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Cromatina / Epigenética

Cromatina / Epigenética

Los inhibidores de cromatina/epigenética son compuestos que modulan la estructura y función de la cromatina o interfieren con modificaciones epigenéticas, como la metilación del ADN y la modificación de histonas. Estos inhibidores son herramientas esenciales para estudiar la regulación de la expresión génica y el papel de la epigenética en enfermedades como el cáncer, los trastornos neurológicos y las anomalías del desarrollo. Al dirigirse a los procesos epigenéticos, estos inhibidores pueden alterar los patrones de expresión génica y ofrecer nuevas vías terapéuticas. En CymitQuimica, ofrecemos una amplia selección de inhibidores de cromatina/epigenética de alta calidad para apoyar su investigación en biología molecular, genética y epigenética.

Subcategorías de "Cromatina / Epigenética"

Se han encontrado 2238 productos de "Cromatina / Epigenética"

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  • KAT6-IN-2


    <p>KAT6-IN-2 is a potent inhibitor of KAT6, showing promise for use in cancer research.</p>
    Forma y color:Odour Solid
  • Tyrosine Protein Kinase JAK 2 (Phospho-Tyr8, 9)

    CAS:
    <p>Tyrosine Protein Kinase JAK 2 (Phospho-Tyr8, 9) is a peptide derived from mouse JAK2, specifically composed of amino acids 475 to 491.</p>
    Fórmula:C88H138N20O34P2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:2082.1
  • Lys-CoA TFA


    <p>Lys-CoA TFA: p300 HAT inhibitor, IC50 50-500 nM, &gt;100x selective vs PCAF, inhibits p300-dependent transcription.</p>
    Fórmula:C33H54F3N10O21P3S
    Forma y color:Solid
    Peso molecular:1108.82
  • VPC-70063

    CAS:
    <p>VPC-70063 (Thiourea, N-[3,5-bis(trifluoromethyl)phenyl]-N'-(phenylmethyl)-) is an inhibitor of c-Myc-MAX.</p>
    Fórmula:C16H12F6N2S
    Pureza:99.98%
    Forma y color:Solid
    Peso molecular:378.34
  • Biguanide

    CAS:
    <p>Biguanide can reduce oxidative stress in rats with hyperglycemia.</p>
    Fórmula:C2H7N5
    Forma y color:Solid
    Peso molecular:101.11
  • BRD3067

    CAS:
    <p>BRD3067, a Tubacin derivative, inhibits HDAC6 (IC50 15 nM) and acts as a negative control for Tubacin A, showing anticancer and anti-inflammatory effects.</p>
    Fórmula:C21H23N3O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:349.43
  • Bryostatin 3

    CAS:
    <p>Bryostatin 3 is a protein kinase C activator.</p>
    Fórmula:C46H64O17
    Pureza:98%
    Forma y color:Solid
    Peso molecular:888.99
  • MSC2504877

    CAS:
    <p>MSC2504877 inhibits tankyrase, boosts CDK4/6 inhibitors, blocks Cyclin D2/E2 upregulation, and strengthens phospho-Rb suppression.</p>
    Fórmula:C17H18N2O2
    Pureza:99.72%
    Forma y color:Soild
    Peso molecular:282.34
  • pan-BET/BD2-IN-1


    <p>Pan-BET/BD2-IN-1 (compound 6b) is a selective BET protein inhibitor with BRDT-1Ki of 1.05 μM and BRD4-1Ki of 0.68 μM. It effectively inhibits the growth of MM.1S cancer cells with an IC50 value of 2.6 μM.</p>
    Forma y color:Odour Solid
  • POI ligand 1


    <p>POI ligand 1 serves as a template for the non-selective HDAC inhibitor Vorinostat. It functions as a target protein ligand (PROTAC target protein ligand) in the creation of PROTAC HDAC degraders with anti-tumor properties. Additionally, POI ligand 1 is utilized in the synthesis of FF2049.</p>
    Fórmula:C14H21N3O3
    Forma y color:Solid
    Peso molecular:279.335
  • CD532 hydrochloride


    <p>CD532 hydrochloride, potent Aurora A inhibitor (IC50=45 nM), hampers MYCN protein, changes AURKA's shape, aids cancer research.</p>
    Forma y color:Solid
  • BRD4 degrader AT1

    CAS:
    <p>BRD4 degrader AT1 is a highly selective Brd4 degrader based on PROTAC technology, with a Kd of 44 nM for Brd4BD2 in cells.</p>
    Fórmula:C48H58ClN9O5S3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:972.68
  • Malantide

    CAS:
    <p>Malantide, a synthetic dodecapeptide, boosts and measures PKA activity by undergoing PKA-induced phosphorylation.</p>
    Fórmula:C72H124N22O21
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1633.89
  • CAY10591

    CAS:
    <p>SIRT1 activated by CAY10591, mimics caloric restriction, extends lifespan, inhibits apoptosis, suppresses TNF-α, and promotes fat mobilization.</p>
    Fórmula:C20H25N5O2
    Forma y color:Solid
    Peso molecular:367.44
  • UNC6864 (Kei)


    <p>UNC6864, an ethylisopropyllysine-containing ligand, exhibits binding affinity to wild-type CBX5, demonstrating a dissociation constant (K D) of 3.3 μM.</p>
    Fórmula:C42H59N7O11
    Forma y color:Solid
    Peso molecular:837.96
  • FTX-6058 hydrochloride

    CAS:
    <p>FTX-6058 hydrochloride is a potent EED inhibitor, induces HbF, and aids sickle cell and β-thalassemia research.</p>
    Fórmula:C22H19ClFN5O2
    Forma y color:Solid
    Peso molecular:439.87
  • PROTAC BRD4 Degrader-1

    CAS:
    <p>PROTAC BRD4 Degrader-1 is an efficacious degrader of BRD4(BRD4 BD1,IC50 of 41.8 nM).</p>
    Fórmula:C40H37N9O8
    Pureza:98%
    Forma y color:Solid
    Peso molecular:771.78
  • JAK1/TYK2-IN-1

    CAS:
    <p>JAK1/TYK2-IN-1 is a dual inhibitor of TYK2 and JAK1 ( IC 50 = 29 and 41 nM respectively).</p>
    Fórmula:C18H20F3N7O
    Forma y color:Solid
    Peso molecular:407.401
  • HDAC-IN-26

    CAS:
    <p>HDAC-IN-26 is a highly selective class I HDAC inhibitor with an EC 50 value of 4.7 nM.</p>
    Fórmula:C24H28FN5O3
    Forma y color:Solid
    Peso molecular:453.518
  • Biotinylated-JQ1

    CAS:
    <p>Biotin-JQ1 is a bromodomain BRD4 binder; inhibits MM1.S cell growth with EC50 of 0.4μM.</p>
    Fórmula:C39H53ClN8O6S2
    Forma y color:Solid
    Peso molecular:829.47