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ADN metiltransferasa

ADN metiltransferasa

Las metiltransferasas de ADN (DNMT) son enzimas que catalizan la adición de grupos metilo a los residuos de citosina en el ADN, lo que lleva al silenciamiento génico. La metilación aberrante del ADN está asociada con diversas enfermedades, incluido el cáncer. Los inhibidores de DNMT bloquean la actividad de estas enzimas, lo que lleva a la reactivación de genes silenciados y la inducción de apoptosis en células cancerosas. Los inhibidores de DNMT se utilizan ampliamente en la investigación epigenética y la terapia contra el cáncer. En CymitQuimica, ofrecemos una gama de inhibidores de DNMT de alta calidad para apoyar su investigación en epigenética, metilación del ADN y biología del cáncer.

Se han encontrado 422 productos de "ADN metiltransferasa"

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  • GSK591

    CAS:
    <p>GSK591 (GSK3203591), Alternative Names are EPZ015866, GSK3203591, is a potent selective inhibitor of the arginine methyltransferase PRMT5 (IC50=11 nM).</p>
    Fórmula:C22H28N4O2
    Pureza:99.35% - 99.45%
    Forma y color:Solid
    Peso molecular:380.48
  • Succinic acid sodium

    CAS:
    <p>Succinic acid sodium is an orally active anxiolytic.</p>
    Fórmula:C4H6O4·xNa
    Forma y color:Solid
  • Piribedil

    CAS:
    <p>Piribedil (Trivastan) is a dopamine D2 agonist, used in the treatment of Parkinson's disease.</p>
    Fórmula:C16H18N4O2
    Pureza:99.79% - 99.82%
    Forma y color:Solid
    Peso molecular:298.34
  • CM-272

    CAS:
    <p>CM-272 is a dual G9a/DNA methyltransferases (DNMTs) inhibitor.</p>
    Fórmula:C28H38N4O3
    Pureza:97.83%
    Forma y color:Solid
    Peso molecular:478.63
  • 3-deazaneplanocin A HCl

    CAS:
    <p>3-deazaneplanocin A HCl is both an S-adenosyl-l-homocysteine hydrolase inhibitor and an enhancer of zeste homolog 2(EZH2) inhibitor.</p>
    Fórmula:C12H15ClN4O3
    Pureza:93.24% - 98.9%
    Forma y color:Solid
    Peso molecular:298.73
  • UNC3866 TFA(1872382-47-2 free base)

    CAS:
    <p>UNC3866 TFA is a potent antagonist of the CBX7-H3 interaction as determined by AlphaScreen.</p>
    Fórmula:C45H67F3N6O10
    Pureza:98.43%
    Forma y color:Solid
    Peso molecular:909.04
  • EPZ005687

    CAS:
    <p>EPZ005687 is a potent and selective inhibitor of EZH2.</p>
    Fórmula:C32H37N5O3
    Pureza:97.06% - 99.64%
    Forma y color:Solid
    Peso molecular:539.67
  • Amodiaquine

    CAS:
    <p>Amodiaquine is a synthetic aminoquinoline, used to treat malaria.</p>
    Fórmula:C20H22ClN3O
    Pureza:99.78% - 99.99%
    Forma y color:Crystals From Absolute Ethanol Solid
    Peso molecular:355.86
  • GSK3685032

    CAS:
    <p>GSK3685032 is a non-covalent and selective DNMT1 inhibitor(IC50 = 36 nM).</p>
    Fórmula:C22H24N6OS
    Pureza:98.56% - 99.49%
    Forma y color:Solid
    Peso molecular:420.53
  • SETDB1-TTD-IN-1 TFA


    <p>SETDB1-TTD-IN-1 TFA: potent, selective SETDB1-TTD inhibitor (Kd: 88 nM), useful for related biological research.</p>
    Fórmula:C30H32F3N5O4
    Forma y color:Solid
    Peso molecular:583.6
  • GSK126

    CAS:
    <p>GSK126 (GSK2816126A) is a excellently specific EZH2 methyltransferase inhibitor ( IC50=9.9 nM).</p>
    Fórmula:C31H38N6O2
    Pureza:98% - 99.67%
    Forma y color:Solid
    Peso molecular:526.67
  • EED226

    CAS:
    <p>EED226 is a potent, selective, and orally bioavailable embryonic ectoderm development (EED) inhibitor with an IC50 of 22 nM.</p>
    Fórmula:C17H15N5O3S
    Pureza:98.14% - 99.33%
    Forma y color:Solid
    Peso molecular:369.4
  • GSK3326595

    CAS:
    <p>GSK3326595 (EPZ015938) is an inhibitor of protein arginine methyltransferase 5 (PRMT5)(IC50:6.2 nM.).</p>
    Fórmula:C24H32N6O3
    Pureza:97.7% - 99.63%
    Forma y color:Solid
    Peso molecular:452.55
  • A-196

    CAS:
    <p>A-196 is a potent and selective inhibitor of SUV420 h1 and SUV420 h2 with IC50 values of 0.025 and 0.144 μM, respectively; more than 100-fold selective over</p>
    Fórmula:C18H16Cl2N4
    Pureza:99.92%
    Forma y color:Solid
    Peso molecular:359.25
  • JNJ-64619178

    CAS:
    <p>JNJ-64619178: selective, oral, pseudo-irreversible PRMT5 inhibitor (IC50: 0.14 nM), effective in lung cancer.</p>
    Fórmula:C22H23BrN6O2
    Pureza:98.44% - 99.63%
    Forma y color:Solid
    Peso molecular:483.36
  • MM-102 TFA

    CAS:
    <p>MM-102 TFA is a potent WDR5/MLL inhibitor with IC50 of 2.4 nM; it disrupts MLL1-WDR5 interaction, impeding H3K4 HMT activity.</p>
    Fórmula:C37H50F5N7O6
    Pureza:99.4% - 99.78%
    Forma y color:Solid
    Peso molecular:783.83
  • JQEZ5

    CAS:
    <p>JQEZ5 is an inhibitor of EZH2 lysine methyltransferase (IC50 = 11.1 nM).</p>
    Fórmula:C30H38N8O2
    Pureza:98.14% - ≥98%
    Forma y color:Solid
    Peso molecular:542.68
  • WDR5-0103

    CAS:
    <p>WDR5-0103 (WD-Repeat Protein 5-0103) is an effective and specific WD repeat-containing protein 5 (WDR5) antagonist (Kd: 450 nM).</p>
    Fórmula:C21H25N3O4
    Pureza:98% - 99.61%
    Forma y color:Solid
    Peso molecular:383.44
  • C-7280948

    CAS:
    <p>C-7280948 is a PRMT1 inhibitor.</p>
    Fórmula:C14H16N2O2S
    Pureza:99.55% - ≥95%
    Forma y color:Solid
    Peso molecular:276.35
  • MIV-6R

    CAS:
    <p>MIV-6R inhibits Menin-MLL interaction (IC50: 56 nM) and can be used to study leukemia.</p>
    Fórmula:C27H35N3O
    Pureza:99.81% - 99.88%
    Forma y color:Solid
    Peso molecular:417.59