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Chromatin/Epigenetics

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 2235 products of "Chromatin/Epigenetics"

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  • NSC 228155
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    NSC 228155

    CAS:
    <p>NSC 228155 is an activator of EGFR, binding to the sEGFR dimerization domain II and modulate EGFR tyrosine phosphorylation.</p>
    Formula:C11H6N4O4S
    Purity:99.84%
    Color and Shape:Solid
    Molecular weight:290.25

    Ref: TM-T6908

  • PF-CBP1
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    PF-CBP1

    CAS:
    <p>PF-CBP1 HCl is a highly selective inhibitor of the bromodomain of CREB-binding protein(CREBBP).</p>
    Formula:C29H36N4O3
    Purity:99.45%
    Color and Shape:Solid
    Molecular weight:488.62

    Ref: TM-T3973

  • 653-47
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    653-47

    CAS:
    <p>653-47 enhances the effects of 666-15 on inhibiting CREB and is a mild CREB inhibitor itself (IC50: 26.3μM).</p>
    Formula:C20H19ClN2O3
    Color and Shape:Solid
    Molecular weight:370.83

    Ref: TM-T8889

  • PF 477736
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    PF 477736

    CAS:
    <p>PF 477736 (PF-736,PF-00477736) is a specifc, effective and ATP-competitive Chk1 inhibitor (Ki: 0.49 nM ) and also inhibits FGFR3, Aurora-A, VEGFR2, Flt3, Fms (</p>
    Formula:C22H25N7O2
    Purity:97.58% - 99.94%
    Color and Shape:Solid
    Molecular weight:419.48

    Ref: TM-T6028

  • Paris saponin VII
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    Paris saponin VII

    CAS:
    <p>Paris saponin VII (Dioscini) shows inhibitory effects on cell proliferation.</p>
    Formula:C51H82O21
    Purity:99.51% - 99.63%
    Color and Shape:Solid
    Molecular weight:1031.18

    Ref: TM-T4085

  • CPI-637
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    CPI-637

    CAS:
    <p>CPI-637 is a selective and cell-active benzodiazepinone CBP/EP300 bromodomain inhibitor.</p>
    Formula:C22H22N6O
    Purity:99.89% - 99.95%
    Color and Shape:Solid
    Molecular weight:386.45

    Ref: TM-T6811

  • 6-Bromo-3-methyl-1,4-dihydroquinazolin-2-one
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    6-Bromo-3-methyl-1,4-dihydroquinazolin-2-one

    CAS:
    <p>CHEMBRDG-BB 7118966 is an inhibitor of Bromodomain-containing protein 4 (human).</p>
    Formula:C9H9BrN2O
    Purity:99.28%
    Color and Shape:Solid
    Molecular weight:241.08

    Ref: TM-T8609

  • Cerdulatinib
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    Cerdulatinib

    CAS:
    <p>Cerdulatinib (PRT2070) is an novel oral dual Syk/JAK inhibitor.</p>
    Formula:C20H27N7O3S
    Purity:98.74% - 99.49%
    Color and Shape:Solid
    Molecular weight:445.54

    Ref: TM-T2487

  • UNC1079
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    UNC1079

    CAS:
    <p>UNC1079 is an selective L3MBTL3 domain inhibitor</p>
    Formula:C28H42N4O2
    Purity:99.48%
    Color and Shape:Solid
    Molecular weight:466.66

    Ref: TM-T8453

  • EPZ015666
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    EPZ015666

    CAS:
    <p>EPZ015666 (GSK3235025) is an orally available inhibitor of PRMT5 enzymatic activity.</p>
    Formula:C20H25N5O3
    Purity:98% - 99.64%
    Color and Shape:Solid
    Molecular weight:383.44

    Ref: TM-T6076

  • BI-9564
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    BI-9564

    CAS:
    <p>BI-9564, a specific cell-permeable BRD9 BD inhibitor. The Kd for BRD9 is 5.9 nM, and IC50 for BET family is &gt; 100 μM.</p>
    Formula:C20H23N3O3
    Purity:99.38%
    Color and Shape:Solid
    Molecular weight:353.41

    Ref: TM-T6786

  • PF-9363
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    PF-9363

    CAS:
    <p>PF-9363 (CTX-3648) is a potent and high selective KAT6A/KAT6B inhibitor. PF-9363 can be used for the research of cancer.</p>
    Formula:C20H20N4O6S
    Purity:99.03% - 99.7%
    Color and Shape:Solid
    Molecular weight:444.46

    Ref: TM-T9167

  • Anacardic Acid
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    Anacardic Acid

    CAS:
    <p>Anacardic Acid (6-pentadecylsalicylic Acid) is an effective inhibitor of p300 and p300/CBP-associated factor histone acetyltranferases.</p>
    Formula:C22H36O3
    Purity:97.47% - 99.87%
    Color and Shape:Solid
    Molecular weight:348.52

    Ref: TM-T6389

  • 666-15
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    666-15

    CAS:
    <p>666-15 is a selective CREB inhibitor with an IC50 of 81 nM. 666-15 can effectively inhibit the growth of breast cancer.Cost-effective and quality-assured.</p>
    Formula:C33H31Cl2N3O5
    Purity:99.41% - 99.88%
    Color and Shape:Solid
    Molecular weight:620.52

    Ref: TM-T5318

  • KDM4D-IN-1
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    KDM4D-IN-1

    CAS:
    <p>KDM4D-IN-1 is a KDM4D inhibitor (IC50: 0.41±0.03 μM).</p>
    Formula:C11H7N5O
    Purity:99.51% - >99.99%
    Color and Shape:Solid
    Molecular weight:225.21

    Ref: TM-T4214

  • Nicotinamide riboside chloride
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    Nicotinamide riboside chloride

    CAS:
    <p>NR, also SRT647, is a B3 vitamin form; precursor to NAD+.</p>
    Formula:C11H15ClN2O5
    Purity:98.92% - 99.86%
    Color and Shape:Solid
    Molecular weight:290.7

    Ref: TM-T6220

  • LLY-507
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    LLY-507

    CAS:
    <p>LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.</p>
    Formula:C36H42N6O
    Purity:99.58% - 99.93%
    Color and Shape:Solid
    Molecular weight:574.76

    Ref: TM-T6879

  • 4-amino-1,8-Naphthalimide
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    4-amino-1,8-Naphthalimide

    CAS:
    <p>4-amino-1,8-Naphthalimide (4-ANI) is a PARP inhibitor with IC50 of 180 nM</p>
    Formula:C12H8N2O2
    Purity:95.13%
    Color and Shape:Yellow Solid Powder
    Molecular weight:212.2

    Ref: TM-T21524

  • Ro 31-8220
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    Ro 31-8220

    CAS:
    <p>Ro 31-8220: potent PKC inhibitor (IC50: 5-27 nM). Affects MAPKAP-K1b, MSK1, S6K1, GSK3β (IC50: 3-38 nM), not MKK3/4/6/7.</p>
    Formula:C25H23N5O2S
    Color and Shape:Solid
    Molecular weight:457.55

    Ref: TM-T6643L

  • Bobcat339
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    Bobcat339

    CAS:
    <p>Bobcat339 is a novel cytosine-based TET enzyme inhibitor (IC50s: 33/73 uM for TET1/2), but not DNMT3a, does not inhibit the DNA methyltransferase DNMT3a.</p>
    Formula:C16H12ClN3O
    Purity:97.79% - 99.24%
    Color and Shape:Solid
    Molecular weight:297.74

    Ref: TM-T5198