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 2548 products of "Chromatin/Epigenetics"
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HAT-IN-1
CAS:HAT-IN-1 is an inhibitor of HAT used in the research of cancer.Formula:C23H18BrF4N3O4Purity:98%Color and Shape:SolidMolecular weight:556.3A2AAR/HDAC-IN-2
CAS:A2AAR/HDAC-IN-2: potent dual A2AAR/HDAC inhib., Ki 10.3 nM, IC50 18.5 nM, anti-tumor potential.Formula:C23H26N6O4Color and Shape:SolidMolecular weight:450.49FNDR-20123 free base
CAS:FNDR-20123 is a safe, oral first-in-class anti-malarial HDAC inhibitor with low IC50s against Plasmodium and human HDACs.Formula:C21H23N5O2Color and Shape:SolidMolecular weight:377.44Galegine hydrochloride
CAS:Galegine hydrochloride, from G. officinalis, leads to weight loss, activates AMPK in various cells, and has antibacterial properties.Formula:C6H14ClN3Color and Shape:SolidMolecular weight:163.65Bromodomain inhibitor-10
CAS:Bromodomain inhibitor-10 (compound 128) suppresses BRD4-1/2 with Kd 15 nM/2.5 μM and curbs IL12p40 production.Formula:C20H20N4O3Color and Shape:SolidMolecular weight:364.4MAT2A-IN-7
CAS:MAT2A-IN-7 inhibits MAT2A in various cancers, especially MTAP-deficient cancer cells, with potential for research use.Formula:C17H13ClF3N3O2Color and Shape:SolidMolecular weight:383.75AMPK activator 4
CAS:Potent, selective AMPK activator 4 enhances glucose tolerance and insulin sensitivity without affecting mitochondrial complex I.Formula:C24H21ClN2O3Purity:99.97% - 99.99%Color and Shape:SolidMolecular weight:420.89Ref: TM-T62238
1mg86.00€5mg173.00€10mg334.00€25mg563.00€50mg802.00€100mg1,099.00€500mg2,187.00€1mL*10mM (DMSO)203.00€ART-IN-1
CAS:ART-IN-1 (compound 7) is a selective inhibitor of PARP with IC 50 s of 19, 22, 2.4, >100, 1.1 μM for PARP2, TNKS2, PARP10, PARP14, PARP15, respectively [1].Formula:C14H13NO2SColor and Shape:SolidMolecular weight:259.32Furamidine
CAS:Furamidine is a PRMT1-selective, cell-permeable inhibitor (IC50: 9.4μM), also targeting TDP-1, and is an antiparasitic bisbenzamidine derivative.Formula:C18H16N4OPurity:98%Color and Shape:SolidMolecular weight:304.35UMB-32
CAS:UMB-32: Potent, selective BRD4 inhibitor, Kd 550 nM, IC50 637 nM, also targets TAF1.Formula:C21H23N5OColor and Shape:SolidMolecular weight:361.44JFD00244
CAS:JFD00244 is an inhibitor of sirtuin 2 (SIRT2). It has an anti-tumor effect.Formula:C30H26N2O4Purity:98%Color and Shape:SolidMolecular weight:478.54JAK-2/3-IN-2
CAS:JAK-2/3-IN-2 (Compound 3h) is a potent JAK2 & JAK3 inhibitor with IC50s of 23.85 nM (JAK2) & 18.9 nM (JAK3).Formula:C19H19ClN2OSColor and Shape:SolidMolecular weight:358.89HDAC6/8/BRPF1-IN-1
CAS:HDAC6/8/BRPF1-IN-1 is a cancer-research inhibitor for HDAC6, HDAC8, BRPF1 with IC50: 344-908 nM and Kd: 175.2 nM.Formula:C18H17N3O5SColor and Shape:SolidMolecular weight:387.411,2-Didecanoylglycerol
CAS:1,2-Didecanoylglycerol has functions as bioregulator of protein kinase C in human platelets.Formula:C23H44O5Color and Shape:SolidMolecular weight:400.59ZLD1039
CAS:ZLD1039, an oral EZH2 inhibitor, shows strong PRC2 inhibition at low nanomolar IC50s, and halts breast cancer growth and spread.Formula:C36H48N6O3Purity:99.5%Color and Shape:SolidMolecular weight:612.8A2B57
CAS:A2B57 is a selective SIRT2 inhibitor.Formula:C22H19N5OPurity:98%Color and Shape:SolidMolecular weight:369.42Tripartin
CAS:Tripartin specifically inhibits the histone H3 lysine 9 demethylase KDM4 in HeLa cells.Formula:C10H8Cl2O4Color and Shape:SolidMolecular weight:263.07GNA002
CAS:GNA002 is a highly potent, specific, and covalent EZH2 (Enhancer of zeste homolog 2) inhibitor (IC50: 1.1 μM).Formula:C42H55NO8Purity:98%Color and Shape:SolidMolecular weight:701.89BRD4 Inhibitor-26
BRD4 Inhibitor-26: blocks BRD4 (BD1 and BD2) with IC50 of 0.82 μM & 1.94 μM; used in ovarian cancer research.Formula:C29H27N5O6SColor and Shape:SolidMolecular weight:573.62KDM2B-IN-3
CAS:KDM2B-IN-3, from patent WO2016112284A1 as compound 183c, potently inhibits histone demethylase KDM2B, with cancer research potential.Formula:C25H30N2O2Color and Shape:SolidMolecular weight:390.52
