Cell Cycle

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  1. LIMK1/LIMK2 inhibitor

    TH-257 is a potent inhibitor of LIMK1 and LIMK2 with IC50 values of 84 nM and 39 nM for LIMK1 and LIMK2, respectively, and it can be used as a chemical probe for LIMK1 and LIMK2.
  2. dual inhibitor of CDK12/CDK13

    SR-4835 is a potent, highly selective and ATP competitive dual inhibitor of CDK12/CDK13 (CDK12: IC50=99 nM, Kd=98 nM; CDK13: Kd=4.9 nM).
  3. CDK8 and CDK19 inhibitor

    AS2863619 is a potent, orally active cyclin-dependent kinase 8 (CDK8) and CDK19 inhibitor with IC50s of 0.61 nM and 4.28 nM, respectively.
  4. MRTF pathway inhibitor

    CCG-222740 is an orally active and selective Rho/myocardin-related transcription factor (MRTF) pathway inhibitor. CCG-222740 is also a potent inhibitor of alpha-smooth muscle actin protein expression.
  5. dual inhibitor of protein kinase and CDK

    6-(Dimethylamino)purine is a dual inhibitor of protein kinase and CDK.
  6. CHK1 inhibitor

    SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an IC50 of 13.3 nM for human CHK1.
  7. MYC inhibitor

    MYCi361 (NUCC-0196361) is a MYC inhibitor with the Kd of 3.2 μM for binding to MYC. MYCi361 (NUCC-0196361) suppresses tumor growth and enhances anti-PD1 immunotherapy.
  8. MYC inhibitor

    MYCi975 (NUCC-0200975) is an orally active MYC inhibitor, which disrupts MYC/MAX interaction, promotes MYC T58 phosphorylation and MYC degradation, and impairs MYC driven gene expression.
  9. PLK4 inhibitor

    CFI-400437 is a potent and selective inhibitor of polo-like kinase 4 (PLK4).
  10. protein-protein interactions inhibitor

    NSC-92828, also known as 3-Phenanthrenebutyric acid, is a Protein-protein interaction inhibitor (PP inhibitor or PPI).

  11. RAD51 inhibitor

    Bractoppin is a potent and selective inhibitor of phosphopeptide recognition by the BRCA1 tBRCT domain.
  12. S-IIP inhibitor/KRASG12C Probe

    ARS-1323-Alkyne is a novel KRASG12C occupancy probe.
  13. MYC:MAX protein interactions inhibitor

    MYCMI-6 (NSC354961) is a potent and selective endogenous MYC:MAX protein interactions inhibitor.
  14. ATF6α inhibitor

    Ceapin-A7 is a selective blocker of ATF6α signaling in response to ER stress, with an IC50 of 0.59 μM. 

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