PLK4-IN-25

PLK4-IN-25 : Inhibitor of PLK4

Structure

Information

  • PLK4
  • Inhibitor
  • up to 500 nM

In Vitro Validations

Uniprot ID: O00444
Target Class: Kinase
Target SubClass: Ser/Thr Kinase
Potency: IC50
Potency Value: 7.9 ± 4.0 nM
Potency Assay: ADP-Glo assay
PDB ID for probe-target interaction (3D structure): 9Y9N
Target aliases:
Serine/threonine-protein kinase PLK4, STK18, SAK, ...

DOI Reference: 10.1021/acs.jmedchem.5c02200

In Cell Validations

In Vivo Data

Off-Target Selectivity Assesments

Potency assay (off target): Eurofins KinaseProfile Selectivity Panel Data for Compound 25 at 1 µM
Probe Selectivity in Vitro:
A Eurofins KinaseProfiler selectivity panel containing 435 kinases was conducted to gain additional confidence in the experimental kinase selectivity assays. Fewer than 10% of the kinases screened were inhibited at greater than 50% at a single-point concentration of 1 μM.
Potency assay (off target): Biochemical assays with recombinant AURKB (ADP-Glo IC50 653 nM) and KDR (HTRF IC50 1600 nM ) confirmed selectivity against these targets.
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