Chromatin/Epigenetics
Chromatin/epigenetics inhibitors are compounds that modulate the structure and function of chromatin or interfere with epigenetic modifications, such as DNA methylation and histone modification. These inhibitors are essential tools for studying gene expression regulation and the role of epigenetics in diseases like cancer, neurological disorders, and developmental abnormalities. By targeting epigenetic processes, these inhibitors can alter gene expression patterns and offer new therapeutic avenues. At CymitQuimica, we provide a wide selection of high-quality chromatin/epigenetics inhibitors to support your research in molecular biology, genetics, and epigenetics.
Subcategories of "Chromatin/Epigenetics"
Found 2441 products of "Chromatin/Epigenetics"
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HDAC6 degrader 9c
CAS:HDAC6 degrader 9c is a small molecule histone deacetylase 6 (HDAC6) degrader that can be used to study cancer or other diseases.Formula:C37H45N9O10Purity:>99.99%Color and Shape:SolidMolecular weight:775.81ZEN-2759
CAS:ZEN-2759 is a potent BET small molecule inhibitor of BRD4(BD1), BRD4(BD2) and BRD4(BD1BD2).Formula:C17H16N2O2Purity:99.36%Color and Shape:SolidMolecular weight:280.32AGI-43192
CAS:<p>AGI-43192: potent MAT2A inhibitor, crosses blood-brain barrier, may help study SAM in CNS and treat cancer.</p>Formula:C23H16ClF3N6OPurity:99.89%Color and Shape:SolidMolecular weight:484.86PU139
CAS:<p>PU139 is a novel inhibitor of histone acetyltransferase (HAT).</p>Formula:C12H7FN2OSPurity:99.96%Color and Shape:SolidMolecular weight:246.26Procainamide
CAS:Procainamide: DNMT1 inhibitor, Class 1A antiarrhythmic, promising for cancer and arrhythmia research.Formula:C13H21N3OPurity:99.79% - 99.92%Color and Shape:SolidMolecular weight:235.33CEP-9722
CAS:CEP-9722 is a PARP-1 and PARP-2 inhibitor with anticancer activity and is used in the study of ovarian cancer.Formula:C24H26N4O3Purity:98.38% - 98.56%Color and Shape:SolidMolecular weight:418.49OXFBD04
CAS:OXFBD04: Potent BRD4 inhibitor, IC50=166nM, acts on BET bromodomains; moderate CREBBP affinity; anti-cancer properties.Formula:C17H16N2O3Purity:99.56%Color and Shape:SolidMolecular weight:296.32Ref: TM-T12338
1mg52.00€2mg78.00€5mg115.00€10mg182.00€25mg339.00€50mg505.00€100mg685.00€200mg944.00€1mL*10mM (DMSO)126.00€BAY-299
CAS:BAY-299 inhibits BRPF2, TAF1, and TAF1L with IC50s of 67, 8, and 106 nM.Formula:C25H23N3O4Purity:99.53%Color and Shape:SolidMolecular weight:429.47NSC 694623
CAS:NSC 694623: Potent HAT inhibitor, IC50=15.9 μM against PCAF, anti-cancer properties.Formula:C16H16N2OSPurity:99.9%Color and Shape:SolidMolecular weight:284.38CD532
CAS:CD532: Potent Aurora A inhibitor, IC50=45 nM, blocks kinase activity, degrades MYCN, interacts with AURKA, studies cancer.Formula:C26H25F3N8OPurity:99.99%Color and Shape:SolidMolecular weight:522.52Cedazuridine
CAS:Cedazuridine ((4R)-2'-Deoxy-2',2'-difluoro-3,4,5,6-tetrahydrouridine) is an oral inhibitor of cytidine deaminase with antineoplastic properties.Formula:C9H14F2N2O5Purity:99.66%Color and Shape:SolidMolecular weight:268.21AGI-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 inFormula:C24H24N4O2Purity:98.55%Color and Shape:SolidMolecular weight:400.47Ref: TM-T14141
1mg70.00€5mg154.00€10mg235.00€25mg378.00€50mg540.00€100mg747.00€200mg1,035.00€1mL*10mM (DMSO)207.00€KRH102140
CAS:KRH102140 is a PHD2 activator that reduces angiogenesis by inhibiting HIF-1alpha, used in cardiovascular disease research.Formula:C25H24FNOPurity:98.31% - 99.61%Color and Shape:SolidMolecular weight:373.46GSK-690
CAS:<p>GSK-690 is a potent, reversible and selective inhibitors of Lysine Specific Demethylase 1.</p>Formula:C24H23N3OPurity:98.65%Color and Shape:SolidMolecular weight:369.46R 59-022 hydrochloride
CAS:<p>R 59-022 hydrochloride is a 5-HT antagonist, PKC activator, DGK inhibitor (IC50: 2.8 µM), and modulates lipid production in platelets and neutrophils.</p>Formula:C27H27ClFN3OSPurity:97.7%Color and Shape:SolidMolecular weight:496.04JAK-STAT-IN-1
CAS:JAK-STAT-IN-1 is a specific JAK-STAT inhibitor indicated for the study of autoimmune diseases.Formula:C21H21N5O2Purity:99.59%Color and Shape:SolidMolecular weight:375.42SK-575
CAS:SK-575 is a potent PARP1-degrading agent effective against BRCA1/2 mutant cancers, even at low doses, and enhances tumor inhibition in mice.Formula:C47H53FN8O8Purity:99.39%Color and Shape:SolidMolecular weight:876.97Crebinostat
CAS:Crebinostat: potent HDAC inhibitor, boosts synapsin-1 in neurons, enhances memory and gene Egr1 expression in mice.Formula:C20H23N3O3Purity:99.49%Color and Shape:SolidMolecular weight:353.41DW14800
CAS:DW14800 is an inhibitor of PRMT5 (IC50 = 17 nM), enhances the transcription of HNF4α, and reduces the level of H4R3me2s.Formula:C31H36N4O3Purity:99.55% - 99.68%Color and Shape:SolidMolecular weight:512.64Ref: TM-T11131
1mg87.00€2mg130.00€5mg216.00€10mg378.00€25mg717.00€50mg948.00€100mg1,415.00€1mL*10mM (DMSO)245.00€PARP10-IN-2
CAS:<p>PARP10-IN-2 is a potent inhibitor of PARP10, a mono-ADP-ribosyltransferase, with an IC50 value of 3.64 μM for human PARP10.PARP10-IN-2 also inhibited PARP2 and</p>Formula:C14H10N2O2Purity:99.27%Color and Shape:SolidMolecular weight:238.24
