
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"
- Apoptosis inducer
- ASK
- BCL
- Caspase
- c-RET
- FOXO1
- IAP
- Mdm2
- p53
- PD-1/PD-L1
- PDK
- PERK
- Serine/threonin kinase
- Survivin
- TNF
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Products of "Apoptosis"
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RX-3117
CAS:RX-3117 (fluorocyclopentenylcytosine) is a novel a cytidine analog.Formula:C10H12FN3O4Purity:99.55%Color and Shape:SolidMolecular weight:257.22Ref: TM-T16813
1mg157.00€2mg212.00€5mg309.00€10mg444.00€25mg728.00€50mg1,017.00€100mg1,378.00€1mL*10mM (DMSO)319.00€Mouse IL9(Interleukin 9) ELISA Kit
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mouse IL9. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse IL9. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mouse IL9, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse IL9 in the samples is then determined by comparing the OD of the samples to the standard curve.Color and Shape:Colourless TransparentliquidNavtemadlin
CAS:Navtemadlin (AMG232) is a potent, selective and orally available inhibitor of p53-MDM2 interaction (IC50: 0.6 nM).Cost-effective and quality-assured.Formula:C28H35Cl2NO5SPurity:95.55% - 98.86%Color and Shape:SolidMolecular weight:568.5517-Demethoxy-reblastatin
CAS:17-Demethoxy-reblastatin (17-DR) acts as an inhibitor of heat shock protein 90 (Hsp90). It suppresses the proliferation of HepG2 and SMMC7721 cancer cells, diminishes colony formation, and triggers apoptosis via a mitochondria and caspase-mediated pathway.Formula:C28H42N2O7Color and Shape:SolidMolecular weight:518.64Rat TNFRSF1B(Tumor Necrosis Factor Receptor Superfamily, Member 1B) ELISA Kit
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat TNFRSF1B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat TNFRSF1B. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat TNFRSF1B, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat TNFRSF1B in the samples is then determined by comparing the OD of the samples to the standard curve.Color and Shape:Colourless TransparentliquidPolygalacin D
CAS:Polygalacin D shows anti- proliferation, anti-inflammary, and hepatoprotective activities, it can inhibit the expression of lipopolysaccharide (LPS)-inducedFormula:C57H92O27Purity:99.77% - ≥98%Color and Shape:SolidMolecular weight:1209.4Mouse ERK1/2(Extracellular Signal Regulated Kinase 1/2) ELISA Kit
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mouse ERK1/2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse ERK1/2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mouse ERK1/2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse ERK1/2 in the samples is then determined by comparing the OD of the samples to the standard curve.Color and Shape:Colourless TransparentliquidNPS-1034
CAS:NPS-1034 is a dual Met/Axl inhibitor with IC50 of 48 nM and 10.3 nM, respectively.Formula:C31H23F2N5O3Purity:98.48%Color and Shape:SolidMolecular weight:551.54L-Glutamic acid monosodium salt monohydrate
CAS:L-Glutamic acid monosodium salt monohydrate (MSG monohydrate) is an important food additive with gastrointestinal protective effects.Formula:C5H10NNaO5Purity:99.95%Color and Shape:SolidMolecular weight:187.13Dabuzalgron
CAS:Dabuzalgron (Ro 115-1240) is an orally active selective alpha-1A adrenergic receptor agonist used to treat urinary incontinence.Formula:C12H16ClN3O3SPurity:98.35%Color and Shape:SolidMolecular weight:317.79Ref: TM-T10952
1mg58.00€5mg124.00€10mg216.00€25mg351.00€50mg527.00€100mg758.00€1mL*10mM (DMSO)137.00€Safflor Yellow A
CAS:Safflor Yellow A protects cultured rat cardiomyocytes against A/R injury, maybe via inhibiting cellular oxidative stress and apoptosis.Formula:C27H30O15Purity:98%Color and Shape:SolidMolecular weight:594.52AQ4
CAS:AQ4 is a topoisomerase II inhibitor and DNA-inserting agent that inhibits proliferation and induces apoptosis in two cell lines.Formula:C22H28N4O4Purity:96.64% - 98.29%Color and Shape:SolidMolecular weight:412.48KT5823
CAS:KT5823 is a cGMP-dependent protein kinase (PKG) inhibitor that increases iodide ion uptake by regulating the expression of sodium iodide symporter protein.Formula:C29H25N3O5Purity:95%Color and Shape:SolidMolecular weight:495.53DT2216
CAS:DT2216 inhibits various Bcl-XL-dependent leukemias and cancer cells, but is significantly less toxic to platelets.DT2216 is a selective B-cell lymphoma, extremely large (BCL-XL), proteolytic targeting chimera (PROTAC).DT2216 targets bcl-XL to the Von HippFormula:C77H96ClF3N10O10S4Purity:99.63% - 99.78%Color and Shape:SolidMolecular weight:1542.36Angelicin
CAS:Angelicin (Isopsoralen), is a furanocoumarin with anti-Y, antiviral, anti-inflammatory activity.Formula:C11H6O3Purity:99.89% - 99.98%Color and Shape:White SolidMolecular weight:186.16AGN 192870
CAS:AGN 192870 is a potent retinoic acid receptor (RAR) antagonist.AGN 192870 can be used to study cell growth arrest, differentiation and apoptosis.Formula:C27H22O2Purity:99.22%Color and Shape:SolidMolecular weight:378.46PARP1/BRD4-IN-3
PARP1/BRD4-IN-3 (compound HF4) is an effective inhibitor of BRD4 and PARP1, with IC50 values of 1210 nM and 2019 nM respectively. The compound exhibits antiproliferative activity, induces apoptosis (apoptosis) and cell cycle arrest at the G0/G1 phase. Additionally, PARP1/BRD4-IN-3 causes DNA damage and reduces the expression of the Rad51 protein, demonstrating anti-tumor activity.Color and Shape:Odour SolidTTNPB
CAS:TTNPB (Ro 13-7410,AGN-191183), a potent RAR agonist, inhibits binding of [3H]tRA of human RARα (IC50: 5.1 nM), β (IC50: 4.5 nM), and γ (IC50: 9.3 nM),Formula:C24H28O2Purity:99.55%Color and Shape:White SolidMolecular weight:348.48Ref: TM-T1288
2mg39.00€5mg57.00€10mg87.00€25mg162.00€50mg306.00€100mg464.00€500mg1,008.00€1mL*10mM (DMSO)59.00€Taurolidine
CAS:Taurolidine is a synthetic taurine analog with antimicrobial and anti-neoplastic actions. It displays broad bactericidal and fungicidal activity.Formula:C7H16N4O4S2Purity:98% - 99.79%Color and Shape:SolidMolecular weight:284.36Apoptosis inducer 27
Apoptosisinducer 27 (compound 1c) is a potent inhibitor of MDA-MB-231 breast cancer cells, demonstrating an IC50 of 12.8 μM and inducing early apoptosis in these cells. Additionally, it can bind to DNA molecules as well as Bax and Bcl-2 proteins, thereby inducing DNA damage.Formula:C29H37BrN2Color and Shape:SolidMolecular weight:493.52