Cromatina/Epigenética
Os inibidores de cromatina/epigenética são compostos que modulam a estrutura e função da cromatina ou interferem em modificações epigenéticas, como a metilação do DNA e a modificação de histonas. Esses inibidores são ferramentas essenciais para estudar a regulação da expressão gênica e o papel da epigenética em doenças como o câncer, distúrbios neurológicos e anomalias do desenvolvimento. Ao direcionar os processos epigenéticos, esses inibidores podem alterar os padrões de expressão gênica e oferecer novas vias terapêuticas. Na CymitQuimica, oferecemos uma ampla seleção de inibidores de cromatina/epigenética de alta qualidade para apoiar sua pesquisa em biologia molecular, genética e epigenética.
Subcategorias de "Cromatina/Epigenética"
Foram encontrados 2616 produtos de "Cromatina/Epigenética"
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MAT2A-IN-9
CAS:MAT2A-IN-9, a 2-oxoquinazoline, inhibits MAT2A with antitumor effects on lymphomas and solid cancers.Fórmula:C14H8ClF3N4OPureza:99.17%Cor e Forma:SolidPeso molecular:340.69JAK-STAT-IN-1
CAS:JAK-STAT-IN-1 is a specific JAK-STAT inhibitor indicated for the study of autoimmune diseases.Fórmula:C21H21N5O2Pureza:99.59%Cor e Forma:SolidPeso molecular:375.42HDAC8-IN-20a
CAS:HDAC8-IN-20a (HDAC8 inhibitor-20a) is a potent and selective HDAC8 inhibitor with an IC50 of 27 nM.Fórmula:C15H15NO4Pureza:98.24% - 99.22%Cor e Forma:SolidPeso molecular:273.28Ref: TM-T24133
1mg173,00€1mL*10mM (DMSO)380,00€5mg424,00€10mg585,00€25mg873,00€50mg1.134,00€100mg1.468,00€200mg1.963,00€EB-47
CAS:EB-47 imitates NAD+, spans nicotinamide to adenosine sites, inhibits PARP-1 (IC50: 45 nM) and is less effective on ARTD5 (IC50: 410 nM).Fórmula:C24H27N9O6Pureza:99.81%Cor e Forma:SolidPeso molecular:537.53TM2-115
CAS:TM2-115 is a inhibitor of malaria parasite histone methyltransferases that results in rapid and irreversible parasite death [1].Fórmula:C28H38N6O2Pureza:97.67%Cor e Forma:SolidPeso molecular:490.64ZEN-3411
CAS:ZEN-3411 is an BET inhibitor that inhibits BRD4(BD1), BRD4(BD2), and BRD4(BD1BD2) and suppresses the growth of tumor cells overproducing BET proteins.Fórmula:C21H20N4O2Pureza:97.51% - 98.84%Cor e Forma:SolidPeso molecular:360.41Bisaramil hydrochloride
CAS:Bisaramil hydrochloride (Bisaramil) is an antiarrhythmic compound that inhibits free radical production.Fórmula:C17H24Cl2N2O2Pureza:98.64% - 99.48%Cor e Forma:SolidPeso molecular:359.29LEM-14
CAS:LEM-14 is a potent NSD2-specific inhibitor (IC50:132 μM).LEM-14 may be used in the study of multiple myeloma.
Fórmula:C25H26N4O4SPureza:98.3%Cor e Forma:SolidPeso molecular:478.56KRH102140
CAS:KRH102140 is a PHD2 activator that reduces angiogenesis by inhibiting HIF-1alpha, used in cardiovascular disease research.Fórmula:C25H24FNOPureza:98.31% - 99.61%Cor e Forma:SolidPeso molecular:373.46Crebinostat
CAS:Crebinostat: potent HDAC inhibitor, boosts synapsin-1 in neurons, enhances memory and gene Egr1 expression in mice.Fórmula:C20H23N3O3Pureza:99.49%Cor e Forma:SolidPeso molecular:353.41STS-E412
CAS:STS-E412 is a tissue-protective and selective EPOR/CD131 receptor activator for the study of neurological disorders.Fórmula:C15H15ClN4O2Pureza:99.01%Cor e Forma:SolidPeso molecular:318.76BRD2492
CAS:BRD2492 is an HDAC1 and HDAC2 inhibitor with antiproliferative activity, inhibits HDAC1/2 and induces apoptosis.Fórmula:C20H18N4O2Pureza:99.56%Cor e Forma:SolidPeso molecular:346.38Butyrolactone 3
CAS:Butyrolactone 3 (MB-3) is a Gcn5 inhibitor with weak affinity for CBP.Butyrolactone 3 has antimicrobial activity and can be used in cancer.Fórmula:C9H12O4Pureza:98.99% - 99.5%Cor e Forma:SolidPeso molecular:184.19Butyzamide
CAS:Butyzamide: oral Mpl activator, non-peptide, antagonizes TPO receptors, boosts hMpl, Ba/F3 cells, and enhances platelets in mice.Fórmula:C29H32Cl2N2O5SPureza:99.39% - 99.83%Cor e Forma:SoildPeso molecular:591.55Ref: TM-T67894
1mg149,00€5mg253,00€1mL*10mM (DMSO)329,00€10mg371,00€25mg573,00€50mg862,00€100mg1.305,00€200mg1.755,00€EZH2-IN-13
CAS:EZH2-IN-13 is a potent EZH2 inhibitor with potential anticancer activity.EZH2-IN-13 may be used to study diseases associated with EZH2 activity.Fórmula:C34H45N5O3Pureza:98.3%Cor e Forma:SolidPeso molecular:571.75AGI-24512
CAS:AGI-24512 is a inhibitor of methionine adenosyltransferase 2A (MATA2 ).It is useful for treatment of cancer and blocks growth of MTAP-deleted cancer cells inFórmula:C24H24N4O2Pureza:98.55%Cor e Forma:SolidPeso molecular:400.47Ref: TM-T14141
1mg66,00€5mg145,00€1mL*10mM (DMSO)195,00€10mg224,00€25mg358,00€50mg512,00€100mg707,00€200mg982,00€Cedazuridine
CAS:Cedazuridine ((4R)-2'-Deoxy-2',2'-difluoro-3,4,5,6-tetrahydrouridine) is an oral inhibitor of cytidine deaminase with antineoplastic properties.Fórmula:C9H14F2N2O5Pureza:99.66%Cor e Forma:SolidPeso molecular:268.21OXF BD 02
CAS:OXF BD 02 is a potent and selective BRD4(1) inhibitor (IC50: 382 nM) with anticancer and anti-inflammatory activity.Fórmula:C18H17NO3Pureza:98.25%Cor e Forma:SolidPeso molecular:295.33Bobcat339 hydrochloride
CAS:Bobcat339 hydrochloride is a 10 11 translocation (TET) dioxygenase inhibitor that inhibits both TET1 and TET2.Fórmula:C16H13Cl2N3OPureza:99.22%Cor e Forma:SolidPeso molecular:334.2Ref: TM-T61012
2mg34,00€5mg50,00€1mL*10mM (DMSO)55,00€10mg80,00€25mg152,00€50mg236,00€100mg353,00€200mg517,00€AAPK-25
CAS:AAPK-25, a dual Aurora/PLK inhibitor, disrupts mitosis, induces apoptosis, and has antitumor properties.Fórmula:C21H13Cl2N3O2SPureza:97.05%Cor e Forma:SolidPeso molecular:442.32Ref: TM-T10215
1mg54,00€5mg118,00€1mL*10mM (DMSO)131,00€10mg172,00€25mg313,00€50mg469,00€100mg680,00€
