Apoptose
Os inibidores da apoptose são compostos que previnem ou retardam o processo de morte celular programada, conhecido como apoptose. Esses inibidores são vitais no estudo dos mecanismos de sobrevivência celular e são usados para investigar doenças onde a apoptose é desregulada, como câncer, distúrbios neurodegenerativos e doenças autoimunes. Ao modular a apoptose, esses inibidores podem ajudar no desenvolvimento de terapias destinadas a controlar a morte celular. Na CymitQuimica, oferecemos uma ampla seleção de inibidores da apoptose de alta qualidade para apoiar sua pesquisa em biologia celular, oncologia e áreas relacionadas.
Subcategorias de "Apoptose"
- ASK(9 produtos)
- BCL(11 produtos)
- Caspase(144 produtos)
- FOXO1(3 produtos)
- IAP(67 produtos)
- Mdm2(12 produtos)
- PD-1/PD-L1(139 produtos)
- PDK(9 produtos)
- PERK(26 produtos)
- Serina/treonina quinase(18 produtos)
- Survivina(14 produtos)
- TNF(93 produtos)
- c-RET(62 produtos)
- p53(63 produtos)
Exibir 6 mais subcategorias
Foram encontrados 6068 produtos de "Apoptose"
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RS1-PDK1 inhibitor
CAS:<p>RS1-PDK1 inhibitor (RS 1) is a selective inhibitor of the protein kinase PDK1 that can be used to treat and prevent disease or disorders.</p>Fórmula:C15H9ClN2O2S3Pureza:98.12%Cor e Forma:SolidPeso molecular:380.89Mepazine
CAS:Mepazine, a MALT1 inhibitor, blocks GSTMALT1 (IC50: 0.83μM) and GSTMALT1 325-760 (IC50: 0.42μM), promoting apoptosis and reducing cell viability.Fórmula:C19H22N2SPureza:99.88% - 99.92%Cor e Forma:SolidPeso molecular:310.46Ref: TM-T16040
10mg39,00€25mg60,00€50mg93,00€100mg116,00€200mg177,00€500mgA consultar1mL*10mM (DMSO)35,00€Prinomastat
CAS:Prinomastat: orally active, crosses blood-brain barrier, inhibits MMP-1/2/3/9, Ki/IC50s: 0.05-0.3/5.0-79 nM, antitumor.Fórmula:C18H21N3O5S2Pureza:99.23%Cor e Forma:SolidPeso molecular:423.51Ref: TM-T12539L
1mg73,00€2mg117,00€5mg240,00€10mg432,00€25mg697,00€50mg938,00€100mg1.293,00€200mg1.738,00€BC 11 hydrobromide
CAS:The compound is a selective urokinase inhibitor (IC50 = 8.2 μM). It also inhibits clot lysis with no effect on clot formation.Fórmula:C8H12BBrN2O2SPureza:98.07%Cor e Forma:SolidPeso molecular:290.97RET-IN-23
CAS:RET-IN-23 is an orally available and highly potent RET inhibitor with significant antitumor activity for the study of non-small cell lung cancer.Fórmula:C28H28FN11Pureza:97.46%Cor e Forma:SolidPeso molecular:537.59eIF4A3-IN-1
CAS:<p>eIF4A3-IN-1 is an inhibitor of eukaryotic initiation factor 4A3 (eIF4A3). eIF4A3-IN-1 inhibits cytosolic nonsense-mediated RNA decay at high concentrations.</p>Fórmula:C29H23BrClN5O2Pureza:99.49% - 99.89%Cor e Forma:SolidPeso molecular:588.88HS38
CAS:HS38: DAPK-specific ATP-competitive inhibitor; Kds: DAPK1 (300 nM), PIM3 (200 nM), ZIPK (280 nM); useful in smooth muscle disorder research.Fórmula:C14H12ClN5O2SPureza:98.19%Cor e Forma:SolidPeso molecular:349.8Ciglitazone
CAS:Ciglitazone: potent PPARγ agonist, EC50 3 μM, oral hypoglycemic; reduces insulin, blood pressure, Th17 cells, VEGF; halts gastric cancer growth.Fórmula:C18H23NO3SPureza:98.23% - 99.84%Cor e Forma:White Cyrstalline SolidPeso molecular:333.45A09-003
CAS:A09-003 Inhibits the proliferation of leukemia cell lines and inhibits the increase of leukemia sequence-1 protein in HI bone marrow cells.Fórmula:C23H26N4OPureza:99.61%Cor e Forma:SolidPeso molecular:374.48MMRi64
CAS:MMRi64 inhibits Mdm2-MdmX, boosts p53, triggers apoptosis, and is used in cancer research.Fórmula:C22H17Cl2N3OPureza:99.93%Cor e Forma:SolidPeso molecular:410.3Tubulin inhibitor 32
CAS:Tubulin inhibitor 32 is a microtubule inhibitor with antiproliferative and antitumor activity that induces apoptosis and cell cycle arrest in the G2/M phase.Fórmula:C18H19N3O3Pureza:99.92%Cor e Forma:SolidPeso molecular:325.361G244
CAS:1G244 is an inhibitor of DPP8/9 with antiatherosclerotic and antimyeloma properties.Fórmula:C29H30F2N4O2Pureza:99.14%Cor e Forma:SolidPeso molecular:504.57UCB-5307
CAS:UCB-5307 inhibits TNFR1, binds TNFα with 9 nM KD, shows slow kinetics (KD=6 nM), and penetrates hTNF/hTNFR1 complexes.Fórmula:C22H21N3OPureza:98.76%Cor e Forma:SolidPeso molecular:343.42Sarmustine
CAS:<p>SarCNU is an alkylating anticancer drug targeting prostate cancer through p53 pathways and selects P140K MGMT-transduced CD34(+) cells.</p>Fórmula:C6H11ClN4O3Pureza:98.29% - 99.71%Cor e Forma:SolidPeso molecular:222.63Triciribine phosphate
CAS:Triciribine phosphate (VD 002) is an AKT inhibitor that inhibits neovascularization and can be used in the study of leukemia.Fórmula:C13H17N6O7PPureza:97.94%Cor e Forma:SolidPeso molecular:400.28CCT020312
CAS:CCT020312 (0-9 µM, 24 h) treatment of medium HT29 cells for 24 h resulted in a concentration-dependent loss of P-S608-pRB.Cost-effective and quality-assured.Fórmula:C31H30Br2N4O2Pureza:98.63%Cor e Forma:SolidPeso molecular:650.4Ref: TM-T14902
1mg62,00€5mg140,00€10mg240,00€25mg408,00€50mg603,00€100mg838,00€500mg1.738,00€1mL*10mM (DMSO)188,00€Droloxifene
CAS:Droloxifene, a tamoxifen derivative and oral SERM, induces p53 and apoptosis; Fluroxifene protects bone, blocks estrogen and implantation.Fórmula:C26H29NO2Pureza:99.86% - 99.97%Cor e Forma:Solid PowderPeso molecular:387.51Ref: TM-T11098
1mg54,00€5mg116,00€10mg170,00€25mg283,00€50mg419,00€100mg562,00€500mgA consultar1mL*10mM (DMSO)133,00€EM-12
CAS:EM-12, a Thalidomide analogue, is more active, stable, and boosts rat colon cancer studies.Fórmula:C13H12N2O3Pureza:99.34%Cor e Forma:SolidPeso molecular:244.25XX-650-23
CAS:XX-650-23 is a CREB inhibitor that induces apoptosis and cell cycle arrest in AML cells and can be used to study acute myeloid leukemia (AML).Fórmula:C18H12N2O2Pureza:97.01%Cor e Forma:SolidPeso molecular:288.3Ref: TM-T24212
1mg47,00€5mg92,00€10mg145,00€25mg283,00€50mg472,00€100mg658,00€500mg1.378,00€1mL*10mM (DMSO)97,00€iCRT-5
CAS:iCRT-5 is a potent inhibitor of the Wnt pathway. iCRT-5 has antiproliferative activity and can be used in the study of multiple myeloma.Fórmula:C16H17NO5S2Pureza:99.68%Cor e Forma:SolidPeso molecular:367.44
