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Apoptosis Inducers

  • 1-β-D-Arabinofuranosylcytosine
    An antimetabolic agent which inhibits DNA polymerases α, δ, and ε, and RNA polymerases resulting in suppression of DNA synthesis and repair.
    Katalog #CAS NummerSummenformelMenge
    sc-201628147-94-4C9H13N3O51 g
  • 1,4-Benzoquinone
    Katalog #CAS NummerSummenformelMenge
    sc-202873106-51-4C6H4O2100 g
  • 1α,25-Dihydroxyvitamin D3 (Calcitriol)
    A metabolite of vitamin D3 and the active form of the hormone. Regulates transport and use of calcium in bone development. Signaling agent in a range of developmental pathways.
    Katalog #CAS NummerSummenformelMenge
    sc-20041932222-06-3C27H44O350 µg
  • 2-Amino-N-quinolin-8-yl-benzenesulfonamide
    An apoptosis inducer that inhibits cell cycle at G2 phase.
    Katalog #CAS NummerSummenformelMenge
    sc-21375016082-64-7C15H13N3O2S5 mg
  • 2-Chloro-2′-deoxyadenosine
    A deoxyadenosine analog that induces apoptosis in chronic lymphocytic leukemia (CLL) cells.
    Katalog #CAS NummerSummenformelMenge
    sc-2023994291-63-8C10H12ClN5O310 mg
  • 2,3-DCPE
    2,3 DCPE displays anticancer agent properties and induces ERK activation. Induces S-phase arrest and upregulates p21.
    Katalog #CAS NummerSummenformelMenge
    sc-200139418788-90-6C11H15Cl2NO2 ·HCl5 mg/25 mg
  • 3,3'-Diindolylmethane
    Anticancer and antineoplastic agent. Induces apoptosis in human cancer cells. Activator of cytochrome P450 and partial agonist of aryl hydrocarbon receptor (AhR). Dimer of indole-3-carbinol (sc-202662).
    Katalog #CAS NummerSummenformelMenge
    sc-2046241968-05-4C17H14N2100 mg/500 mg
  • 4-Hydroxyphenylretinamide
    A synthetic retinoid analog of all trans retinoic acid, which displays antiproliferative effects on cultured human breast cancer cells.
    Katalog #CAS NummerSummenformelMenge
    sc-20090065646-68-6C26H33NO25 mg/25 mg
  • 5-[(1Z)-2-(3,5-dimethoxyphenyl)ethenyl]-2-methoxy-phenol
    Resveratrol is a natural polyphenolic antioxidant that has anti-cancer properties. This chemical is an analog of resveratrol which is a potent inducer of apoptosis in promyelocytic leukemia HL-60 cells (IC50 = 40 nM versus 50 μM for resveratrol). In addition, it induces apoptosis (IC50 = 30 nM) in HL60R, a cell line derived from HL-60 that expresses a multidrug-resistance phenotype (resistant to daunorubicin, etoposide, and citarabine).
    Katalog #CAS NummerSummenformelMenge
    sc-290709586410-08-4C17H18O4500 µg/1 mg
  • 5′-Deoxy-5′-methylthioadenosine
    A naturally-occurring co-product of polyamine biosynthesis that acts as a substrate of methylthioadenosine phosphorylase.
    Katalog #CAS NummerSummenformelMenge
    sc-2024272457-80-9C11H15N5O3S50 mg
  • 7BIO
    A 3′ substituted kinase inhibitory bis-indole, which functions as a caspase independent nonapoptotic cell death inducer.
    Katalog #CAS NummerSummenformelMenge
    sc-221118n.n.C16H10BrN3O25 mg/25 mg
  • 10058-F4
    A c-Myc inhibitor that prevents c-Myc/Max dimerization. Also shown to arrest cell growth at G0/G1 phase and eventually lead to apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-213577403811-55-2C12H11NOS25 mg/25 mg
  • 13(S)-HPODE
    13(S)-HPODE is a hydroperoxide shown to be a potent suppressor of platelets.
    Katalog #CAS NummerSummenformelMenge
    sc-20096433964-75-9C18H32O450 µg/1 mg
  • A23187
    Highly selective calcium ionophore. Tool useful for increasing intracellular Ca2+ concentrations. Shown to induce cell activation, differentiation or proliferation.
    Katalog #CAS NummerSummenformelMenge
    sc-359152665-69-7C29H37N3O61 mg/10 mg
  • AAPH
    AAPH is a commonly applied free radical initiator for experimental use.
    Katalog #CAS NummerSummenformelMenge
    sc-2020342997-92-4C8H18N6 ·2HCl1 g
  • Adapalene
    Retinoic acid analog that is a RARβ and RARγ agonist (AC50 values are 2.2, 9.3, 22 and > 1000 nM for RARβ, RARγ, RARα and RXRα receptors respectively). Inhibits proliferation and induces apoptosis in colorectal cancer cell in vitro. Displays comedolytic activity.
    Katalog #CAS NummerSummenformelMenge
    sc-203803106685-40-9C28H28O310 mg/50 mg
  • Adenosine
    Induces apoptosis in human leukemia HL-60 cells. Has anti-arrhythmic properties.
    Katalog #CAS NummerSummenformelMenge
    sc-29183858-61-7C10H13N5O41 g/5 g
  • Alendronate, Sodium Salt
    A nitrogen-containing bisphosphate that acts as a robust inhibitor of bone resorption and induces apoptosis, and is a selective inhibitor of farnesyl diphosphate synthase.
    Katalog #CAS NummerSummenformelMenge
    sc-202049121268-17-5C4H12NNaO7P2 ·3H2O100 mg
  • AM 80
    Retinoic acid receptor α (RARα) agonist that induces differentiation (ED50 = 0.79 nM) and apoptosis of HL-60 cells in vitro. Displays anticancer activity against acute promyelocytic leukemia in vivo and exhibits antiproliferative effects against a variety of human tumor cells lines (mean values of 35, 40 and 60% growth inhibition at 0.1, 1 and 10 μM respectively).
    Katalog #CAS NummerSummenformelMenge
    sc-20381694497-51-5C22H25NO310 mg/50 mg
  • Antimycin A
    An antibiotic that induces apoptosis, inhibits the mitochondrial electron transport chain from cytochrome b to cytochrome C1, and generates ROS.
    Katalog #CAS NummerSummenformelMenge
    sc-2024671397-94-0C28H40N2O95 mg/10 mg
  • API-1
    Katalog #CAS NummerSummenformelMenge
    sc-36110636707-00-3C13H15N5O610 mg
  • Apoptolidin
    A selective polyketide, apoptosis inducer produced by Nocardiopsis mainly inducing cell death in E1A-transformed cells and inhibiting the enzymatic activity of mitochondrial F0F1-ATPase.
    Katalog #CAS NummerSummenformelMenge
    sc-202062194874-06-1C58H96O21100 µg
  • Apoptosis Activator 2
    Cell-permeable indoledione compound that activates caspases in a cytochrome c-dependent manner.
    Katalog #CAS NummerSummenformelMenge
    sc-20295679183-19-0C15H9Cl2NO25 mg
  • Apoptosis Activator VII, Apoptozole
    A cell-permeable imidazole compound that directly binds anti-apoptotic chaperone Hsc70 and its inducible homologue Hsp70.
    Katalog #CAS NummerSummenformelMenge
    sc-221257n.n.C33H24F6N3O310 mg
  • Atractyloside Dipotassium Salt
    Katalog #CAS NummerSummenformelMenge
    sc-363293102130-43-8C30H44K2O16S21 mg
  • Auraptene
    A compound with anti-inflammatory, chemopreventive, apoptotic, cancer cell line suppression, PPAR agonism and MMP-7 translational control properties.
    Katalog #CAS NummerSummenformelMenge
    sc-202477495-02-3C19H22O35 mg/25 mg
  • Baccatin III
    Katalog #CAS NummerSummenformelMenge
    sc-20463727548-93-2C31H38O115 mg/25 mg
  • Bcl-2 Inhibitor
    This contains a mixture of two tautomers (A and B). A potent, cell-permeable, Bcl-2 inhibitor that competes with Bak BH3 peptide for binding to Bcl-2 and Bcl-x in vitro (IC50 10 µM and 7 µM, respectively). It also reduces cell viability and growth in HL-60 cell lines with high Bcl-2 expression (IC50= 4 µM). Also induces apoptosis in a dose-dependent manner in cancer cells exhibiting high Bcl-2 expression with little effect on cancer cells with low Bcl-2 expression.
    Katalog #CAS NummerSummenformelMenge
    sc-221286383860-03-5C16H16N2O45 mg
  • Bcl-2 Inhibitor II, YC137
    A cell-permeable naphthoquinone compound that selectively induces apoptosis of Bcl-2-overexpressing cells with little effect on a variety of primary cells.
    Katalog #CAS NummerSummenformelMenge
    sc-221287n.n.C24H21N3O6S25 mg
  • Bcl-2 Inhibitor III, EM20-25
    A cell-permeable pyrimidine-trione compound that sensitizes apoptosis-resistant, Bcl-2-overexpressing leukemic cells to cytotoxic drugs. It has shown to bind to Bcl-2, disrupt its interaction with Bax as well as activate caspase-9. It also induces PTP (permeability transition pore) opening in both isolated mitochondria and intact cells, without any effect on respiration.
    Katalog #CAS NummerSummenformelMenge
    sc-221288141266-44-6C15H9CLN4O610 mg
  • Benzalkonium Bromide
    This compound functions as an ulcerative agent and preservative in most ophthalmic topical solutions. On epithelial conjunctival cells in vitro, cells die by necrosis at high concetrations and by apoptosis at low concentration.
    Katalog #CAS NummerSummenformelMenge
    sc-20560091080-29-4C21H38BrN100 g/500 g
  • Berberine hemisulfate
    Berberine Hemisulfate is a compound that exhibits anti-inflammatory, anti-diabetic, pro-cardiovascular, cholesterol lowering, anti-tumor and anti- depressant activity.
    Katalog #CAS NummerSummenformelMenge
    sc-202496633-66-9C20H18NO4•½SO41 g
  • Bestatin Methyl Ester
    A cell-permeable derivative of Bestatin which displays slightly stronger inhibition of neutral aminopeptidase than Bestatin, but has much weaker activity against basic aminopeptidase. It also augments Fas- or TNF-α-induced apoptosis in solid tumor cell lines.
    Katalog #CAS NummerSummenformelMenge
    sc-22135065322-89-6C17H26N2O45 mg
  • Betamethasone
    Katalog #CAS NummerSummenformelMenge
    sc-204647378-44-9C22H29FO5100 mg/500 mg
  • BH3I-1
    This is a cell permeable BH3 mimetic that binds to Bcl-XL.
    Katalog #CAS NummerSummenformelMenge
    sc-221352300817-68-9C15H14BrNO3S25 mg
  • BH3I-1"
    This is a cell permeable BH3 mimetic that binds to Bcl-XL.
    Katalog #CAS NummerSummenformelMenge
    sc-221354n.n.C15H15NO3S25 mg
  • BH3I-2'
    A cell-permeable BH3 mimetic that induces apoptosis by specifically preventing BH3 domain-mediated interaction between pro-apoptotic and anti-apoptotic members of the Bcl-2 family. Reported to block the interaction between Bak BH3 and Bcl-x by targeting the Bcl-x binding pocket.
    Katalog #CAS NummerSummenformelMenge
    sc-221355315195-18-7C19H11Cl3INO4S1 mg
  • C2 Ceramide (N-Acetylsphingosine, D-erythro)
    A cell-permeable ceramide and potent modulator of cell proliferation and differentiation.
    Katalog #CAS NummerSummenformelMenge
    sc-2013753102-57-6C20H39NO35 mg/25 mg
  • C75
    Inhibitor of fatty acid synthase (FAS) reducing food intake and body weight in mice. Exhibits irreversible slow-binding biphasic inactivation of fatty acid synthase.
    Katalog #CAS NummerSummenformelMenge
    sc-202511191282-48-1C14H22O41 mg/5 mg
  • CD 2665
    A selective RARβ/γ antagonist (KD values are 110, 306 and > 1000 nM for RARγ, RARβ and RARα respectively). Shown to block retinoic acid-induced apoptosis ex vivo.
    Katalog #CAS NummerSummenformelMenge
    sc-293988170355-78-9C31H34O5•xH2O10 mg/50 mg
  • CD 437
    Cell-permeable retinoid-related molecule. Induces tumor growth arrest and apoptosis. The mechanism is not yet understood. Studies suggest CD437/AHPN functions as an ER stress inducer.
    Katalog #CAS NummerSummenformelMenge
    sc-202527125316-60-1C27H26O35 mg
  • Chaetocin
    An inhibitor of lysine-specific histone methyltransferase effects, which are essential for gene expression patterns during cell differentiation. Also reported to induce apoptosis in some murine cancer cells.
    Katalog #CAS NummerSummenformelMenge
    sc-20089328097-03-2C30H28N6O6S4200 µg
  • Chlorambucil
    A nitrogen mustard bifunctional alkylating agent. Displays antineoplastic and immunosuppressant effect. Induces apoptosis in chronic lymphocytic leukemia cells.
    Katalog #CAS NummerSummenformelMenge
    sc-204682305-03-3C14H19Cl2NO2250 mg/1 g
  • CHM 1
    Katalog #CAS NummerSummenformelMenge
    sc-361147154554-41-3C16H10FNO310 mg/50 mg
  • CHM-1 hydrate
    A potent, selective antitumor agent in human hepatocellular carcinoma. CHM-1 induces apoptosis, and it binds tubulin and inhibits tubulin polymerization.
    Katalog #CAS NummerSummenformelMenge
    sc-214686154554-41-3 (anhydrous)C16H10FNO3 ·H2O5 mg/25 mg
  • Chrysin
    Antioxidant flavonoid. Displays anti-inflammatory and antitumor properties. Inhibits hypoxia-inducible factor-1α (HIF-1α) and induces apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-204686480-40-0C15H10O41 g
  • CIL-102
    A semisynthetic alkaloid derivative, which inhibits cell growth in a wide variety of cancer cell lines in a dose dependent manner.
    Katalog #CAS NummerSummenformelMenge
    sc-214722479077-76-4C19H14N2O210 mg
  • Citrinin
    Katalog #CAS NummerSummenformelMenge
    sc-358726518-75-2C13H14O55 mg/25 mg
  • cis-3,4',5-Trimethoxy-3'-aminostilbene
    A Resveratrol derivative which shows apoptotic activity at nanomolar concentrations. Has an IC50= 0.3. It showed activity toward resistant HL60R cells and their activity was higher than that of several classic chemotherapeutic agents.
    Katalog #CAS NummerSummenformelMenge
    sc-217910586410-12-0C17H19NO310 mg
  • Clodronate, Disodium Salt
    A first-generation bisphosphonate and strong inhibitor of osteoclast-mediated bone resorption. Contains cytotoxic effects towards macrophages.
    Katalog #CAS NummerSummenformelMenge
    sc-20254722560-50-5CH2Cl2O6P2Na2 ·xH2O10 mg
  • Colcemid
    A cell synchronizing agent that induces coordination of nuclear and cytoplasmic events during cell growth. Also an anti-tubulin agent which blocks cell growth at the mitotic level.
    Katalog #CAS NummerSummenformelMenge
    sc-202550477-30-5C21H25NO55 mg
  • Colchicine
    An apoptosis reagent that affects microtubule polymerization and disrupts cytoskeletal formation. Also known to interfere with tissue plasminogen activators.
    Katalog #CAS NummerSummenformelMenge
    sc-20300564-86-8C22H25NO61 g/5 g
  • Concanavalin A
    A plant lectin that is a T cell mitogen. It induces apoptosis in human fibroblasts.
    Katalog #CAS NummerSummenformelMenge
    sc-20300711028-71-0n.n.50 mg/250 mg
  • Cyclophosphamide
    Katalog #CAS NummerSummenformelMenge
    sc-36116550-18-0C7H15Cl2N2O2P50 mg
  • Cyclophosphamide Monohydrate
    A widely used antineoplastic agent that also displays immuno-suppressant activity. Induces apoptotic cell death in rat thymus throught Fas/Fas ligand pathway.
    Katalog #CAS NummerSummenformelMenge
    sc-2021176055-19-2C7H15Cl2N2O2P ·H2O1 g
  • Cyproterone Acetate
    A hepatomitogen and tumor promoter. Induces apoptosis in hepatocytes.
    Katalog #CAS NummerSummenformelMenge
    sc-204703427-51-0C24H29ClO4100 mg/250 mg
  • D-erythro-N,N-Dimethylsphingosine
    N,N-Dimethylsphingosine inhibits sphingosine kinase, blocking the conversion of sphingosine to sphingosine-1 phosphate.
    Katalog #CAS NummerSummenformelMenge
    sc-201373119567-63-4C20H41NO25 mg/25 mg
  • D-α-Tocopheryl Succinate
    An apoptosis agent that triggers caspase-mediated apoptosis at high concentrations and prevents cell proliferation at low concentrations.
    Katalog #CAS NummerSummenformelMenge
    sc-2001414345-03-3C33H54O51 g
  • Deguelin
    A natural product that displays profound antiproliferative activity in many tumor cell lines.
    Katalog #CAS NummerSummenformelMenge
    sc-200657522-17-8C23H22O65 mg/25 mg
  • Dexamethasone Sodium Phosphate
    A systemic corticosteroid. It induces apoptosis and inhibits sodium phosphate symporter. Used in the treatment of emetic effects of cancer therapy and epicondylitis.
    Katalog #CAS NummerSummenformelMenge
    sc-2047152392-39-4C22H28FO8PNa2100 mg/500 mg
  • Dicoumarol
    Reductase inhibitor possessing anticoagulant properties. Aids in apoptosis induction via stimulation of SAPK-JNK and NF-κB pathway blocking. This has no effect on the phosphorylation of P38 or activation of AKT. Also shown to block brefeldin A-dependent mono-ADP-ribosylation in vitro and Golgi disassembly in living cells.
    Katalog #CAS NummerSummenformelMenge
    sc-20564766-76-2C19H12O6500 mg
  • Diethylstilbestrol
    A synthetic estrogen that induces apoptosis in hormone-insensitive prostate cancer cells.
    Katalog #CAS NummerSummenformelMenge
    sc-20472056-53-1C18H20O21 g/5 g
  • Difluoromethylornithine
    An irreversible inhibitor of ornithine decarboxylase which has antiangiogenic activity, inhibits carcinogenesis and induces apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-20472367037-37-0C6H12F2N2O210 mg/25 mg
  • Disulfiram
    A DNA demethylating agent which inhibits prostate cancer cell growth by inhibition of DNA methyltransferase. In addition, studies indicate that Disulfiram inhibits aldehyde dehydrogenase (ALDH) resulting in the accumulation of acetaldehyde upon ethanol ingestion.
    Katalog #CAS NummerSummenformelMenge
    sc-20565497-77-8C10H20N2S450 g/100 g
  • DMXAA
    Apoptosis inducer. Anti-vascular.
    Katalog #CAS NummerSummenformelMenge
    sc-207592117570-53-3C17H14O45 mg/25 mg
  • Docetaxel
    A semi-synthetic analog of Taxol. Stabilizes microtubules and inhibits mitosis, leading to apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-201436114977-28-5C43H53NO145 mg/25 mg/250 mg
  • Dolastatin 15
    A marine natural product with anti-neoplastic, weak microtubule inhibitor, tubulin inhibitor, hematopoietc progenitor cell inhibitor, as well as immunoglobulin production and leukemia cell proliferation inhibitor
    Katalog #CAS NummerSummenformelMenge
    sc-201449123884-00-4C45H68N6O91 mg
  • Eeyarestatin I
    An endoplasmic reticulum associated degradation inhibitor that suppresses protein translocation and therefore limits the elimination of misfolded proteins from the ER.
    Katalog #CAS NummerSummenformelMenge
    sc-358130412960-54-4C27H25Cl2N7O710mg
  • Embelin
    Shown to be an antinociceptive and antiinflammatory agent with antioxidative capabilities. Also been reported to induce apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-201555550-24-3C17H26O410 mg/50 mg
  • Enhancer for Receptors
    Katalog #CAS NummerSummenformelMenge
    sc-221586n.n.n.n.20 µg
  • (-)Epicatechin gallate
    A polyphenol apoptosis inducer in tumor cells commonly found in green tea. Studies suggest that (-)Epicatechin gallate causes anti-proliferative and anti-inflammatory effects on pancreatic ductal adenocarcinoma cells.
    Katalog #CAS NummerSummenformelMenge
    sc-2047391257-08-5C22H18O101 mg/5 mg
  • Erucin
    An isothiocyanate from cruciferous vegetable. It is effective inapoptosis induction and mitochondrial potiential dissipation.
    Katalog #CAS NummerSummenformelMenge
    sc-2047414430-36-8C6H11NS225 mg/50 mg
  • Estren
    A steroid ligand that exhibits lower binding affinity for estrogen receptor and has no classical transcriptional activity. Shown to attenuate osteoblast apoptosis, stimulate osteoclast apoptosis, and increase bone mass and strength with no affect to reproductive organs in a non-sex-specific mechanism of action. Possibly useful in studies pertaining to hormone replacement therapy for osteoporosis.
    Katalog #CAS NummerSummenformelMenge
    sc-20474535950-87-9C18H28O210 mg
  • Farnesol
    Polyprenyl alcohol found in plant essential oils. Induces apoptosis in cell cultures.
    Katalog #CAS NummerSummenformelMenge
    sc-2047484602-84-0C15H26O50 ml/100 ml
  • Fludarabine
    Prodrug converted to free nucleoside 9-β-D-arabinosyl-2-fluoroadenine (F-ara-A). F-ara-A enters cells and accumulates as 5’-triphosphate. Interferes with DNA synthesis and repair. Induces apoptosis of cancer cells and RNA transcription inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-20475521679-14-1C10H12FN5O45 mg/25 mg
  • Gambogic Acid
    Shown to induce apoptosis without affecting the cell cycle. Also reported to decrease Bcl-2 and Bax gene as well as transferrin receptors, which may result in apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-2001372752-65-0C38H44O85 mg/25 mg
  • Gemcitabine Hydrochloride
    Deoxycytidine analog with cytotoxic effects. Inhibits DNA synthesis and induces apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-204763122111-03-9C9H11F2N3O4 ·HCl25 mg/100 mg
  • Geranylgeraniol
    An intermediate in the mevalonate pathway, that has been shown to prevent bone re-adsorption, inhibition of osteoclast formation, and kinase activation in vitro; reduce toxic effects of statins, without inhibiting cholesterol production.
    Katalog #CAS NummerSummenformelMenge
    sc-20085824034-73-9C20H34O20 mg/100 mg
  • GGTI-298
    A cell-permeable, prodrug form of the GGTase I inhibitor GGTI-297. Inhibits the processing of Rap 1A but has no effect on the processing of H-Ras. Also arrests cells in the G0/G1 phase of the cell cycle, induces apoptosis, and enhances iNOS induction by IL-1β.
    Katalog #CAS NummerSummenformelMenge
    sc-221673180977-44-0C27H33N3O3S250 µg
  • Gingerol
    Shown to activate cardiac and skeletal SR Ca2+-ATPase with apoptosis inducing, antiinflammatory, and antioxidant characteristics.
    Katalog #CAS NummerSummenformelMenge
    sc-20151923513-14-6C17H26O45 mg/20 mg
  • HA14-1
    A small, cell-permeable nonpeptidic ligand that binds to the Bcl-2 surface pocket and blocks its biological action. Induces apoptosis in HL-60 leukemic cells overexpressing Bcl-2 and in NIH 3T3 cells via the activation of caspases by a mechanism that is distinct from Fas-mediated apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-20591165673-63-4C17H17BrN2O55 mg/25 mg
  • Hexamethylene Biscetamide
    Prototype of hybrid polar inducers of apoptosis of various transformed cells.
    Katalog #CAS NummerSummenformelMenge
    sc-2047723073-59-4C10H20N2O225 g/50 g
  • Hinokitiol
    Shown to be a potent iron chelator that inhibits UV B-induced apoptosis in keratinocytes of murine skin. Also demonstrates antimicrobial characteristics.
    Katalog #CAS NummerSummenformelMenge
    sc-200812499-44-5C10H12O250 mg/250 mg
  • HLI 373
    HLI 373 is an inhibitor of Hdm2 ubiquitin ligase (E3) which blocks Hdm2-mediated ubiquitylation, proteasomal degradation of p53 and activates p53-dependent transcription.
    Katalog #CAS NummerSummenformelMenge
    sc-358833502137-98-6C18H23N5O2 ·2HCl ·xH2O10 mg/50 mg
  • HMBA
    An inhibitor of microtubule polymerization. An apoptosis inducer.
    Katalog #CAS NummerSummenformelMenge
    sc-300799n.n.C22H16O310 mg
  • Homoharringtonine
    Cephalotaxine alkaloid. Inhibits the formation of diphenylalanine and acetylphenylalanyl-puromycin in liver ribosomes. Has promising activity in hematologic malignancies. Lowers telomerase levels.
    Katalog #CAS NummerSummenformelMenge
    sc-20265226833-87-4C29H39NO91 mg/5 mg/10 mg
  • Honokiol
    Biphenyl neolignan and active part of Magnolia extract that displays anti-angiogenic, anti-tumor and anxiolytic properties. Blocks VEGFR2 autophosphorylation and subsequent rac activation.
    Katalog #CAS NummerSummenformelMenge
    sc-20265335354-74-6C18H18O210 mg/100 mg
  • Idarubicin Hydrochloride
    A hydrochloride salt preparation of Idarubicin and an anthracycline analog of daunorubicin. Shown to be an apoptosis inducer that triggers ROS production.
    Katalog #CAS NummerSummenformelMenge
    sc-20477457852-57-0C26H27NO9 ·HCl1 mg/5 mg
  • Indanocine
    A potent cytostatic and cytotoxic indanone that inhhibits tubulin polymerization. Induces apoptotic cell death in stationary-phase multidrug-resistant cancer cells.
    Katalog #CAS NummerSummenformelMenge
    sc-221750n.n.C20H21NO41 mg
  • Ionomycin
    Highly selective and potent calcium ionophore which serves as a useful tool for increasing intracellular Ca2+ concentrations. A non-fluorescent antibiotic and more effective than A23187 (sc-3591).
    Katalog #CAS NummerSummenformelMenge
    sc-359256092-82-1C41H70CaO91 mg/5 mg
  • Iron Chelator, Dp44mT
    A cell-permeable di-2-pyridyl thiosemicarbazone (DpT) based tridentate ligand that displays potent and selective antiproliferative properties in neoplastic cells and minimally affects normal cells. Prevents aggressive growth of M109 lung carcinoma in mice. Shown to mobilize cellular iron effectively, and generate ROS leading to apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-221764n.n.C14H15N5S25 mg
  • Isoapoptolidin
    A ring expanded isomer of apoptolidin. In water, an equilibrium mixture of apoptolidin:isoapoptolidin (~1.5:1) is formed within hours. Used for F0F1-ATPase assays.
    Katalog #CAS NummerSummenformelMenge
    sc-202187476647-30-0C58H96O21100 µg
  • Jasplakinolide
    Binds to F-actin competitively with Phalloidin. Stabilizes F-actin and promotes actin polymerization. Produces antiproliferative and cytotoxic effects.
    Katalog #CAS NummerSummenformelMenge
    sc-202191102396-24-7C36H45BrN4O650 µg/100 µg
  • Kainic acid
    An agonist of the glutamate-recognizing ionotropic kainate receptors. Employed as a tool for inducing excitotoxicity and producing seizures in neurotransmission models.
    Katalog #CAS NummerSummenformelMenge
    sc-200454487-79-6C10H15NO45 mg/25 mg
  • LE 135
    Retinoic acid receptor antagonist; displays moderate selectivity for RARβ over RARα; highly selective over RARγ and RXRα. Inhibits human HL-60 leukemia cell differentiation induced by the retinoid Am80.
    Katalog #CAS NummerSummenformelMenge
    sc-204053155877-83-1C29H30N2O210 mg/50 mg
  • Lipopolysaccharide, Salmonella typhimurium
    Katalog #CAS NummerSummenformelMenge
    sc-221857n.n.n.n.5 mg
  • Lovastatin
    A hypocholesterolemic statin, inhibits HMGCR and mevalonate biosynthesis. Mevalonate reduction confers inhibition of cholesterol biosynthesis and blocks isoprenylation modification of ras proteins.
    Katalog #CAS NummerSummenformelMenge
    sc-20085075330-75-5C24H36O55 mg/25 mg
  • Methylprednisolone
    An apoptosis inducer used in the treatment of lupus nephritis and was also found to inhibit human small cell lung cancer cell growth.
    Katalog #CAS NummerSummenformelMenge
    sc-20574983-43-2C22H30O5100 mg/500 mg
  • Mevastatin (Compactin)
    An inhibitor of isoprenoid biosynthesis via inhibition of HMG-CoA reductase, and an inducer of neurite outgrowth in neuroblastomas.
    Katalog #CAS NummerSummenformelMenge
    sc-20085373573-88-3C23H34O510 mg/50 mg
  • Mevastatin Sodium
    This is the active carboxylate form of mevastatin. It is active in whole cells as well as in cell free assays.
    Katalog #CAS NummerSummenformelMenge
    sc-205752n.n.C23H35NaO65 mg/25 mg
  • Miltefosine
    A PI3K/Akt inhibitor that also inhibits anti-IgE induced histamine release from skin mast cells. Has been shown to also reduce cytokines IL-1β, IL-4, and IL-6 in certain skin tissue cells.
    Katalog #CAS NummerSummenformelMenge
    sc-20313558066-85-6C21H46NO4P50 mg
  • MIRA-1
    Restores wild-type conformation, function and DNA binding activity to mutant p53. Induces p53 transcriptional transactivation of p21, MDM2 and PUMA. Promotes tumor cell death by apoptosis in a mutant p53-dependent manner in vitro (IC50 = 10μM).
    Katalog #CAS NummerSummenformelMenge
    sc-20408772835-26-8C8H9NO410 mg/50 mg
  • Mitomycin C (4% in NaCl)
    A reagent used to generate mitotically inactive feeder cells in culture. Mitomycin C (4% in NaCl) is a DNA crosslinking agent which inhibits DNA synthesis and causes apoptosis via a p53-dependent pathway.
    Katalog #CAS NummerSummenformelMenge
    sc-28696450-07-7 (non-salt)C15H18N4O5 ·xNaCl50 mg
  • Narciclasine
    Katalog #CAS NummerSummenformelMenge
    sc-36127129477-83-6C14H13NO71 mg
  • Necrosis Inhibitor, IM-54
    A cell-permeable mono-indolylmaleimide compound that selectively blocks oxidative stress-induced necrotic cell death (~3 µM IM-54 prevented ~50% cell death in HL60 cells exposed to 100 µM H2O2). Does not offer protection against Etoposide induced apoptosis or display antioxidant properties. Does not affect the kinase activities of S6K1 and PKC isozymes even at concentrations as high as 50 µM.
    Katalog #CAS NummerSummenformelMenge
    sc-222053861891-50-1C19H23N3O25 mg
  • Nigericin•Na
    Nigericin, a polyether antibioitc K+ and Na+ ionophore, stimulates Ca2+ release from mitochondria and stimulates ATPase activity.
    Katalog #CAS NummerSummenformelMenge
    sc-20151828380-24-7C40H67O11··Na5 mg/1 mg
  • Nutlin-3
    The most commonly used nutlin, nutlin-3 inhibits p53-Mdm2 interaction resulting in antiproliferative activity in treated cells.
    Katalog #CAS NummerSummenformelMenge
    sc-45061548472-68-0C30H30Cl2N4O41 mg
  • Noscapine hydrochloride
    Opioid alkaloid binds to arresting cells in mitosis, inducing apoptosis and tubulin. Also is an antagonist at bradykinin receptors (pA2 = 6.68), inhibits carbachol-stimulated phosphoinositol turnover and enhances forskolin-stimulated increases in cAMP levels in CNS tissues. Clinically used antitussive agent.
    Katalog #CAS NummerSummenformelMenge
    sc-203650912-60-7C22H23NO7•HCl•xH2O100 mg
  • Oligomycin
    A macrolide that acts as a specific inhibitor of the mitochondrial ATP-synthase and blocks oxidative phosphorylation.
    Katalog #CAS NummerSummenformelMenge
    sc-2033421404-19-9C45H74O1110 mg
  • Oncrasin 1
    Proapoptotic substance. Induces abnormal nuclear aggregation of PKCι and suppressing RNA transcription. Displays antiproliferative effects against various human tumor cell lines. Shown to inhibit human xenograft growth by 75% in vivo.
    Katalog #CAS NummerSummenformelMenge
    sc-20414675629-57-1C16H12CINO10 mg/50 mg
  • P-Glycoprotein Inhibitor, C-4
    A cell-permeable cinnamoyl compound that reversibly inhibits P-gp (P-glycoprotein) efflux function. Also reverses the MDR (multidrug resistance) phenotype with no effect on P-gp expression. Significantly enhance Paclitaxel- and Vincristine- induced cytotoxicity as well as apoptosis in P-gp expressing KBV20C cells.
    Katalog #CAS NummerSummenformelMenge
    sc-222109n.n.C23H18ClNO410 mg
  • p53 Activator III, RITA
    A trycyclic thiophene derivative that binds and activates p53 and induces apoptosis. Renal carcinoma research has demonstrated that RITA induces DNA damage, and DNA-DNA, DNA-protein crosslinks.
    Katalog #CAS NummerSummenformelMenge
    sc-202753213261-59-7C14H12O3S21 mg
  • PAC 1
    Procaspase-activating compound; activates procaspase-3 to produce caspase-3. Less efficiently activates procaspase-7.
    Katalog #CAS NummerSummenformelMenge
    sc-203174315183-21-2C23H28N4O210 mg/50 mg
  • PDK1/Akt/Flt Dual Pathway Inhibitor
    A cell-permeable compound that selectively induces apoptosis in AML (Acute Myelogenous Leukemia) with little effect on normal CD34+ AML progenitor cells. Directly inhibit both PDK1 and Akt activities in in vitro kinase assays in a dose-dependent manner and block cellular phosphorylation of Akt at both Ser473 and Thr308. The dual inhibition nature against both PDK1/Akt and Flt3/PIM signaling pathways allows effective elimination of AML cells that are otherwise resistant to inhibitors that target only the PDK1/Akt pathway.
    Katalog #CAS NummerSummenformelMenge
    sc-222144n.n.C10H4N6O5 mg
  • (-)-Perillyl Alcohol
    A monoterpene derived from Lavender, that induces apoptosis in colon tumor cells. Inhibits mammary cancer by inducing hepatocyte phase II enzymes, glutathione-S-transferase.
    Katalog #CAS NummerSummenformelMenge
    sc-20579818457-55-1C10H16O10 g/50 g
  • (+)-Perillyl alcohol
    Katalog #CAS NummerSummenformelMenge
    sc-36218957717-97-2C10H16O1 g
  • PHA 767491 hydrochloride
    Potent, ATP-competitive dual cdc7/cdk9 inhibitor (IC50 values are 10 and 34 nM respectively) that prevents initiation of DNA replication. Induces apoptosis in a p53-independent manner in vivo and Inhibits cell proliferation in a variety of human cell lines (IC50 ~ 0.86 - 5.87 μM). Also inhibits mitogen-activated protein kinase-activated protein kinase-2 (MK-2) (IC50 = 171 nM).
    Katalog #CAS NummerSummenformelMenge
    sc-204187845714-00-3C12H11N3O.ClH10 mg
  • Phenylethyl 3-methylcaffeate
    Has chemopreventive property against chemically induced colon carcinogenesis. Also amplifies apoptosis in azoxymethane induced colon tumors.
    Katalog #CAS NummerSummenformelMenge
    sc-20580471835-85-3C18H18O450 mg/100 mg
  • PIT 1
    Katalog #CAS NummerSummenformelMenge
    sc-36129353501-41-0C14H10ClN3O4S10 mg/50 mg
  • PPAHV
    Non-pungent resiniferatoxin-type phorboid vanilloid. Agonist of rat TRPV1 but virtually inactive with human TRPV1. Induces apoptosis through a TRPV-independent mechanism. Tumor promotor.
    Katalog #CAS NummerSummenformelMenge
    sc-202296175796-50-6C39H44O111 mg/5 mg
  • Pregnenolone
    Endogenous neurosteroid that inhibits GABA-gated chloride currents by enhancing receptor desensitization. Modulates NMDA receptors resulting in delayed apoptotic retinal cell death.Stimulates prostate LNCaP cell proliferation through binding to the mutated androgen receptor.
    Katalog #CAS NummerSummenformelMenge
    sc-204860145-13-1C21H32O25 g/25 g
  • PRIMA-1MET
    Katalog #CAS NummerSummenformelMenge
    sc-3612955291-32-7C10H17NO310 mg
  • Prodigiosin
    A water insoluble, potent proapoptotic compound that belongs to a family of Prodigions isolated from gram-negative bacteria. Also described as a red-pigmented antibiotic produced by Serratia marcescens strains.
    Katalog #CAS NummerSummenformelMenge
    sc-20229882-89-3C20H25N3O500 µg
  • Quercetin
    A hydroxylated flavonoid that causes reversible inhibition of fatty acid synthase. Furthermore, Quercetin has been reported to reduce de novo synthesis of long chain fatty acids.
    Katalog #CAS NummerSummenformelMenge
    sc-206089117-39-5C15H10O7100 mg/500 mg
  • Raltitrexed monohydrate
    This is a folate-based inhibitor of thymidylate synthase (TS) that is rapidly metabolized to its more potent polyglutamate derivatives.
    Katalog #CAS NummerSummenformelMenge
    sc-311520n.n.C21H22N4O6S•H2O10 mg
  • Reveromycin A
    The dominant analogue of a complex of spiroketals isolated from Streptomyces. Inhibits the mitogenic activity of EGF. G1 phase cell cycle inhibitor, selectively inhibiting isoleucyl-tRNA synthetase.
    Katalog #CAS NummerSummenformelMenge
    sc-202314134615-37-5C36H52O11100 µg/500 µg
  • RGD peptide (GRGDNP)
    An inhibitor of integrin-ligand interactions. It can induce apoptosis in the absence of signals and integrin-mediated cell clustering.
    Katalog #CAS NummerSummenformelMenge
    sc-201176114681-65-1C23H38N10O105 mg
  • (S)-a-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
    Active enantiomer of AMPA that induces apoptotic cell death in cortical neurons. Does not exhibit any affinity for NMDA receptors.
    Katalog #CAS NummerSummenformelMenge
    sc-20325083643-88-3C7H10N2O45 mg
  • Saikosaponin D
    Saikosaponin D inhibits cell growth of human cancer cells by inducing apoptosis and blocking cell cycle progression in the G1 phase. Saikosaponin D was found to stimulate corticotropin-releasing factor (CRF) gene expression and CRF release.
    Katalog #CAS NummerSummenformelMenge
    sc-30178620874-52-6C42H68O131 mg
  • Simvastatin, Sodium Salt
    Carboxylate form of Simvastatin which is active in whole cells and in cell-free preparations.
    Katalog #CAS NummerSummenformelMenge
    sc-22231212009-77-6C25H39O6•Na5 mg
  • SJ 172550
    SJ 172550 is an MDMX inhibitor which reversibly binds MDMX and inhibits MDMX-p53 interaction in cell cultures.
    Katalog #CAS NummerSummenformelMenge
    sc-357403431979-47-4C22H21ClN2O510mg /50mg
  • Sodium Butyrate
    Shown to cause hyperacetylation of histones via inhibition of histone deacetylase. Also reported to induce differentiation, gene expression, and prevent proliferation.
    Katalog #CAS NummerSummenformelMenge
    sc-202341156-54-7C4H7O2Na250 mg/25 g
  • SU11652
    A potent cell-permeable pyrrole-indolinone compound that acts as an ATP-competitive tyrosine kinase receptor and angiogenic inhibitor that exhibits greater selectivity for PDGFRβ (IC50 = 3 nM), VEGFR2 (IC50 = 27 nM), FGFR1 (IC50 = 170 nM), and Kit family members (IC50 ~ 10-500 nM) over EGFR (IC50 >20 µM). Display anti-proliferative and pro-apoptotic properties in tumor cells.
    Katalog #CAS NummerSummenformelMenge
    sc-204310326914-10-7C22H27ClN4O2500 µg
  • Sulindac
    Inhibits the NF-κB pathway. Non-steroidal anti-inflammatory drug. Reduces the level and activity of several cyclin-dependent kinases (CDKs) and induces apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-20282338194-50-2C20H17FO3S1 g
  • Taxol
    An antineoplastic and microtubule affecting agent that causes apoptotic cell death, internucleosomal DNA fragmentation, and inhibition of protein isoprenylation.
    Katalog #CAS NummerSummenformelMenge
    sc-20143933069-62-4C47H51NO145 mg/25 mg/250 mg
  • Teniposide
    Glycoside-derivative of podophyllotoxin. Has cytostatic effect. Inhibits topoisomerase II while induces apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-20491029767-20-2C32H32O13S25 mg/100 mg
  • Tetracycline
    Used for treatment of chronic inflammatory cells. Tetracycline derivatives induce apoptosis in osteoclasts, Jurkat T lymphocyte cells and in cultured monocytes and macrophages.
    Katalog #CAS NummerSummenformelMenge
    sc-20585860-54-8C22H24N2O810 g/25 g
  • Thiocolchicine
    Inhibitor of microtubules by specific binding to tubulin. Modulator of axonal cytoskeleton. Induces apoptosis. Topoisomerase I inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-2028382730-71-4C22H25NO5S100 mg/1 g
  • TPEN
    A cell permeable, high-affinity heavy metal chelator that exhibits low affinity for Mg2+ and Ca2+. A useful tool for chelation of intracellular Zn2+.
    Katalog #CAS NummerSummenformelMenge
    sc-20013116858-02-9C26H28N6100 mg
  • Triamcinolone
    A glucocorticoid capable of sustaining neuromuscular transmission during early motor nerve degeneration. It is also known to induce apoptosis in T lymphocytes.
    Katalog #CAS NummerSummenformelMenge
    sc-204924124-94-7C21H27FO650 mg/250 mg
  • Tubeimoside I
    A triterpenoid saponin isolated from tubers of bolbostemma paniculatum, Franquet, a traditional Chinese medicine "Tu-Bei-Mu". Used as anti-tumor agent, induces cell cycle arrest and apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-204931102040-03-9C63H98O2910 mg/25 mg
  • TW-37
    Katalog #CAS NummerSummenformelMenge
    sc-361387877877-35-5C33H35NO6S10 mg/50 mg
  • UA62784
    A specific inhibitor of centromere protein E (CENPE) kinesin-like protein mitotic inhibitor. CENP-E is a kinesin-like motor protein that localizes to the kinetochore during mitosis and is essential for bipolar spindle formation. UA62784 is a novel specific inhibitor of CENP-E, which likely binds within the motor domain of CENP-E. UA62784 causes reversible cell cycle arrest in mitosis before metaphase, which leads to apoptosis. The compound is not interacting with microtubules directly.
    Katalog #CAS NummerSummenformelMenge
    sc-216036313367-92-9C23H15NO35 mg/25 mg
  • Valinomycin
    Ionophore selective to potassium. Used to induce mitochondrial swelling, CHO apoptotic induction and antagonism of endothelin-induced vasoconstriction.
    Katalog #CAS NummerSummenformelMenge
    sc-2009912001-95-8C54H90N6O1825 mg
  • VER-49009
    A pyrazole compound that inhibits Hsp90 with an IC50 value of 47 nM; produces a cellular antiproliferative GI50 value of 685 nM when tested against a human cancer cell line panel.
    Katalog #CAS NummerSummenformelMenge
    sc-357409940289-57-6C19H18ClN3O4500 µg/1 mg
  • Vinblastine Sulfate
    The sulfate of an alkaloid with anti-neoplastic, anti-mitotic, immunosuppressive and apoptotic activity. The compound’s methods of action revolves around inhibition of microtubule assembly and depolymerization of microtubules.
    Katalog #CAS NummerSummenformelMenge
    sc-201447143-67-9C46H58N4O9 ·H2SO410 mg/50 mg
  • Vincristine Sulfate
    Shown to bind tubulin via a protein self association reaction. Also shown to contain anti-proliferative characteristics via induction of apoptosis of cells.
    Katalog #CAS NummerSummenformelMenge
    sc-2014342068-78-2C46H56N4O10 ·H2SO45 mg/25 mg
  • Xanthorrhizol
    An antibacterial and an anti-inflammatory compound that can induce apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-20285530199-26-9C15H22O1 mg
  • Zearalenone
    A phytoestrogenic mycotoxin usually produced by Fusarium species. Also shown to be an anti-proliferative agent that causes mitochondrial release of Cytochrome c and production of ROS.
    Katalog #CAS NummerSummenformelMenge
    sc-20494317924-92-4C18H22O510 mg/50 mg