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(27 products)
- Serine/threonin kinase(18 products)
- Survivin(14 products)
- TNF(93 products)
- c-RET(62 products)
- p53(63 products)
Show 6 more subcategories
Found 6063 products of "Apoptosis"
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1,4-Dideoxy-1,4-epithio-D-ribitol
CAS:1,4-Dideoxy-1,4-epithio-D-ribitol is a purine nucleoside analog that targets malignant tumors of the inert lymphatic system and possesses a broad spectrum ofFormula:C5H10O3SPurity:99.76%Color and Shape:SolidMolecular weight:150.2Cobimetinib hemifumarate
CAS:Cobimetinib hemifumarate is a potent and selective MEK1 inhibitor with an IC50 value of 4.2 nM for MEK1.Formula:C46H46F6I2N6O8Color and Shape:SolidMolecular weight:1178.707Isoquinoline
CAS:Compound PDK0035, with CAS No. 119-65-3, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound PDK0035 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.Formula:C9H7NMolecular weight:129.15Pyraclostrobin (Standard)
CAS:Pyraclostrobin (Standard) is the standard substance of Pyraclostrobin, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Pyraclostrobin is one of the most heavily used fungicides that inhibits mitochondrial complex III of fungal and mammalian cells.Formula:C19H18ClN3O4Molecular weight:387.82Tacrolimus-13C-d2
CAS:Tacrolimus-13C-d2 is the 13C and deuterated compound of Tacrolimus.Formula:C44H67D2NO12Molecular weight:807.02Iodoacetyl-LC-Biotin
CAS:Iodoacetyl-LC-Biotin (Iaa-Biotin) is a sulfhydryl-responsive probe that forms irreversible thioether bonds at alkaline pH, label protein cysteines.Formula:C18H31IN4O3SPurity:97.47%Color and Shape:SolidMolecular weight:510.43Palmatine hydroxide
CAS:<p>Palmatine hydroxide: oral IDO-1 inhibitor (IC50: 3-157μM), targets WNV protease, has anti-cancer/viral and neuroprotective properties.</p>Formula:C21H23NO5Color and Shape:SolidMolecular weight:369.41Zinc pyrithione (Standard)
CAS:Zinc pyrithione (Standard) is an analytical standard and reference sample. Zinc pyrithione (OM-1563) disrupts membrane transport by inhibiting proton pumps.Formula:C10H8N2O2S2ZnMolecular weight:317.71PT-262
CAS:PT-262: ROCK inhibitor, causes cytoskeleton change, halts lung cancer cell migration.Formula:C14H13ClN2O2Purity:98%Color and Shape:SolidMolecular weight:276.72Diafenthiuron (Standard)
CAS:Diafenthiuron (Standard) is the standard substance of Diafenthiuron, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Diafenthiuron is a widely utilized thiourea-based pesticide that effectively hinders mitochondrial activity in insect pests.Formula:C23H32N2OSMolecular weight:384.58Monensin sodium salt (Standard)
CAS:Monensin sodium salt (Standard) is the standard substance of Monensin sodium salt, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Monensin sodium is an antiprotozoal agent produced by Streptomyces cinnamonensis.Monensin sodium salt (Monensin A sodium salt) causes a marked enlargement of the MVBs and regulates exosome secretionFormula:C36H61NaO11Molecular weight:692.85PARG-IN-4
CAS:PARG-IN-4 (compound A) is an orally active and cell-membrane permeable PARG inhibitor (EC50=1.9 nM) that inhibits tumour growth in mice with antitumour .Formula:C20H25F2N7O2S2Purity:98.51%Color and Shape:SolidMolecular weight:497.592'-Aminoacetophenone
CAS:Compound Fr14273 is a natural product for research related to life sciences. The catalog number is Fr14273 and the CAS number is 551-93-9.Formula:C8H9NOPurity:99.88%Color and Shape:Pale Yellow Solid Solid CrystallineMolecular weight:135.17Melatonin-d4
CAS:Melatonin D5, a deuterium-labeled version of melatonin, is a hormone produced by the pineal gland, known for its role as a selective ATF-6 inhibitor that promotes apoptosis in human hepatoma cells via COX-2 downregulation. Additionally, it activates melatonin receptors and exhibits antioxidative and anti-inflammatory properties.Formula:C13H16N2O2Purity:98%Color and Shape:SolidMolecular weight:236.3TH1834
CAS:TH1834 is a specific inhibitor of Tip60/KAT5 histone acetyltransferase. TH1834 induces apoptosis and DNA damage in MCF.Formula:C33H40N6O3Purity:99.96%Color and Shape:SolidMolecular weight:568.71Furazolidone (Standard)
CAS:Furazolidone (Standard) is the standard substance of Furazolidone, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Furazolidone (Furoxone), a nitrofuran derivative, inhibits AML1-ETO transformed cells with IC50 value of 12.7 μM. It is antibacterial and antiprotozoal activity,Formula:C8H7N3O5Molecular weight:225.16Tubulin inhibitor 1
CAS:Tubulin inhibitor 1 blocks tubulin polymerization, with strong anti-tumor effects, induces apoptosis and G2/M mitotic arrest.Formula:C21H24N2O4Purity:98%Color and Shape:SolidMolecular weight:368.43Br-DAPI
CAS:IST5-002 (N6-Benzyladenosine-5'-phosphate) is a Stat5a/b inhibitor with anticancer activity and is used in cancer research.Formula:C16H14BrN5Purity:100%Color and Shape:SolidMolecular weight:356.22M47
CAS:<p>M47 is a selective CRY1 (Cryptochrome 1) degradator that enhances nuclear degradation of CRY1, thereby extending the lifespan of p53 knockout mice.</p>Formula:C28H22ClNO4Color and Shape:SolidMolecular weight:471.93Givinostat
CAS:Givinostat (ITF-2357) is a non-selective, orally active HDAC inhibitor capable of inhibiting STAT5 phosphorylation which is antitumour and anti-inflammatory .Formula:C24H27N3O4Purity:98.56%Color and Shape:SolidMolecular weight:421.5
