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(91 products)
- c-RET(61 products)
- p53(63 products)
Show 6 more subcategories
Found 6039 products of "Apoptosis"
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Biotin-PEG6-Thalidomide
CAS:Biotin-PEG6-Thalidomide is a PROTAC linker based on PEG.Formula:C37H53N5O12SPurity:98%Color and Shape:SolidMolecular weight:791.91(E)-C-HDMAPP (ammonium salt)
CAS:<p>Alkyl phosphates like (E)-C-HDMAPP activate γδ-T cells, resist hydrolysis, and boost TNF-α synthesis and γδ-T cell count in vivo.</p>Formula:C6H23N3O7P2Color and Shape:SolidMolecular weight:311.21DB0614
CAS:DB0614 degrades 26 kinases including AAK1 and CDK6, targeting aberrant activity in disease research.Formula:C41H42N8O7S2Color and Shape:SolidMolecular weight:822.95Waltonitone
CAS:<p>Waltonitone is a natural ursane-type pentacyclic triterpene isolated from Gentian waltonii Burkill.</p>Formula:C30H48O2Purity:98%Color and Shape:SolidMolecular weight:440.7Ferroptosis-IN-13
Ferroptosis-IN-13 (compound NY-26) is an inhibitor of ferroptosis. It effectively suppresses RSL3-induced ferroptosis in 786-O cells, with an EC50 value of 62 nM.Formula:C32H30F2N4O3Color and Shape:SolidMolecular weight:556.6021,8-Cineole
CAS:<p>Eucalyptol, a natural monoterpenoid and cyclic ether found in eucalyptus species, effectively controls excessive airway mucus secretion and asthma by inhibiting pro-inflammatory cytokines. It serves as an efficacious treatment for non-purulent sinusitis, reducing inflammation and pain when applied topically, and demonstrating leukemic cell-killing capabilities in vitro.</p>Formula:C10H18OPurity:97.44% - 97.44%Color and Shape:SolidMolecular weight:154.25VK-28
CAS:VK-28 is a brain permeable iron chelator with neuroprotection. VK-28 inhibits basal as well as iron-induced mitochondrial lipid peroxidation.Formula:C16H21N3O2Purity:99.87%Color and Shape:SolidMolecular weight:287.36AUNP-12
CAS:AUNP-12, a new immune checkpoint modulator, is an inhibitor of the PD-1 pathway.Formula:C142H226N40O48Purity:98%Color and Shape:SolidMolecular weight:3261.55K-252c
CAS:<p>K-252c is a staurosporine analog isolated from Nocardiopsis sp.</p>Formula:C20H13N3OPurity:98%Color and Shape:SolidMolecular weight:311.34Mangafodipir trisodium
CAS:Mangafodipir trisodium can enhance contrast in magnetic resonance imaging (MRI) of the liver, is a contrast agent delivered intravenously.Formula:C22H27MnN4Na3O14P2Purity:98%Color and Shape:SolidMolecular weight:757.32Tauro-β-muricholic acid
CAS:Tauro-β-muricholic acid (TβMCA), a trihydroxylated bile acid, acts as a competitive and reversible FXR antagonist (IC 50 = 40 μM) and exhibits antiapoptoticFormula:C26H45NO7SPurity:98%Color and Shape:SolidMolecular weight:515.78-Bromo-cAMP
CAS:<p>8-Bromo-cAMP is a cell-permeable cAMP analogue and activator of CAMP-dependent protein kinase A that induces cell death and reduces proliferation.</p>Formula:C10H11BrN5O6PPurity:97.30%Color and Shape:SolidMolecular weight:408.1Diphenhydramine hydrochloride
CAS:<p>DPH: antihistamine for cough, nausea, itching, allergy, Parkinson's, sleep aid, cold remedy.</p>Formula:C17H22ClNOPurity:99.84%Color and Shape:Taste Ph (5% Aqueous Solution) 4-6 (Ntp 1992)Molecular weight:291.82MYC-RIBOTAC
MYC-RIBOTAC, a ribonuclease-targeting chimera (RIBOTAC) specific to the MYC internal ribosome entry site (IRES), comprises an MYC mRNA-binding element tetheredFormula:C55H58N10O11SPurity:98%Color and Shape:SolidMolecular weight:1067.17TAPI 0
CAS:ADAM-17 (TACE) and MMP inhibitor; attenuates TNF-α processing. Acts in concert with GM6001 to inhibit Chlamydia trachomatis growth.Formula:C24H32N4O5Purity:98%Color and Shape:SolidMolecular weight:456.54EGFR-IN-86
<p>EGFR-IN-86 (compound 4i), an EGFR inhibitor (IC50: 1.5 nM), demonstrates potent activity against glioblastoma by inducing apoptosis and causing G2/M phase cell</p>Formula:C20H21N7O2SPurity:98%Color and Shape:SolidMolecular weight:423.49Z-VDVA-(DL-Asp)-FMK
CAS:Z-VDVA-(DL-Asp)-FMK is a derivative compound of Z-VDVAD-FMK specifically designed as an inhibitor targeting caspase-2.Formula:C32H46FN5O11Color and Shape:SolidMolecular weight:695.742Thalidomide-O-amido-C6-NH2
CAS:<p>Thalidomide-O-amido-C6-NH2 is a synthetic E3 ligase used for PROTAC creation, containing cereblon ligand and linker.</p>Formula:C21H26N4O6Color and Shape:SolidMolecular weight:430.45Ganoderic acid Mk
CAS:GA-Mk is a triterpenoid from Ganoderma lucidum mycelia, inhibits HeLa cell growth, and induces apoptosis via mitochondria; used in cervical cancer studies.Formula:C34H50O7Color and Shape:SolidMolecular weight:570.76YW-N-7 TFA
YW-N-7 (TFA) is a PROTAC designed to target, inhibit, and degrade RET kinase, demonstrating a DC50 of 88 nM. It exhibits antitumor activity in xenograft mouse models driven by KIF5B-RET, making it a valuable compound for cancer research.Formula:C58H63F3N12O9Color and Shape:SolidMolecular weight:1129.19
