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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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  • PKC-9

    CAS:
    <p>PKC-9 is a PKC-zeta inhibitor 9.</p>
    Fórmula:C25H25N7
    Forma y color:Solid
    Peso molecular:423.51
  • JTK-101

    CAS:
    <p>JTK-101 is a potent and selective Tat-dependent HIV-1 replication inhibitor.</p>
    Fórmula:C25H23N3O3
    Forma y color:Solid
    Peso molecular:413.47
  • EGFR/CDK2-IN-1

    CAS:
    <p>EGFR/CDK2-IN-1, an inhibitor of both EGFR and CDK2, demonstrates effective cytotoxicity towards MCF7 and HepG2 cells, suggesting its potential application in</p>
    Fórmula:C19H12BrClO2
    Forma y color:Solid
    Peso molecular:387.65
  • Ulecaciclib

    CAS:
    Ulecaciclib: oral, BBB-permeable CDK inhibitor; favorable pharmacokinetics; ki: 0.62 μM (CDK2/A), 3 nM (CDK6/D3), 0.2 nM (CDK4/D1), 0.63 μM (CDK7/H).
    Fórmula:C25H33FN8S
    Forma y color:Solid
    Peso molecular:496.65
  • Cdc7-IN-13

    CAS:
    <p>Cdc7-IN-13 (compound 84) is a highly potent CDC7 inhibitor, exhibiting an IC50 value of &lt;1 nM. This compound holds promise for cancer research [1].</p>
    Fórmula:C18H20N4O2S
    Forma y color:Solid
    Peso molecular:356.44
  • (S)-LY3177833 hydrate

    CAS:
    <p>(S)-LY3177833 ((S)-Example 2) hydrate, an orally active CDC7 kinase inhibitor, exhibits extensive in vitro anticancer efficacy.</p>
    Fórmula:C16H14FN5O2
    Forma y color:Solid
    Peso molecular:327.31
  • CDK4/6-IN-9

    CAS:
    <p>CDK4/6-IN-9 selectively inhibits CDK4/6 (IC50: 905 nM); potential for MM research.</p>
    Fórmula:C22H23FN8
    Forma y color:Solid
    Peso molecular:418.47
  • CDK1-IN-1

    CAS:
    <p>CDK1-IN-7 inhibits CDK1 at 161.2 nM, triggers p53-dependent apoptosis, and selectively targets tumor growth.</p>
    Fórmula:C27H23N5O3
    Forma y color:Solid
    Peso molecular:465.5
  • Indirubin-5-sulfonate

    CAS:
    <p>Indirubin-5-sulfonate inhibits GSK-3β &amp; CDKs with IC50: 55/35/150/300/65 nM for CDK1/B, 2/A&amp;E, 4/D1, 5/p35.</p>
    Fórmula:C16H10N2O5S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:342.33
  • FLT3/CDK4-IN-1

    CAS:
    <p>FLT3/CDK4-IN-1: Oral FLT3 (7 nM IC50) &amp; CDK4 (11 nM IC50) inhibitor with strong in vivo anti-cancer properties.</p>
    Fórmula:C25H28F2N8
    Forma y color:Solid
    Peso molecular:478.54
  • Crozbaciclib fumarate

    CAS:
    <p>Crozbaciclib fumarate is a CDK4/6 inhibitor with IC 50 s of 3 and 1 nM, respectively.</p>
    Fórmula:C32H34F2N6O4
    Forma y color:Solid
    Peso molecular:604.65
  • Cdc7-IN-14

    CAS:
    <p>Cdc7-IN-14 (compound 82) is a potent CDC7 inhibitor with an IC50 &lt; 1 nM, promising for cancer research.</p>
    Fórmula:C18H20N4O2S
    Forma y color:Solid
    Peso molecular:356.44
  • KH-CB19

    CAS:
    <p>KH-CB19 is an effective and highly specific inhibitor of the CDC2-like kinase isoforms 1 and 4 (CLK1/CLK4).</p>
    Fórmula:C15H13Cl2N3O2
    Forma y color:Solid
    Peso molecular:338.19
  • CDK8-IN-6

    CAS:
    <p>CDK8-IN-6 (compound 9) is a potent inhibitor of cyclin-dependent kinase 8 (CDK8) (Kd: 13 nM), CDK8-IN-6 showed potential research value in AML cancers.</p>
    Fórmula:C26H37ClN2
    Forma y color:Solid
    Peso molecular:413.04
  • Ipivivint

    CAS:
    <p>Ipivivint: orally active, potent CLK inhibitor; hinders CLK1, CLK2, &amp; CLK3; curbs Wnt signaling &amp; SRSF phosphorylation for cancer research.</p>
    Fórmula:C26H21FN8
    Forma y color:Solid
    Peso molecular:464.5
  • CDK7-IN-8

    CAS:
    <p>CDK7-IN-8 is a potent inhibitor of CDK7 (IC50: 54.29 nM) and exhibits inhibitory activity against several cancer cells and in vivo tumor models.</p>
    Fórmula:C25H38N8O3
    Forma y color:Solid
    Peso molecular:498.62
  • CDK4/6-IN-8

    CAS:
    <p>CDK4/6-IN-8 (Compound 7p) is a selective inhibitor of CDK4 (IC50=5.01 nM) and CDK6 (IC50=3.97 nM).</p>
    Fórmula:C18H18N6O5
    Forma y color:Solid
    Peso molecular:398.37
  • (S)-CR8

    CAS:
    <p>(S)-CR8 is an effective second-generation cyclin-dependent kinase inhibitor.</p>
    Fórmula:C24H29N7O
    Forma y color:Solid
    Peso molecular:431.53
  • CCT068127

    CAS:
    <p>CCT068127 is a potent CDK2 and CDK9 inhibitor.</p>
    Fórmula:C19H27N7O
    Forma y color:Solid
    Peso molecular:369.46
  • MFH290

    CAS:
    <p>MFH290 is a selective CDK12/13 inhibitor, covalently bonding with CDK12 Cys-1039, blocks Pol II CTD phosphorylation, and enhances olaparib's efficacy.</p>
    Fórmula:C26H31N5O3S2
    Forma y color:Solid
    Peso molecular:525.69