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(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 6084 produtos de "Apoptose"
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C6 Ceramide
CAS:<p>C6 Ceramide (N-hexanoylsphingosine) is an activator of the ceramide pathway that arrests cells in the G0/G1 phase by activating ERK.</p>Fórmula:C24H47NO3Pureza:99.67%Cor e Forma:SolidPeso molecular:397.63NM-3
CAS:NM-3, an oral anti-angiogenic and anti-tumor agent, modulates radiation and blocks VEGF to curb endothelial growth and induce apoptosis.Fórmula:C13H12O6Pureza:99.89%Cor e Forma:SolidPeso molecular:264.23Ref: TM-T33701
1mg180,00€5mg457,00€10mg652,00€25mg1.026,00€50mg1.406,00€100mg1.890,00€500mg3.725,00€1mL*10mM (DMSO)416,00€Anticancer agent 110
CAS:Anticancer Agent 110 exhibits potent in vitro anti-leukemia activity, demonstrating high cytotoxicity against K-562 lineage chronic myelogenous leukemia cellsFórmula:C18H13FN6OSPureza:98%Cor e Forma:SolidPeso molecular:380.4VAS 3947
CAS:VAS 3947: NOX inhibitor, induces platelet apoptosis via UPR, not linked to NOX inhibition.Fórmula:C14H10N6OSPureza:99.25%Cor e Forma:SolidPeso molecular:310.33Ref: TM-T29097
1mg48,00€5mg97,00€10mg170,00€25mg295,00€50mg424,00€100mg562,00€200mg743,00€1mL*10mM (DMSO)105,00€CCT020312
CAS:CCT020312 (0-9 µM, 24 h) treatment of medium HT29 cells for 24 h resulted in a concentration-dependent loss of P-S608-pRB.Cost-effective and quality-assured.Fórmula:C31H30Br2N4O2Pureza:98.63%Cor e Forma:SolidPeso molecular:650.4Ref: TM-T14902
1mg62,00€5mg140,00€10mg240,00€25mg408,00€50mg603,00€100mg838,00€500mg1.738,00€1mL*10mM (DMSO)188,00€HS-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€LDCA
CAS:LDCA inhibits LDH-A, disrupts mitochondrial function, induces apoptosis in cancer cells, and is non-toxic.Fórmula:C8H5Cl3FNOPureza:99.19%Cor e Forma:SolidPeso molecular:256.49CUDC-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:564.7Vamotinib
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€UNC0321
CAS:UNC0321 is an effective inhibitor of histone methyltransferase G9a with a Ki of 63 pM and with IC50s 9 nM and 6 nM in ECSD and CLOT assays.Fórmula:C27H45N7O3Pureza:99.80%Cor e Forma:SolidPeso molecular:515.69Alethine
CAS:Alethine is a small antitumor compound used to treat cancers and infections, boosting T-cell cytotoxicity by raising TNFα.Fórmula:C10H22N4O2S2Pureza:99.78%Cor e Forma:SolidPeso molecular:294.44Prinomastat
CAS:Prinomastat: orally active, crosses blood-brain barrier, inhibits MMP-1/2/3/9, Ki/IC50s: 0.05-0.3/5.0-79 nM, antitumor.Fórmula:C18H21N3O5S2Pureza:99.23%Cor e Forma:SolidPeso molecular:423.51Ref: TM-T12539L
1mg73,00€2mg117,00€5mg240,00€10mg432,00€25mg697,00€50mg938,00€100mg1.293,00€200mg1.738,00€W146
CAS:W146 is an S1PR1 antagonist that induces a significant but transient decrease in blood lymphocytes in mice.Fórmula:C16H27N2O4PPureza:99.37%Cor e Forma:SolidPeso molecular:342.37Mepazine
CAS:Mepazine, a MALT1 inhibitor, blocks GSTMALT1 (IC50: 0.83μM) and GSTMALT1 325-760 (IC50: 0.42μM), promoting apoptosis and reducing cell viability.Fórmula:C19H22N2SPureza:99.88% - 99.92%Cor e Forma:SolidPeso molecular:310.46Ref: TM-T16040
10mg39,00€25mg60,00€50mg93,00€100mg116,00€200mg177,00€500mgA consultar1mL*10mM (DMSO)35,00€GSK854
CAS:GSK854 is a selective TNNI3K inhibitor reducing heart damage and stress post-infarction in mice.Fórmula:C18H19ClN6O4S2Pureza:98.91%Cor e Forma:SolidPeso molecular:482.96Ref: TM-T24115
1mg97,00€5mg235,00€10mg378,00€25mg748,00€50mg1.121,00€100mg1.776,00€500mg3.562,00€1mL*10mM (DMSO)259,00€CP 461
CAS:CP 461 is a PDE2A inhibitor that promotes apoptosis in cancer cells without affecting normal cells or COX-1/2.Fórmula:C25H22ClFN2OPureza:99.82%Cor e Forma:SolidPeso molecular:420.91XX-650-23
CAS:XX-650-23 is a CREB inhibitor that induces apoptosis and cell cycle arrest in AML cells and can be used to study acute myeloid leukemia (AML).Fórmula:C18H12N2O2Pureza:97.01%Cor e Forma:SolidPeso molecular:288.3Ref: TM-T24212
1mg47,00€5mg92,00€10mg145,00€25mg283,00€50mg472,00€100mg658,00€500mg1.378,00€1mL*10mM (DMSO)97,00€RS1-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:380.89ZDLD20
CAS:ZDLD20 is a CDK4 inhibitor with anti-HCT116 and anticancer activity that inhibits colony formation and blocks the G1 phase of the cell cycle.Fórmula:C22H22N6OPureza:98.59%Cor e Forma:SolidPeso molecular:386.45Ciglitazone
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:333.45
