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 2553 products of "Chromatin/Epigenetics"
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SIRT5 inhibitor 5
CAS:SIRT5 inhibitor 5 is a selective and substrate-competitive SIRT5 inhibitor, which does not occupy the NAD+ binding pocket,cancer and metabolism-related disease.Formula:C21H14ClN3O3SPurity:99.33%Color and Shape:SolidMolecular weight:423.87Valemetostat tosylate
CAS:Valemetostat tosylate is a dual inhibitor of EZH1/2 and used in the research of relapsed/refractory peripheral T-cell lymphoma.Formula:C33H42ClN3O7SPurity:98%Color and Shape:SolidMolecular weight:660.22KP-302
CAS:KP-302 is a selective PAD inhibitor, reversing physical disability in multiple sclerosis (MS) mice and clearing T-cell infiltration in the brain.
Formula:C20H23N5O2Purity:99.77%Color and Shape:SolidMolecular weight:365.43Ref: TM-T88080
1mg60.00€5mg127.00€10mg202.00€25mg416.00€50mg677.00€100mg1,074.00€200mg1,454.00€1mL*10mM (DMSO)140.00€GSK360A
CAS:GSK360A is a novel prolyl hydroxylase (PHD) domain-containing enzyme inhibitor.Formula:C17H17FN2O5Purity:98%Color and Shape:SolidMolecular weight:348.33ZYJ-34c
CAS:ZYJ-34c is a potent oral antitumor activities histone deacetylase inhibitor (HDACi).Formula:C31H42N4O7Purity:98%Color and Shape:SolidMolecular weight:582.69SIRT1-IN-3
CAS:SIRT1-IN-3 (compound 3j) is a potent and selective inhibitor of silent information regulator 1 (SIRT1) with an IC 50 of 4.2 μM [1].Formula:C13H15BrN2OColor and Shape:SolidMolecular weight:295.17DC_C66
CAS:DC_C66 selectively inhibits CARM1 with IC50 of 1.8μM; also affects PRMT1, 6, 5. It's cell-permeable.Formula:C28H22NO2Purity:98%Color and Shape:SolidMolecular weight:404.48LSD1-IN-5
CAS:LSD1-IN-5, a reversible LSD1 inhibitor, boosts H3K4me2 without affecting LSD1 expression; IC50: 121 nM.Formula:C15H13BrN2O3Purity:98%Color and Shape:SolidMolecular weight:349.18Tripolin A
CAS:Tripolin A is a specific non-ATP competitive inhibitor of Aurora A kinase(Aurora A and Aurora B with IC50 values of 1.5 μM and 7 μM, respectively)Formula:C15H11NO3Purity:98%Color and Shape:SolidMolecular weight:253.25CM-579
CAS:CM-579 is a dual inhibitor of G9a and DNMT( IC50:16 nM, 32 nM for G9a and DNMT). It has potent in vitro cellular activity in a wide range of cancer cells.Formula:C29H40N4O3Purity:99.23%Color and Shape:SolidMolecular weight:492.65Ref: TM-T10840L
1mg52.00€5mg90.00€10mg131.00€25mg207.00€50mg303.00€100mg447.00€1mL*10mM (DMSO)117.00€LP99
CAS:LP99 is an epigenetic probe.Formula:C26H30ClN3O4SPurity:99.74%Color and Shape:SolidMolecular weight:516.05Ref: TM-T15784
1mg43.00€5mg96.00€10mg145.00€25mg305.00€50mg442.00€100mgTo inquire1mL*10mM (DMSO)97.00€TM6089
CAS:TM6089 is an inhibitor of Prolyl Hydroxylase that stimulates HIF activity without iron chelation, induces angiogenesis, and protects organ against ischemia.Formula:C13H14N4O3SPurity:99.70%Color and Shape:SolidMolecular weight:306.34Ref: TM-T17105
1mg52.00€5mg115.00€10mg167.00€25mg301.00€50mg452.00€100mg658.00€200mg884.00€1mL*10mM (DMSO)123.00€PRMT4-IN-1
CAS:PRMT4-IN-1 is a selective inhibitor of PRMT4, demonstrating an IC50 value of 3.2 nM, and has been shown to reduce the relative viability of MCF7 cells [1].Formula:C23H28FN3OPurity:98%Color and Shape:SolidMolecular weight:381.49BET bromodomain inhibitor 3
CAS:BET Bromodomain Inhibitor 3 is a BET bromodomain inhibitor with an inhibitory Ki value of >40 µM against BrdT.Formula:C18H17N3O4Purity:98%Color and Shape:SolidMolecular weight:339.35Angiogenesis agent 1
CAS:Compound C-31, a salidroside-based glycoside, activates HIF-1α and may aid in diabetic limb ischemia studies.Formula:C20H24O7Purity:98%Color and Shape:SolidMolecular weight:376.4Eleven-Nineteen-Leukemia Protein IN-1
CAS:ENL-IN-1: Potent ENL YEATS domain inhibitor with 14.5 nM IC50, enhances thermal stability in vitro.Formula:C27H33N7O2Purity:98%Color and Shape:SolidMolecular weight:487.6JAK-IN-30
CAS:JAK-IN-30 (compound 31) is a water-soluble inhibitor of Janus kinases (JAKs), demonstrating inhibitory potency with half-maximal inhibitory concentration (IC50Formula:C19H26N8SPurity:98%Color and Shape:SolidMolecular weight:398.53JAK-IN-28
CAS:JAK-IN-28 (Compound 111) is a Janus kinase (JAK) inhibitor potentially applicable in the research of cancer and inflammatory diseases [1].Formula:C20H18ClN7OPurity:98%Color and Shape:SolidMolecular weight:407.86EPZ032597
CAS:EPZ032597 is a novel selective inhibitor of SMYD2 with an IC50 of 16 nM. EPZ032597 has anticancer activity and prevent and treat pancreatic cancerFormula:C20H23N7OPurity:99.70%Color and Shape:SolidMolecular weight:377.44(2R/S)-6-PNG
CAS:(2R/S)-6-PNG (6-Prenylnaringenin) from hops is a natural histone deacetylase inhibitor that blocks T-type calcium channels reducing neurogenicity in mice.Formula:C20H20O5Purity:98%Color and Shape:SolidMolecular weight:340.37
