Apoptosis
Apoptosis inhibitors are compounds that prevent or delay the process of programmed cell death, known as apoptosis. These inhibitors are vital in studying cell survival mechanisms and are used to investigate diseases where apoptosis is dysregulated, such as cancer, neurodegenerative disorders, and autoimmune diseases. By modulating apoptosis, these inhibitors can help in the development of therapies aimed at controlling cell death. At CymitQuimica, we provide a comprehensive selection of high-quality apoptosis inhibitors to support your research in cell biology, oncology, and related fields.
Subcategories of "Apoptosis"
- ASK(9 products)
- BCL(5 products)
- Caspase(151 products)
- FOXO1(2 products)
- IAP(67 products)
- Mdm2(12 products)
- PD-1/PD-L1(105 products)
- PDK(9 products)
- PERK(26 products)
- Serine/threonin kinase(18 products)
- Survivin(14 products)
- TNF(58 products)
- c-RET(61 products)
- p53(63 products)
Show 6 more subcategories
Found 6043 products of "Apoptosis"
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1,2-Di-13(Z)-Docosenoyl-3-Oleoyl-rac-glycerol
CAS:1,2-Di-13(Z)-docosenoyl-3-oleoyl-rac-glycerol is a triacylglycerol composed of 13(Z)-docosenoic acid at both the sn-1 and sn-2 positions and oleic acid at the sn-3 position.Formula:C65H120O6Color and Shape:SolidMolecular weight:997.64Atiprimod (free base)
CAS:Atiprimod: an oral azaspirane inhibiting STAT3, blocking IL-6/VEGF pathways, and promoting apoptosis by downregulating Bcl-2 and Mcl-1.Formula:C22H44N2Color and Shape:SolidMolecular weight:336.6RET-IN-25
CAS:RET-IN-25 (compound 6b) is an anticancer RET kinase inhibitor that demonstrates efficacy against medullary thyroid carcinoma (MTC), exhibiting half-maximalFormula:C22H17N3O5SColor and Shape:SolidMolecular weight:435.45MOTS-c
CAS:MOTS-c is a mitochondria-derived polypeptide (MDP) that has anti-damage and anti-inflammatory effects by activating the AMPK pathway and inhibiting the MAPFormula:C101H152N28O22S2Color and Shape:SolidMolecular weight:2174.6DC_AC50
CAS:"DC_AC50 inhibits Atox1/CCS to reduce cancer cell growth and prevent chemotherapy resistance."Formula:C17H12BrF2N3OSPurity:99.84% - 99.9%Color and Shape:SolidMolecular weight:424.264E2RCat
CAS:4E2RCat is an inhibitor of eIF4E-eIF4G interaction (IC50 = 13.5 μM) and is capable of blocking coronavirus replication as monitored by viral protein expressionFormula:C22H14ClNO4S2Purity:98.44%Color and Shape:SolidMolecular weight:455.93PD-1/PD-L1-IN-27
CAS:PD-1/PD-L1-IN-27: potent anti-cancer, IC50 134nM, minimal T cell harm, boosts CD8+ T cells, reduces fatigue.Formula:C44H35NO6Purity:98%Color and Shape:SolidMolecular weight:673.7515-Deoxy-Δ12,14-prostaglandin A1
CAS:15-Deoxy-Δ12,14-Prostaglandin A1, a deoxyanalog of prostaglandins, inhibits NF-κB signaling and induces apoptosis. It also prevents TNF-α-induced upregulation of inflammatory endothelial cell adhesion molecules (CAM) and reduces monocyte arrest [1].Formula:C20H30O3Color and Shape:SolidMolecular weight:318.457Ezatiostat hydrochloride
CAS:Ezatiostat HCl (TLK199) inhibits glutathione S-transferase, GSTP1-1 specifically, and may treat cytopenias.Formula:C27H36ClN3O6SPurity:98%Color and Shape:SolidMolecular weight:566.11Ref: TM-T22776
2mg58.00€5mg82.00€10mg120.00€25mg200.00€50mg306.00€100mg517.00€200mg777.00€500mg1,165.00€1mL*10mM (DMSO)118.00€PLK1/BRD4-IN-1
CAS:PLK1/BRD4-IN-1 (9b) is an orally active dual inhibitor of PLK1 (IC50: 22 nM) and BRD4 (IC50: 109 nM).Formula:C31H43N9O2Color and Shape:SolidMolecular weight:573.73BAI1 hydrochloride
CAS:BAI1 hydrochloride is a selective inhibitor of the apoptosis factor BAX, functioning through an allosteric mechanism. By binding to BAX, it allosterically inhibits its activation, showcasing potential applications in the research of diseases mediated by BAX-dependent cell death [1].Formula:C19H23Br2Cl2N3OColor and Shape:SolidMolecular weight:540.12Immunosuppressant-1
CAS:Immunosuppressant-1 (Compound 31) suppresses T-cell proliferation triggered by anti-CD3/anti-CD28 co-stimulation and demonstrates immunosuppressive effects,Formula:C14H12BrNO3Purity:98%Color and Shape:SolidMolecular weight:322.15Vepafestinib
CAS:Vepafestinib is a RET inhibitor with potential antineoplastic activity[1].Formula:C26H30N6O3Purity:98.56%Color and Shape:SolidMolecular weight:474.55MS-177
CAS:MS-177 is a PROTAC EZH2 degrader that promotes cholangiocarcinoma growth through the EZH2-mediated WNT7B/β-catenin pathway.Formula:C48H55N11O8Color and Shape:SolidMolecular weight:914.02Ref: TM-T69771
1mg84.00€5mg177.00€10mg281.00€25mg557.00€50mg893.00€100mg1,341.00€1mL*10mM (DMSO)358.00€Ferroptocide
CAS:Ferroptocide is a thioredoxin inhibitor that induces iron death in cancer cells and can be used in breast cancer research.Formula:C30H36ClN3O7Color and Shape:SolidMolecular weight:586.08YM281
CAS:YM281 is a potent EZH2 inhibitor, causes apoptosis and G0/G1 arrest, has antitumor activity in vivo, and may be researched for lymphoma.Formula:C56H71N7O9SColor and Shape:SolidMolecular weight:1018.27RUNX-IN-2
CAS:RUNX-IN-2 (Compound Conjugate 3) covalently attaches to RUNX-binding sequences, preventing RUNX proteins from associating with their targets, thereby inhibitingFormula:C71H88Cl2N24O11Purity:98%Color and Shape:SolidMolecular weight:1524.52ST1074
CAS:ST1074, a dual inhibitor of CerS2 and CerS4, promotes apoptosis and is applicable in cancer research [1].Formula:C20H36ClNO3Purity:98%Color and Shape:SolidMolecular weight:373.96AAPK-25
CAS:AAPK-25, a dual Aurora/PLK inhibitor, disrupts mitosis, induces apoptosis, and has antitumor properties.Formula:C21H13Cl2N3O2SPurity:97.05%Color and Shape:SolidMolecular weight:442.32Ref: TM-T10215
1mg57.00€5mg125.00€10mg182.00€25mg329.00€50mg495.00€100mg718.00€1mL*10mM (DMSO)138.00€Antitumor agent-97
CAS:Antitumor agent-97 (compound 42), an anticancer agent, effectively inhibits proliferation and autophagy in MGC 803 cells, induces apoptosis, and enhances ROSFormula:C24H34O3Purity:98%Color and Shape:SolidMolecular weight:370.52
