Apoptosis
Los inhibidores de la apoptosis son compuestos que previenen o retrasan el proceso de muerte celular programada, conocido como apoptosis. Estos inhibidores son vitales para estudiar los mecanismos de supervivencia celular y se utilizan para investigar enfermedades donde la apoptosis está desregulada, como el cáncer, los trastornos neurodegenerativos y las enfermedades autoinmunes. Al modular la apoptosis, estos inhibidores pueden ayudar en el desarrollo de terapias dirigidas a controlar la muerte celular. En CymitQuimica, ofrecemos una amplia selección de inhibidores de la apoptosis de alta calidad para apoyar su investigación en biología celular, oncología y campos relacionados.
Subcategorías de "Apoptosis"
- ASK(9 productos)
- BCL(8 productos)
- Caspasa(144 productos)
- FOXO1(3 productos)
- IAP(67 productos)
- Mdm2(12 productos)
- PD-1 / PD-L1(139 productos)
- PDK(9 productos)
- PERK(26 productos)
- Serina / treonina quinasa(18 productos)
- Survivin(14 productos)
- TNF(93 productos)
- c-RET(61 productos)
- p53(63 productos)
Mostrar 6 subcategorías más
Se han encontrado 6084 productos de "Apoptosis"
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JMJD3/HDAC-IN-1
CAS:Compound A5b, also known as JMJD3/HDAC-IN-1, is a dual inhibitor that targets both JMJD3 (Jumonji domain-containing protein demethylase 3) and HADC1 (histoneFórmula:C21H30N6O2Pureza:98%Forma y color:SolidPeso molecular:398.5AM-8735
CAS:AM-8735 is an inhibitor of MDM2 ( IC50: 25 nM).Fórmula:C27H31Cl2NO6SPureza:98%Forma y color:SolidPeso molecular:568.51TL02-59
CAS:TL02-59: Fgr inhibitor (IC50=0.03nM), also targets Lyn (0.1nM), Hck (160nM), halts acute myelogenous leukemia growth.Fórmula:C32H34F3N5O4Pureza:98.77%Forma y color:SolidPeso molecular:609.64Ref: TM-T13186
1mg49,00€2mg62,00€5mg93,00€10mg133,00€25mg260,00€50mg401,00€100mg557,00€200mg790,00€1mL*10mM (DMSO)111,00€WYE-132
CAS:WYE-125132: potent mTOR inhibitor, IC50 0.19 nM, selective over PI3Ks/hSMG1/ATR.Fórmula:C27H33N7O4Pureza:99.16%Forma y color:SolidPeso molecular:519.6SM-1295
CAS:SM-1295: IAP antagonist, Kd 3077 nM XIAP-BIR3, 3.2 nM c-IAP1-BIR3, 9.5 nM c-IAP2-BIR3.Fórmula:C29H36BrN5O4Forma y color:SolidPeso molecular:598.53Lepadin H
CAS:Lepadin H, a marine alkaloid and ferroptosis inducer, exhibits significant cytotoxicity by promoting p53 expression, escalating ROS production, and enhancingFórmula:C26H45NO3Pureza:98%Forma y color:SolidPeso molecular:419.64Antitumor agent-92
CAS:Antitumor Agent-92, a derivative of Icaritin, halts cell cycle, triggers cell death, and is promising for liver cancer study.Fórmula:C33H41NO10Pureza:98%Forma y color:SolidPeso molecular:611.68Antitumor agent-110
CAS:Antitumor Agent-110 (Compound 13), an imidazotetrazine anticancer agent, exhibits excellent permeability.Fórmula:C10H6N6OSPureza:98%Forma y color:SolidPeso molecular:258.26Lepadin E
CAS:Lepadin E, a notably cytotoxic compound, effectively stimulates ferroptosis via the canonical p53-SLC7A11-GPX4 pathway.Fórmula:C26H47NO3Pureza:98%Forma y color:SolidPeso molecular:421.66PD-1/PD-L1-IN-22
CAS:PD-1/PD-L1-IN-22 is a small molecule inhibitor of PD-1/PD-L1 protein-protein interactions that blocks PD-1/PD-L1 interactions (IC50: 0.732 μM).Fórmula:C25H26BrClN2O3Forma y color:SolidPeso molecular:517.84Cerivastatin
CAS:Cerivastatin is an HMG-CoA reductase inhibitor with anticancer and lipid-lowering effects and can be used to study primary hyperlipidemia.Fórmula:C26H34FNO5Pureza:97.80% - 99.56%Forma y color:SolidPeso molecular:459.55Eeyarestatin I
CAS:Eeyarestatin I blocks ER protein degradation, hinders p97/atx3 processes, and induces anticancer proteins.Fórmula:C27H25Cl2N7O7Pureza:98% - 98.99%Forma y color:SolidPeso molecular:630.44MP7
CAS:MP7 (PDK1 inhibitor) is a inhibitor of phosphoinositide-dependent kinase-1 (PDK1).Fórmula:C28H22F2N4O4Pureza:99.89%Forma y color:SolidPeso molecular:516.5Anticancer agent 128
CAS:Anticancer agent 128 (compound 1) is an IAP inhibitor that covalently binds to the BIR3 domains of XIAP, cIAP1, and cIAP2, exhibiting IC50 values of 24.9 nM, 19Fórmula:C26H38N4O4Pureza:98%Forma y color:SolidPeso molecular:470.6Anticancer agent 105
CAS:Anticancer agent 105, a thienopyrimidine scaffold-based compound, exhibits selective toxicity towards melanoma and induces apoptosis.Fórmula:C25H24KN3O6SPureza:98%Forma y color:SolidPeso molecular:533.64Anticancer agent 127
CAS:<p>Anticancer agent 127 (142D6), an IAP inhibitor, covalently binds to the BIR3 domains of XIAP, cIAP1, and cIAP2, with IC50 values of 12 nM, 14 nM, and 9 nM,</p>Fórmula:C26H37FN4O6SPureza:98%Forma y color:SolidPeso molecular:552.66BQZ-485
CAS:BQZ-485, a potent GDI2 inhibitor, interacts with Tyr245 to disrupt the native GDI2-Rab1A interaction.Fórmula:C32H39NO3Pureza:98%Forma y color:SolidPeso molecular:485.66IK-862
CAS:<p>IK-862 is a selective TACE inhibitor with potential anti-inflammatory and anticancer activity for the study of neuritis.</p>Fórmula:C25H27N3O4Pureza:97.75% - 98.29%Forma y color:SolidPeso molecular:433.5Methyl 12-methyltridecanoate
CAS:Methyl 12-methyltridecanoate ((R)-betaxolol hydrochloride), a biosurfactant derived from Brevibacterium casei LS14, enhances the biocompatibility ofFórmula:C15H30O2Pureza:98%Forma y color:SolidPeso molecular:242.4eIF4A3-IN-17
CAS:eIF4A3-IN-17, a silvestrol analogue, disrupts eIF4F assembly; EC50: 0.9-15 nM. Used in cancer pathogenesis research.Fórmula:C28H25NO7Forma y color:SolidPeso molecular:487.5
