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Assay Detail

CHEMBL5736583

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Binding
Enzyme Inhibitory Assay: R206H: An overview of evaluation of an inhibitory effect of a compound of the present invention with respect to ALK2 (R206H) is as follows.In a buffer solution (20 mM HEPES, pH 7.5, 10 mM MgCl2, 2 mM MnCl2, 1 mM EGTA, 0.02% Brij 35, 0.02 mg/mL BSA, 0.1 mM Na3VO4, 2 mM DTT, 1% DMSO), human ALK2 (http://www.expasy.org/uniprot/Q04771) in which Arg206 was mutated with His, and a substrate (20 μM casein) were incubated at room temperature for 20 minutes together with a test compound, 33P-ATP (specific radioactivity: 10 Ci/L) was then added thereto so that the final ATP concentration was 10 μM, and the mixture was additionally incubated at room temperature for 2 hours. The reaction mixture was filtered using a P81 ion exchange filter, and a kinase activity was determined by measuring a radioactivity bound to the filter. An inhibitory effect was determined using test compounds with respective concentrations, and a concentration (IC50) indicating 50% of the maximum inhibitory concentration was calculated.
228
Total Activities
76
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Activin receptor type-1 (CHEMBL5903)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

BMP-signal-inhibiting compound
(2021)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 76 7.80 8.89
kon 76 - -
k_off 76 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5961222 3 8.89
CHEMBL6007636 3 8.57
CHEMBL6047714 3 8.52
CHEMBL5936597 3 8.27
CHEMBL5972606 3 8.26
CHEMBL5851101 3 8.25
CHEMBL5843386 3 8.25
CHEMBL6004497 3 8.24
CHEMBL5813932 3 8.21
CHEMBL6033191 3 8.20
CHEMBL5951625 3 8.17
CHEMBL5883349 3 8.15
CHEMBL5775099 3 8.12
CHEMBL5968166 3 8.12
CHEMBL5992279 3 8.10
CHEMBL5885412 3 8.04
CHEMBL5752456 3 8.03
CHEMBL5886480 3 8.03
CHEMBL5994005 3 8.00
CHEMBL6007911 3 7.97
CHEMBL6026040 3 7.96
CHEMBL5823049 3 7.96
CHEMBL5781360 3 7.96
CHEMBL5824341 3 7.94
CHEMBL5759999 3 7.94
CHEMBL5919859 3 7.90
CHEMBL5913989 3 7.88
CHEMBL5893945 3 7.87
CHEMBL5793047 3 7.87
CHEMBL5914490 3 7.87

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5961222 IC50 = 1.3 nM 8.89
CHEMBL6007636 IC50 = 2.7 nM 8.57
CHEMBL6047714 IC50 = 3.0 nM 8.52
CHEMBL5936597 IC50 = 5.4 nM 8.27
CHEMBL5972606 IC50 = 5.5 nM 8.26
CHEMBL5843386 IC50 = 5.6 nM 8.25
CHEMBL5851101 IC50 = 5.6 nM 8.25
CHEMBL6004497 IC50 = 5.7 nM 8.24
CHEMBL5813932 IC50 = 6.1 nM 8.21
CHEMBL6033191 IC50 = 6.3 nM 8.20
CHEMBL5951625 IC50 = 6.7 nM 8.17
CHEMBL5883349 IC50 = 7.1 nM 8.15
CHEMBL5968166 IC50 = 7.5 nM 8.12
CHEMBL5775099 IC50 = 7.5 nM 8.12
CHEMBL5992279 IC50 = 8.0 nM 8.10
CHEMBL5885412 IC50 = 9.2 nM 8.04
CHEMBL5886480 IC50 = 9.4 nM 8.03
CHEMBL5752456 IC50 = 9.4 nM 8.03
CHEMBL5994005 IC50 = 9.9 nM 8.00
CHEMBL6007911 IC50 = 10.7 nM 7.97
CHEMBL5781360 IC50 = 11.0 nM 7.96
CHEMBL5823049 IC50 = 11.0 nM 7.96
CHEMBL6026040 IC50 = 10.9 nM 7.96
CHEMBL5759999 IC50 = 11.5 nM 7.94
CHEMBL5824341 IC50 = 11.6 nM 7.94
CHEMBL5919859 IC50 = 12.6 nM 7.90
CHEMBL5913989 IC50 = 13.2 nM 7.88
CHEMBL5893945 IC50 = 13.5 nM 7.87
CHEMBL5914490 IC50 = 13.6 nM 7.87
CHEMBL5793047 IC50 = 13.5 nM 7.87
CHEMBL5950412 IC50 = 13.9 nM 7.86
CHEMBL5818543 IC50 = 14.5 nM 7.84
CHEMBL6019285 IC50 = 14.3 nM 7.84
CHEMBL5826606 IC50 = 14.7 nM 7.83
CHEMBL6058646 IC50 = 15.1 nM 7.82
CHEMBL6057564 IC50 = 16.0 nM 7.80
CHEMBL5868335 IC50 = 16.3 nM 7.79
CHEMBL5918848 IC50 = 16.3 nM 7.79
CHEMBL5978827 IC50 = 17.1 nM 7.77
CHEMBL5947703 IC50 = 17.0 nM 7.77
CHEMBL5765854 IC50 = 17.0 nM 7.77
CHEMBL5890533 IC50 = 17.3 nM 7.76
CHEMBL6009394 IC50 = 17.7 nM 7.75
CHEMBL5907765 IC50 = 18.7 nM 7.73
CHEMBL5922240 IC50 = 18.7 nM 7.73
CHEMBL5951725 IC50 = 18.5 nM 7.73
CHEMBL5956568 IC50 = 21.0 nM 7.68
CHEMBL5871650 IC50 = 22.3 nM 7.65
CHEMBL5829740 IC50 = 23.8 nM 7.62
CHEMBL5965129 IC50 = 24.9 nM 7.60