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(8 produtos)
- Caspase(145 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(92 produtos)
- c-RET(61 produtos)
- p53(63 produtos)
Exibir 6 mais subcategorias
Foram encontrados 6093 produtos de "Apoptose"
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AQ4
CAS:AQ4 is a topoisomerase II inhibitor and DNA-inserting agent that inhibits proliferation and induces apoptosis in two cell lines.Fórmula:C22H28N4O4Pureza:96.28% - 97.15%Cor e Forma:SolidPeso molecular:412.48RS1-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:380.89R306465
CAS:R306465 (JNJ-16241199) is an HDAC 1 inhibitor with broad-spectrum anti-tumor activity, inducing apoptosis, and can be used to study solid tumors.Fórmula:C19H19N5O4SPureza:98.46% - 99.54%Cor e Forma:SolidPeso molecular:413.45A09-003
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:374.48Miclxin
CAS:Miclxin (DS37262926) is a novel MIC60 inhibitor that induces apoptosis through mitochondrial stress in mutant tumor cells via β-catenin.Miclxin is a potentFórmula:C26H27N5O2Pureza:99.17% - 99.99%Cor e Forma:SolidPeso molecular:441.52Ref: TM-T73415
1mg64,00€5mg140,00€10mg192,00€25mg324,00€50mg452,00€100mg620,00€200mg835,00€1mL*10mM (DMSO)156,00€GS-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:734.82Vamotinib
CAS:Vamotinib (PF-114) is a tyrosine kinase inhibitor with antiproliferative and antitumor activity.Vamotinib is used in the study of Alzheimer's disease.Fórmula:C29H27F3N6OPureza:99.64%Cor e Forma:SolidPeso molecular:532.56Ref: TM-T63746
1mg106,00€5mg259,00€10mg424,00€25mg757,00€50mg1.035,00€100mg1.415,00€200mg1.882,00€1mL*10mM (DMSO)304,00€LQZ-7F
CAS:LQZ-7F is a survivin dimerization inhibitor with anticancer activity.LQZ-7F induces proteasome-dependent survivin degradation and inhibits human tumor growth.Fórmula:C14H7N9O3Pureza:98.64%Cor e Forma:SolidPeso molecular:349.26F16
CAS:F16 ((E)-4-(3-indolylvinyl)-N-methylpyridinium iodide) inhibits the growth of neu-overexpressing cells and the proliferation of mammary epithelial.Fórmula:C16H15IN2Pureza:99.89%Cor e Forma:SolidPeso molecular:362.21GSK2983559 free acid
CAS:GSK2983559 free acid selectively inhibits RIP2, reducing inflammatory cytokines in human bowel disease.Fórmula:C21H23N4O7PS2Pureza:97.8700% - 99.56%Cor e Forma:SolidPeso molecular:538.53Bomedemstat 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:864.02UCB-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:343.42CZL55
CAS:CZL55 is a potent caspase-1 inhibitor with an IC50 value of 0.024 μM.CZL55 has low cytotoxicity and can be used in the study of febrile seizures (FS).Fórmula:C20H22N2O6Pureza:98.19%Cor e Forma:SolidPeso molecular:386.4Necrostatin-5
CAS:Necrostatin-5 (Nec-5) inhibits RIP1 kinase, prevents cell necrosis, and protects Fadd-deficient Jurkat cells with an EC50 of 240 nM.Fórmula:C19H17N3O2S2Pureza:99.40%Cor e Forma:SolidPeso molecular:383.49Ciglitazone
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:333.45HS-276
CAS:HS-276, a selective oral TAK1 inhibitor (Ki: 2.5 nM), also targets CLK2, GCK, ULK2, MAP4K5; potential for RA research.Fórmula:C24H29N5O2Pureza:97.67% - 98.81%Cor e Forma:SolidPeso molecular:419.52Ref: TM-T62209
1mg66,00€5mg144,00€10mg219,00€25mg430,00€50mg690,00€100mg1.064,00€200mg1.434,00€1mL*10mM (DMSO)170,00€CUDC-427
CAS:CUDC-427 (GDC-0917) is an orally bioactive and pan antagonist of inhibitor of apoptosis proteins(IAPs). CUDC-427 can be used in research on cancers.Fórmula:C29H36N6O4SPureza:99.92%Cor e Forma:SolidPeso molecular:564.7HS38
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:349.8AOH1160
CAS:AOH1160 is an inhibitor of proliferating cell nuclear antigen (PCNA).Fórmula:C25H20N2O3Pureza:98.46% - 99.52%Cor e Forma:SolidPeso molecular:396.44Imipramine
CAS:Imipramine (Dimipressin) is a Fascin1 inhibitor with antitumor activity and induces apoptosis.Fórmula:C19H24N2Pureza:99.4%Cor e Forma:White To Off-White /Hydrochloride/ SolidPeso molecular:280.41
