • LSD1-IN-14
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    LSD1-IN-14

    CAS:
    <p>LSD1-IN-14: potent LSD1 inhibitor, IC50 0.89 μM; hinders A549/THP-1 cell growth, induces tumor cell apoptosis.</p>
    Formula:C21H24FN5
    Colore e forma:Solid
    Peso molecolare:365.45

    Ref: TM-T61405

  • SPRC
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    SPRC

    CAS:
    <p>"SPRC, a synthetic antioxidant, boosts H2S production, activates STAT3, and guards against doxorubicin heart damage."</p>
    Formula:C6H9NO2S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:159.21

    Ref: TM-T19728

  • Nafamostat hydrochloride
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    Nafamostat hydrochloride

    CAS:
    <p>Nafamostat hydrochloride is a synthetic serine protease inhibitor and is an anticoagulant.</p>
    Formula:C19H19Cl2N5O2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:420.29

    Ref: TM-T23051

  • ARN5187 trihydrochloride
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    ARN5187 trihydrochloride

    CAS:
    <p>ARN5187 trihydrochloride: a REV-ERBβ inhibitor that blocks transcription, autophagy, and induces apoptosis with lysosomal cytotoxicity.</p>
    Formula:C24H35Cl3FN3O
    Colore e forma:Solid
    Peso molecolare:506.912

    Ref: TM-T63476

  • SMBA1
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    SMBA1

    CAS:
    <p>SMBA1 is a Bax agonist with antitumor activity that can induce cell cycle arrest and apoptosis in malignant glioma cells.</p>
    Formula:C20H13NO3
    Purezza:99.2%
    Colore e forma:Solid
    Peso molecolare:315.32

    Ref: TM-T8792

  • Antitumor agent-45
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    Antitumor agent-45

    CAS:
    <p>Antitumor agent-45 has an inhibitory effect on c-Met expression and is able to block A549 cells in the G0/G1 and G2/M phases and induce apoptosis.</p>
    Formula:C28H17BrFN5O3
    Colore e forma:Solid
    Peso molecolare:570.37

    Ref: TM-T64034

  • MI-192
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    MI-192

    CAS:
    <p>MI-192: Selective HDAC2/3 inhibitor, IC50=30/16 nM, induces apoptosis in myeloid leukemia, potential in leukemia/anti-stroke treatment.</p>
    Formula:C24H21N3O2
    Colore e forma:Solid
    Peso molecolare:383.44

    Ref: TM-T21898

  • HIOC
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    HIOC

    CAS:
    <p>TrkB agonist; shields neurons &amp; retinas; crosses blood-brain &amp; retinal barriers.</p>
    Formula:C16H19N3O3
    Colore e forma:Solid
    Peso molecolare:301.34

    Ref: TM-T37081

  • LWG-301
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    LWG-301

    <p>LWG-301, a GLS1 allosteric inhibitor, IC50 7 nM, impedes glutamine metabolism and prompts apoptosis; shows antitumor effects.</p>
    Formula:C28H38N8O3S
    Colore e forma:Solid
    Peso molecolare:566.72

    Ref: TM-T73458

  • EGFR-IN-52
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    EGFR-IN-52

    CAS:
    <p>EGFR-IN-52, a potent EGFR inhibitor, has IC50s: 0.358 μM (wild-type), 86.02 μM (L858R-TK), 432.67 μM (T790M-TK); induces cancer cell apoptosis.</p>
    Formula:C19H18N4O3S
    Colore e forma:Solid
    Peso molecolare:382.44

    Ref: TM-T61646