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 6064 produtos de "Apoptose"
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HBV-IN-23
CAS:HBV-IN-23: HBV replication inhibitor, IC50 0.58μM, affects resistant strains, induces HepG2 apoptosis, anti-HCC.Fórmula:C25H27N3O3SCor e Forma:SolidPeso molecular:449.57PERK-IN-3
CAS:PERK-IN-3 is a potent inhibitor of PERK(IC50 of 7.4 nM).Fórmula:C22H16F2N4O2Pureza:98%Cor e Forma:SolidPeso molecular:406.38TNF-α-IN-18
CAS:TNF-α-IN-18 is a small molecule TNF-α inhibitor that blocks NF-κB translocation, alleviates sepsis in models, and protects against rheumatoid arthritis in mice.Fórmula:C16H7ClF2O4Pureza:99.77%Cor e Forma:SolidPeso molecular:336.67Metallo-β-lactamase-IN-5
CAS:Metallo-β-lactamase-IN-5 (compound 5c) is a powerful inhibitor of metallo-β-lactamases (MBLs).Fórmula:C19H16N4O3Cor e Forma:SolidPeso molecular:348.36GLUT4-IN-2
CAS:GLUT4-IN-2, selective GLUT4 blocker; IC50: 6.8μM (GLUT4), 11.4μM (GLUT1). Induces apoptosis, G0/G1 arrest, has antitumor effects.Fórmula:C17H11N3O4S2Pureza:99.90%Cor e Forma:SolidPeso molecular:385.42PD-1/PD-L1-IN-25
CAS:"PD-1/PD-L1-IN-25 blocks PD-1/PD-L1 (IC50: 16.17 nM), boosting T-cell anti-tumor immunity, useful for cancer research."Fórmula:C26H24ClN3O5Cor e Forma:SolidPeso molecular:493.94CCT128930
CAS:'CCT128930, potent Akt2 inhibitor (IC50=6 nM), 28x more selective over PKA.'Fórmula:C18H20ClN5Pureza:99.07% - 99.18%Cor e Forma:SolidPeso molecular:341.84Ref: TM-T6303
2mg42,00€5mg65,00€10mg94,00€25mg170,00€50mg273,00€100mg409,00€200mg652,00€1mL*10mM (DMSO)71,00€MPT0B214
CAS:MPT0B214, a potent microtubule inhibitor, disrupts tubulin polymerization and kills various cancer cells, including drug-resistant types.Fórmula:C20H20N2O5Cor e Forma:SolidPeso molecular:368.38PD-1/PD-L1-IN-29
CAS:PD-1/PD-L1-IN-29 (S4-1) is a potent inhibitor of the PD-1/PD-L1 interaction, with an IC50 value of 6.1 nM.Fórmula:C26H24N2O6Cor e Forma:SolidPeso molecular:460.48Ludartin
CAS:Ludartin activates TRPA1, induces DNA damage, and lowers mitochondrial potential, yielding anticancer effects.Fórmula:C15H18O3Cor e Forma:SolidPeso molecular:246.3APPA
CAS:APPA, an aldose reductase inhibitor, demonstrates efficacy in preventing apoptosis and symptoms of Streptozotocin-induced diabetes in rats through inhibition ofFórmula:C14H13NO3Pureza:98%Cor e Forma:SolidPeso molecular:243.26Ormeloxifene
CAS:estrogen receptor modulatorFórmula:C30H35NO3Pureza:98%Cor e Forma:SolidPeso molecular:457.6Zoledronate disodium
CAS:Zoledronate disodium inhibits osteoclasts, lowers bone turnover, stabilizes matrix, and has anti-tumor effects in osteosarcoma.Fórmula:C5H8N2Na2O7P2Cor e Forma:SolidPeso molecular:316.0531R-547 mesylate
CAS:R547 Mesylate is a potent ATP-competitive inhibitor of CDK1, CDK2, CDK4 with Ki value of 2 nM, 3 nM, 1 nM respectively.Fórmula:C19H25F2N5O7S2Cor e Forma:SolidPeso molecular:537.56Nanatinostat 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:508.43CHS-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:494.97RSH-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:436.49Bomedemstat ditosylate
CAS:<p>Bomedemstat (IMG-7289) is an LSD1 inhibitor for acute myeloid leukemia, MDS, and Myelofibrosis; induces apoptosis by regulating p53, PUMA, and BCLXL.</p>Fórmula:C42H50FN7O8S2Pureza:99.05%Cor e Forma:SolidPeso molecular:864.02GS-9191
CAS:GS-9191 is a potent inhibitor of DNA polymerase alpha and ß , a prodrug of the novel nucleoside analogue 9-(2-phosphonomethoxyethyl)guanine (PMEG) , whichFórmula:C37H51N8O6PPureza:98.01 - 99.28%Cor e Forma:SolidPeso molecular:734.82UC-112
CAS:UC-112 is a novel potent IAP inhibitor and potently inhibits cell growth in two human melanoma and two human prostate cancer cell lines (IC50=0.7-3.4 uM).Fórmula:C22H24N2O2Pureza:99.54%Cor e Forma:SolidPeso molecular:348.44Ref: TM-T17195
1mg35,00€2mg47,00€5mg73,00€10mg104,00€25mg213,00€50mg329,00€100mg470,00€500mgA consultar1mL*10mM (DMSO)82,00€
