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(11 products)
- Caspase(144 products)
- FOXO1(3 products)
- IAP(67 products)
- Mdm2(12 products)
- PD-1/PD-L1(139 products)
- PDK(9 products)
- PERK(26 products)
- Serine/threonin kinase(18 products)
- Survivin(14 products)
- TNF(93 products)
- c-RET(62 products)
- p53(63 products)
Show 6 more subcategories
Found 6064 products of "Apoptosis"
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LQZ-7F
CAS:LQZ-7F is a survivin dimerization inhibitor with anticancer activity.LQZ-7F induces proteasome-dependent survivin degradation and inhibits human tumor growth.Formula:C14H7N9O3Purity:98.64%Color and Shape:SolidMolecular weight:349.26MJN68390
CAS:MJN68390 has an apparent IC50 value of 15 μM against CASP8 and shows no activity against CASP10.Formula:C24H28ClN3O3Purity:98.86%Color and Shape:SolidMolecular weight:441.95Erastin2
CAS:<p>Erastin2 is an iron death inducer that induces cell death by binding to the lipophilic free radical trapping antioxidant ferrostatin-1 or the iron chelator DFO.</p>Formula:C36H35ClN4O4Purity:99.63%Color and Shape:SolidMolecular weight:623.14Alethine
CAS:Alethine is a small antitumor compound used to treat cancers and infections, boosting T-cell cytotoxicity by raising TNFα.Formula:C10H22N4O2S2Purity:99.78%Color and Shape:SolidMolecular weight:294.44Cot inhibitor-1
CAS:Cot inhibitor-1 selectively blocks Tpl2 kinase, reducing TNF-alpha in blood (IC50: 5.7 nM). It may treat arthritis, IBD, and certain cancers.Formula:C27H27Cl2FN8Purity:98.87%Color and Shape:SolidMolecular weight:553.46Ref: TM-T10865
1mg77.00€5mg160.00€10mg235.00€25mg424.00€50mg635.00€100mg935.00€200mg1,283.00€1mL*10mM (DMSO)187.00€STAT3-IN-13
CAS:STAT3-IN-13 is a STAT3 inhibitor with antiproliferative activity that induces apoptosis and can be used to study breast and liver cancer.Formula:C21H20N6O3SPurity:98.89%Color and Shape:SolidMolecular weight:436.49Anticancer agent 110
CAS:Anticancer Agent 110 exhibits potent in vitro anti-leukemia activity, demonstrating high cytotoxicity against K-562 lineage chronic myelogenous leukemia cellsFormula:C18H13FN6OSPurity:98%Color and Shape:SolidMolecular weight:380.4A 419259 trihydrochloride
CAS:A 419259 trihydrochloride (RK 20449 trihydrochloride) is an Src family kinases inhibitor (IC50s: 9 nM, 3 nM and 3 nM for Src, Lck and Lyn).Formula:C29H37Cl3N6OPurity:99.75% - 99.96%Color and Shape:SolidMolecular weight:592GCN2-IN-1
CAS:<p>GCN2-IN-1 (A-92) is an effective GCN2 inhibitor and can be used in research on the treatment of cancer as a chemotherapeutic agent.</p>Formula:C19H18N10OPurity:99.49% - 99.64%Color and Shape:SolidMolecular weight:402.41BCL6-IN-7
CAS:BCL6-IN-7 (BCL6 inhibitor-7) is a BCL6 corepressor-interaction inhibitor with potential antitumor activity, used in lymphoma research.Formula:C18H15ClN6OPurity:99.03%Color and Shape:SolidMolecular weight:366.8SYM 2081
CAS:SYM 2081: Kainate receptor agonist, IC50 of 35 nM, depolarizes muscle, lowers EPSP amplitude.Formula:C6H11NO4Purity:99.63%Color and Shape:SolidMolecular weight:161.16CDK9-IN-7
CAS:CDK9-IN-7: selective, oral CDK9/cyclin T inhibitor with 11 nM IC50, stronger than CDK4/6.Formula:C29H37N7O2SPurity:98.08%Color and Shape:SolidMolecular weight:547.71Ref: TM-T10745
1mg90.00€5mg208.00€10mg304.00€25mg457.00€50mg630.00€100mg845.00€200mg1,121.00€1mL*10mM (DMSO)229.00€Benitrobenrazide
CAS:Benitrobenrazide (Hexokinase 2 inhibitor 1) is a novel orally available hexokinase 2 (HK2) inhibitor with anticancer and antitumor activity for cancer research.Formula:C14H11N3O6Purity:96.87%Color and Shape:SolidMolecular weight:317.25Droloxifene
CAS:Droloxifene, a tamoxifen derivative and oral SERM, induces p53 and apoptosis; Fluroxifene protects bone, blocks estrogen and implantation.Formula:C26H29NO2Purity:99.86% - 99.97%Color and Shape:Solid PowderMolecular weight:387.51Ref: TM-T11098
1mg54.00€5mg116.00€10mg170.00€25mg283.00€50mg419.00€100mg562.00€500mgTo inquire1mL*10mM (DMSO)133.00€LDCA
CAS:LDCA inhibits LDH-A, disrupts mitochondrial function, induces apoptosis in cancer cells, and is non-toxic.Formula:C8H5Cl3FNOPurity:99.19%Color and Shape:SolidMolecular weight:256.49HS-276
CAS:HS-276, a selective oral TAK1 inhibitor (Ki: 2.5 nM), also targets CLK2, GCK, ULK2, MAP4K5; potential for RA research.Formula:C24H29N5O2Purity:97.67% - 98.81%Color and Shape:SolidMolecular weight:419.52Ref: TM-T62209
1mg66.00€5mg144.00€10mg219.00€25mg430.00€50mg690.00€100mg1,064.00€200mg1,434.00€1mL*10mM (DMSO)170.00€Bomedemstat ditosylate
CAS:<p>Bomedemstat (IMG-7289) is an LSD1 inhibitor for acute myeloid leukemia, MDS, and Myelofibrosis; induces apoptosis by regulating p53, PUMA, and BCLXL.</p>Formula:C42H50FN7O8S2Purity:99.05%Color and Shape:SolidMolecular weight:864.02P505-15 Acetate
CAS:<p>P505-15 Acetate inhibits spleen tyrosine kinase, reduces immune response and inflammation, and lowers arthritis severity.</p>Formula:C21H27N9O3Purity:99.99%Color and Shape:SolidMolecular weight:453.5Tubulin inhibitor 11
CAS:Potent, oral Tubulin inhibitor 11 hinders polymerization, targets Colchicine site, induces mitotic block, and apoptosis.Formula:C22H23N3O3SPurity:99.93%Color and Shape:SoildMolecular weight:409.5Ref: TM-T67935
1mg35.00€5mg80.00€10mg116.00€25mg259.00€50mg383.00€100mg545.00€200mg740.00€1mL*10mM (DMSO)96.00€Ro 08-2750
CAS:Ro 08-2750: A non-peptide NGF inhibitor binding NGF (~1 µM IC50) & selectively inhibits p75NTR over TRKA and MSI RNA-binding (2.7 µM IC50).Formula:C13H10N4O3Purity:98.795%Color and Shape:SolidMolecular weight:270.24
