| | 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 Nummer | Summenformel | Menge |
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| sc-223742 | 300675-28-9 | C10H5Cl2NO3 | 1 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 Nummer | Summenformel | Menge |
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| sc-352980 | 137346-42-0 | C25H26N4O4 | 1 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 Nummer | Summenformel | Menge |
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| sc-221221 | 581797-29-7 | C18H13F3N2O3 | 10 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 Nummer | Summenformel | Menge |
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| sc-205595 | 54135-60-3 | C13H16O4 | 10 mg |
- Apoptosis Inhibitor II, NS3694
A cell-permeable diarylurea compound that suppresses the formation of the apoptosome Apaf-1.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203823 | 426834-38-0 | C15H10ClF3N2O3 | 10 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 Nummer | Summenformel | Menge |
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| sc-3525 | 4431-00-9 | C22H14O9 | 100 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 Nummer | Summenformel | Menge |
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| sc-221285 | n.n. | C19H21Br2N3O ·2CF3CO2H | 5 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 Nummer | Summenformel | Menge |
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| sc-205606 | 11076-19-0 | C28H38O7 ·3NH3 | 100 µg |
- Bongkrekic Acid, Triammonium Salt
A ligand of the adenine nucleotide translocator.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-311298 | 1177154-51-6 | C28H35O7 ·3NH4 | 500 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 Nummer | Summenformel | Menge |
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| sc-3545 | 121263-19-2 | C44H38O14 | 100 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 Nummer | Summenformel | Menge |
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| sc-223865 | n.n. | C32H32F3N3O2 | 500 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 Nummer | Summenformel | Menge |
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| sc-205238 | 19231-60-8 | C10H3I4NO4 | 1 mg/10 mg |
- Chlorogenic Acid
An analog of Caffeic Acid (sc-200499) that displays antioxidant, analgesic, antipyretic and chemopreventive activity.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204683 | 327-97-9 | C16H18O9 | 500 mg/1 g |
- Colivelin
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-361153 | 867021-83-8 | C119H206N32O35 | 500 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 Nummer | Summenformel | Menge |
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| sc-221655 | n.n. | C38H45NO7 | 1 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 Nummer | Summenformel | Menge |
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| sc-202172 | 40732-48-7 | C10H11N5O7P ·Na | 25 mg |
- (±)-Huperzine A
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-218582 | 120786-18-7 | C15H18N2O | 1 mg |
- (-)-Huperzine A
An inhibitor of AChE. Antagonist of NMDA receptors. Protects against glutamate-mediated excitotoxicity.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-200183 | 102518-79-6 | C15H18N2O | 1 mg/5 mg |
- Hypericin
Inhibits PKC, CKII, MAP Kinase, Insulin R, EGFR, PI-3 Kinase and also noted to possess antiviral activity.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-3530 | 548-04-9 | C30H16O8 | 1 mg/5 mg |
- iMAC2
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-362750 | 335166-36-4 | C19H20Br2FN3.2HCl | 10 mg/50 mg |
- Linomide
Immunomodulator with antitumour properties. Inhibits apoptosis of T-cells in vivo and angiogenesis in rats.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204057 | 84088-42-6 | C18H16N2O3 | 10 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 Nummer | Summenformel | Menge |
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| sc-221873 | 4373-41-5 | C30H48O4 | 1 mg/5 mg |
- Mdivi-1
A compound that inhibits the mitochondrial division dynamin-related GTPase.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-215291 | 338967-87-6 | C15H10Cl2N2O2S | 5 mg/25 mg |
- Me-7BIO
Control compound for 6BIOand 7BIO.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-221878 | n.n. | C17H12BrN3O2 | 1 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 Nummer | Summenformel | Menge |
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| sc-203443 | 10236-47-2 (anhydrous) | C27H32O14 ·xH2O | 10 g/50 g |
- Necrostatin-1
An inhibitor of necroptosis, a non-apoptotic cell death pathway. Does not affect Fas/TNFR-triggered apoptosis.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-200142 | 4311-88-0 | C13H13N3OS | 20 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 Nummer | Summenformel | Menge |
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| sc-204815 | 64419-92-7 | C12H11N3OS | 5 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 Nummer | Summenformel | Menge |
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| sc-301483 | n.n. | C38H40N10•xH2O | 5 mg |
- Orsellinic acid
Benzoic acid. Blocks PAF-mediated neuronal apoptosis. Shows free radical scavenging activity.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-202752 | 480-64-8 | C8H8O4 | 1 mg |
- Pidotimod
A synthetic dipeptide with immunological modulatory activity on both the adaptive and innate immune responses.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204846 | 121808-62-6 | C9H12N2O4S | 1 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 Nummer | Summenformel | Menge |
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| sc-222230 | n.n. | C26H25F2N3O6 | 5 mg |
- R5C3
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-215783 | 753504-14-2 | C33H28N2O6 | 5 mg |
- Razoxane
Inhibits topoisomerase II without inducing DNA strand breaks (topo II catalytic inhibitor). | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-253425 | 21416-67-1 | C11H16N4O4 | 5 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 Nummer | Summenformel | Menge |
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| sc-253617 | 331852-66-5 | C17H16O7 | 10 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 Nummer | Summenformel | Menge |
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| sc-224304 | 24150-24-1 | C22H30O4 | 50 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 Nummer | Summenformel | Menge |
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| sc-222351 | n.n. | C21H46NO3PS | 1 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 Nummer | Summenformel | Menge |
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| sc-222372 | 95933-74-7 | C7H8N2O4 | 5 mg/10 mg |
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