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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 2242 products of "Chromatin/Epigenetics"

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  • 3-methyl-1,2,3,4-tetrahydroquinazolin-2-one
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    3-methyl-1,2,3,4-tetrahydroquinazolin-2-one

    CAS:
    <p>3-methyl-1,2,3,4-tetrahydroquinazolin-2-one is a inhibitor of BRD4 .</p>
    Formula:C9H10N2O
    Purity:99.3% - 99.64%
    Color and Shape:Solid
    Molecular weight:162.19

    Ref: TM-T50006

  • SHR0302
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    SHR0302

    CAS:
    <p>SHR0302 (ARQ252) is a JAK inhibitor that binds JAK1 with stronger affinity than others (Selectivity for JAK1 is more than 10 times for JAK2, 77 times for JAK3,</p>
    Formula:C18H22N8O2S
    Purity:99.11%
    Color and Shape:Solid
    Molecular weight:414.48

    Ref: TM-T9195

  • HJ-PI01
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    HJ-PI01

    CAS:
    <p>HJ-PI01 (HJ-PI01) is a Pim-2 inhibitor. HJ-PI01 (HJ-PI01) induces apoptosis and autophagic cell death in triple-negative human breast cancer.</p>
    Formula:C14H11NO2
    Purity:98.92%
    Color and Shape:Solid
    Molecular weight:225.24

    Ref: TM-T9583

  • Tubacin
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    Tubacin

    CAS:
    Tubacin is a highly potent and selective, reversible, cell-permeable HDAC6 inhibitor with an IC50 of 4 nM, approximately 350-fold selectivity over HDAC1.
    Formula:C41H43N3O7S
    Purity:97.62% - 98.75%
    Color and Shape:Solid
    Molecular weight:721.86

    Ref: TM-T6327

  • VX-11e
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    VX-11e

    CAS:
    VX-11e (TCS ERK 11e) is a potent, selective, and orally bioavailable ERK(Extracellular Signal-Regulated Kinase) inhibitor; antitumor agent.
    Formula:C24H20Cl2FN5O2
    Purity:98.92% - ≥98%
    Color and Shape:Solid
    Molecular weight:500.35

    Ref: TM-T3166

  • JNJ-42041935
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    JNJ-42041935

    CAS:
    <p>JNJ-42041935 (HIF-PHD Inhibitor II) is a potent (pKi = 7.3-7.9), 2-oxoglutarate competitive, reversible, and selective inhibitor of PHD enzymes.</p>
    Formula:C12H6ClF3N4O3
    Purity:99.58% - ≥95%
    Color and Shape:Solid
    Molecular weight:346.65

    Ref: TM-T3180

  • BYK204165
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    BYK204165

    CAS:
    <p>BYK204165 (RT-017290) is a potent PARP inhibitor (PARP1; IC50 = 44.67 nM for human recombinant PARP1 in an enzyme assay)</p>
    Formula:C15H12N2O2
    Purity:99.61%
    Color and Shape:Solid
    Molecular weight:252.27

    Ref: TM-T7896

  • J-147
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    J-147

    CAS:
    <p>J-147, a curcumin derivative, is an experimental drug with reported effects against both Alzheimer's disease and ageing in mouse models of accelerated aging.</p>
    Formula:C18H17F3N2O2
    Purity:99.61% - >99.99%
    Color and Shape:Solid
    Molecular weight:350.33

    Ref: TM-T1993

  • Alobresib
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    Alobresib

    CAS:
    <p>Alobresib (Vorolanib) is an inhibitor of BET bromodomain,is an antineoplastic drug candidate.</p>
    Formula:C26H23N5O2
    Purity:97.63%
    Color and Shape:Solid
    Molecular weight:437.49

    Ref: TM-T8495

  • M1001
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    M1001

    CAS:
    <p>M1001 is a HIF-2α agonist.</p>
    Formula:C17H17N3O2S
    Purity:98.83%
    Color and Shape:Solid
    Molecular weight:327.4

    Ref: TM-T7802

  • UPF 1069
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    UPF 1069

    CAS:
    <p>UPF 1069 is a specific PARP2 inhibitor ( IC50: 0.3 μM). It is ~27-fold selective against PARP1.</p>
    Formula:C17H13NO3
    Purity:98.80% - 99.88%
    Color and Shape:Solid
    Molecular weight:279.29

    Ref: TM-T6181

  • Apabetalone
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    Apabetalone

    CAS:
    <p>Apabetalone (RVX000222) , an effective BET bromodomain inhibitor, has been investigated for the treatment of diabetes, atherosclerosis, and coronary artery</p>
    Formula:C20H22N2O5
    Purity:98.08% - ≥98%
    Color and Shape:Solid
    Molecular weight:370.4

    Ref: TM-T2480

  • Chlorogenic Acid
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    Chlorogenic Acid

    CAS:
    <p>Chlorogenic acid is a natural phenol. Chlorogenic acid has anti-inflammatory, antitumor, and antimicrobial effects. Cost-effective and quality-assured.</p>
    Formula:C16H18O9
    Purity:98.84% - 99.67%
    Color and Shape:Solid
    Molecular weight:354.31

    Ref: TM-T2805

  • Ruxolitinib (S enantiomer)
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    Ruxolitinib (S enantiomer)

    CAS:
    <p>Ruxolitinib S enantiomer (INCB18424) is the S-enantiomer of Ruxolitinib. Ruxolitinib is the first potent, selective JAK1/2 inhibitor.</p>
    Formula:C17H18N6
    Purity:99.37% - 99.79%
    Color and Shape:Solid
    Molecular weight:306.36

    Ref: TM-T6156

  • ML367
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    ML367

    CAS:
    <p>ML367 inhibits ATAD5 stabilization with low micromolar activity, serving as a probe molecule.</p>
    Formula:C19H12F2N4
    Purity:99.39%
    Color and Shape:Solid
    Molecular weight:334.32

    Ref: TM-T5425

  • GSK484 hydrochloride
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    GSK484 hydrochloride

    CAS:
    <p>GSK484 hydrochloride (GTPL8577) is a reversible peptidyl-arginine deiminase 4 (PAD4) inhibitor.Cost-effective and quality-assured.</p>
    Formula:C27H32ClN5O3
    Purity:98.32% - 99.62%
    Color and Shape:Solid
    Molecular weight:510.03

    Ref: TM-TQ0067

  • Nicotinamide Hydrochloride
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    Nicotinamide Hydrochloride

    CAS:
    <p>Nicotinamide Hydrochloride, a vitamin B3 form, inhibits SIRT2 and melanoma growth, enhancing NAD+, ATP, ROS, and survival in melanoma mice.</p>
    Formula:C6H7ClN2O
    Color and Shape:Solid
    Molecular weight:158.59

    Ref: TM-T72188

  • Momelotinib HCl
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    Momelotinib HCl

    CAS:
    <p>Momelotinib HCl is a JAK1/2 inhibitor, reducing anemia in myelofibrosis (MF) patients.</p>
    Formula:C23H24Cl2N6O2
    Color and Shape:Solid
    Molecular weight:487.38

    Ref: TM-T70823

  • BCI-121
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    BCI-121

    CAS:
    <p>BCI-121 is a substrate-competitive SMYD3 inhibitor that inhibits the proliferation of the cancer cell.</p>
    Formula:C14H18BrN3O2
    Purity:99.67%
    Color and Shape:Solid
    Molecular weight:340.22

    Ref: TM-T5322

  • JNJ-7706621
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    JNJ-7706621

    CAS:
    <p>JNJ-7706621 is a potent aurora kinase inhibitor, and also inhibits CDK1 and CDK2.</p>
    Formula:C15H12F2N6O3S
    Purity:99.1% - 99.85%
    Color and Shape:Solid
    Molecular weight:394.36

    Ref: TM-T6126