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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ENMD-2076
CAS:ENMD-2076, a multi-targeted kinase inhibitor, has specific activity against Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, PDGFRα.Formula:C21H25N7Purity:97.63% - ≥95%Color and Shape:SolidMolecular weight:375.47(E/Z)-TG003
CAS:(E/Z)-TG003 is a potent and ATP-competitive Cdc2-like kinase (Clk) inhibitor.Formula:C13H15NO2SPurity:98% - 99.04%Color and Shape:SolidMolecular weight:249.33Ref: TM-T1901
2mg42.00€5mg52.00€10mg92.00€25mg164.00€50mg271.00€100mg399.00€200mg567.00€1mL*10mM (DMSO)52.00€Ro-3306
CAS:RO-3306: ATP-competitive CDK1 inhibitor, Ki 20 nM, >15x more selective than other human kinases.Formula:C18H13N3OS2Purity:97.67% - 99.79%Color and Shape:SolidMolecular weight:351.45K858 (Racemic)
CAS:K858 Racemic (K858) is a selective mitotic kinesin Eg5 inhibitor which acts in an ATP-noncompetitive manner.Formula:C13H15N3O2SPurity:>99.99%Color and Shape:SolidMolecular weight:277.34PKD-IN-1 dihydrochloride (956121-30-5 free base)
CAS:CRT0066101 dihydrochloride is an inhibitor of PKD.Formula:C18H21Cl3N4OPurity:99.5%Color and Shape:SolidMolecular weight:415.752-Hydroxychalcone
CAS:2-Hydroxychalcone (2-(2-Hydroxybenzal)Acetophenone) can be used as antiparasitic hit compounds when Methoxylated. It inhibits invasion of breast cancer cells.Formula:C15H12O2Purity:99.6%Color and Shape:SolidMolecular weight:224.25Echinocystic acid
CAS:EA, a natural triterpene, is found in herbs; it has anti-inflammatory and antioxidant properties.Formula:C30H48O4Purity:98% - 99.57%Color and Shape:SolidMolecular weight:472.70GW 5074
CAS:GW 5074 (Raf1 Kinase Inhibitor I)(IC50=9 nM) is an effective and specific c-Raf inhibitor.Formula:C15H8Br2INO2Purity:99.32%Color and Shape:SolidMolecular weight:520.94Malabaricone B
CAS:Malabaricone B is a Spice-derived phenolic, it induces mitochondrial damage in lung cancer cells via a p53-independent pathway.Formula:C21H26O4Purity:99.84% - 99.91%Color and Shape:SolidMolecular weight:342.43Maduramicin ammonium
CAS:Maduramicin ammonium (Maduramycin Ammonium) is an anticoccidial agent for the the treatment of Eimeria spp., E.Formula:C47H83NO17Purity:99.83%Color and Shape:White Crystalline PowderMolecular weight:934.20Tanespimycin
CAS:Tanespimycin (KOS 953) is an Hsp90 inhibitor (IC50=5 nM) and is selective. Tanespimycin depletes intracellular STK38/NDR1. High-Quality, Low-Cost!Formula:C31H43N3O8Purity:98.24% - 99.83%Color and Shape:Dark Purple SolidMolecular weight:585.69AT7519
CAS:AT7519 is a CDK1/2/4/6/9 inhibitor (IC50: 10-210 nM). It is less effective to CDK3 and little active to CDK7.Formula:C16H17Cl2N5O2Purity:98.88% - 99.65%Color and Shape:SolidMolecular weight:382.24Tauroursodeoxycholate
CAS:Tauroursodeoxycholate (UR 906), a hydrophilic bile acid, low in humans, may treat PBC, insulin resistance, and ALS.Formula:C26H45NO6SPurity:98.77% - 99.93%Color and Shape:White SolidMolecular weight:499.7Terameprocol
CAS:Terameprocol (EM-1421), a synthetic NDGA derivative, shows potent anti-HIV, antiangiogenic, and anticancer properties.Formula:C22H30O4Purity:99.38%Color and Shape:SolidMolecular weight:358.47PEAQX
CAS:<p>PEAQX (NVP-AAM077) is an oral NMDA antagonist, inhibits 1A/2A receptors (IC50: 270 nM), less so 1A/2B (IC50: 29,600 nM).</p>Formula:C17H17BrN3O5PPurity:98% - 99.9%Color and Shape:SolidMolecular weight:454.21Telekin
CAS:<p>Telekin, a sesquiterpene lactone from Carpesium divaricatum, strongly inhibits cancer cell growth.</p>Formula:C15H20O3Purity:99.86% - 99.97%Color and Shape:SolidMolecular weight:248.32Dexrazoxane
CAS:Dexrazoxane (ICRF-187) is a mitosis-blocking anticancer drug, iron chelator, and anthracycline cardioprotectant.Formula:C11H16N4O4Purity:99.88%Color and Shape:SolidMolecular weight:268.27AR42
CAS:<p>AR42 (OSU-HDAC42) is an HDAC inhibitor (IC50: 30 nM).</p>Formula:C18H20N2O3Purity:98.46% - 98.96%Color and Shape:SolidMolecular weight:312.36Glycochenodeoxycholic Acid
CAS:<p>Glycochenodeoxycholic Acid (Lithocholylglycine) is a glycine conjugate of lithocholic acid, a bile acid.</p>Formula:C26H43NO5Purity:97% - 99.97%Color and Shape:SolidMolecular weight:449.62A-1210477
CAS:A-1210477 is an effective and specific MCL-1 and Bcl-2 inhibitor (Ki/IC50: 0.454/26.2 nM).Formula:C46H55N7O7SPurity:99.17% - 99.37%Color and Shape:SolidMolecular weight:850.04Thalidomide-O-amido-C4-NH2 TFA
CAS:Thalidomide-O-amido-C4-NH2 TFA (E3 ligase Ligand-Linker Conjugates 19 TFA) is a synthesized E3 ligase ligand-linker conjugate.Formula:C21H23F3N4O8Purity:95%Color and Shape:SolidMolecular weight:516.42Etomoxir sodium salt
CAS:Etomoxir sodium salt ((R)-Etomoxir sodium salt) is a carnitine palmitoyltransferase 1a (CPT-1a) inhibitor that blocks fatty acid synthesis.Formula:C15H18ClO4·NaPurity:99.34% - 99.82%Color and Shape:SolidMolecular weight:320.74Ref: TM-T4535
1mg35.00€2mg43.00€5mg60.00€10mg87.00€25mg153.00€50mg264.00€100mg432.00€200mg635.00€1mL*10mM (DMSO)To inquireO6-Benzylguanine
CAS:O6-Benzylguanine is a guanine analog with antineoplastic activity,and is a potent O6-alkylguanine DNA alkyltransferase (AGT) inactivator.Formula:C12H11N5OPurity:98.9%Color and Shape:Solid CrystallineMolecular weight:241.25Torkinib
CAS:Torkinib (PP 242) (PP 242) is a selective and ATP-competitive mTOR inhibitor (IC50: 8 nM). It also inhibits mTORC1/2 (IC50s: 30/58 nM).Formula:C16H16N6OPurity:99.11%Color and Shape:SolidMolecular weight:308.34Ref: TM-T2414
5mg57.00€10mg74.00€25mg96.00€50mg136.00€100mg227.00€200mg338.00€500mg560.00€1mL*10mM (DMSO)63.00€Pyraclostrobin
CAS:Pyraclostrobin is one of the most heavily used fungicides that inhibits mitochondrial complex III of fungal and mammalian cells.Formula:C19H18ClN3O4Purity:99.89%Color and Shape:SolidMolecular weight:387.82LW6
CAS:LW6 (HIF-1α inhibitor) is a novel HIF-1 inhibitor.Formula:C26H29NO5Purity:98.1% - 98.22%Color and Shape:SolidMolecular weight:435.51Ref: TM-T3494
2mg47.00€5mg69.00€10mg89.00€25mg183.00€50mg298.00€100mg449.00€500mg938.00€1mL*10mM (DMSO)69.00€Wogonin
CAS:<p>Wogonin (Vogonin) is a cell-permeable and orally available flavonoid that displays anti-inflammatory and anticancer properties.</p>Formula:C16H12O5Purity:98% - 99.8%Color and Shape:Yellow CrystalMolecular weight:284.264'-bromo-Resveratrol
CAS:<p>4'-bromo-Resveratrolis a potent inhibitor of the deacetylases sirtuin 1 (SIRT1) and 3 (SIRT3)</p>Formula:C14H11BrO2Purity:99.00%Color and Shape:SolidMolecular weight:291.14Formosanin C
CAS:Formosanin C (Polyphyllin B) is a compound isolated from Rhizoma Paridis, showed pro-apoptosis and immunoregulation with antitumor activity.Formula:C51H82O20Purity:98.98% - >99.99%Color and Shape:SolidMolecular weight:1015.18Cyasterone
CAS:Cyasterone (Cyasteron), a natural EGFR inhibitor, can inhibit the growth of A549 and MGC823 cells, via regulating EGFR signaling pathway, it may be a promisingFormula:C29H44O8Purity:99.32% - 99.70%Color and Shape:SolidMolecular weight:520.65Panobinostat
CAS:<p>Panobinostat (NVP-LBH589) is a broad-spectrum HDAC inhibitor (IC50=5 nM) with oral activity and non-selectivity.</p>Formula:C21H23N3O2Purity:97.2% - 99.81%Color and Shape:Yellow SolidMolecular weight:349.43SHR0302
CAS:SHR0302 (ARQ252) is a JAK inhibitor that binds JAK1 with stronger affinity than others (Selectivity for JAK1 is more than 10 times for JAK2, 77 times for JAK3,Formula:C18H22N8O2SPurity:99.11%Color and Shape:SolidMolecular weight:414.48Ref: TM-T9195
1mg80.00€5mg183.00€10mg298.00€25mg512.00€50mg817.00€100mg1,311.00€1mL*10mM (DMSO)167.00€RRX-001
CAS:RRx-001 is a potent inhibitor ofglucose 6-phosphate dehydrogenase(G6PD) and with potent antimalarial activityFormula:C5H6BrN3O5Purity:99.91% - ≥95%Color and Shape:SolidMolecular weight:268.02Ref: TM-T7400
1mg52.00€2mg77.00€5mg115.00€10mg153.00€25mg279.00€50mg487.00€100mg710.00€500mg1,483.00€1mL*10mM (DMSO)127.00€Loganin
CAS:Loganin inhibits Cox-1, suppresses TNF-α, and has antioxidant and anti-melanogenic properties.Formula:C17H26O10Purity:99.01% - 99.9%Color and Shape:White PowderMolecular weight:390.38(Z)-Mirin
CAS:<p>(Z)-Mirin is a potent Mre11–Rad50–Nbs1 (MRN) complex inhibitor, and inhibits Mre11-associated exonuclease activity.</p>Formula:C10H8N2O2SPurity:99.67% - 99.76%Color and Shape:SolidMolecular weight:220.25Stattic
CAS:Stattic (STAT3 Inhibitor V) is a STAT3 inhibitor (IC50=5.1 μM) that selectively inhibits STAT3 activation, dimerization, and nuclear translocation.Formula:C8H5NO4SPurity:98.32% - 99.76%Color and Shape:SolidMolecular weight:211.19Ref: TM-T6308
5mg35.00€10mg51.00€25mg85.00€50mg124.00€100mg187.00€200mg279.00€500mg465.00€1mL*10mM (DMSO)55.00€TT-232 TFA(147159-51-1 free base)
CAS:<p>TT2-32 TFA induces a biphasic activation of phosphotyrosine phosphatase activity in human colon tumor cell line, SW620</p>Formula:C47H59F3N10O11S2Purity:99.27% - 99.8%Color and Shape:SolidMolecular weight:1061.16Ref: TM-T23479L
1mg86.00€2mg111.00€5mg172.00€10mg259.00€25mg425.00€50mg598.00€100mg810.00€200mg1,074.00€L67
CAS:<p>L67 (DNA Ligase Inhibitor) is a competitive human DNA ligase inhibitor, inhibits DNA ligases I and III (IC50: 10 μM).</p>Formula:C16H14Br2N4O4Purity:98.34% - 99.56%Color and Shape:SolidMolecular weight:486.11Bufotalin
CAS:<p>1. Bufotalin (Bufotaline)e is a kind of poisonous secretions of toads.</p>Formula:C26H36O6Purity:99.45% - 99.91%Color and Shape:White To Off-White SolidMolecular weight:444.56Masitinib mesylate
CAS:Masitinib mesylate (AB-1010 mesylate) is a selective and orally bioavailable c-Kit inhibitor (IC50 of 200 nM,540/800 nM,510 nM for human recombinant c-Kit;Formula:C29H34N6O4S2Purity:97.67% - 98.44%Color and Shape:SolidMolecular weight:594.75Pifithrin-α hydrobromide
CAS:Pifithrin-α hydrobromide (Pifithrin-α hydrobromide) is a p53 inhibitor, inhibiting p53-dependent transactivation of p53-responsive genes.Formula:C16H18N2OS·HBrPurity:97.71% - >99.99%Color and Shape:SolidMolecular weight:367.3GSK-2256098 HCl
CAS:GSK-2256098 HCl is a focal adhesion kinase-1 (FAK) inhibitor with potential antiangiogenic and antineoplastic activities.Formula:C20H24Cl2N6O2Color and Shape:SolidMolecular weight:451.35Amantadine
CAS:<p>Amantadine (1-Aminoadamantane), an antiviral, is a weak antagonist of the NMDA-type glutamate receptor, increases dopamine release and blocks dopamine reuptake.</p>Formula:C10H17NPurity:99.73% - 99.94%Color and Shape:Hexakistetrahedral Crystals By Sublimation SolidMolecular weight:151.25Nitidine chloride
CAS:1.Formula:C21H18ClNO4Purity:96.59% - 99.55%Color and Shape:SolidMolecular weight:383.82MAZ51
CAS:MAZ51 is a VEGFR-3 (Flt-4) tyrosine kinase inhibitor.Formula:C21H18N2OPurity:98.53%Color and Shape:SolidMolecular weight:314.38MPI-0479605
CAS:MPI-0479605 is an ATP competitive and selective inhibitor.Formula:C22H29N7OPurity:97.59% - >99.99%Color and Shape:SolidMolecular weight:407.51TCS-PIM-1-4a
CAS:SMI-4a, a Pim inhibitor, activates AMPK, halts mTORC1, and kills various myeloid/lymphoid cells (IC50=0.8-40μM).Formula:C11H6F3NO2SPurity:99.89%Color and Shape:SolidMolecular weight:273.23Dihydrorotenone
CAS:Dihydrorotenone is a potent mitochondrial inhibitor and probably induces Parkinsonian syndrome.Formula:C23H24O6Purity:98.98% - 99.58%Color and Shape:SolidMolecular weight:396.43Ref: TM-TN1586
1mg97.00€5mg264.00€10mg420.00€25mg697.00€50mg938.00€100mg1,264.00€1mL*10mM (DMSO)270.00€MPP dihydrochloride (289726-02-9 Free base)
CAS:MPP dihydrochloride is a highly selective antagonist of estrogen receptor alpha (ERα).Formula:C29H33Cl2N3O3Color and Shape:SolidMolecular weight:542.5C646
CAS:<p>C646, a histone acetyltransferase inhibitor, inhibits p300 (Ki: 400 nM, in a cell-free assay).</p>Formula:C24H19N3O6Purity:98% - 99.21%Color and Shape:SolidMolecular weight:445.42Ref: TM-T2452
2mg48.00€5mg69.00€10mg97.00€25mg195.00€50mg380.00€100mg562.00€500mg1,206.00€1mL*10mM (DMSO)69.00€
