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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KU-0058948
CAS:KU-0058948: PARP inhibitor, triggers cell cycle arrest and apoptosis in myeloid leukemia cells in vitro.Formula:C21H21FN4O2Color and Shape:SolidMolecular weight:380.42BRD4 Inhibitor-15
CAS:BRD4 Inhibitor-15 targets BRD4 with 18 nM IC50, induces apoptosis in 22RV1 cells, and lowers c-Myc, aiding prostate cancer research.Formula:C22H21N3O2Color and Shape:SolidMolecular weight:359.42TSI-13-57
CAS:TSI-13-57 is a MyD88 inhibitor or pan-TLR inhibitor that suppresses MyD88 TIR domain dimerization ,inhibits LPS-induced TNF-α (IC50 = 6.73 mM).Formula:C28H29N3O3Purity:99.63%Color and Shape:SolidMolecular weight:455.55Arecaidine propargyl ester (hydrobromide)
CAS:Arecaidine propargyl ester: selective M2 muscarinic receptor agonist, induces guinea pig atrium contraction, lowers cat blood pressure, toxic to flies.Formula:C10H14BrNO2Color and Shape:SolidMolecular weight:260.13PDGFR-IN-1
CAS:PDGFR-IN-1 is a platelet-derived growth factor receptor (PDGFR) inhibitor, strongly inhibiting PDGFRα and PDGFRβ, useful for studying solid tumors.Formula:C25H30N8OPurity:99.13% - 99.49%Color and Shape:SolidMolecular weight:458.56Ref: TM-T62872
1mg170.00€5mg432.00€10mg655.00€25mg1,153.00€50mg1,665.00€100mg2,250.00€1mL*10mM (DMSO)434.00€CRA-026440
CAS:CRA-026440(PCI-34051) is a highly potent HDAC inhibitor with inhibitory effects on HDAC1, HDAC2, HDAC3, HDAC6, HDAC8 and HDAC10 with Ki values of 4,14,11,15,7Formula:C23H24N4O4Purity:96.42%Color and Shape:SolidMolecular weight:420.46SGC-STK17B-1
CAS:SGC-STK17B-1 is a potent and selective inhibitor of STK17B/DRAK2 kinase.Formula:C16H10N2O2S3Color and Shape:SolidMolecular weight:358.46AMXT1501
CAS:AMXT1501 is a polyamine uptake inhibitor, also inhibiting the putrescine transport in epimastigotes (the insect stage of t. cruzi)Formula:C32H68N6O2Color and Shape:SolidMolecular weight:568.92UA 62784
CAS:Blocks microtubule growth, spurs cell apoptosis, enhances vinblastine's effect in HeLa cells, mistakenly seen as CENP-E ATPase inhibitor.Formula:C23H15NO3Color and Shape:SolidMolecular weight:353.37Mcl1-IN-4
CAS:Mcl1-IN-4 is an inhibitor of Mcl1 ( IC50:0.2 μM).Formula:C28H26N2O5SPurity:98%Color and Shape:SolidMolecular weight:502.58Didesmethylrocaglamide
CAS:Didesmethylrocaglamide, a Rocaglamide derivative, is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor that exhibits strong growth-inhibitory effects,Formula:C27H27NO7Color and Shape:SolidMolecular weight:477.51Semapimod
CAS:Semapimod is an inhibitor of proinflammatory cytokine production, capable of suppressing TNF-α, IL-1β, and IL-6.Formula:C34H52N18O2Color and Shape:SolidMolecular weight:744.9DC-CPin711
CAS:DC-CPin711: Potent, selective CBP bromodomain inhibitor, IC50=0.0626 μM; arrests G1 cell cycle, induces apoptosis.Formula:C23H22N4O2Color and Shape:SolidMolecular weight:386.45Melflufen
CAS:Melflufen, a dipeptide prodrug of Melphalan, is an alkylating agent with strong antitumor activity in MM, causing DNA damage and cytotoxicity.Formula:C24H30Cl2FN3O3Purity:97.056%Molecular weight:498.42AZD-5991 Racemate
CAS:AZD-5991 Racemate is the racemate of AZD-5991. (Rac)-AZD-5991 is a novel Mcl-1 inhibitor induces upregulation of BCL2,BCL-XL, CMYC and MCL1 in AML cell lines.Formula:C35H34ClN5O3S2Color and Shape:SolidMolecular weight:672.26PI3K/AKT-IN-2
CAS:PI3K/AKT-IN-2 inhibits PI3K/AKT, EMT, induces apoptosis, and blocks tubulin polymerization.Formula:C32H27BrO10Color and Shape:SolidMolecular weight:651.45Mcl1-IN-11
CAS:Mcl1-IN-11 (Compound G) is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.06 and 4.2 μM, respectively.Formula:C38H41N3O5S2Purity:98%Color and Shape:SolidMolecular weight:683.88IKK2-IN-4
CAS:IKK2-IN-4(IKK2 Inhibitor VI) is a highly potent IKK-2 inhibitor with an IC50 value of 25 nM. IKK2-IN-4 inhibited the production of TNF-α in PBMC induced by LPS.Formula:C12H11N3O2SPurity:99.83%Color and Shape:SolidMolecular weight:261.3Ref: TM-T36524
1mg108.00€5mg261.00€10mg401.00€25mg622.00€50mg837.00€100mg1,125.00€200mg1,504.00€500µg82.00€VMY-1-103
CAS:VMY-1-103: a strong CDK inhibitor better than purvalanol B; halts prostate/breast cancer cell growth, induces apoptosis, may treat medulloblastoma.Formula:C34H42ClN9O4SColor and Shape:SolidMolecular weight:708.27PDK4-IN-1
CAS:PDK4-IN-1 is an anthraquinone derivative and a potent and orally active inhibitor of pyruvate dehydrogenase kinase 4 (PDK4)(IC50 value of 84 nM).Formula:C22H19N3O2Purity:98%Color and Shape:SolidMolecular weight:357.41
