
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(6 products)
- BCL(11 products)
- Caspase(127 products)
- FOXO1(3 products)
- IAP(66 products)
- Mdm2(12 products)
- PD-1/PD-L1(126 products)
- PDK(9 products)
- PERK(23 products)
- Serine/threonin kinase(15 products)
- Survivin(13 products)
- TNF(91 products)
- c-RET(51 products)
- p53(62 products)
Show 6 more subcategories
Found 5618 products of "Apoptosis"
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HNPMI
CAS:<p>HNPMI is an epidermal growth factor receptor inhibitor that promotes apoptosis and is used in the study of colorectal cancer.</p>Formula:C22H20N2O3Purity:97.19%Color and Shape:SoildMolecular weight:360.41RMC-9805
CAS:<p>RMC-9805(Zoldonrasib) is a KRAS G12D inhibitor with anti-tumor and anti-proliferative activity for the study of pancreatic cancer.</p>Formula:C63H88F3N11O7Purity:98.10% - 99.51%Color and Shape:SolidMolecular weight:1168.44Nrf2 activator 19
<p>Nrf2 activator 19 is a compound capable of crossing the blood-brain barrier and acts as an NRF2/HO-1 activator, offering potent antioxidant and neuroprotective effects. It effectively reduces brain damage and minimizes the accumulation of Reactive Oxygen Species (ROS). Additionally, Nrf2 activator 19 inhibits neuronal apoptosis, aiding in the recovery of neural function and motor skills. It has demonstrated significant potential in ischemic stroke research.</p>Color and Shape:Odour SolidZ-Ala-Ala-Asp-CMK
CAS:<p>Z-Ala-Ala-Asp-CMK (Z-AAD-CMK) is a selective granzyme B inhibitor that blocks granzyme B protease activity, for inflammatory diseases and tumours.</p>Formula:C19H24ClN3O7Purity:99.967%Color and Shape:SolidMolecular weight:441.86Spexin TFA
<p>Spexin TFA: GAL2/GAL3 agonist (EC50: 45.7/112.2 nM), no activity at GAL1, reduces appetite, fatty acid uptake, and LH secretion; anxiolytic.</p>Formula:C76H115F3N20O21SColor and Shape:SolidMolecular weight:1733.9YB-0158 ammonium
<p>YB-0158 ammonium (Wnt pathway inhibitor 2 ammonium) is a reverse-rotation peptidomimetic with translation-enhancing potential and anticancer activity.</p>Formula:C32H40N9O7PPurity:99.14% - 99.18%Color and Shape:SolidMolecular weight:693.69Chaetoglobosin A
CAS:Chaetoglobosin A, the active compound extracted of Penicillium aquamarinium, is a member of the cytochalasan family. It preferentially induces apoptosis.Formula:C32H36N2O5Purity:98%Color and Shape:SolidMolecular weight:528.6492-Acetamidophenol
CAS:<p>2-Acetamidophenol (Orthocetamol) has analgesic and antipyretic effects. 2-Acetamidophenol is an isomer of Paracetamol (4-acetamidophenol).</p>Formula:C8H9NO2Purity:>99.99%Color and Shape:Light Brown PowderMolecular weight:151.16Reproxalap
CAS:<p>Reproxalap (NS-2) is a dry eye treatment that neutralizes aldehydes like malondialdehyde.</p>Formula:C12H13ClN2OPurity:99.4% - 99.97%Color and Shape:SolidMolecular weight:236.7Oxatomide
CAS:<p>Oxatomide: Dual H1/P2X7 antagonist, antihistamine, anti-allergic, treats immune diseases, IC50: 0.95 μM (P2X7), 0.43 μM (5-HT).</p>Formula:C27H30N4OPurity:98.82% - 99.72%Color and Shape:White PowderMolecular weight:426.55Waltonitone
CAS:<p>Waltonitone is a natural ursane-type pentacyclic triterpene isolated from Gentian waltonii Burkill.</p>Formula:C30H48O2Purity:98%Color and Shape:SolidMolecular weight:440.7Enniatin complex
CAS:<p>Enniatin complex: fungal cyclohexadepsipeptides inhibit enzymes, induce cancer cell apoptosis, and have ionophoric, antibiotic, and hypolipidemic effects.</p>Purity:98%Color and Shape:SolidFerroptosis-IN-13
<p>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.</p>Formula:C32H30F2N4O3Color and Shape:SolidMolecular weight:556.602FPR1 antagonist 2
<p>Compound 25b, an FPR1 antagonist, exhibits potent inhibition of the formyl peptide receptor 1 with an IC50 of 70 nM.</p>Formula:C25H25F3O5Color and Shape:SolidMolecular weight:462.46Ianalumab
CAS:<p>Ianalumab (VAY-736) is a decarboxylated humanized antibody against BAFF-R.</p>Purity:100% (SEC-HPLC) - > 95%Color and Shape:LiquidMolecular weight:146.44 kDaKB03-SLF
CAS:<p>KB03-SLF is a protease with the capability to target specific proteins and regulate intracellular protein levels by inducing protein degradation. This mechanism renders KB03-SLF potentially valuable in the suppression of related diseases.</p>Formula:C50H63ClF3N5O12Color and Shape:SolidMolecular weight:1018.51WAY-118959-A
CAS:<p>WAY-118959-A is a potential microtubule acetylation inhibitor.</p>Formula:C16H14N4OS2Purity:99.92%Color and Shape:SolidMolecular weight:342.44Sorafenib-d4
CAS:<p>Sorafenib D4 is deuterium-labeled Sorafenib, a multi-kinase inhibitor (Raf-1, B-Raf, VEGFR-3) with IC50s: 6, 20, 22 nM.</p>Formula:C21H16ClF3N4O3Purity:98%Color and Shape:SolidMolecular weight:468.85Thalidomide-PEG2-NH2
CAS:<p>Thalidomide-PEG2-NH2: synthetic E3 ligase ligand-linker, combines Thalidomide-based cereblon and PROTAC linker.</p>Formula:C17H19N3O6Color and Shape:SolidMolecular weight:361.354Taltirelin acetate
CAS:<p>Taltirelin acetate (TA-0910 acetate) is a superagonist at thyrotropin-releasing hormone receptor (TRH-R)(IC50 of 910 nM and EC50 of 36 nM for stimulating an</p>Formula:C19H27N7O7Purity:99.21%Color and Shape:SolidMolecular weight:465.46Neocarzinostatin
CAS:<p>Neocarzinostatin is an effective DNA-damaging, anti-tumor antibiotic.</p>Purity:98%Color and Shape:SolidMolecular weight:N/A1,8-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:154.25MTX-23
CAS:MTX-23, an AR-targeted Proteolysis Targeting Chimera (PROTAC), effectively degrades both AR-V7 and AR-FL, inhibiting the proliferation of CaP cells and inducingFormula:C43H53F2N7O7S2Color and Shape:SolidMolecular weight:882.05(R)-JAK2/STAT3-IN-10a
CAS:<p>(R)-JAK2/STAT3-IN-10a is the R-isomer of JAK2/STAT3-IN-1.JAK2/STAT3-IN-1 is a structural domain inhibitor of GP130 D1 with antitumor activity.</p>Formula:C34H35BrF3N5O2Purity:97.99%Color and Shape:SoildMolecular weight:682.57NMC-001
<p>NMC-001 is a human IgG1 monoclonal antibody (mAb) that targets MDM2. It is useful for pancreatic cancer research. The recommended isotype control is HumanIgG1kappa, Isotype Control.</p>Color and Shape:Odour LiquidConophylline
CAS:<p>Conophylline, an alkaloid from Ervatamia microphylla, induces pancreatic cell differentiation and apoptosis, and suppresses HSC.</p>Formula:C44H50N4O10Purity:98%Color and Shape:SolidMolecular weight:794.89Verdinexor
CAS:<p>Verdinexor (KPT-335) (KPT-335), a specific XPO1/CRM1 inhibitor, are orally bioavailable.</p>Formula:C18H12F6N6OPurity:98% - 99.68%Color and Shape:SolidMolecular weight:442.32HTR2A antagonist 1
<p>HTR2A antagonist 1 (Compound 15f) is an HTR2A antagonist with an IC50 of 42.79 nM. It induces sub-G1 cell cycle arrest and apoptosis in colorectal cancer cells by activating the p53/p21/caspase 3 signaling pathway. HTR2A antagonist 1 exhibits good liver microsomal stability and is useful for colorectal cancer research.</p>Formula:C35H43Cl2F2N5O4Color and Shape:SolidMolecular weight:706.65Resolvin D2 n-3 DPA
CAS:<p>RvD2 n-3 DPA is an SPM made from docosapentaenoic acid in human leukocytes, inhibiting neutrophil chemotaxis and adhesion.</p>Formula:C22H34O5Color and Shape:SolidMolecular weight:378.509PD-1/PD-L1-IN-49
<p>PD-1/PD-L1-IN-49 (compound 1c) is a potent inhibitor of PD-1/PD-L1 with an IC50 of 77 nM. This compound can activate Jurkat T cells and effectively block the PD-1/PD-L1 immune checkpoint.</p>Formula:C27H32N4O5Color and Shape:SolidMolecular weight:492.567Azadirone
CAS:<p>Azadirone, a limonoid, sensitizes cancer cells to TRAIL by modulating DR4/DR5, survival, and apoptotic proteins.</p>Formula:C9H15N3O5Color and Shape:SolidMolecular weight:245.23Streptonigrin
CAS:<p>Streptonigrin, from Streptomyces flocculus, has anti-tumor and anti-bacterial properties, inhibiting PAD1-4.</p>Formula:C25H22N4O8Purity:98%Color and Shape:SolidMolecular weight:506.46Kusunokinin
<p>Kusunokinin is a useful organic compound for research related to life sciences and the catalog number is T124612.</p>Formula:C21H22O6Color and Shape:SolidMolecular weight:370.401TRBP-IN-1
<p>TRBP-IN-1 (Compound 13j) is an orally active inhibitor of TAR RNA-binding protein 2 (TRBP) with an IC50 of 12.72 μM. It exhibits significant anti-hepatocellular carcinoma (HCC) activity, effectively suppressing proliferation and metastasis of HCC cells [HCCLM3 cells (IC50: 18.96 μM) and SK-Hep-1 cells (IC50: 16.45 μM)]. TRBP-IN-1 modulates miRNA biosynthesis by targeting TRBP, inhibiting the expression of oncogenic miRNAs. It induces apoptosis and pyroptosis in HCC cells by decreasing miRNA levels. TRBP-IN-1 is suitable for research on targeted HCC therapy.</p>Formula:C25H23F3N2O5SColor and Shape:SolidMolecular weight:520.12798VK-28
CAS:<p>VK-28 is a brain permeable iron chelator with neuroprotection. VK-28 inhibits basal as well as iron-induced mitochondrial lipid peroxidation.</p>Formula:C16H21N3O2Purity:99.87%Color and Shape:SolidMolecular weight:287.36(E/Z)-10-Hydroxy-2-decenoic acid
CAS:<p>(E/Z)-10-Hydroxy-2-decenoic acid is a useful organic compound for research related to life sciences.</p>Formula:C10H18O3Color and Shape:SolidMolecular weight:186.251CST626
CAS:<p>CST626 is a PROTAC degrader that targets XIAP, cIAP1, and cIAP2.</p>Formula:C61H82N8O9SPurity:95.87%Color and Shape:SolidMolecular weight:1103.42NQO2-IN-1
CAS:NQO2-IN-1, a resveratrol analog, is a potent NQO2 inhibito,antitumor,generation of ROS and up-regulation of DR5 (death receptor 5) to promote apoptosis.Formula:C18H18N2O3Purity:99.83%Color and Shape:SoildMolecular weight:310.35AUNP-12
CAS:<p>AUNP-12, a new immune checkpoint modulator, is an inhibitor of the PD-1 pathway.</p>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:311.34CNDAC hydrochloride
CAS:<p>CNDAC hydrochloride, a nucleoside analog, is a metabolite of the sapacitabine.</p>Formula:C10H13ClN4O4Purity:99.45%Color and Shape:SolidMolecular weight:288.69Ceftiofur hydrochloride
CAS:<p>Ceftiofur hydrochloride (U-67279A) is a stable, broad-spectrum 3rd-gen cephalosporin with antibacterial properties.</p>Formula:C19H17N5O7S3·HClPurity:99.51%Color and Shape:Off-White SolidMolecular weight:560.02Albicanol
CAS:<p>Albicanol is a biochemical.</p>Formula:C15H26OColor and Shape:SolidMolecular weight:222.372Methylene Violet 3RAX
CAS:<p>Methylene Violet 3RAX is a cationic dye that is a potential photosensitizer in photodynamic therapy and has antitumor activity.</p>Formula:C22H23ClN4Purity:97.03% - 97.17%Color and Shape:SolidMolecular weight:378.9Bax inhibitor peptide, negative control
CAS:<p>The compound is a negative control peptide for the Bax inhibitor peptides V5 and P5.</p>Formula:C28H52N6O6SPurity:98%Color and Shape:SolidMolecular weight:600.81Thalidomide-NH-C10-COOH
<p>Compound 6b is a synthetic Thalidomide-VHL E3 ligase-linker for PROTACs.</p>Formula:C24H31N3O6Purity:98%Color and Shape:SolidMolecular weight:457.52PPIA-IN-1
<p>PPIA-IN-1 (Compound 20b) is an inhibitor of peptidyl-prolyl isomerase A (PPIA) with a KD of 0.52 μM. It demonstrates antiproliferative activity across various cancer cell lines, including an IC50 of 0.69 μM in HCT116 cells, induces cell cycle arrest at the G0/G1 phase, and exhibits antimetastatic effects in HCT116 cells. PPIA-IN-1 elevates ROS levels, causing DNA damage, ER stress, and mitochondrial dysfunction, and induces apoptosis in HCT116 cells via the MAPK pathway. Additionally, PPIA-IN-1 shows antitumor activity in a CT26 xenograft mouse model.</p>Formula:C23H21Cl2FN4O7Color and Shape:SolidMolecular weight:555.34AKT-IN-18
<p>AKT-IN-18, an Akt inhibitor, demonstrates an IC50 value of 69.45 μM in A549 cells, effectively impeding Akt activity.</p>Formula:C19H14ClN5O2SPurity:98%Color and Shape:SolidMolecular weight:411.86Mangafodipir trisodium
CAS:<p>Mangafodipir trisodium can enhance contrast in magnetic resonance imaging (MRI) of the liver, is a contrast agent delivered intravenously.</p>Formula:C22H27MnN4Na3O14P2Purity:98%Color and Shape:SolidMolecular weight:757.32Tauro-β-muricholic acid
CAS:<p>Tauro-β-muricholic acid (TβMCA), a trihydroxylated bile acid, acts as a competitive and reversible FXR antagonist (IC 50 = 40 μM) and exhibits antiapoptotic</p>Formula:C26H45NO7SPurity:98%Color and Shape:SolidMolecular weight:515.7

