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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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  • N-Desmethyltamoxifen hydrochloride
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    N-Desmethyltamoxifen hydrochloride

    CAS:
    <p>N-Desmethyltamoxifen hydrochloride is the major tamoxifen metabolite in humans.</p>
    Formula:C25H28ClNO
    Purity:99.15%
    Color and Shape:Solid
    Molecular weight:393.95

    Ref: TM-T12148

  • Lin28-let-7a antagonist 1
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    Lin28-let-7a antagonist 1

    CAS:
    <p>Lin28-let-7a antagonist 1, with an IC50 of 4.03 μM for Lin28A-let-7a-1 interaction，and shows a clear antagonistic effect against the Lin28-let-7a interaction.</p>
    Formula:C31H29N5O7
    Purity:99.44%
    Color and Shape:Solid
    Molecular weight:583.59

    Ref: TM-T11851

  • PT2399
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    PT2399

    CAS:
    <p>PT2399, an oral HIF-2 inhibitor, blocks HIF-2α/1β dimerization, showing strong in vivo antitumor effects.</p>
    Formula:C17H10F5NO4S
    Purity:98.8% - 99.45%
    Color and Shape:Solid
    Molecular weight:419.32

    Ref: TM-T12675L

  • (R)​-​CR8
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    (R)​-​CR8

    CAS:
    <p>(R)-CR8 ((R)-Isomer) is a potent and selective CDK inhibitor.</p>
    Formula:C24H29N7O
    Purity:98.41%
    Color and Shape:Solid
    Molecular weight:431.53

    Ref: TM-T12617L

  • Diflunisal
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    Diflunisal

    CAS:
    <p>Diflunisal (Dolobid) is a cyclooxygenase (COX) Inhibitor, used as an anti-inflammatory analgesic.</p>
    Formula:C13H8F2O3
    Purity:98.92% - 99.42%
    Color and Shape:Solid
    Molecular weight:250.20

    Ref: TM-T0808

  • BMS-986158
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    BMS-986158

    CAS:
    <p>BMS-986158: BET inhibitor, IC50 of 6.6 nM in SCLC, 5 nM in TNBC cells.</p>
    Formula:C30H33N5O2
    Purity:98.78%
    Color and Shape:Solid
    Molecular weight:495.62

    Ref: TM-T14685

  • LIN28 inhibitor LI71
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    LIN28 inhibitor LI71

    CAS:
    <p>LIN28 inhibitor LI71 is a potent and cell-permeable LIN28 inhibitor, which abolishes LIN28-mediated oligouridylation with an IC50 of 7 uM.</p>
    Formula:C21H21NO3
    Purity:95.88%
    Color and Shape:Solid
    Molecular weight:335.4

    Ref: TM-T11850

  • ODM-207
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    ODM-207

    CAS:
    <p>ODM-207 (BET-IN-4) is a potent BRD4 inhibitor.</p>
    Formula:C22H21N3O3
    Purity:99.75%
    Color and Shape:Solid
    Molecular weight:375.42

    Ref: TM-T10521

  • Chitosan oligosaccharide
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    Chitosan oligosaccharide

    CAS:
    <p>Chitosan oligosaccharide (COS) is an oligomer of β-(1→4)-linked D-glucosamine.</p>
    Formula:C12H24N2O9
    Purity:98%
    Color and Shape:Solid
    Molecular weight:340.327

    Ref: TM-T10789

  • JAK2 Inhibitor V
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    JAK2 Inhibitor V

    CAS:
    <p>JAK2 Inhibitor V (JAK2 Inhibitor V Z3) is a novel specific inhibitor of Jak2, inhibiting Jak2-V617F and Jak2-WT autophosphorylation in a dose-dependent manner.</p>
    Formula:C23H24N2O
    Purity:98.36% - 99.15%
    Color and Shape:Solid
    Molecular weight:344.45

    Ref: TM-T3042

  • Fenbendazole
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    Fenbendazole

    CAS:
    <p>Fenbendazole (Fenbendazol) is an antinematodal benzimidazole used in veterinary medicine.</p>
    Formula:C15H13N3O2S
    Purity:99.74%
    Color and Shape:White To Yellowish Powder
    Molecular weight:299.35

    Ref: TM-T1141

  • Uzansertib phosphate
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    Uzansertib phosphate

    CAS:
    <p>Uzansertib phosphate (INCB053914 phosphate) is an orally active, ATP-competitive inhibitor of pan-PIM kinase, inhibiting PIM1, PIM2 and PIM3.</p>
    Formula:C26H29F3N5O7P
    Purity:99.75% - 99.79%
    Color and Shape:Solid
    Molecular weight:611.51

    Ref: TM-T12477

  • Levetiracetam
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    Levetiracetam

    CAS:
    <p>Levetiracetam (SIB-S1) is a relatively unique anticonvulsant that is typically used in combination with other antiepileptic medications for partial onset</p>
    Formula:C8H14N2O2
    Purity:99.67% - 99.86%
    Color and Shape:White Crystalline Powder
    Molecular weight:170.21

    Ref: TM-T0192

  • MAK683
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    MAK683

    CAS:
    <p>MAK683 is an inhibitor of embryonic ectoderm development (EED) (IC50s: 59, 89, 26 nM in EED Alphascreen binding, LC-MS and ELISA assay).</p>
    Formula:C20H17FN6O
    Purity:98.25% - 99.92%
    Color and Shape:Solid
    Molecular weight:376.39

    Ref: TM-T15201

  • MS402
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    MS402

    CAS:
    <p>MS402 is a novel BD1-selective BET BrD inhibitor.</p>
    Formula:C20H19ClN2O3
    Purity:99.72%
    Color and Shape:Solid
    Molecular weight:370.83

    Ref: TM-T12112

  • Minocycline hydrochloride
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    Minocycline hydrochloride

    CAS:
    <p>Minocycline HCl: tetracycline antibiotic, treats bacterial infections and acne, may cause acute or chronic hepatitis.</p>
    Formula:C23H28ClN3O7
    Purity:99.28% - >99.99%
    Color and Shape:Bright Yellow-Orange Amorphous Solid Crystalline Yellow
    Molecular weight:493.94

    Ref: TM-T1101

  • VTP50469
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    VTP50469

    CAS:
    <p>VTP50469 is a highly selective and orally active small molecule inhibitor of the Menin-MLL protein-protein interaction.Cost-effective and quality-assured.</p>
    Formula:C32H47FN6O4S
    Purity:98.31% - 99.55%
    Color and Shape:Solid
    Molecular weight:630.82

    Ref: TM-T13336

  • A-395
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    A-395

    CAS:
    <p>A-395 blocks PRC2 (EZH2-EED-SUZ12) interactions, strongly inhibiting the complex with an IC50 of 18 nM.</p>
    Formula:C26H35FN4O2S
    Purity:98.43%
    Color and Shape:Solid
    Molecular weight:486.65

    Ref: TM-T10205

  • Golidocitinib
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    Golidocitinib

    CAS:
    <p>Golidocitinib (AZD4205) is a selective JAK1 inhibitor (IC50: 73 nM) and weakly inhibits JAK2/JAK3 (IC50: &gt;14.7, &gt;30 μM).</p>
    Formula:C25H31N9O2
    Purity:98.87% - 99.88%
    Color and Shape:Solid
    Molecular weight:489.57

    Ref: TM-T10431

  • Nicotinamide riboside
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    Nicotinamide riboside

    CAS:
    <p>Nicotinamide riboside increases NAD[+] levels and activates SIRT1 and SIRT3, culminating in enhanced oxidative metabolism and protection against high fat diet-</p>
    Formula:C11H15N2O5
    Purity:98.82% - 99.58%
    Color and Shape:Solid
    Molecular weight:255.25

    Ref: TM-T13795