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(1 produtos)
- Caspase(154 produtos)
- FOXO1(2 produtos)
- IAP(67 produtos)
- Mdm2(12 produtos)
- PD-1/PD-L1(109 produtos)
- PDK(9 produtos)
- PERK(26 produtos)
- Serina/treonina quinase(18 produtos)
- Survivina(14 produtos)
- TNF(64 produtos)
- c-RET(61 produtos)
- p53(63 produtos)
Exibir 6 mais subcategorias
Foram encontrados 6100 produtos de "Apoptose"
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Necrostatin-7
CAS:Necrostatin-7 (Necrostatin 7) is a necrotic apoptosis inhibitor with cardioprotective effects that inhibits RANK-NFATc1 signaling.Fórmula:C16H10FN5OS2Pureza:98.71%Cor e Forma:SolidPeso molecular:371.41Telomerase-IN-5
CAS:Telomerase-IN-5 is a potent inhibitor of telomerase with antiproliferative properties, and it induces apoptosis [1].Fórmula:C22H20N4OS2Pureza:98%Cor e Forma:SolidPeso molecular:420.55TNF-α-IN-1
CAS:TNF-α-IN-1 is a TNF-α inhibitor.Fórmula:C16H14ClN3O5Pureza:98.82%Cor e Forma:SolidPeso molecular:363.75Ref: TM-T13175
1mg56,00€5mg120,00€10mg178,00€25mg330,00€50mg505,00€100mg713,00€1mL*10mM (DMSO)203,00€F5446
CAS:F5446 is a selective small molecule SUV39H1 methyltransferase inhibitor, promotes apoptosis in colorectal cancer cells by inhibiting the deposition of H3K9me3.Fórmula:C26H17ClN2O8SPureza:98.56%Cor e Forma:SolidPeso molecular:552.94NSC745887
CAS:NSC745887 (compound 25) is an anticancer agent that demonstrates dose-dependent inhibition of proliferation across 60 cancer cell lines [1].Fórmula:C16H8N2O2Cor e Forma:SolidPeso molecular:260.25VII-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:427.51ADU-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:690.54Dinoprost
CAS:Dinoprost (Prostaglandin F2a) is a naturally occurring prostaglandin. It is used in medicine to induce labor and as an abortifacient.Fórmula:C20H34O5Pureza:97.94% - 98.04%Cor e Forma:White To Off-White Crystalline SolidPeso molecular:354.48Ref: TM-T15133
5mg49,00€10mg74,00€25mg137,00€50mg205,00€100mg326,00€200mg485,00€1mL*10mM (DMSO)54,00€C1A
CAS:C1A is an inhibitor of HDAC6 which modulates downstream autophagy substrates and leads to growth inhibition of a diverse set of cancer cell lines.Fórmula:C22H25Cl2N3O4SCor e Forma:SolidPeso molecular:498.42STAT3-IN-11
CAS:STAT3-IN-11 is a STAT3 inhibitor.STAT3-IN-11 promotes apoptosis in cancer cells and is a candidate compound for the treatment of cancer.Fórmula:C20H17NO4Pureza:98.3%Cor e Forma:SolidPeso molecular:335.35p-MPPF dihydrochloride
CAS:p-MPPF dihydrochloride is a 5-HT antagonist that can be used to study neurological diseases.Fórmula:C25H29Cl2FN4O2Pureza:99.55%Cor e Forma:SolidPeso molecular:507.43CHS-828 nicotinate
CAS:CHS-828, or GMX-1778, is a potent NAMPT inhibitor with anticancer properties, active against tumors and enhanced by certain drugs.Fórmula:C25H27ClN6O3Cor e Forma:SolidPeso molecular:494.97BIM-46174
CAS:BIM-46174 has anticancer activity, inhibits the growth of a large number of human cancer cell lines, and induces caspase-3-dependent cancer cell apoptosis.Fórmula:C22H30N4OSCor e Forma:SolidPeso molecular:398.57FKBP51F67V-selective antagonist Ligand2
CAS:FKBP51F67V-selective antagonist Ligand2 (example 3-3), a potent ligand, selectively binds to the FKBP51 F67V variant, with no affinity for wild-type FKBP51 orFórmula:C43H56N2O10Pureza:98%Cor e Forma:SolidPeso molecular:760.91Nanatinostat TFA
CAS:Nanatinostat (Tractinostat, CHR-3996, VRx-3996) is a second-gen oral HDAC inhibitor with potential cancer treatment properties.Fórmula:C22H20F4N6O4Cor e Forma:SolidPeso molecular:508.43IDH1 Inhibitor 9
CAS:IDH1 Inhibitor 9 (compound 11S) (2, 4, 8, 10 µM) induces apoptosis and causes cell cycle arrest in the S phase in a dose-dependent manner.Fórmula:C26H30N4O3Cor e Forma:SolidPeso molecular:446.54MBC-11
CAS:MBC-11: First bone-targeting bisphosphonate-etidronate conjugate with araC, may treat TIBD.Fórmula:C11H20N3O14P3Pureza:>99.99% - >99.99%Cor e Forma:SolidPeso molecular:511.21MC-70
CAS:MC-70, P-gp and ABC transporter inhibitor (EC50=0.69 µM), interacts with ABCB1/G2/C1, inhibits colon cancer growth and induces apoptosis.Fórmula:C24H25NO3Pureza:99.94%Cor e Forma:SolidPeso molecular:375.46KS106
CAS:KS106 inhibits ALDH (1A1: 334 nM, 2: 2137 nM, 3A1: 360 nM), has anti-cancer properties, raises ROS, and promotes aldehyde build-up.Fórmula:C18H15BrF3N3O2SPureza:99.31%Cor e Forma:SolidPeso molecular:474.3RI-962
CAS:RI-962 is a potent and selective inhibitor of RIPK1 that protects cells from necrotic apoptosis by inhibiting RIPK1, RIPK3, and MLKL phosphorylation.Fórmula:C28H28N6O2Pureza:99.39%Cor e Forma:SoildPeso molecular:480.56
