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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CPUY074020
CAS:CPUY074020 is a potent and orally bioavailable inhibitor of histone methyltransferase G9a (IC50: 2.18 μM) with anti-proliferative activity.Formula:C25H28N4O2Purity:98.64%Color and Shape:SolidMolecular weight:416.52Ref: TM-T10882
1mg74.00€5mg156.00€10mg215.00€25mg338.00€50mg475.00€100mg620.00€200mg848.00€1mL*10mM (DMSO)168.00€Butyrolactone 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.Formula:C9H12O4Purity:98.99% - 99.5%Color and Shape:SolidMolecular weight:184.19Flosequinan
CAS:<p>Flosequinan is an arteriovenous vasodilator, which can effectively treat acute heart failure.</p>Formula:C11H10FNO2SPurity:99.95%Color and Shape:SolidMolecular weight:239.27TM2-115
CAS:TM2-115 is a inhibitor of malaria parasite histone methyltransferases that results in rapid and irreversible parasite death [1].Formula:C28H38N6O2Purity:97.67%Color and Shape:SolidMolecular weight:490.64MAT2A-IN-9
CAS:MAT2A-IN-9, a 2-oxoquinazoline, inhibits MAT2A with antitumor effects on lymphomas and solid cancers.Formula:C14H8ClF3N4OPurity:99.17%Color and Shape:SolidMolecular weight:340.69ZEN-3219
CAS:ZEN-3219 is a BET inhibitor, which has inhibitory effect on BRD4(BD1), BRD4(BD2) and BRD4(BD1BD2).Formula:C19H18N2O3Purity:99.86%Color and Shape:SolidMolecular weight:322.36Bisaramil hydrochloride
CAS:Bisaramil hydrochloride (Bisaramil) is an antiarrhythmic compound that inhibits free radical production.Formula:C17H24Cl2N2O2Purity:98.64% - 99.48%Color and Shape:SolidMolecular weight:359.29EZH2-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.Formula:C34H45N5O3Purity:98.3%Color and Shape:SolidMolecular weight:571.75TGP-377/421
CAS:TGP-377/421 (Targapre-miR-377/421) is a potent miR-377 and miR-421 dual inhibitor that inhibits miR-377 and miR-421 by binding to their functional sites.Formula:C20H16N6Purity:97.02%Color and Shape:SolidMolecular weight:340.38Ref: TM-T61085
1mg66.00€5mg144.00€10mg227.00€25mg454.00€50mg733.00€100mg1,026.00€500mg2,052.00€1mL*10mM (DMSO)159.00€CMP-5
CAS:CMP-5 is a PRMT5 inhibitor with antiviral activity, inhibits PRMT5 methyltransferase activity, and can be used in the study of SARS virus infection.Formula:C21H21N3Purity:98.68%Color and Shape:SolidMolecular weight:315.41Ref: TM-T10850
1mg47.00€5mg97.00€10mg144.00€25mg236.00€50mg354.00€100mg520.00€500mg1,111.00€1mL*10mM (DMSO)106.00€Izencitinib
CAS:Izencitinib (JNJ-8398) is a JAK inhibitor with potential anti-inflammatory activity for the study of ulcerative colitis and Crohn;s disease.Formula:C22H26N8Purity:99.82%Color and Shape:SolidMolecular weight:402.50Ref: TM-T35898
1mg88.00€5mg187.00€10mg298.00€25mg597.00€50mg938.00€100mg1,510.00€200mg2,072.00€1mL*10mM (DMSO)207.00€OUL232
CAS:OUL232 is a potent single ARTs PARP7, PARP10, PARP11, PARP12, PARP14 and PARP15 inhibitor for cancer and tumour research.Formula:C10H10N4O2SPurity:99.04%Color and Shape:SolidMolecular weight:250.28JAK1-IN-8
CAS:<p>JAK1-IN-8, a specific inhibitor of Janus kinase 1 (JAK1, IC50<500 nM).</p>Formula:C22H23FN4O3SPurity:98.4%Color and Shape:SolidMolecular weight:442.51PF-249
CAS:PF-249 (PF-06685249) is a β1-selective AMPK with an EC50 of 12 nM for AMPK α1β1γ1 and can be used in studies about diabetic nephropathy.Formula:C17H16ClN3O3Purity:97.01%Color and Shape:SolidMolecular weight:345.78Ref: TM-T24626
1mg48.00€5mg97.00€10mg156.00€25mg250.00€50mg363.00€100mg510.00€200mg700.00€1mL*10mM (DMSO)105.00€LEM-14
CAS:<p>LEM-14 is a potent NSD2-specific inhibitor (IC50:132 μM).LEM-14 may be used in the study of multiple myeloma.</p>Formula:C25H26N4O4SPurity:98.3%Color and Shape:SolidMolecular weight:478.56MS0124
CAS:<p>MS0124 is a potent and selective G9A-like protein (GLP) inhibitor with IC50 values of 13±4 nM and 440±63 nM, respectively.</p>Formula:C20H29N5O3Purity:98.97%Color and Shape:SolidMolecular weight:387.48EB-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).Formula:C24H27N9O6Purity:99.81%Color and Shape:SolidMolecular weight:537.53Butyzamide
CAS:<p>Butyzamide: oral Mpl activator, non-peptide, antagonizes TPO receptors, boosts hMpl, Ba/F3 cells, and enhances platelets in mice.</p>Formula:C29H32Cl2N2O5SPurity:99.51% - 99.83%Color and Shape:SoildMolecular weight:591.55Ref: TM-T67894
1mg158.00€5mg266.00€10mg393.00€25mg605.00€50mg909.00€100mg1,378.00€200mg1,853.00€1mL*10mM (DMSO)346.00€TNG908
CAS:TNG908, a brain-penetrant PRMT5 inhibitor, is 15x more selective for MTAP mutant vs WT lines, useful in cancer studies.Formula:C21H23N5O2SPurity:98.08% - 98.24%Color and Shape:SolidMolecular weight:409.51Ref: TM-T73494
1mg70.00€5mg154.00€10mg235.00€25mg378.00€50mg540.00€100mg747.00€1mL*10mM (DMSO)166.00€β-NF-JQ1
CAS:β-NF-JQ1 is a PROTAC that recruits aryl hydrocarbon receptor E3 (AhR E3) ligase to target proteins.Formula:C45H42ClN5O6SPurity:97.58% - 99.15%Color and Shape:SolidMolecular weight:816.36
