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Apoptosis Inhibitors

  • 7,8-dichloro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
    Casein kinase 2 (CK2) is a threonine/serine-selective protein kinase involved in many signal transduction pathways. CK2 is known to negatively regulate apoptosis and its activity is increased in many tumors and proliferating tissues, which lends promise as an anti-cancer drug target. This chemical inhibits CK2 with an IC50 value of 0.8 µM.
    Katalog #CAS NummerSummenformelMenge
    sc-223742300675-28-9C10H5Cl2NO31 mg/5 mg
  • 7-nitro-10-octyl-3-phenyl-pyrimido[4,5-b]quinoline-2,4(3H,10H)-dione
    An antagonist of the interaction between survivin and the apoptosis-promoting protein Smac/Diablo, exhibiting an IC50 value of 2.2 µM; inhibits the interaction of survivin with INCENP less effectively with an IC50 value of 20 µM; cell-permeable and sensitizes cells to the induction of apoptosis by doxorubicin.
    Katalog #CAS NummerSummenformelMenge
    sc-352980137346-42-0C25H26N4O41 mg/5 mg
  • AG 490, m-CF3
    A cell-permeable, m-trifluoromethyl derivative of AG 490 that displays apoptotic and antiproliferative properties. Inhibits IL-7-induced JAK3 tyrosine phosphorylation in 2E8 cells in vitro and significantly decreases lymph node cellularity in a murine B and T cell lymphoma model in vivo.
    Katalog #CAS NummerSummenformelMenge
    sc-221221581797-29-7C18H13F3N2O310 mg
  • Apoptosis Inhibitor
    Cell-permeable inhibitor of apoptosis induction. Does not directly inhibit caspase-3, but effects are attributable to the inhibition of caspase-3 activation.
    Katalog #CAS NummerSummenformelMenge
    sc-20559554135-60-3C13H16O410 mg
  • Apoptosis Inhibitor II, NS3694
    A cell-permeable diarylurea compound that suppresses the formation of the apoptosome Apaf-1.
    Katalog #CAS NummerSummenformelMenge
    sc-203823426834-38-0C15H10ClF3N2O310 mg
  • Aurintricarboxylic Acid
    Inhibits Apoptosis. Potent inhibitor of DNA topoisomerase II. Stimulates tyrosine phosphorylation of MAP Kinases, Shc proteins, PI-3 Kinase and PLC-γ
    Katalog #CAS NummerSummenformelMenge
    sc-35254431-00-9C22H14O9100 mg
  • Bax Channel Blocker
    A cell-permeable dibromocarbazolo-piperazinyl derivative that displays anti-apoptotic properties. Effectively blocks Bid-induced cyctochrome c release from HeLa cell mitochondria by inhibiting Bax channel-forming activity.
    Katalog #CAS NummerSummenformelMenge
    sc-221285n.n.C19H21Br2N3O ·2CF3CO2H5 mg
  • Bongkrekic acid
    A mitochondrial permeability transition pore blocker that acts as an inhibitory ligand of the mitochondrial adenine nucleotide translocator. This compound has been shown to inhibit apoptosis by preventing PARP cleavage and DEVDase activity.
    Katalog #CAS NummerSummenformelMenge
    sc-20560611076-19-0C28H38O7 ·3NH3100 µg
  • Bongkrekic Acid, Triammonium Salt
    A ligand of the adenine nucleotide translocator.
    Katalog #CAS NummerSummenformelMenge
    sc-3112981177154-51-6C28H35O7 ·3NH4500 µg
  • Calphostin C
    Cell permeable, light dependent, potent and highly selective inhibitor of PKC. Inhibits PC-PLD1, PC-PLD2 and induces apoptotic DNA fragmentation.
    Katalog #CAS NummerSummenformelMenge
    sc-3545121263-19-2C44H38O14100 µg/1 mg
  • CAY10500
    Tumor necrosis factor α (TNFα) inhibitor that prevents binding to the TNF Receptor 1 (TNFR1).6 Binds to the biologically active TNFα trimer and promotes accelerated displacement of a single subunit to rapidly inactivate the cytokine. In a cell based assay, compound inhibited TNFα-mediated stimulation of IKB degradation.
    Katalog #CAS NummerSummenformelMenge
    sc-223865n.n.C32H32F3N3O2500 µg/1 mg
  • CAY10578
    CK2 is known to negatively regulate apoptosis, and increased activity has been noted in many proliferating tissues and tumors, which lends promise as an anticancer drug target. CAY10578 is a potent inhibitor of CK2 and is ATP competitive, only minimally inhibiting the activities of other protein kinases.
    Katalog #CAS NummerSummenformelMenge
    sc-20523819231-60-8C10H3I4NO41 mg/10 mg
  • Chlorogenic Acid
    An analog of Caffeic Acid (sc-200499) that displays antioxidant, analgesic, antipyretic and chemopreventive activity.
    Katalog #CAS NummerSummenformelMenge
    sc-204683327-97-9C16H18O9500 mg/1 g
  • Colivelin
    Katalog #CAS NummerSummenformelMenge
    sc-361153867021-83-8C119H206N32O35500 µg
  • Gambogic amide
    A selective agonist for TrkA which mimics the actions of NGF. This compound possesses robust neurotrophic actvity, while it prevents neuronal cell death 1.
    Katalog #CAS NummerSummenformelMenge
    sc-221655n.n.C38H45NO71 mg/5 mg
  • Guanosine 3’5’-cyclic Monophosphate, Sodium Salt
    An important intracellular second messenger that interacts with the extracellular signals NO and natriuretic peptides.
    Katalog #CAS NummerSummenformelMenge
    sc-20217240732-48-7C10H11N5O7P ·Na25 mg
  • (±)-Huperzine A
    Katalog #CAS NummerSummenformelMenge
    sc-218582120786-18-7C15H18N2O1 mg
  • (-)-Huperzine A
    An inhibitor of AChE. Antagonist of NMDA receptors. Protects against glutamate-mediated excitotoxicity.
    Katalog #CAS NummerSummenformelMenge
    sc-200183102518-79-6C15H18N2O1 mg/5 mg
  • Hypericin
    Inhibits PKC, CKII, MAP Kinase, Insulin R, EGFR, PI-3 Kinase and also noted to possess antiviral activity.
    Katalog #CAS NummerSummenformelMenge
    sc-3530548-04-9C30H16O81 mg/5 mg
  • iMAC2
    Katalog #CAS NummerSummenformelMenge
    sc-362750335166-36-4C19H20Br2FN3.2HCl10 mg/50 mg
  • Linomide
    Immunomodulator with antitumour properties. Inhibits apoptosis of T-cells in vivo and angiogenesis in rats.
    Katalog #CAS NummerSummenformelMenge
    sc-20405784088-42-6C18H16N2O310 mg/50 mg
  • Maslinic Acid
    A pentacyclic triterpene with antioxidant and anti-inflammatory properties. Shown to block the generation of nitric oxide, and inhibits the secretion of IL-6 and TNF-α induced by lipopolysaccharides
    Katalog #CAS NummerSummenformelMenge
    sc-2218734373-41-5C30H48O41 mg/5 mg
  • Mdivi-1
    A compound that inhibits the mitochondrial division dynamin-related GTPase.
    Katalog #CAS NummerSummenformelMenge
    sc-215291338967-87-6C15H10Cl2N2O2S5 mg/25 mg
  • Me-7BIO
    Control compound for 6BIOand 7BIO.
    Katalog #CAS NummerSummenformelMenge
    sc-221878n.n.C17H12BrN3O21 mg
  • Naringin hydrate
    A citrus bioflavonoid found to inhibit cytochrome P450 monooxygenase activity in mouse liver. It prevents toxin-induced cytoskeletal disruption and apoptotic liver cell death.
    Katalog #CAS NummerSummenformelMenge
    sc-20344310236-47-2 (anhydrous)C27H32O14 ·xH2O10 g/50 g
  • Necrostatin-1
    An inhibitor of necroptosis, a non-apoptotic cell death pathway. Does not affect Fas/TNFR-triggered apoptosis.
    Katalog #CAS NummerSummenformelMenge
    sc-2001424311-88-0C13H13N3OS20 mg/100 mg
  • Necrostatin-1, Inactive Control
    A cell-permeable N-demethylated thiohydantoin analog of Nec-1, devoid of anti-necroptotic properties and serves as a suitable inactive control.
    Katalog #CAS NummerSummenformelMenge
    sc-20481564419-92-7C12H11N3OS5 mg
  • NSC348884 hydrate
    This product is a nucleolar phosphoprotein that displays several biological activities in ribosome biogenesis, cell proliferation, cytoplasmic/nuclear shuttle transportation, nucleic acid binding, ribonucleic cleavage, centrosome duplication and molecular chaperoning, and is found in higher levels in tumor cells. Overexpression has been shown to lead to inhibition of apoptosis. NSC34884 upregulates p53.
    Katalog #CAS NummerSummenformelMenge
    sc-301483n.n.C38H40N10•xH2O5 mg
  • Orsellinic acid
    Benzoic acid. Blocks PAF-mediated neuronal apoptosis. Shows free radical scavenging activity.
    Katalog #CAS NummerSummenformelMenge
    sc-202752480-64-8C8H8O41 mg
  • Pidotimod
    A synthetic dipeptide with immunological modulatory activity on both the adaptive and innate immune responses.
    Katalog #CAS NummerSummenformelMenge
    sc-204846121808-62-6C9H12N2O4S1 g/5 g
  • Q-VD-OPH
    A selective, brain and cell permeable, highly potent and irreversible inhibitor of caspase-3, caspase-1, caspase-8 and caspase-9.
    Katalog #CAS NummerSummenformelMenge
    sc-222230n.n.C26H25F2N3O65 mg
  • R5C3
    Katalog #CAS NummerSummenformelMenge
    sc-215783753504-14-2C33H28N2O65 mg
  • Razoxane
    Inhibits topoisomerase II without inducing DNA strand breaks (topo II catalytic inhibitor).
    Katalog #CAS NummerSummenformelMenge
    sc-25342521416-67-1C11H16N4O45 mg
  • Suptopin-2
    Suppressor of topoisomerase II inhibition. Reverses cell cycle arrest; bypass of checkpoint function. Has inherent fluorescence and a distinct advantage in identification of molecule targets; effective concentraion in the µM range.
    Katalog #CAS NummerSummenformelMenge
    sc-253617331852-66-5C17H16O710 mg
  • tetramethyl Nordihydroguaiaretic Acid
    A synthetic derivative of NDGA and a non-selective lipoxygenase inhibitor. It inhibits Sp1 transcription factor binding at the HIV long terminal repeat promoter and at the α-ICP4 promoter (a gene essential for HSV replication).
    Katalog #CAS NummerSummenformelMenge
    sc-22430424150-24-1C22H30O450 mg/100 mg
  • thio-Miltefosine
    A sulfur-containing derivative of miltefosine. Miltefosine is an inhibitor of phosphocholine cytidylyl transferase (CTP) and has antimetastatic properties. At concentrations of 3 and 25 µM, miltefosine inhibits proliferation of HaCaT cells (immortalized human keratinocyte cell line) by 50% and 94%, respectively. The mechanism of action of miltefosine is not well established, but the antiproliferative effect may be mediated by an increase in cellular ceramide which results in apoptosis. Miltefosine is more than 90% effective in eradicating visceral infections of Leishmania species (kala azar), but the mechanism of this antiprotozoal activity is also poorly understood.
    Katalog #CAS NummerSummenformelMenge
    sc-222351n.n.C21H46NO3PS1 mg/5 mg
  • Trimidox
    A specific ribonucleotide reductase inhibitor that reduces levels of dGTP and dCTP in HL-60 cells, inducing apoptosis via activation of caspases without altering the cell cycle distribution. Trimidox inhibits growth of human promyelocytic leukemia HL-60 cells with an IC50 value of 35 µM.
    Katalog #CAS NummerSummenformelMenge
    sc-22237295933-74-7C7H8N2O45 mg/10 mg