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Assay Detail

CHEMBL5735285

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
PKR KinaseGlo Assay: Commercially available recombinant human GST-PKR (SignalChem, Canada; 1.5 uM-2 uM stock) is diluted to 500 nM in assay buffer (20 mM Tris-HCl, pH 7.2, 10 mM KCl, 10 mM MgCl2, 10% glycerol). Preactivated PKR is dispensed to 384/96-well black plates at 3.125/12.5 uls/well using the liquid handler Janus. Appropriate dilutions of inhibitors are added to 384/96-well plate followed by 6.6 uM ATP (final) and incubated for 10 minutes at room temperature. The remaining ATP/well is determined by adding 6.25/25 uls/well Kinase-Glo assay mix (Promega) and luminescence is measured on EnVision luminescence plate reader (integration time, 0.2 sec; Perkin-Elmer, Mass., USA). The % inhibition for the compounds is calculated using ATP only (100% inhibition) and PKR +ATP (0% inhibition). IC50 values are determined by plotting % activity versus inhibitor concentration. Curves are fitted using Activity base XLfit (IDBS, UK).
12
Total Activities
4
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Publication

Pyridyl benzothiophenes as kinase inhibitors
(2020)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 6.65 7.16
kon 4 - -
k_off 4 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5783751 3 7.16
CHEMBL6029379 3 6.78
CHEMBL5854149 3 6.41
CHEMBL5878808 3 6.26

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5783751 IC50 = 69.0 nM 7.16
CHEMBL6029379 IC50 = 167.0 nM 6.78
CHEMBL5854149 IC50 = 390.0 nM 6.41
CHEMBL5878808 IC50 = 551.0 nM 6.26
CHEMBL5783751 kon = - -
CHEMBL5783751 k_off = - s-1 -
CHEMBL6029379 kon = - -
CHEMBL6029379 k_off = - s-1 -
CHEMBL5878808 kon = - -
CHEMBL5878808 k_off = - s-1 -
CHEMBL5854149 kon = - -
CHEMBL5854149 k_off = - s-1 -