
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 2592 products of "Chromatin/Epigenetics"
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PT-1
CAS:PT-1 is an AMPKα1 activator that dose-dependently activates AMPK α1394, α1335, and α2398 and enhances AMPK phosphorylation.Formula:C23H16ClN3O6SPurity:99.62%Color and Shape:SolidMolecular weight:497.91Niraparib (R-enantiomer)
CAS:Niraparib R-enantiomer (MK 4827 R-enantiomer) is an inhibitor of PARP1(IC50 of 2.4 nM).
Formula:C19H20N4OPurity:99.83%Color and Shape:SolidMolecular weight:320.39BMS-986158
CAS:BMS-986158: BET inhibitor, IC50 of 6.6 nM in SCLC, 5 nM in TNBC cells.Formula:C30H33N5O2Purity:98.78%Color and Shape:SolidMolecular weight:495.62Ref: TM-T14685
1mg87.00€5mg259.00€10mg465.00€25mg745.00€50mg1,026.00€100mg1,388.00€1mL*10mM (DMSO)283.00€Abexinostat
CAS:Abexinostat (PCI-24781) is a pan-HDAC inhibitor, strongest on HDAC1; less so on HDACs 2, 3, 6, 10. Very select for HDAC8. In Phase 1/2 trials.Formula:C21H23N3O5Purity:98.19% - 98.43%Color and Shape:SolidMolecular weight:397.42Hydroxycitric acid tripotassium hydrate
CAS:Hydroxycitric acid tripotassium hydrate (Potassium citrate monohydrate) effectively inhibits HIF, has antioxidation, anti-inflammation, and anti-tumor effects.Formula:C6H7K3O8Purity:99.85%Color and Shape:White Solid CrystallineMolecular weight:324.41PKC β pseudosubstrate acetate
PKC β pseudosubstrate acetate (PKC β pseudosubstrate acetate (172308-76-8 Free base)) is a selective cell-permeable inhibitor of PKC.Purity:95.42%Color and Shape:SoildLIN28 inhibitor LI71
CAS:LIN28 inhibitor LI71 is a potent and cell-permeable LIN28 inhibitor, which abolishes LIN28-mediated oligouridylation with an IC50 of 7 uM.Formula:C21H21NO3Purity:95.88%Color and Shape:SolidMolecular weight:335.4Ref: TM-T11850
1mg107.00€5mg255.00€10mg414.00€25mg745.00€50mg1,063.00€100mg1,459.00€1mL*10mM (DMSO)341.00€Fenbendazole
CAS:Fenbendazole (Fenbendazol) is an antinematodal benzimidazole used in veterinary medicine.Formula:C15H13N3O2SPurity:99.74%Color and Shape:White To Yellowish PowderMolecular weight:299.35AES-135
CAS:AES-135 is a potent HDAC inhibitor, inhibits HDAC3, HDAC6, HDAC11 (IC50s: 654, 190, and 636 nM) with anti-tumor activity.Formula:C33H29F6N3O5SPurity:97.72%Color and Shape:SolidMolecular weight:693.66Ref: TM-T10255
1mg79.00€5mg152.00€10mg250.00€25mg424.00€50mg583.00€100mg803.00€1mL*10mM (DMSO)225.00€A-3 hydrochloride
CAS:A-3 hydrochloride: potent, reversible kinase antagonist; permeable; inhibits PKC, CKI, PKA, CKII, MLCK; Ki: 4.3-80 μM.Formula:C12H14Cl2N2O2SPurity:99.32%Color and Shape:SolidMolecular weight:321.22Ref: TM-T14069
1mg34.00€5mg63.00€10mg90.00€25mg161.00€50mg260.00€100mg416.00€500mg888.00€1mL*10mM (DMSO)95.00€ODM-207
CAS:ODM-207 (BET-IN-4) is a potent BRD4 inhibitor.Formula:C22H21N3O3Purity:99.75%Color and Shape:SolidMolecular weight:375.42Ref: TM-T10521
1mg44.00€5mg92.00€10mg133.00€25mg235.00€50mg339.00€100mg480.00€200mg660.00€1mL*10mM (DMSO)90.00€Citric acid trilithium salt tetrahydrate
CAS:Citric acid trilithium salt tetrahydrate (Lithium citrate tribasic tetrahydrate) , the active component of Lithium, is a medicine used in the therapy ofFormula:C6H13Li3O11Purity:99.88%Color and Shape:White Crystalline PowderMolecular weight:281.98Chloramphenicol
CAS:Chloramphenicol (Chloromycetin) is a broad-spectrum antibiotic that inhibits the biosynthesis of bacterial proteins. Cost-effective and quality-assured.
Formula:C11H12Cl2N2O5Purity:99.6% - 99.84%Color and Shape:Needles Or Elongated Plates From Water Or Ethylene Dichloride SolidMolecular weight:323.13EBI-2511
CAS:EBI-2511 is a highly potent and orally active inhibitor of EZH2 (IC50: 6 nM in Pfeffiera cell lines).Formula:C34H48N4O4Purity:99.74%Color and Shape:SolidMolecular weight:576.77Decitabine
CAS:Decitabine (Deoxycytidine) is a deoxycytidine analog, a DNA methyltransferase inhibitor with oral activity.Formula:C8H12N4O4Purity:98.06% - 99.87%Color and Shape:Physical Description Fine White Crystalline Powder Used As A DrugMolecular weight:228.21M-89
CAS:M-89, a potent menin inhibitor (Kd 1.4 nM), disrupts Menin-MLL interaction, offering possible MLL leukemia treatment.
Formula:C37H47N5O4SPurity:98.38%Color and Shape:SolidMolecular weight:657.87Enarodustat
CAS:Enarodustat (JTZ-951) is an orally active factor inhibitor of prolyl hydroxylase (EC50: 0.22 μM) and has the potential for renal anemia treatment.Formula:C17H16N4O4Purity:99.73% - 99.75%Color and Shape:SolidMolecular weight:340.33Ref: TM-T15219
1mg37.00€2mg52.00€5mg74.00€10mg109.00€25mg178.00€50mg295.00€100mg439.00€1mL*10mM (DMSO)86.00€MOZ-IN-2
CAS:MOZ-IN-2 is an protein MOZ inhibitor(IC50 of 125 μM).
Formula:C17H13FN4O3SPurity:99.17%Color and Shape:SolidMolecular weight:372.37RBN-2397
CAS:RBN-2397 is a potent, selective and orally active accross species NAD+ competitive PARP7 inhibitor with IC50 less than 3 nM.Formula:C20H23F6N7O3Purity:98.48% - 99.8%Color and Shape:SolidMolecular weight:523.43Ref: TM-T12695
1mg90.00€2mg132.00€5mg215.00€10mg349.00€25mg708.00€50mg888.00€100mg1,224.00€200mg1,648.00€1mL*10mM (DMSO)248.00€AW68
CAS:AW68 is a potential small molecule BRD4 inhibitor that prevents and treats BRD4-related diseases and can be used in cancer research.Formula:C22H21ClN6Purity:98.52% - 98.52%Color and Shape:SoildMolecular weight:404.89
