
Apoptose
Sous-catégories appartenant à la catégorie "Apoptose"
- ASK(9 produits)
- BCL(1 produits)
- Caspase(154 produits)
- FOXO1(2 produits)
- IAP(67 produits)
- Mdm2(12 produits)
- PD-1/PD-L1(134 produits)
- PDK(9 produits)
- PERK(23 produits)
- Sérine/thréonine kinase(17 produits)
- Survivant(14 produits)
- TNF(93 produits)
- c-RET(61 produits)
- p53(63 produits)
6222 produits trouvés pour "Apoptose"
Avasimibe
CAS :Applications Avasimibe is a selective inhibitor of Cholesterol Acyltransferase 1 and CYP2C9. Avasimibe is known to induce apoptosis of glioma cell lines as a model of glioblastoma.
References Bemlih, S., et al.: Cancer. BIol. Therap., 9, 1025 (2010); Fahmi, O.A., et al.: Drug. Meta. Disp. 38, 1605 (2010);Formule :C29H43NO4SCouleur et forme :White SolidMasse moléculaire :501.72Vamifeport
CAS :Vamifeport (VIT-2763), an inhibitor targeting iron transport proteins, improves anemia and erythropoiesis and can be studied β-thalassemiaFormule :C21H21FN6O2Degré de pureté :99.91%Couleur et forme :SolidMasse moléculaire :408.43Acivicin
CAS :Produit contrôléApplications Azaserine and Acivicin are classical and irreversible inhibitors of γ-Glutamyltranspeptidase (GGT). Acivicin is a potent antitumor antibiotic that induces apoptosis in human lymphoblastoid cells.
References Hanigan, M., et al.: Biochemistry, 32, 6302 (1993); Suzuki, H., et al.: J. Bacteriol., 175, 6038 (1993); Suzuki, H., et al.: J. Biol. Chem., 277, 43536 (2002); Magdalena, L., et al.: Biochem. Pharma., 77, 76 (2009)Formule :C5H7ClN2O3Couleur et forme :Off White SolidMasse moléculaire :178.57Dapolsertib
CAS :Dapolsertib (SEL24-B489) is an orally active and efficient PIM and FLT3-ITD inhibitor, reducing PIM-specific substrate phosphorylation.Formule :C15H18Br2N4O2Degré de pureté :99.61%Couleur et forme :SolidMasse moléculaire :446.14Meloxicam
CAS :Meloxicam (Metacam) is a Nonsteroidal Anti-inflammatory Drug.Formule :C14H13N3O4S2Degré de pureté :97.09% - 99.60%Couleur et forme :Light Yellow SolidMasse moléculaire :351.40Rabeprazole
CAS :Rabeprazole (LY307640) is an H+/K+-ATPase inhibitor that inhibits cell proliferation in gastric epithelial cells and can be used in the study of gastric ulcers.Formule :C18H21N3O3SDegré de pureté :97.06%Couleur et forme :White To Yellowish Crystalline PowderMasse moléculaire :359.44Sodium oleate
CAS :Sodium oleate (cis-9-Octadecenoic acid sodium salt) (Oleic acid sodium) is an abundant monounsaturated fatty acid sodium.Formule :C18H33NaO2Degré de pureté :98.11%Couleur et forme :SolidMasse moléculaire :304.44Envafolimab
CAS :Envafolimab (ASC 22) is a humanized antibody targeting PD-L1, with anticancer activity, blocking the PD-L1 and PD-1 interaction.Degré de pureté :95%Couleur et forme :LiquidMasse moléculaire :80 kDaN6-(2-Hydroxyethyl)adenosine
CAS :N6-(2-Hydroxyethyl)adenosine is a sedative, Ca2+ antagonist, and anti-inflammatory, affecting brain and heart blood flow.Formule :C12H17N5O5Degré de pureté :99.47%Couleur et forme :SolidMasse moléculaire :311.29EasyStep Human GDF15(Growth Differentiation Factor 15) ELISA Kit
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human GDF15, and the Human GDF15 standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human GDF15. After TMB substrate solution is added, only those wells that contain Human GDF15 and HRP-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human GDF15 in the samples is then determined by comparing the OD of the samples to the standard curve.Couleur et forme :Colourless Transparentliquid(R)-Thalidomide
CAS :(R)-Thalidomide is a COX 1/2 inhibitor that induces apoptosis in MCF-7, IM-9, HS-Sultan, KB and other cancer cells.Formule :C13H10N2O4Degré de pureté :99.87%Couleur et forme :SolidMasse moléculaire :258.23Cholesteryl Hemisuccinate
CAS :Cholesteryl Hemisuccinate (Cholesterol hydrogen succinate) is a highly soluble cholesterol analogue often used in polar solutions for its hepatoprotective,Formule :C31H50O4Degré de pureté :97.09% - 99.98%Couleur et forme :White PowderMasse moléculaire :486.73FINO2
CAS :FINO2, a strong ferroptosis trigger, blocks GPX4, oxidizes Fe2+, stable in different pH, causes lipid peroxidation.Formule :C15H28O3Degré de pureté :97.27%Couleur et forme :SoildMasse moléculaire :256.38Doxorubicin
CAS :Doxorubicin (Adriamycin) is a Topoisomerase II (Top2) inhibitor with antineoplastic activity.Formule :C27H29NO11Degré de pureté :99.31%Couleur et forme :Red Crystalline Solid SolidMasse moléculaire :543.52Socazolimab
CAS :Socazolimab (ZKAB001) is a monoclonal antibody targeting PD-L1 with antitumor activity, used in studies of recurrent or metastatic cervical cancer.Degré de pureté :95%Couleur et forme :LiquidMasse moléculaire :143.06 kDaSeribantumab
CAS :Seribantumab (MM 121) is a humanized monoclonal antibody targeting HER3, inhibiting cancer cell proliferation.Degré de pureté :>95%Couleur et forme :LiquidMasse moléculaire :143.14 kDaPOMHEX
CAS :Pomhex, a cell-penetrating ENO2 inhibitor, thwarts glycolysis to combat ENO1-deficient tumors.Formule :C17H30NO9PDegré de pureté :99.28%Couleur et forme :SolidMasse moléculaire :423.4L-Cystine dihydrochloride
CAS :L-Cystine dihydrochloride, a sulfur-based glutathione precursor, maintains GSH balance, used in cell culture.Formule :C6H14Cl2N2O4S2Degré de pureté :99.58%Couleur et forme :SolidMasse moléculaire :313.22Demecolcine
CAS :Stability Hygroscopic
Applications An antimitotic agent that disrupts microtubles by binding to tubulin and preventing its polymerization. Stimulates the intrinsic GTPase activity of tubulin. Induces apoptosis in several normal and tumor cell lines and activates the JNK/SAPK signaling pathway.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Lunduena, R.F., et al.: Curr. Opin. Cell Biol., 4, 53 (1992), Ceccatelli, S., et al.: Neuroreport, 8, 3779 (1997), Want, T.H., et al.: J. Biol. Chem., 273, 4928 (1998), Andreu, J.M., et al.: Biochemistry, 37, 8356 (1998), Jordan, A., et al.: Med. Res. Rev., 18, 259 (1998),Formule :C21H25NO5Couleur et forme :NeatMasse moléculaire :371.43Tulisokibart
CAS :Tulisokibart (PRA023) is a humanized anti-TNFSF15 monoclonal antibody used to study colon cancer.Degré de pureté :98.38% (SEC-HPLC) - > 95%Couleur et forme :LiquidMasse moléculaire :143.96 kDa4-Vinylphenol
CAS :4-Vinylphenol, a metabolite from lactic acid bacteria in wine, induces apoptosis. Found in Hedyotis diffusa Willd.Formule :C8H8ODegré de pureté :97.07%Couleur et forme :SolidMasse moléculaire :120.156-Chloroisatin
CAS :Produit contrôléApplications 6-Chloroisatin (cas# 6341-92-0) is a useful research chemical.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the packageFormule :C8H4NO2ClCouleur et forme :NeatMasse moléculaire :181.58Maslinic Acid
CAS :Applications Maslinic Acid is an apoptosis inducer in lung cancer cells, occuring under normoxic and hypoxic conditions.
References Hsia, T. et al.: Molecules., 19, 19892 (2014);Formule :C30H48O4Couleur et forme :NeatMasse moléculaire :472.7Scutellarin
CAS :Applications Scutellarin is an active flavonoid component from the medical plant Erigeron breviscapus (Vant) Hand-Mazz. Scutellarin is used as a micrpcirculation promoter for the treatment of cardio-cerebrovascular diseases. Studies suggest that Scutellarin has anti-cancer properties and has been shown to enhance apoptosis of tumor cells.
References Gao, C. et al.: Drug Metab. Dispos., 39, 2034 (2011); Chan, J.Y. et al.: Anticancer Res., 29, 3043 (2009); Wang, C.-Z. et al.: Phytomedicine, 17, 63 (2010);Formule :C21H18O12Couleur et forme :NeatMasse moléculaire :462.36(S)-(-)-Perillyl alcohol
CAS :"(S)-(−)-Perillyl alcohol, a lavender monoterpene, inhibits Ras farnesylation, promotes apoptosis, and has anti-cancer effects."Formule :C10H16ODegré de pureté :98.22%Couleur et forme :SolidMasse moléculaire :152.23AOH1996
CAS :AOH1996: Oral PCNA ligand, disrupts TRC, triggers DNA stress, apoptosis, and enhances DNA damage agent effects.Formule :C26H22N2O4Degré de pureté :98.63% - 99.62%Couleur et forme :SoildMasse moléculaire :426.46TAS1553
CAS :TAS1553, an oral PPI inhibitor with 0.0396 μM IC50, blocks DNA replication, reduces dATP levels, and induces apoptosis in cancer research.Formule :C20H20ClFN4O5SDegré de pureté :99.13%Couleur et forme :SoildMasse moléculaire :482.91Ref: TM-T60217
1mg50,00€5mg105,00€1mL*10mM (DMSO)113,00€10mg170,00€25mg334,00€50mg467,00€100mg647,00€Selumetinib sulfate
CAS :Selumetinib sulfate (AZD6244 sulfate) is a MEK1/2 inhibitor that inhibits MEK1/2 phosphorylation.Formule :C17H17BrClFN4O7SDegré de pureté :99.65%Couleur et forme :SolidMasse moléculaire :555.76BC-1471
CAS :BC-1471 is a STAMBP deubiquitinase inhibitor that blocks NALP7 inflammasome activity.Formule :C27H32N4O4SDegré de pureté :99.98%Couleur et forme :SolidMasse moléculaire :508.63Ref: TM-T8553
1mg58,00€5mg128,00€1mL*10mM (DMSO)144,00€10mg187,00€25mg323,00€50mg482,00€100mg658,00€200mg888,00€Morusin
CAS :Produit contrôléStability Light Sensitive
Applications Morusin is an inhibitor of human cervical cancer stem cell growth, attenuating NF-kB activity, and initiating apoptosis.
References Wang, L. et al.: Mol. Cell. Biochem., 379, 7 (2013);Formule :C25H24O6Couleur et forme :NeatMasse moléculaire :420.45GDC 0152
CAS :Produit contrôléApplications GDC 0152 is a peptidomimetic small molecule antagonist of inhibitor of apoptosis (IAP) proteins with antitumor activity.
References Yue, Q., et. al.: Drug Metab. Dispos., 41, 508 (2013)Formule :C25H34N6O3SCouleur et forme :NeatMasse moléculaire :498.64Sabutoclax
CAS :Sabutoclax (BI-97C1)(BI-97C1) is a pan-Bcl-2 inhibitor, including Bcl-xL, Bcl-2, Mcl-1 and Bfl-1 with IC50 of 0.31 μM, 0.32 μM, 0.20 μM and 0.62 μM,Formule :C42H40N2O8Degré de pureté :99.3%Couleur et forme :SolidMasse moléculaire :700.78p53 Activator 7
CAS :p53 Activator 7 is a highly potent and cell-permeable activator of the p53 mutation Y220C (MDM-2/p53), which induces apoptosis.Formule :C27H32F3N4OPDegré de pureté :98.16% - 99.25%Couleur et forme :SolidMasse moléculaire :516.538Cinnabarinic Acid
CAS :Produit contrôléFormule :C14H8N2O6Couleur et forme :NeatMasse moléculaire :300.22CPUY192018
CAS :CPUY192018 is an inhibitor of Keap1-Nrf2 protein-protein interactions, and can be used to study mitochondrial autophagy.Formule :C28H26N2O10S2Degré de pureté :98.9%Couleur et forme :SolidMasse moléculaire :614.64Taurodeoxycholic Acid Sodium Salt
CAS :Produit contrôléApplications Deoxycholyltaurine rescues human colon cancer cells from apoptosis by activating EGFR-dependent PI3K/Akt signaling.
References Cheng, K., et al.: Biochem. J., 330, 353 (1998), Cheng, K., et al.: Cancer Res., 63, 6744 (2003), Bellacosa, A., et al.: Adv. Cancer Res., 94, 29 (2005), Cheng, K., et al.: Biochem. Pharmacol., 70, 1035 (2005), Fang, D., et al.: J. Biol. Chem., 282, 11221 (2007),Formule :C26H44NO6S·NaCouleur et forme :Off-WhiteMasse moléculaire :521.69Fructose L-Arginine Adduct Hydrochloride, >80%
CAS :Produit contrôléStability Hygroscopic
Applications α-Fructose L-Arginine is an analogue of Fructose-leucine, an amadori compound having the potential to alter cellular adhesion, inhibit cancer metastasis and induce apoptosis.
References Slatter, D. et al.: Int. J. Biochem. Cell Biol., 40, 2253 (2008); Horiuchi, T., et al.: Agric. Biol. Chem., 55, 333 (1991), Glinsky, G., et al.: Cancer Res., 56, 5319 (1996); Srinivas, S. et al.: J. Agri Food Chem., 60, 1522 (2012);Formule :C12H24N4O7•x(HCl)Degré de pureté :>80%Couleur et forme :NeatMasse moléculaire :372.8Solasodine Hydrochloride
CAS :Produit contrôléApplications Solasodine Hydrochloride enhances the effect of As2O3 in inducing apoptosis in HeLa cell, which is related to its inhibiting telomerase activity in HeLa cells.
References Ai, J., et al.: Chin. J. Endemiol., 30, 279 (2011)Formule :C27H43NO2·HClCouleur et forme :NeatMasse moléculaire :413.64Tirabrutinib
CAS :Tirabrutinib, an oral Btk inhibitor (IC50=6.8 nM), crosses the BBB and halts B cell signaling for autoimmune and hematologic studies.Formule :C25H22N6O3Degré de pureté :99.64%Couleur et forme :SolidMasse moléculaire :454.485'-Amino-5'-deoxyadenosine
CAS :5'-Amino-5'-deoxyadenosine (NH2dAdo) is an adenosine kinase inhibitor targeting malignant tumors of the inert lymphatic system with antitumor and anticancerFormule :C10H14N6O3Degré de pureté :99.72%Couleur et forme :SolidMasse moléculaire :266.26Eurycomanone
CAS :Produit contrôléApplications Eurycomanone is known as a cytotoxic compound found in Eurycoma Longifolia Jack. Previous studies had noted its cytotoxic effects against various cancer cell lines. More recent research demonstrated the ability of Eurycomanone to suppress the expression of lung cancer cell tumor markers, prohibitin, annexin 1 and endoplasmic reticulum protein 28. Eurycomanone was shown to also exerts the ability to induce apoptosis through the up-regulation of p53 in human cervical carcinoma cells.
References Wong, P.F., et al.: Phytomed., 19, 138 (2012); Nurkhasanah, M., et al., Medunion Press., 4, 109 (2008); Zakaria, Y., et al.: Cancer Cell Intern., 9, (2009);Formule :C20H24O9·2H2ODegré de pureté :>90%Couleur et forme :NeatMasse moléculaire :444.43IACS-010759 hydrochloride
CAS :IACS-010759 hydrochloride is an orally potent and selective OXPHOS inhibitor that inhibits proliferation and induces apoptosis AML and solid tumours.Formule :C25H26ClF3N6O4SDegré de pureté :98.81%Couleur et forme :SolidMasse moléculaire :599.03Ref: TM-T27568
1mg50,00€5mg113,00€1mL*10mM (DMSO)150,00€10mg166,00€25mg268,00€50mg395,00€100mg583,00€200mg833,00€Snail/HDAC-IN-1
CAS :Snail/HDAC-IN-1 is a Snail/HDAC inhibitor with antimicrobial and anticancer activity, known to reduce Snail protein expression and induce apoptosis, making it useful for the study of solid tumors.Formule :C24H21FN8OSDegré de pureté :97.08% - 98.83%Couleur et forme :SolidMasse moléculaire :488.5425R-3α,7α,12α-Trihydroxy-5β-cholestanoic Acid
CAS :Produit contrôléApplications 25R-3α,7α,12α-Trihydroxy-5β-cholestanoic acid is an intermediate in the synthesis of (25R)-3β,7α,12α-Trihydroxy-5-cholestenoic Acid (T795130), which is an oxysterol, an oxidized derivatives of cholesterol (C432501), which may be important in many biological processes, including cholesterol homeostasis, atherosclerosis, sphingolipid metabolism, platelet aggregation, apoptosis, and protein prenylation,[1] though their roles are poorly understood.
References Schroepfer, G., et al.: Physiol. Rev., 80, 361 (2000); Bjorkhem, I.: J. Clin. Invest., 6, 725(2002); Bjorkhem, I., et al.: Arterio. hromb. Vascul. Biol., 22, 734 (2002)Formule :C27H46O5Couleur et forme :NeatMasse moléculaire :450.65FK866
CAS :Applications FK866 is a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase (NMPRTase), that induces tumor cell apoptosis, and thus is a potential anticancer drug.
References Hasmann, M., Schemainda, I.: Cancer Res., 63, 7436 (2003); Khan, J., et a.: Nat. Struct. Mol. Biol., 13, 582 (2006);Formule :C24H29N3O2Couleur et forme :NeatMasse moléculaire :391.51Anticancer agent 43
CAS :Anticancer agent 43 is a potent anticancer agent that induces apoptosis through caspase 3, PARP1, and Bax protein-dependent pathways.Anticancer agent 43 induces
Formule :C14H9FN2O3S2Degré de pureté :98.88%Couleur et forme :SolidMasse moléculaire :336.36BTT-3033
CAS :BTT-3033 is an α2β1 inhibitor that induces apoptosis and can be used to study prostate cancer, inflammation and cardiovascular disease.Formule :C23H20FN5O3SDegré de pureté :98.91% - 99.36%Couleur et forme :SolidMasse moléculaire :465.5PF-543 Citrate
CAS :PF-543 Citrate is an SPHK1 inhibitor and also an inhibitor of S1P formation, exhibiting anticancer, antifibrotic, and anti-inflammatory activities.Formule :C33H39NO11SDegré de pureté :99.33%Couleur et forme :SolidMasse moléculaire :657.73Jaceosidin
CAS :Produit contrôléFormule :C17H14O7Couleur et forme :Light YellowMasse moléculaire :330.29Hydronidone
CAS :Hydronidone (F-351) is Non-Steroidal Antiinflammatory Drugs. It potentially for the treatment of hepatic fibrosis.Formule :C12H11NO2Degré de pureté :99.74% - 99.84%Couleur et forme :SolidMasse moléculaire :201.22Ref: TM-T19694
5mg57,00€1mL*10mM (DMSO)60,00€10mg93,00€25mg166,00€50mg260,00€100mg385,00€500mg873,00€EasyStep Human VEGFA(Vascular Endothelial Growth Factor A) ELISA Kit
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human VEGFA, and the Human VEGFA standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human VEGFA. After TMB substrate solution is added, only those wells that contain Human VEGFA and HRP-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human VEGFA in the samples is then determined by comparing the OD of the samples to the standard curve.Couleur et forme :Colourless TransparentliquidCCT241161
CAS :CCT241161: oral pan-RAF inhibitor; IC50s: LCK (3 nM), CRAF (6), SRC (10), V600E-BRAF (15), BRAF (30); fights BRAF/NRAS melanomas, anti-proliferative.Formule :C28H27N7O3SDegré de pureté :99.76% - 99.77%Couleur et forme :SolidMasse moléculaire :541.62Meclizine
CAS :Meclizine, also known as Meclozine, is a piperazine class H1 antagonist with antihistamine properties that inhibits the interaction of histamine at H1 receptorsFormule :C25H27ClN2Degré de pureté :99.55%Couleur et forme :SolidMasse moléculaire :390.95CSRM617 hydrochloride
CAS :CSRM617 hydrochloride: selective OC2 inhibitor, Kd 7.43 uM, binds OC2-HOX, induces apoptosis, tolerable in mouse prostate cancer.Formule :C10H14ClN3O5Degré de pureté :99.59%Couleur et forme :SoildMasse moléculaire :291.694-Benzyloxy-3-methoxybenzoic Acid
CAS :Produit contrôléApplications 4-Benzyloxy-3-methoxybenzoic Acid is used in the synthesis of Hsp90 inhibitors as EGCG analogues. Also used in the preparation of vanillates exhibiting cytostatic properties towards cancel cells resistant to pro-apoptotic stimuli.
References Khandelwal, A. et al.: J. Org. Chem., 78, 7859 (2013); Lamoral-Theys, D. et al.: Bioorg. Med. Chem., 18, 3823 (2010);Formule :C15H14O4Couleur et forme :NeatMasse moléculaire :258.27Tapotoclax
CAS :Tapotoclax (AMG-176) is an orally active MCL1 inhibitor for the study of myeloid leukemia.Formule :C33H41ClN2O5SDegré de pureté :98.8%Couleur et forme :SolidMasse moléculaire :613.21(S)-(+)-Ibuprofen
CAS :(S)-(+)-Ibuprofen (Dexibuprofen) , is a non-steroidal anti-inflammatory drug (NSAID), inhibiting cyclooxygenase (COX).Formule :C13H18O2Degré de pureté :99.51% - 99.86%Couleur et forme :Colourless Crystalline SolidMasse moléculaire :206.28Pyropheophorbide A Methyl Ester
CAS :Produit contrôléStability Light Sensitive
Applications Pyropheophorbide A Methyl Ester is a chlorophyll (C379815) analog for studies of photosynthesis. Methyl pyropheophorbide a (Pyropheophorbide-a methyl ester), a chlorophyll-a derivative, and is a potent photosensitizer that can be used in photodynamic therapy (PDT) of cancer. Methyl pyropheophorbide a has photodynamic activity and can induce apoptosis and inhibit tumor growth.
References Bensasson, R., et al.: Nature, 290, 329 (1981); Moore, A., et al.: Science, 216, 982 (1982)Formule :C34H36N4O3Couleur et forme :NeatMasse moléculaire :548.67ARB-272572
CAS :ARB-272572 is a PD-L1 signaling inhibitor that produces immunostimulatory activity in human primary cells.Formule :C32H36N6O4Degré de pureté :97.36% - 98.07%Couleur et forme :SolidMasse moléculaire :568.67Ref: TM-T39914
1mg123,00€5mg295,00€1mL*10mM (DMSO)353,00€10mg425,00€25mg712,00€50mg1.035,00€100mg1.485,00€200mg1.998,00€Dracorhodin Perchlorate
CAS :Produit contrôléFormule :C17H15O3·ClO4Couleur et forme :NeatMasse moléculaire :366.75Tamsulosin
CAS :Tamsulosin: an alpha1A blocker for easing urination in BPH by relaxing prostate and bladder muscles.Formule :C20H28N2O5SDegré de pureté :99.93%Couleur et forme :White CrystalsMasse moléculaire :408.51Docetaxel-d9
CAS :Docetaxel-d9 is a deuterated compound of Docetaxel. Docetaxel has a CAS number of 114977-28-5. Docetaxel is a microtubule inhibitor that inhibits microtubule disassembly (IC50: 0.2 μM).Formule :C43H44D9NO14Couleur et forme :SolidMasse moléculaire :816.93Glyphosate-13C2-15N
CAS :Glyphosate-13C2-15N is the 13C and 15N labeled compound of Glyphosate. Glyphosate has a CAS number of 1071-83-6. Glyphosate is an herbicide. It also is a possible carcinogen to humans.Formule :C2C1D0H8NO5PCouleur et forme :SolidMasse moléculaire :172.05Lovastatin-d3
CAS :Lovastatin-d3 is a deuterated compound of Lovastatin. Lovastatin has a CAS number of 75330-75-5. Lovastatin is an HMG-CoA Reductase Inhibitor, used for lowering cholesterol.Formule :C24H33D3O5Couleur et forme :SolidMasse moléculaire :407.56Mebendazole-d3
CAS :Mebendazole-d3 is a deuterated compound of Mebendazole. Mebendazole has a CAS number of 31431-39-7. Mebendazole is a hedgehog inhibitor, used as an antihelminthic.Formule :C16H10D3N3O3Couleur et forme :SolidMasse moléculaire :298.31Tauroursodeoxycholic-2,2,3,4,4-d5 Acid
CAS :Tauroursodeoxycholic-2,2,3,4,4-d5 Acid is a deuterated compound of Tauroursodeoxycholic Acid. Tauroursodeoxycholic Acid has a CAS number of 14605-22-2. Tauroursodeoxycholate, also known as ursodoxicoltaurine, is a highly hydrophilic tertiary bile acid that is produced in humans at a low concentration. Tauroursodeoxycholate is the more hydrophilic form of ursodeoxycholic acid, which is the more abundant naturally produced bile acid in humans.Tauroursodeoxycholate is being investigated for use in several conditions such as Primary Biliary Cirrhosis (PBC), insulin resistance, amyloidosis, Cystic Fibrosis, Cholestasis, and Amyotrophic Lateral Sclerosis.Formule :C26H40D5NO6SCouleur et forme :SolidMasse moléculaire :504.73Vildagliptin-d7
CAS :Vildagliptin-d7 is a deuterated compound of Vildagliptin. Vildagliptin has a CAS number of 274901-16-5. Vildagliptin is a cyanopyrrolidine-based, orally bioavailable inhibitor of dipeptidyl peptidase 4 (DPP-4), with hypoglycemic activity. Vildagliptin's cyano moiety undergoes hydrolysis and this inactive metabolite is excreted mainly via the urine.Formule :C17H18D7N3O2Couleur et forme :SolidMasse moléculaire :310.44Flubendazole-d3 (methyl-d3)
CAS :Flubendazole-d3 (methyl-d3) is a deuterated compound of Flubendazole. Flubendazole has a CAS number of 31430-15-6. Flubendazole is available OTC in Europe that is an anthelmintic using to treat worm infection in humans.Formule :C16H9D3FN3O3Couleur et forme :SolidMasse moléculaire :316.30Sulfasalazine-d4
CAS :Sulfasalazine-d4 is a deuterated compound of Sulfasalazine. Sulfasalazine has a CAS number of 599-79-1. Sulfasalazine is a synthetic salicylic acid derivative with affinity for connective tissues containing elastin and formulated as a prodrugFormule :C18H10D4N4O5SCouleur et forme :SolidMasse moléculaire :402.42Verapamil-d7 Hydrochloride
CAS :Verapamil-d7 Hydrochloride is a deuterated compound of Verapamil Hydrochloride. Verapamil Hydrochloride has a CAS number of 152-11-4. Verapamil hydrochloride is a calcium channel blocker that is a class IV anti-arrhythmia agent.Formule :C27H32D7ClN2O4Couleur et forme :SolidMasse moléculaire :498.11ZZW-115
CAS :ZZW-115: NUPR1 inhibitor, Kd 2.1 μM, TFP derivative, dose-linked tumor shrinkage, no neuro effects, triggers necroptosis & apoptosis.Formule :C24H31F3N4SDegré de pureté :99.17%Couleur et forme :SoildMasse moléculaire :464.59Verubulin
CAS :Verubulin (MPC 6827) is a microtubule blocking agent with cytotoxic and potentially anticancer activity that disrupts newly formed blood vessels in xenografts.Formule :C17H17N3ODegré de pureté :99.98%Couleur et forme :SolidMasse moléculaire :279.34Pitavastatin
CAS :Pitavastatin (NK-104) is an HMG-CoA reductase inhibitor with hypocholesterolemic and neuroprotective activities.Formule :C25H24FNO4Degré de pureté :97.17%Couleur et forme :SolidMasse moléculaire :421.46Dehydrotrametenolic acid
CAS :Dehydrotrametenolic acid (Dehydroeburicoic acid) induces necrotic cell death that involves Ca(2+) overload, mitochondrial dysfunction, and calpain activation inFormule :C31H48O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :468.71β-NETA
CAS :β-NETA (α-NETA) is a stable, noncompetitive, slowly reversible choline acetyltransferase (ChAT) inhibitor with an IC50 of 9 μM and is a potent chemokine-likeFormule :C16H20INODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :369.24Puerarin 6''-O-Xyloside
CAS :Puerarin 6''-O-xyloside possesses significant anti-osteoporotic activity on ovariectomy mice, it has significant antitumour activities, the mechanisms areFormule :C26H28O13Degré de pureté :98% - 98.67%Couleur et forme :SolidMasse moléculaire :548.49Ref: TM-T5S2083
1mg87,00€5mg177,00€1mL*10mM (DMSO)222,00€10mg264,00€25mg447,00€50mg650,00€100mg888,00€Fasnall
CAS :Fasnall: FASN inhibitor with anti-tumor effect in HER2(+) breast cancer, enhanced by carboplatin.Formule :C19H22N4SDegré de pureté :90% - 99.58%Couleur et forme :SolidMasse moléculaire :338.47Ilexsaponin A
CAS :1. Ilexsaponin A (Ilexsaponin A1) shows protective effects on ischemia-reperfusion-induced myocardial injury through anti-apoptotic pathway.Formule :C36H56O11Degré de pureté :98.28% - 99.76%Couleur et forme :SolidMasse moléculaire :664.82Ref: TM-T2S0500
1mg94,00€5mg222,00€1mL*10mM (DMSO)325,00€10mg356,00€25mg583,00€50mg820,00€100mg1.099,00€200mg1.485,00€TIC10
CAS :TIC10 (ONC-201) inactivates Akt and ERK to induce TRAIL through Foxo3a, possesses superior drug properties: delivery across the blood-brain barrier, superiorFormule :C24H26N4ODegré de pureté :99.72% - 99.98%Couleur et forme :SolidMasse moléculaire :386.49Ref: TM-T7001
5mg52,00€1mL*10mM (DMSO)55,00€10mg63,00€25mg96,00€50mg109,00€100mg169,00€200mg259,00€500mg437,00€1g623,00€Colcemid
CAS :Colcemid (NSC-3096) is a microtubule polymerization inhibitor,main target being Tubulin and an IC50 of 2.4 μM. induce apoptosis. High-Quality, Low-Cost!Formule :C21H25NO5Degré de pureté :99.65% - 99.83%Couleur et forme :SolidMasse moléculaire :371.43BGT226 maleate
CAS :BGT226 maleate (NVP-BGT226) is a class I PI3K/mTOR inhibitor for PI3Kα/β/γ (IC50: 4/63/38 nM) .Formule :C28H25F3N6O2·C4H4O4Degré de pureté :97.75% - 98.77%Couleur et forme :SolidMasse moléculaire :650.6Ref: TM-T6072
1mg35,00€5mg73,00€1mL*10mM (DMSO)94,00€10mg108,00€25mg230,00€50mg339,00€100mg485,00€200mg665,00€α-Eleostearic Acid
CAS :Produit contrôléStability Light Sensitive
Applications α-Eleostearic Acid, is a conjugated polyunsaturated fatty acid commonly found in plant seed oil. It has shown potential as a tumor growth suppressor. In colon cancer Caco-2 cells, α-ESA induced apoptosis through up-regulation of GADD45, p53, and PPARγ.
References Yasui, Y., et al.: Prostaglandins, Leukotrienes and Essential Fatty Acids 75, 113-119 (2005).;Formule :C18H30O2Couleur et forme :Off-WhiteMasse moléculaire :278.43Sodium Chromate
CAS :Produit contrôléApplications Sodium Chromate is used in the induction of apoptosis in human cells. Genotoxic agent.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Cavallo, D. et al.: J. App. Toxicol., 30, 218 (2010); Holmes, A. et al.: Mut. Res. Genetic Toxicol. Env Mutagen., 610, 8 (2006);Formule :CrNa2O4Couleur et forme :NeatMasse moléculaire :161.973-Hydroxy-4-((R)-6-methylhept-5-en-2-yl)cyclohexanone
Produit contrôléApplications 3-Hydroxy-4-((R)-6-methylhept-5-en-2-yl)cyclohexanone is an impurity in the synthesis of Xanthorrhizol (X742050), a natural sesquiterpenoid from the rhizome of Curcuma xanthorrhiza that induces apoptosis.
Formule :C14H24O2Couleur et forme :NeatMasse moléculaire :224.339(3Alpha,5Beta,7Alpha,12Alpha)-3,7,12-Trihydroxy-cholest-24-en-26-oic Acid Ethyl Ester
CAS :Produit contrôléApplications (3α,5β,7α,12α)-3,7,12-Trihydroxy-cholest-24-en-26-oic Acid Ethyl Ester is an intermediate in the synthesis of (25R)-3β,7α,12α-Trihydroxy-5-cholestenoic Acid (T795130), which is an oxysterol, an oxidized derivatives of cholesterol (C432501), which may be important in many biological processes, including cholesterol homeostasis, atherosclerosis, sphingolipid metabolism, platelet aggregation, apoptosis, and protein prenylation,[1] though their roles are poorly understood.
References Schroepfer, G., et al.: Physiol. Rev., 80, 361 (2000); Bjorkhem, I.: J. Clin. Invest., 6, 725(2002); Bjorkhem, I., et al.: Arterio. hromb. Vascul. Biol., 22, 734 (2002)Formule :C29H48O5Couleur et forme :NeatMasse moléculaire :476.35N-[1-Deoxy-2,3:4,5-bis-O-(1-methylethylidene)-β-D-fructopyranos-1-yl]-L-alanine
CAS :Produit contrôléFormule :C15H25NO7Couleur et forme :NeatMasse moléculaire :331.364-(4,4-Dimethyl-2,5-dioxo-1-imidazolidinyl)-2-(trifluoromethyl)benzonitrile
CAS :Produit contrôléApplications 4-(4,4-Dimethyl-2,5-dioxo-1-imidazolidinyl)-2-(trifluoromethyl)benzonitrile is an intermediate in the synthesis of Oxo-MDV 3100 (Oxo-enzalutamide) (O857800), which is an impurity of Enzalutamide (M199800), which is an androgen-receptor antagonist that blocks androgens from binding to the androgen receptor and prevents nuclear translocation and co-activator recruitment of the ligand-receptor complex. Enzalutamide has been shown to induce tumor cell apoptosis, and is used for the treatment of castration-resistant prostate cancer.
References Scher, H.I. et al.: Lancet, 375, 1437 (2010); Bellmunt, J. et al.: Ther. Adv. Med. Oncol., 2, 189 (2010); Ryan, C.J. et al.: J. Clin. Oncol., 29, 3651 (2011); Ma, X., et al.: J. Pharm. Biomed. Anal., 131, 436 (2016);Formule :C13H10F3N3O2Couleur et forme :NeatMasse moléculaire :297.23(3β,5β,7α,12α,24E)-3,7,12-Trihydroxy-cholest-24-en-26-oic Acid
Produit contrôléApplications (3β,5β,7α,12α,24E)-3,7,12-Trihydroxy-cholest-24-en-26-oic Acid is an intermediate in the synthesis of (25R)-3β,7α,12α-Trihydroxy-5-cholestenoic Acid (T795130), which is an oxysterol, an oxidized derivatives of cholesterol (C432501), which may be important in many biological processes, including cholesterol homeostasis, atherosclerosis, sphingolipid metabolism, platelet aggregation, apoptosis, and protein prenylation,[1] though their roles are poorly understood.
References Schroepfer, G., et al.: Physiol. Rev., 80, 361 (2000); Bjorkhem, I.: J. Clin. Invest., 6, 725(2002); Bjorkhem, I., et al.: Arterio. hromb. Vascul. Biol., 22, 734 (2002)Formule :C27H44O5Couleur et forme :NeatMasse moléculaire :448.64(3α,5β,7α,12α)-3,7,12-Tris(ethoxymethoxy)-cholan-24-ol
Produit contrôléApplications (3α,5β,7α,12α)-3,7,12-Tris(ethoxymethoxy)-cholan-24-ol is an intermediate in the synthesis of (25R)-3β,7α,12α-Trihydroxy-5-cholestenoic Acid (T795130), which is an oxysterol, an oxidized derivatives of cholesterol (C432501), which may be important in many biological processes, including cholesterol homeostasis, atherosclerosis, sphingolipid metabolism, platelet aggregation, apoptosis, and protein prenylation,[1] though their roles are poorly understood.
References Schroepfer, G., et al.: Physiol. Rev., 80, 361 (2000); Bjorkhem, I.: J. Clin. Invest., 6, 725(2002); Bjorkhem, I., et al.: Arterio. hromb. Vascul. Biol., 22, 734 (2002)Formule :C33H60O7Couleur et forme :NeatMasse moléculaire :568.83(3α,5β,7α,12α)-3,7,12-Tris(ethoxymethoxy)-cholan-24-oic Acid Methyl Ester
Produit contrôléApplications (3α,5β,7α,12α)-3,7,12-Tris(ethoxymethoxy)-cholan-24-oic Acid Methyl Ester is an intermediate in the synthesis of (25R)-3β,7α,12α-Trihydroxy-5-cholestenoic Acid (T795130), which is an oxysterol, an oxidized derivatives of cholesterol (C432501), which may be important in many biological processes, including cholesterol homeostasis, atherosclerosis, sphingolipid metabolism, platelet aggregation, apoptosis, and protein prenylation,[1] though their roles are poorly understood.
References Schroepfer, G., et al.: Physiol. Rev., 80, 361 (2000); Bjorkhem, I.: J. Clin. Invest., 6, 725(2002); Bjorkhem, I., et al.: Arterio. hromb. Vascul. Biol., 22, 734 (2002)Formule :C34H60O8Couleur et forme :NeatMasse moléculaire :596.84(3α,5β,7α,12α)-3,7,12-Tris(ethoxymethoxy)-cholan-24-al
Produit contrôléApplications (3α,5β,7α,12α)-3,7,12-Tris(ethoxymethoxy)-cholan-24-al is an intermediate in the synthesis of (25R)-3β,7α,12α-Trihydroxy-5-cholestenoic Acid (T795130), which is an oxysterol, an oxidized derivatives of cholesterol (C432501), which may be important in many biological processes, including cholesterol homeostasis, atherosclerosis, sphingolipid metabolism, platelet aggregation, apoptosis, and protein prenylation,[1] though their roles are poorly understood.
References Schroepfer, G., et al.: Physiol. Rev., 80, 361 (2000); Bjorkhem, I.: J. Clin. Invest., 6, 725(2002); Bjorkhem, I., et al.: Arterio. hromb. Vascul. Biol., 22, 734 (2002)Formule :C33H58O7Couleur et forme :NeatMasse moléculaire :566.813,4,5-tris(Acetyloxy)benzoic Acid
CAS :Produit contrôléFormule :C13H12O8Couleur et forme :NeatMasse moléculaire :296.22(3α,5β,7α,12α)-3,7,12-Tris(ethoxymethoxy)-cholest-24-en-26-oic Acid Ethyl Ester
Produit contrôléApplications (3α,5β,7α,12α)-3,7,12-Tris(ethoxymethoxy)-cholest-24-en-26-oic Acid Ethyl Ester is an intermediate in the synthesis of (25R)-3β,7α,12α-Trihydroxy-5-cholestenoic Acid (T795130), which is an oxysterol, an oxidized derivatives of cholesterol (C432501), which may be important in many biological processes, including cholesterol homeostasis, atherosclerosis, sphingolipid metabolism, platelet aggregation, apoptosis, and protein prenylation,[1] though their roles are poorly understood.
References Schroepfer, G., et al.: Physiol. Rev., 80, 361 (2000); Bjorkhem, I.: J. Clin. Invest., 6, 725(2002); Bjorkhem, I., et al.: Arterio. hromb. Vascul. Biol., 22, 734 (2002)Formule :C38H66O8Couleur et forme :NeatMasse moléculaire :650.48(S)-8-bis[(Phenylmethoxy)carbonyl]-3-imino-12,12-dimethyl-10-oxo-4-phenylmethyl Ester 11-Oxa-2,4,9-triazatridecanoic Acid
CAS :Produit contrôléFormule :C34H40N4O8Couleur et forme :NeatMasse moléculaire :632.713,3'-Dimethyl-5,5'-bis(1-methylethyl)-[2,2'-binaphthalene]-1,1',6,6',7,7'-hexol Hexaacetate
CAS :Produit contrôléFormule :C40H42O12Couleur et forme :NeatMasse moléculaire :714.25Linvoseltamab
CAS :Linvoseltamab, a bispecific antibody, targets both BCMA (TNFRSF17) and CD3 epsilon, demonstrating a favorable safety profile and promising efficacy in relapsed/Couleur et forme :LiquidTuvonralimab
CAS :Tuvonralimab, a combo of anti-PD-1/IgG4 and anti-CTLA-4/IgG1 antibodies, blocks dual immune checkpoints.Degré de pureté :95% - 95%Couleur et forme :LiquidAcasunlimab
CAS :Acasunlimab (GEN1046) is a bsAb that targets PD-L1 and 4-1BB, boosting T/NK cells and blocking PD-1/PD-L1 in cancer research.Couleur et forme :LiquidDalnicastobart
CAS :Dalnicastobart (LVGN-7409) is a humanized monoclonal antibody targeting CD40/TNFRSF5 with agonist activity, immunostimulatory and antitumor.Degré de pureté :95% - 97.4% (SDS-PAGE); 97.8% (SEC-HPLC)Couleur et forme :LiquidMasse moléculaire :146.33 kDa



