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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Allethrin
CAS:Allethrin induces oxidative stress, apoptosis and calcium release. Allethrin, a pyrethroid insecticide is a major mosquito repellent agent.Formula:C19H26O3Purity:99.52%Molecular weight:302.41Setafrastat
CAS:Setafrastat is a vascular endothelial growth factor (VEGF) promotor and rotamase inhibitor.Formula:C25H33F2N3O4Color and Shape:SolidMolecular weight:477.54RLX
CAS:RLX (PD 139530) is a PI3K/Akt/FoxO3a signal inhibitor with anticancer,antitussive and anti-asthmatic activity,colon cancer，toxicity toward A549 cells..Formula:C13H14N2OPurity:99.81%Color and Shape:SolidMolecular weight:214.26NSC10010 hydrochloride
CAS:NSC10010 inhibits gammaherpesvirus B-lymphomas by activating NF-κB and c-Myc pathways.Formula:C31H42Cl2N4O2Purity:98%Color and Shape:SolidMolecular weight:573.60Tolbutamide Sodium
CAS:potassium channel blockerFormula:C12H18N2NaO3SPurity:98%Color and Shape:SolidMolecular weight:293.34Ormeloxifene
CAS:estrogen receptor modulatorFormula:C30H35NO3Purity:98%Color and Shape:SolidMolecular weight:457.6Fenoldopam hydrochloride
CAS:<p>Fenoldopam HCl: D1 dopamine receptor agonist, vasodilator, doesn't cross blood-brain barrier, α2-adrenoceptor antagonist.</p>Formula:C16H17Cl2NO3Color and Shape:SolidMolecular weight:342.22MK-886 sodium salt
CAS:MK-886 sodium salt inhibits leukotriene biosynthesis in leukocytes.Formula:C27H33ClNNaO2SColor and Shape:SolidMolecular weight:494.06CFM-5
CAS:CFM-5 has anticonvulsant activity and is used in epilepsy research.Formula:C23H18BrN3OSPurity:98%Color and Shape:SolidMolecular weight:464.38IZTZ-1
CAS:IZTZ-1: c-MYC G4 stabilizer, reduces expression, blocks cell cycle, induces apoptosis, inhibits B16 melanoma growth.Formula:C32H35N7SColor and Shape:SolidMolecular weight:549.73MPT0B002
CAS:MPT0B002 is a microtubule inhibitor that acts by downregulating T315I mutant Bcr-Abl and inducing apoptosis of imatinib-resistant chronic myeloid leukemia cellsFormula:C19H19NO4Purity:98%Color and Shape:SolidMolecular weight:325.36CEP-40125
CAS:CEP-40125 (RXDX-107) is a DNA alkylating agent for the study of advanced solid tumors.Formula:C28H45Cl2N3O2Purity:98.28%Color and Shape:SolidMolecular weight:526.58Anti-inflammatory agent 54
CAS:Anti-inflammatory agent 54 (compound 9c), a Coixol derivative, exhibits anti-inflammatory properties by inhibiting the NF-κB pathway and reducing the expressionFormula:C17H16N2O5Color and Shape:SolidMolecular weight:328.32Thienopyridone
CAS:Thienopyridone: potent, selective PRL phosphatase inhibitor, IC50s: 173/277/128 nM for PRL-1/2/3, induces apoptosis, anticancer.Formula:C13H10N2OSPurity:98%Color and Shape:SolidMolecular weight:242.3PD-1/PD-L1-IN 6
CAS:Compound A13 inhibits PD-1/PD-L1, enhances interferon-γ, lacks toxicity, and boosts immune response in co-culture models. IC50=132.8 nM.Formula:C25H26N2O3Color and Shape:SolidMolecular weight:402.49CFM 4
CAS:CFM 4 is a potent small molecule CARP-1/APC-2 antagonist that prevents CARP-1 from binding to APC-2, contributes to G2M cell cycle arrest, and induces apoptosisFormula:C22H16ClN3OSPurity:98.16%Color and Shape:SolidMolecular weight:405.9HDAC-IN-36
CAS:HDAC-IN-36: Oral HDAC6 inhibitor, IC50 = 11.68 nM, promotes apoptosis & autophagy, anti-tumor & anti-metastatic, for breast cancer research.Formula:C29H39N5O5Color and Shape:SolidMolecular weight:537.65XMD15-44
CAS:XMD15-44, a RET kinase inhibitor, demonstrates potent growth-inhibitory effects on RAT1 cells transformed by RET/C634R and RET/M918T, with IC50 values of 11.5 nM and 8.3 nM, respectively. It effectively inhibits RET kinase activity and signaling in human thyroid cancer cell lines harboring oncogenic RET alleles, thereby reducing cell proliferation.Formula:C29H29F3N4OMolecular weight:506.56Ferroptosis-IN-4
CAS:Ferroptosis-IN-4 (compound 6k), an inhibitor of ferroptosis, exhibits an EC50 of 20 μM and lacks significant cytotoxicity. It demonstrates a protective role in glycerol-induced RM-AKI mice by alleviating kidney dysfunction [1].Formula:C17H24ClN3O2Molecular weight:337.84CCT373567
CAS:<p>CCT373567 is a potent degrader of the transcriptional repressor BCL6 (IC50: 2.9 nM) and exhibits anti-proliferative effects.</p>Formula:C26H29ClF2N6O3Color and Shape:SolidMolecular weight:547
