CG211

CG211 : Inhibitor of RIOK2

Structure

Information

  • RIOK2
  • Inhibitor
  • up to 5 µM

In Vitro Validations

Uniprot ID: Q9BVS4
Target Class: Kinase
Target SubClass: RIO Type
Potency: Kd
Potency Value: 6.1 ± 0.4 nM
Potency Assay: Biochemical assay
PDB ID for probe-target interaction (3D structure): 7VBT
Target aliases:
Serine/threonine-protein kinase RIO2, RIO2, RIOK2, ...

DOI Reference: 10.1021/acs.jmedchem.2c00271

Uniprot ID: Q9BVS4
Target Class: Kinase
Target SubClass: RIO Type
Potency: IC50
Potency Value: 139 ± 46 nM
Potency Assay: ADP-GloTM kinase assay
PDB ID for probe-target interaction (3D structure): 7VBT
Target aliases:
Serine/threonine-protein kinase RIO2, RIO2, RIOK2, ...

DOI Reference: 10.1021/acs.jmedchem.2c00271

In Cell Validations

In Vivo Data

Off-Target Selectivity Assesments

Potency assay (off target): KINOMEscan approach was used to test the specificity of the binding of compound CQ211 to RIOK2 by screening it in a panel of 468 kinases, including 412 wild-type kinases (403 wild-type human kinases) and 56 disease-related mutants. Surprisingly, CQ211 exhibited excellent selectivity to RIOK2, with no interaction being observed between CQ211 and any of the other wild-type kinases (S (35) = 0.002 at 1 μM). CQ211 showed binding interactions only with three FLT3 mutants, FLT3-ITD-D835V, FLT3-ITD-F691L, and FLT3-D835V with percentage of control (%Ctr) of 4, 3.6, and 28, respectively, at 1 μM concentration.
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SERP ratings and comments


SERP Ratings

In Cell Rating
In Model Organisms

SERP Comments:

CQ211 shows adequate potency and selectivity and can be used as a probe in cells, with several reservations. 1) No cytotoxicity data is available in non-malignant cells, and 2) "CQ211 showed poor solubility in H2O and organic solvents. This may lead to poor membrane permeability and a loss of potency when moving into cells." Limited dosage and PK data do not allow for a recommended dose in model organisms to be provided.

(last updated: 3 Apr 2025 )