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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 5599 produtos de "Apoptose"

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  • YX-02-030

    CAS:
    <p>YX-02-030M is a PROTACMDM2 degrader. It inhibits the binding of MDM2 to p53 and VHL to HIF1α, with IC50 values of 63 nM and 1.35 μM, respectively. YX-02-030M binds to MDM2 and recruits the VHL E3 ubiquitin ligase to initiate MDM2 degradation, effectively killing p53 mutant or deficient triple-negative breast cancer (TNBC) cells.</p>
    Fórmula:C66H85Cl2N9O10S
    Peso molecular:1267.41
  • PRMT5-IN-33


    <p>PRMT5-IN-33 (compound A8) is a selective inhibitor of PRMT5 that competes with SAM, exhibiting an IC50 of 10.9 nM. It induces apoptosis and inhibits the proliferation of Z-138 and MOLM-13 cells, demonstrating antitumor activity.</p>
    Fórmula:C25H24BrN5O3S
    Peso molecular:553.07832
  • PD-L1-IN-5


    <p>PD-L1-IN-5 (X22) is an orally active PD-L1 inhibitor with an IC50 of 785.6 nM, demonstrating antitumor activity in vivo.</p>
  • PROTAC EGFR degrader 9

    CAS:
    <p>PROTACEGFRdegrader 9 (Compound C6) is an orally active, CRBN-based PROTAC EGFR degrader. It has a DC50 of 10.2 nM and a Kd of 240.2 nM against EGFRL858R/T790M/C797S. PROTACEGFRdegrader 9 demonstrates effective degradation activity against various EGFR mutants while not affecting EGFRWT.</p>
    Fórmula:C45H48F3N9O6S
    Peso molecular:899.98
  • Antimycobacterial agent-5


    <p>Antimycobacterial agent-5 (compound 27) is an imidazopyridine amide compound that targets the Mycobacterium electron transport chain (ETC) respiratory CIII2CIV2 supercomplex. It acts on Mycobacterium smegmatis CIII2CIV2 with an IC50 of 441 nM.</p>
    Fórmula:C25H34ClN3O
    Peso molecular:427.23904
  • 155H1


    155H1 (Compound 11) is a stapled peptide that covalently binds to hMcl1 (172-323) with an IC50 of 18 nM.
    Fórmula:C79H120FN19O23S
    Peso molecular:1753.85092
  • PROTAC GPX4 degrader-2


    <p>PROTACGPX4 degrader-2 (compound 18a) is a proteolysis-targeting chimera (PROTAC) that targets the degradation of glutathione peroxidase 4 (GPX4), with a DC50, 48h value of 1.68 μM. It induces the accumulation of lipid peroxides and mitochondrial depolarization, subsequently triggering ferroptosis. Additionally, PROTACGPX4 degrader-2 exhibits antiproliferative activity.</p>
    Fórmula:C50H61ClN8O9
    Peso molecular:952.425
  • ECDD-S16


    <p>ECDD-S16 is a potent inhibitor of pyroptosis. It effectively suppresses pyroptosis in Raw264.7 cells activated by surface and endosomal TLR ligands.</p>
    Fórmula:C35H31FO12
    Peso molecular:662.17995
  • DA5-HTL


    <p>DA5-HTL is a compound that combines dasatinib with the HaloTag system, effectively inhibiting the growth of tumor cells, with a GI50 of 1.923 nM.</p>
    Fórmula:C39H58Cl2N8O8S
    Peso molecular:868.34754
  • EGFR-PK/JNK-2-IN-1


    <p>EGFR-PK/JNK-2-IN-1 (Compound 6c) is a dual inhibitor of EGFR-PK and JNK-2, with IC50 values of 2.7 and 3.0 μM, respectively. It can induce apoptosis and cause cell cycle arrest at various stages. This compound is applicable in cancer research.</p>
    Fórmula:C22H17ClN4O3S
    Peso molecular:452.07099
  • Anticancer agent 178


    <p>Anticanceragent 178 (compound C2) is a potent anticancer compound. It effectively inhibits the proliferation and metabolic activity of MDA-MB 231 cells, with IC50 values of 1.1 and 4.2 μM, respectively. Additionally, Anticanceragent 178 induces ferroptosis and necroptosis in cells.</p>
    Fórmula:C32H30ClFeN2O6
    Peso molecular:629.11418
  • LC-1-40


    <p>LC-1-40 is a PROTAC that selectively degrades NUDT1 (DC50=0.97 nM). In mouse models, LC-1-40 selectively inhibits tumor growth induced by MYCN and induces nucleotide damage and apoptosis (cell death) in MYCN-associated tumors. It is applicable for cancer research.</p>
    Fórmula:C49H48N8O6
    Peso molecular:844.36968
  • NCA029


    <p>NCA029 is a potent activator of human caseinolytic protease P (HsClpP) with an EC50 of 0.15 μM. It targets HsClpPP and triggers an ATF3-dependent integrated stress response, resulting in the death of colon cancer cells.</p>
    Fórmula:C22H20F3N3O
    Peso molecular:399.15585
  • RIPK2-IN-4


    <p>RIPK2-IN-4 is a potent and specific inhibitor of RIPK2 with an IC50 value of 5 nM.</p>
    Fórmula:C16H10N6S2
    Peso molecular:350.04084
  • Cu(I) chelator 1


    <p>Cu(I) chelator 1 (Compound LH2) is a chelating agent specifically targeting the Cu(I) redox state. It inhibits the production of ROS.</p>
    Fórmula:C16H27NO4S3
    Peso molecular:393.11022
  • P-gp inhibitor 16


    <p>P-gp inhibitor 16 (compound 14) is an inhibitor of p-glycoprotein. It significantly enhances apoptosis induced by doxorubicin and displays anticancer properties.</p>
    Fórmula:C35H35N5O4
    Peso molecular:589.2689
  • Feladilimab

    CAS:
    <p>Feladilimab (GSK3359609) is an IgG4 monoclonal antibody that is an ICOS agonist.</p>
    Pureza:SDS-PAGE:95% SEC-HPLC:98%
    Cor e Forma:Liquid
    Peso molecular:145.24 kDa
  • Prolgolimab

    CAS:
    <p>Prolgolimab (BCD-100) is an anti-PD-1 antibody used in melanoma research.</p>
    Pureza:>95%
    Cor e Forma:Liquid
  • 4-Nitro-3-cresol

    CAS:
    <p>4-Nitro-3-cresol exhibits ciliate toxicity against Tetrahymena pyriformis and is widely used in biochemical experiments and drug synthesis research.</p>
    Fórmula:C7H7NO3
    Pureza:99.87%
    Cor e Forma:Beige Powder
    Peso molecular:153.14
  • Lipustobart

    CAS:
    <p>Lipustobart is an IgG4-kappa humanized monoclonal antibody targeting PDCD1 (programmed cell death 1, PD1, PD-1, CD279), with immunostimulant and antineoplastic</p>
    Pureza:98%
    Cor e Forma:Liquid