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CDK

CDK

Los inhibidores de las quinasas dependientes de ciclina (CDK) son compuestos que bloquean la actividad de las CDK, un grupo de quinasas de proteínas que regulan el ciclo celular, la transcripción y otros procesos celulares. Las CDK se activan al unirse a las ciclinas, y su actividad es crucial para la progresión de las células a través de las diferentes fases del ciclo celular. Inhibir las CDK puede detener la división celular, provocando la detención del ciclo celular y la apoptosis, especialmente en células cancerosas donde las CDK a menudo están desreguladas. Los inhibidores de CDK se utilizan ampliamente en la investigación del cáncer y tienen un potencial terapéutico en el tratamiento de varios tipos de cáncer. En CymitQuimica, ofrecemos una selección completa de inhibidores de CDK de alta calidad para apoyar su investigación en el control del ciclo celular, el cáncer y el desarrollo terapéutico.

Se han encontrado 501 productos de "CDK"

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  • K 00546

    CAS:
    <p>K00546 inhibits CDK1/cyclin B (IC50: 0.6 nM), CDK2/cyclin A (IC50: 0.5 nM), CLK1 (IC50: 8.9 nM), and CLK3 (IC50: 29.2 nM).</p>
    Fórmula:C15H13F2N7O2S2
    Pureza:99.12%
    Forma y color:Solid
    Peso molecular:425.44
  • SNX2-1-108

    CAS:
    <p>SNX2-1-108 is a selective CDK8 and CDK19 inhibitor.</p>
    Fórmula:C21H16N4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:324.38
  • Metralindole HCl

    CAS:
    <p>Metralindole is a reversible monoamine oxidase A (RIMA) inhibitor, it was investigated as a potential antidepressant.</p>
    Fórmula:C15H18ClN3O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:291.78
  • CDK8-IN-7

    CAS:
    <p>CDK8-IN-7 is a potent CDK8 inhibitor with a Kd of 3.5 nM, showing promise for AML research.</p>
    Fórmula:C30H40N2
    Forma y color:Solid
    Peso molecular:428.65
  • BAY-958

    CAS:
    <p>BAY-958 is a potent and selective inhibitor of PTEFb/CDK9.</p>
    Fórmula:C17H16FN5O3S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:389.4
  • Atuveciclib S-Enantiomer

    CAS:
    <p>Atuveciclib S-Enantiomer is a (S)-form of BAY-1143572; a potent, selective CDK9 inhibitor with an IC50 of 16 nM.</p>
    Fórmula:C18H18FN5O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:387.43
  • Cdc7-IN-15

    CAS:
    <p>Cdc7-IN-15 (Example 108) is an inhibitor of cdc7 kinase that has potential to be used for cancer research [1].</p>
    Fórmula:C12H14N4OS
    Forma y color:Solid
    Peso molecular:262.33
  • CP681301

    CAS:
    <p>CP681301 is a potent CDK5 inhibitor with anti-tumor effects in Drosophila and reduces Glioma stem cells' growth and renewal.</p>
    Fórmula:C17H22N4O
    Forma y color:Solid
    Peso molecular:298.38
  • (E/Z)-BIO-acetoxime

    CAS:
    <p>(E/Z)-BIO-acetoxime: potent GSK-3 α/β inhibitor; IC50: GSK-3α/β 10nM, CDK5/p25 2.4μM, CDK2/A 4.3μM, CDK1/B 63μM.</p>
    Fórmula:C18H12BrN3O3
    Forma y color:Solid
    Peso molecular:398.21
  • CDK-IN-10

    CAS:
    <p>CDK-IN-10 is a cell cycle protein-dependent kinase (CDK) inhibitor with potential anticancer activity for cancer research.</p>
    Fórmula:C18H18N4O2
    Pureza:97.07%
    Forma y color:Solid
    Peso molecular:322.36
  • CDK8-IN-4

    CAS:
    <p>CDK8-IN-4 is an inhibitor of CDK8 (IC50: 0.2 nM).</p>
    Fórmula:C20H18N4O
    Forma y color:Solid
    Peso molecular:330.38
  • CDK12-IN-3

    CAS:
    <p>CDK12-IN-3 is a CDK12 inhibitor with anti-tumor activity and can be used for the study of malignant tumors.</p>
    Fórmula:C23H28F2N8O
    Pureza:99.85%
    Forma y color:Solid
    Peso molecular:470.52
  • NSC 693868

    CAS:
    <p>CDKs and GSK-3 inhibitor</p>
    Fórmula:C9H7N5
    Pureza:98%
    Forma y color:Solid
    Peso molecular:185.19
  • P18IN003

    CAS:
    <p>P18IN003 is a selective and effective p18(INK4C) inhibitor that inhibits the activity of p18 protein and can be used to study in vitro expansion of</p>
    Fórmula:C17H16N2O3
    Pureza:98.77%
    Forma y color:Solid
    Peso molecular:296.32
  • CDK7-IN-15

    CAS:
    <p>CDK7-IN-15, a pyrimidine-based potent CDK7 inhibitor, shows promise for various cancers with defective transcription.</p>
    Fórmula:C21H24F4N6OS
    Forma y color:Solid
    Peso molecular:484.51
  • Cdc7-IN-1

    CAS:
    <p>Cdc7-IN-1: selective ATP-competitive Cdc7 kinase inhibitor; IC50 0.6 nM at 1mM ATP; induces cancer cell death.</p>
    Fórmula:C21H16ClN3O4
    Forma y color:Solid
    Peso molecular:409.82
  • BS-181

    CAS:
    <p>BS-181 is a highly selective CDK7 inhibitor (IC50: 21 nM); &gt;40-fold selective for CDK7 than CDK1/2/4/5/6/9.</p>
    Fórmula:C22H32N6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:380.53
  • CLK1/2-IN-3

    CAS:
    <p>CLK1/2-IN-3 (Cpd-3) is a CLK1 and CLK2 inhibitor with antiproliferative activity that inhibits the activity of CLK and SRPK.</p>
    Fórmula:C21H21N5O2
    Pureza:99.04%
    Forma y color:Solid
    Peso molecular:375.42
  • CDK7-IN-10

    CAS:
    <p>CDK7-IN-10: CDK7 inhibitor, IC50&lt;100 nM, may hinder cell growth, induce apoptosis. (Patent WO2021016388A1, I-1)</p>
    Fórmula:C29H35N7O3
    Forma y color:Solid
    Peso molecular:529.63
  • CGP60474

    CAS:
    <p>CGP60474 is an inhibitor of VEGFR-2 (IC50 = 84 nM) and an inhibitor of ATP-competitive PKC.</p>
    Fórmula:C18H18ClN5O
    Pureza:98.81%
    Forma y color:Solid
    Peso molecular:355.82