YKL-05-099

YKL-05-099 : Inhibitor of SIK1, SIK3, SIK2

Structure

Information

  • SIK1
  • SIK3
  • SIK2
  • Inhibitor
  • up to 1 µM

In Vitro Validations

Uniprot ID: P57059
Target Class: Kinase
Target SubClass: CAMK
Potency: IC50
Potency Value: 10.9 nM
Potency Assay: Competitive binding assay
PDB ID for probe-target interaction (3D structure): --
Target aliases:
Serine/threonine-protein kinase SIK1, SNF1LK, SIK, ...

DOI Reference: 10.1021/acschembio.6b00217

In Cell Validations

In Vivo Data

Off-Target Selectivity Assesments

Potency assay (off target): YKL-05-099 (1 μM) was tested for its ability to inhibit the activity of 144 kinases at the MRC PPU International Center for kinase profiling. In addition, YKL-05-099 (1 μM) was tested for interaction with 468 recombinant kinases using the KINOMEscan active site-directed competitive binding assay (DiscoverRx).
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