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(61 produtos)
- p53(63 produtos)
Exibir 6 mais subcategorias
Foram encontrados 6071 produtos de "Apoptose"
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Cl-Necrostatin-1
CAS:Cl-Necrostatin-1 is an inhibitor of receptor-interacting protein kinase. It inhibits RIPK1 activity.Fórmula:C13H12ClN3OSCor e Forma:SolidPeso molecular:293.77ZK-304709 HCl
CAS:ZK-304709 is an oral multitarget tumor growth inhibitor with activity against cell-cycle progression and angiogenesis.Fórmula:C22H29ClN6O2Cor e Forma:SolidPeso molecular:444.96RSH-7
CAS:RSH-7 is a potent dual inhibitor of BTK and FLT3, with IC50s of 47 and 12 nM, respectively.RSH-7 has antiproliferative and antitumor activities, inducingFórmula:C22H25FN8OPureza:99.43%Cor e Forma:SolidPeso molecular:436.49CAY10406
CAS:CAY10406, a trifluoromethyl isatin sulfonamide, selectively targets and inhibits caspase-3 and -7, key in apoptosis, with no data on its inhibition potency.Fórmula:C27H23F3N2O5SCor e Forma:SolidPeso molecular:544.543,5-dimethyl PIT-1
CAS:PtdIns-(3,4,5)-P3 (PIP3) serves as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains such asFórmula:C16H15N3O4SCor e Forma:SolidPeso molecular:345.37MDH1-IN-2
CAS:MDH1-IN-2 is a potent MDH1 inhibitor with potential anticancer activity for the study of diseases related to the immune system.Fórmula:C25H33NO5Pureza:99.21%Cor e Forma:SolidPeso molecular:427.53Hetrombopag
CAS:Hetrombopag: potent thrombopoietin receptor agonist, well tolerated, safe, promising for immune thrombocytopenia research.Fórmula:C25H22N4O5Cor e Forma:SolidPeso molecular:458.47HJC-0123
CAS:HJC-0123: inhibits STAT3, boosts cleaved caspase-3, hinders cell growth, triggers apoptosis, effective in ER-negative breast/pancreatic cancer.Fórmula:C24H16N2O3SCor e Forma:SolidPeso molecular:412.46CT-1
CAS:<p>CT-1 is a DNA minor groove ligand and causes p53-dependent breast cancer cell apoptosis.</p>Fórmula:C29H23F3N4OPureza:99.79%Cor e Forma:SolidPeso molecular:500.51Paclitaxel Ceribate
CAS:Paclitaxel Ceribate is a mitotic inhibitor used in cancer chemotherapy.Fórmula:C51H57NO18Cor e Forma:SolidPeso molecular:971.99Ceranib-2
CAS:<p>Ceranib-2, a ceramidase inhibitor (IC50: 28 μM, SKOV3), reduces sphingosine/S1P and promotes apoptosis, showing anticancer properties.</p>Fórmula:C25H19NO3Pureza:98.49%Cor e Forma:SolidPeso molecular:381.42KU-0058948
CAS:KU-0058948: PARP inhibitor, triggers cell cycle arrest and apoptosis in myeloid leukemia cells in vitro.Fórmula:C21H21FN4O2Cor e Forma:SolidPeso molecular:380.42TSI-13-57
CAS:TSI-13-57 is a MyD88 inhibitor or pan-TLR inhibitor that suppresses MyD88 TIR domain dimerization ,inhibits LPS-induced TNF-α (IC50 = 6.73 mM).Fórmula:C28H29N3O3Pureza:99.63%Cor e Forma:SolidPeso molecular:455.55SGC-STK17B-1
CAS:SGC-STK17B-1 is a potent and selective inhibitor of STK17B/DRAK2 kinase.Fórmula:C16H10N2O2S3Cor e Forma:SolidPeso molecular:358.46AZD-5991 Racemate
CAS:<p>AZD-5991 Racemate is the racemate of AZD-5991. (Rac)-AZD-5991 is a novel Mcl-1 inhibitor induces upregulation of BCL2,BCL-XL, CMYC and MCL1 in AML cell lines.</p>Fórmula:C35H34ClN5O3S2Cor e Forma:SolidPeso molecular:672.26IKK2-IN-4
CAS:IKK2-IN-4(IKK2 Inhibitor VI) is a highly potent IKK-2 inhibitor with an IC50 value of 25 nM. IKK2-IN-4 inhibited the production of TNF-α in PBMC induced by LPS.Fórmula:C12H11N3O2SPureza:99.83%Cor e Forma:SolidPeso molecular:261.3Ref: TM-T36524
1mg114,00€5mg276,00€10mg424,00€25mg657,00€50mg884,00€100mg1.188,00€200mg1.586,00€500µg87,00€ADU-S100
CAS:ADU-S100 (MIW815) is a STING agonist that significantly induces the production of IFN-β,TNF-α,IL-6,and MCP-1,induces TBK1 and IRF3 phosphorylation,antitumour.Fórmula:C20H24N10O10P2S2Pureza:99.83%Cor e Forma:SolidPeso molecular:690.54VII-31
CAS:VII-31 is an activator of the NEDDylation pathway, capable of inducing apoptosis in MCF-7, PC-3, and MGC-803 cells.Fórmula:C23H25NO5SCor e Forma:SolidPeso molecular:427.51Glucocorticoid receptor modulator 1
CAS:Glucocorticoid receptor modulator 1 is a orally NF-κB and AP-1 inhibitor, inflammatory factors IL-6, IL-1β, TNF-α, and MMP-13, alleviating skin inflammation.Fórmula:C24H23ClN2O4SPureza:99.79%Cor e Forma:SolidPeso molecular:470.97Ref: TM-T72102
1mg64,00€5mg137,00€10mg210,00€25mg424,00€50mg615,00€100mg847,00€1mL*10mM (DMSO)140,00€EP12
CAS:EP12, a c-Myc inhibitor and G4 stabilizer, induces apoptosis and DNA damage in multiple myeloma cells while obstructing P65/P50 nuclear translocation byFórmula:C26H22FN3O2Pureza:98%Cor e Forma:SolidPeso molecular:427.47
