| | 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 Nummer | Summenformel | Menge |
|---|
| sc-201628 | 147-94-4 | C9H13N3O5 | 1 g |
- 1,4-Benzoquinone
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202873 | 106-51-4 | C6H4O2 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-200419 | 32222-06-3 | C27H44O3 | 50 µg |
- 2-Amino-N-quinolin-8-yl-benzenesulfonamide
An apoptosis inducer that inhibits cell cycle at G2 phase.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-213750 | 16082-64-7 | C15H13N3O2S | 5 mg |
- 2-Chloro-2′-deoxyadenosine
A deoxyadenosine analog that induces apoptosis in chronic lymphocytic leukemia (CLL) cells.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202399 | 4291-63-8 | C10H12ClN5O3 | 10 mg |
- 2,3-DCPE
2,3 DCPE displays anticancer agent properties and induces ERK activation. Induces S-phase arrest and upregulates p21.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200139 | 418788-90-6 | C11H15Cl2NO2 ·HCl | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-204624 | 1968-05-4 | C17H14N2 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-200900 | 65646-68-6 | C26H33NO2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-290709 | 586410-08-4 | C17H18O4 | 500 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 Nummer | Summenformel | Menge |
|---|
| sc-202427 | 2457-80-9 | C11H15N5O3S | 50 mg |
- 7BIO
A 3′ substituted kinase inhibitory bis-indole, which functions as a caspase independent nonapoptotic cell death inducer.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-221118 | n.n. | C16H10BrN3O2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-213577 | 403811-55-2 | C12H11NOS2 | 5 mg/25 mg |
- 13(S)-HPODE
13(S)-HPODE is a hydroperoxide shown to be a potent suppressor of platelets.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200964 | 33964-75-9 | C18H32O4 | 50 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 Nummer | Summenformel | Menge |
|---|
| sc-3591 | 52665-69-7 | C29H37N3O6 | 1 mg/10 mg |
- AAPH
AAPH is a commonly applied free radical initiator for experimental use.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202034 | 2997-92-4 | C8H18N6 ·2HCl | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-203803 | 106685-40-9 | C28H28O3 | 10 mg/50 mg |
- Adenosine
Induces apoptosis in human leukemia HL-60 cells. Has anti-arrhythmic properties.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-291838 | 58-61-7 | C10H13N5O4 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-202049 | 121268-17-5 | C4H12NNaO7P2 ·3H2O | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-203816 | 94497-51-5 | C22H25NO3 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-202467 | 1397-94-0 | C28H40N2O9 | 5 mg/10 mg |
- API-1
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361106 | 36707-00-3 | C13H15N5O6 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-202062 | 194874-06-1 | C58H96O21 | 100 µg |
- Apoptosis Activator 2
Cell-permeable indoledione compound that activates caspases in a cytochrome c-dependent manner.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202956 | 79183-19-0 | C15H9Cl2NO2 | 5 mg |
- Apoptosis Activator VII, Apoptozole
A cell-permeable imidazole compound that directly binds anti-apoptotic chaperone Hsc70 and its inducible homologue Hsp70.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-221257 | n.n. | C33H24F6N3O3 | 10 mg |
- Atractyloside Dipotassium Salt
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-363293 | 102130-43-8 | C30H44K2O16S2 | 1 mg |
- Auraptene
A compound with anti-inflammatory, chemopreventive, apoptotic, cancer cell line suppression, PPAR agonism and MMP-7 translational control properties.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202477 | 495-02-3 | C19H22O3 | 5 mg/25 mg |
- Baccatin III
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204637 | 27548-93-2 | C31H38O11 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-221286 | 383860-03-5 | C16H16N2O4 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-221287 | n.n. | C24H21N3O6S2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-221288 | 141266-44-6 | C15H9CLN4O6 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-205600 | 91080-29-4 | C21H38BrN | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-202496 | 633-66-9 | C20H18NO4•½SO4 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-221350 | 65322-89-6 | C17H26N2O4 | 5 mg |
- Betamethasone
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204647 | 378-44-9 | C22H29FO5 | 100 mg/500 mg |
- BH3I-1
This is a cell permeable BH3 mimetic that binds to Bcl-XL.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-221352 | 300817-68-9 | C15H14BrNO3S2 | 5 mg |
- BH3I-1"
This is a cell permeable BH3 mimetic that binds to Bcl-XL.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-221354 | n.n. | C15H15NO3S2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-221355 | 315195-18-7 | C19H11Cl3INO4S | 1 mg |
- C2 Ceramide (N-Acetylsphingosine, D-erythro)
A cell-permeable ceramide and potent modulator of cell proliferation and differentiation.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-201375 | 3102-57-6 | C20H39NO3 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-202511 | 191282-48-1 | C14H22O4 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-293988 | 170355-78-9 | C31H34O5•xH2O | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-202527 | 125316-60-1 | C27H26O3 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-200893 | 28097-03-2 | C30H28N6O6S4 | 200 µg |
- Chlorambucil
A nitrogen mustard bifunctional alkylating agent. Displays antineoplastic and immunosuppressant effect. Induces apoptosis in chronic lymphocytic leukemia cells.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204682 | 305-03-3 | C14H19Cl2NO2 | 250 mg/1 g |
- CHM 1
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361147 | 154554-41-3 | C16H10FNO3 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-214686 | 154554-41-3 (anhydrous) | C16H10FNO3 ·H2O | 5 mg/25 mg |
- Chrysin
Antioxidant flavonoid. Displays anti-inflammatory and antitumor properties. Inhibits hypoxia-inducible factor-1α (HIF-1α) and induces apoptosis.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204686 | 480-40-0 | C15H10O4 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-214722 | 479077-76-4 | C19H14N2O2 | 10 mg |
- Citrinin
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-358726 | 518-75-2 | C13H14O5 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-217910 | 586410-12-0 | C17H19NO3 | 10 mg |
- Clodronate, Disodium Salt
A first-generation bisphosphonate and strong inhibitor of osteoclast-mediated bone resorption. Contains cytotoxic effects towards macrophages.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202547 | 22560-50-5 | CH2Cl2O6P2Na2 ·xH2O | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-202550 | 477-30-5 | C21H25NO5 | 5 mg |
- Colchicine
An apoptosis reagent that affects microtubule polymerization and disrupts cytoskeletal formation. Also known to interfere with tissue plasminogen activators.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203005 | 64-86-8 | C22H25NO6 | 1 g/5 g |
- Concanavalin A
A plant lectin that is a T cell mitogen. It induces apoptosis in human fibroblasts. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203007 | 11028-71-0 | n.n. | 50 mg/250 mg |
- Cyclophosphamide
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361165 | 50-18-0 | C7H15Cl2N2O2P | 50 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 Nummer | Summenformel | Menge |
|---|
| sc-202117 | 6055-19-2 | C7H15Cl2N2O2P ·H2O | 1 g |
- Cyproterone Acetate
A hepatomitogen and tumor promoter. Induces apoptosis in hepatocytes. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204703 | 427-51-0 | C24H29ClO4 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-201373 | 119567-63-4 | C20H41NO2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-200141 | 4345-03-3 | C33H54O5 | 1 g |
- Deguelin
A natural product that displays profound antiproliferative activity in many tumor cell lines.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200657 | 522-17-8 | C23H22O6 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-204715 | 2392-39-4 | C22H28FO8PNa2 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-205647 | 66-76-2 | C19H12O6 | 500 mg |
- Diethylstilbestrol
A synthetic estrogen that induces apoptosis in hormone-insensitive prostate cancer cells.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204720 | 56-53-1 | C18H20O2 | 1 g/5 g |
- Difluoromethylornithine
An irreversible inhibitor of ornithine decarboxylase which has antiangiogenic activity, inhibits carcinogenesis and induces apoptosis.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204723 | 67037-37-0 | C6H12F2N2O2 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-205654 | 97-77-8 | C10H20N2S4 | 50 g/100 g |
- DMXAA
Apoptosis inducer. Anti-vascular.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-207592 | 117570-53-3 | C17H14O4 | 5 mg/25 mg |
- Docetaxel
A semi-synthetic analog of Taxol. Stabilizes microtubules and inhibits mitosis, leading to apoptosis. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-201436 | 114977-28-5 | C43H53NO14 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-201449 | 123884-00-4 | C45H68N6O9 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-358130 | 412960-54-4 | C27H25Cl2N7O7 | 10mg |
- Embelin
Shown to be an antinociceptive and antiinflammatory agent with antioxidative capabilities. Also been reported to induce apoptosis. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-201555 | 550-24-3 | C17H26O4 | 10 mg/50 mg |
- Enhancer for Receptors
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-221586 | n.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 Nummer | Summenformel | Menge |
|---|
| sc-204739 | 1257-08-5 | C22H18O10 | 1 mg/5 mg |
- Erucin
An isothiocyanate from cruciferous vegetable. It is effective inapoptosis induction and mitochondrial potiential dissipation.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204741 | 4430-36-8 | C6H11NS2 | 25 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 Nummer | Summenformel | Menge |
|---|
| sc-204745 | 35950-87-9 | C18H28O2 | 10 mg |
- Farnesol
Polyprenyl alcohol found in plant essential oils. Induces apoptosis in cell cultures. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204748 | 4602-84-0 | C15H26O | 50 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 Nummer | Summenformel | Menge |
|---|
| sc-204755 | 21679-14-1 | C10H12FN5O4 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-200137 | 2752-65-0 | C38H44O8 | 5 mg/25 mg |
- Gemcitabine Hydrochloride
Deoxycytidine analog with cytotoxic effects. Inhibits DNA synthesis and induces apoptosis.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204763 | 122111-03-9 | C9H11F2N3O4 ·HCl | 25 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 Nummer | Summenformel | Menge |
|---|
| sc-200858 | 24034-73-9 | C20H34O | 20 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 Nummer | Summenformel | Menge |
|---|
| sc-221673 | 180977-44-0 | C27H33N3O3S | 250 µg |
- Gingerol
Shown to activate cardiac and skeletal SR Ca2+-ATPase with apoptosis inducing, antiinflammatory, and antioxidant characteristics.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-201519 | 23513-14-6 | C17H26O4 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-205911 | 65673-63-4 | C17H17BrN2O5 | 5 mg/25 mg |
- Hexamethylene Biscetamide
Prototype of hybrid polar inducers of apoptosis of various transformed cells. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204772 | 3073-59-4 | C10H20N2O2 | 25 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 Nummer | Summenformel | Menge |
|---|
| sc-200812 | 499-44-5 | C10H12O2 | 50 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 Nummer | Summenformel | Menge |
|---|
| sc-358833 | 502137-98-6 | C18H23N5O2 ·2HCl ·xH2O | 10 mg/50 mg |
- HMBA
An inhibitor of microtubule polymerization. An apoptosis inducer.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-300799 | n.n. | C22H16O3 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-202652 | 26833-87-4 | C29H39NO9 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-202653 | 35354-74-6 | C18H18O2 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-204774 | 57852-57-0 | C26H27NO9 ·HCl | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-221750 | n.n. | C20H21NO4 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-3592 | 56092-82-1 | C41H70CaO9 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-221764 | n.n. | C14H15N5S | 25 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 Nummer | Summenformel | Menge |
|---|
| sc-202187 | 476647-30-0 | C58H96O21 | 100 µg |
- Jasplakinolide
Binds to F-actin competitively with Phalloidin. Stabilizes F-actin and promotes actin polymerization. Produces antiproliferative and cytotoxic effects.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202191 | 102396-24-7 | C36H45BrN4O6 | 50 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 Nummer | Summenformel | Menge |
|---|
| sc-200454 | 487-79-6 | C10H15NO4 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-204053 | 155877-83-1 | C29H30N2O2 | 10 mg/50 mg |
- Lipopolysaccharide, Salmonella typhimurium
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-221857 | n.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 Nummer | Summenformel | Menge |
|---|
| sc-200850 | 75330-75-5 | C24H36O5 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-205749 | 83-43-2 | C22H30O5 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-200853 | 73573-88-3 | C23H34O5 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-205752 | n.n. | C23H35NaO6 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-203135 | 58066-85-6 | C21H46NO4P | 50 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 Nummer | Summenformel | Menge |
|---|
| sc-204087 | 72835-26-8 | C8H9NO4 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-286964 | 50-07-7 (non-salt) | C15H18N4O5 ·xNaCl | 50 mg |
- Narciclasine
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361271 | 29477-83-6 | C14H13NO7 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-222053 | 861891-50-1 | C19H23N3O2 | 5 mg |
- Nigericin•Na
Nigericin, a polyether antibioitc K+ and Na+ ionophore, stimulates Ca2+ release from mitochondria and stimulates ATPase activity.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-201518 | 28380-24-7 | C40H67O11··Na | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-45061 | 548472-68-0 | C30H30Cl2N4O4 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-203650 | 912-60-7 | C22H23NO7•HCl•xH2O | 100 mg |
- Oligomycin
A macrolide that acts as a specific inhibitor of the mitochondrial ATP-synthase and blocks oxidative phosphorylation.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203342 | 1404-19-9 | C45H74O11 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-204146 | 75629-57-1 | C16H12CINO | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-222109 | n.n. | C23H18ClNO4 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-202753 | 213261-59-7 | C14H12O3S2 | 1 mg |
- PAC 1
Procaspase-activating compound; activates procaspase-3 to produce caspase-3. Less efficiently activates procaspase-7.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203174 | 315183-21-2 | C23H28N4O2 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-222144 | n.n. | C10H4N6O | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-205798 | 18457-55-1 | C10H16O | 10 g/50 g |
- (+)-Perillyl alcohol
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-362189 | 57717-97-2 | C10H16O | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-204187 | 845714-00-3 | C12H11N3O.ClH | 10 mg |
- Phenylethyl 3-methylcaffeate
Has chemopreventive property against chemically induced colon carcinogenesis. Also amplifies apoptosis in azoxymethane induced colon tumors.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-205804 | 71835-85-3 | C18H18O4 | 50 mg/100 mg |
- PIT 1
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361293 | 53501-41-0 | C14H10ClN3O4S | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-202296 | 175796-50-6 | C39H44O11 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-204860 | 145-13-1 | C21H32O2 | 5 g/25 g |
- PRIMA-1MET
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361295 | 5291-32-7 | C10H17NO3 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-202298 | 82-89-3 | C20H25N3O | 500 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 Nummer | Summenformel | Menge |
|---|
| sc-206089 | 117-39-5 | C15H10O7 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-311520 | n.n. | C21H22N4O6S•H2O | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-202314 | 134615-37-5 | C36H52O11 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-201176 | 114681-65-1 | C23H38N10O10 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-203250 | 83643-88-3 | C7H10N2O4 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-301786 | 20874-52-6 | C42H68O13 | 1 mg |
- Simvastatin, Sodium Salt
Carboxylate form of Simvastatin which is active in whole cells and in cell-free preparations.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-222312 | 12009-77-6 | C25H39O6•Na | 5 mg |
- SJ 172550
SJ 172550 is an MDMX inhibitor which reversibly binds MDMX and inhibits MDMX-p53 interaction in cell cultures.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-357403 | 431979-47-4 | C22H21ClN2O5 | 10mg
/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 Nummer | Summenformel | Menge |
|---|
| sc-202341 | 156-54-7 | C4H7O2Na | 250 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 Nummer | Summenformel | Menge |
|---|
| sc-204310 | 326914-10-7 | C22H27ClN4O2 | 500 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 Nummer | Summenformel | Menge |
|---|
| sc-202823 | 38194-50-2 | C20H17FO3S | 1 g |
- Taxol
An antineoplastic and microtubule affecting agent that causes apoptotic cell death, internucleosomal DNA fragmentation, and inhibition of protein isoprenylation.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-201439 | 33069-62-4 | C47H51NO14 | 5 mg/25 mg/250 mg |
- Teniposide
Glycoside-derivative of podophyllotoxin. Has cytostatic effect. Inhibits topoisomerase II while induces apoptosis.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204910 | 29767-20-2 | C32H32O13S | 25 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 Nummer | Summenformel | Menge |
|---|
| sc-205858 | 60-54-8 | C22H24N2O8 | 10 g/25 g |
- Thiocolchicine
Inhibitor of microtubules by specific binding to tubulin. Modulator of axonal cytoskeleton. Induces apoptosis. Topoisomerase I inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202838 | 2730-71-4 | C22H25NO5S | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-200131 | 16858-02-9 | C26H28N6 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-204924 | 124-94-7 | C21H27FO6 | 50 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 Nummer | Summenformel | Menge |
|---|
| sc-204931 | 102040-03-9 | C63H98O29 | 10 mg/25 mg |
- TW-37
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361387 | 877877-35-5 | C33H35NO6S | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-216036 | 313367-92-9 | C23H15NO3 | 5 mg/25 mg |
- Valinomycin
Ionophore selective to potassium. Used to induce mitochondrial swelling, CHO apoptotic induction and antagonism of endothelin-induced vasoconstriction.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200991 | 2001-95-8 | C54H90N6O18 | 25 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 Nummer | Summenformel | Menge |
|---|
| sc-357409 | 940289-57-6 | C19H18ClN3O4 | 500 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 Nummer | Summenformel | Menge |
|---|
| sc-201447 | 143-67-9 | C46H58N4O9 ·H2SO4 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-201434 | 2068-78-2 | C46H56N4O10 ·H2SO4 | 5 mg/25 mg |
- Xanthorrhizol
An antibacterial and an anti-inflammatory compound that can induce apoptosis. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202855 | 30199-26-9 | C15H22O | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-204943 | 17924-92-4 | C18H22O5 | 10 mg/50 mg |
|