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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N6-Cyclopentyladenosine
CAS:N6-Cyclopentyladenosine (CPA) is a selective agonist of the adenosine A1 receptor and can be used to mimic the action of the adenosine A1 receptor, with Ki's ofFórmula:C15H21N5O4Pureza:99.95%Cor e Forma:SolidPeso molecular:335.36F16
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:362.21W146
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:342.37OR-1896
CAS:OR-1896 is a PDE III inhibitor, a vasodilator with partial anti-inflammatory properties, and can be used to study heart failure and vascular dysfunction.Fórmula:C13H15N3O2Pureza:99.33%Cor e Forma:SolidPeso molecular:245.28Ref: TM-T12315
1mg94,00€5mg197,00€10mg325,00€25mg657,00€50mg1.035,00€100mg1.406,00€200mg1.882,00€1mL*10mM (DMSO)217,00€CSN5i-3
CAS:CSN5i-3 is a potent, selective, and orally available inhibitor of the proteolytic subunit of the CSN complex, CSN5, as an anticancer agent.Cost-effective and quality-assured.Fórmula:C28H29F2N5O2Pureza:99.56% - >99.99%Cor e Forma:SolidPeso molecular:505.56Ref: TM-T10895
1mg359,00€5mg772,00€10mg1.169,00€25mg1.738,00€50mg2.347,00€100mg3.163,00€1mL*10mM (DMSO)842,00€CBS9106
CAS:CBS9106 (SL-801) is a CRM1 inhibitor with CRM1-degrading and anti-tumor activity that inhibits CRM1-dependent nuclear export.Fórmula:C18H21ClF3N3O3Pureza:98.98%Cor e Forma:SolidPeso molecular:419.83SYM 2081
CAS:SYM 2081: Kainate receptor agonist, IC50 of 35 nM, depolarizes muscle, lowers EPSP amplitude.Fórmula:C6H11NO4Pureza:99.63%Cor e Forma:SolidPeso molecular:161.16TAI-1
CAS:TAI-1 is a potent and specific Hec1 inhibitor, which disrupts Hec1-Nek2 protein interaction.Fórmula:C24H21N3O3SPureza:99.58%Cor e Forma:SolidPeso molecular:431.51RO-5963
CAS:RO-5963 is a dual inhibitor of p53-MDM2 and p53-MDMX (IC50s: ~17 nM and ~24 nM, respectively).Fórmula:C24H21ClF2N4O5Pureza:99.28%Cor e Forma:SolidPeso molecular:518.9Ref: TM-T16771
1mg70,00€5mg197,00€10mg284,00€25mg434,00€50mg562,00€100mg780,00€200mg1.035,00€1mL*10mM (DMSO)224,00€LCS3
CAS:<p>LCS3 is a reversible and non-competitive synergistic inhibitor of glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) with IC50s of 3.3</p>Fórmula:C11H7ClN2O4Pureza:99.68%Cor e Forma:SolidPeso molecular:266.64DB1976
CAS:DB1976: Selenophene DB270 analog, inhibits PU.1 (IC50=10 nM), disrupts PU.1/DNA (KD=12 nM), induces apoptosis, cell-permeable.Fórmula:C20H16N8SePureza:98.74%Cor e Forma:SolidPeso molecular:447.35EM-12
CAS:EM-12, a Thalidomide analogue, is more active, stable, and boosts rat colon cancer studies.Fórmula:C13H12N2O3Pureza:99.34%Cor e Forma:SolidPeso molecular:244.25EGFR-IN-11
CAS:EGFR-IN-11 selectively blocks EGFR-tyrosine kinase and promotes apoptosis; targets EGFRL858R/T790M/C797S, IC50=18 nM; halts cell cycle at G0/G1.Fórmula:C29H35N9O2SPureza:99.93%Cor e Forma:SolidPeso molecular:573.71VAS 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€Ro24-7429
CAS:Ro24-7429: oral HIV-1 Tat antagonist, RUNX1 inhibitor with anti-HIV, antifibrotic, and anti-inflammatory properties.Fórmula:C14H13ClN4Pureza:99.29% - 99.85%Cor e Forma:SolidPeso molecular:272.73Ref: TM-T28578
1mg92,00€5mg187,00€10mg298,00€25mg507,00€50mg730,00€100mg1.026,00€500mg2.877,00€1mL*10mM (DMSO)215,00€UK-101
CAS:UK-101 is a potent and selective inhibitor of the immunoproteasome LMP2, inhibiting β1i (LMP2), β1c (LMP2), and β5 (LMP2), with IC50s of 104 nM, 15 μM, and 1 μMFórmula:C25H48N2O5SiPureza:98.97% - 99.08%Cor e Forma:SolidPeso molecular:484.74CCT018159
CAS:<p>CCT018159: ATP-competitive HSP90 inhibitor, IC50 3.2 μM (human), 6.6 μM (yeast), blocks invasion, angiogenesis, induces G1 arrest and apoptosis.</p>Fórmula:C20H20N2O4Pureza:98.78% - 99.79%Cor e Forma:SolidPeso molecular:352.38GS-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:734.82Mepazine
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€Benitrobenrazide
CAS:Benitrobenrazide (Hexokinase 2 inhibitor 1) is a novel orally available hexokinase 2 (HK2) inhibitor with anticancer and antitumor activity for cancer research.Fórmula:C14H11N3O6Pureza:96.87%Cor e Forma:SolidPeso molecular:317.25
