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Assay Detail

CHEMBL5736677

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Binding
Test of Small Molecule Compounds for Inhibiting the Activity of C-RAF and B-RAF Kinases: 1. Preparation of test compounds: according to the molecular weight of the compounds, an appropriate volume of DMSO was directly added to dissolve the test compounds. For storing the compound, the concentration of DMSO is 100%, and the final concentration of DMSO in the experimental system is 1%. The compounds were 3-fold serially diluted with DMSO to obtain a total of 8 dilutions, with a maximum concentration of 1000 nM and a minimum concentration of 0.46 nM.2. Preparation of the sorafenib positive control: sorafenib, a selective inhibitor of BRAF and RAF1, was used as the positive control of this experiment, and the dilution method thereof was the same as that of the above test compounds.3. Test Conditions:Enzyme: B-RAF: 0.1 ng/l (the final concentration in the reaction system); C-RAF: 0.1 ng/μl (the final concentration in the reaction system)Substrate and ATP: inactive MEKI: 2 ng/μl (the final concentration in the reaction system); ATP: 35 μM (the final concentration in the reaction system)HPE: the reaction without enzyme (1% DMSO)ZPE: the reaction with enzyme but without compound (1% DMSO)4. Test procedure:a) 1 ul of 10-fold diluted compound or 10% DMSO was added to a 384-well assay plate,b) 4 ul enzyme solution or assay buffer was added to the wells of the assay plate,c) the plate was centrifuged at 1000 rpm for 1 minute to homogeneous,d) 5 ul of ATP-substrate mixture was added to the wells of the assay plate,e) the plate was shaked for mixing for 2 minutes,f) the plate was incubated at 30° C. for 1 hour,g) 10 ul of ADP-Glo reagent was added to the wells of the assay plate, and the plate was incubated for 40 minutes at 27° C.,h) 20 ul of kinase assay solution was added to the wells of the plate, and the plate was incubated for 30 minutes at 27° C.,i) the chemiluminescent signal was read with Envision.5. Analysis of the results: calculation of the compound inhibition rate:Inhibition rate (%)=(control measurement without compound−sample measurement)/(control measurement without compound−control measurement without enzyme)*100%The IC50 values of the positive control compound and the test compounds were calculated using the Prism software according to the variable slope of the curve.
57
Total Activities
19
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

Target

RAF proto-oncogene serine/threonine-protein kinase (CHEMBL1906)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Urea-substituted aromatic ring-linked dioxane-quinazoline and -linked dioxane-quinoline compounds, preparation method therefor and use thereof
(2021)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 6.21 7.33
kon 19 - -
k_off 19 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1336 SORAFENIB 4.0 3 7.33
CHEMBL5887076 3 6.56
CHEMBL6048799 3 6.56
CHEMBL4449250 3 6.56
CHEMBL4528373 3 6.56
CHEMBL4466426 3 6.56
CHEMBL4514617 3 6.56
CHEMBL6001367 3 5.56
CHEMBL5757962 3 5.56
CHEMBL4516513 3 5.56
CHEMBL5821626 3 5.56
CHEMBL5967090 3 5.56
CHEMBL5930162 3 -
CHEMBL5835833 3 -
CHEMBL5815669 3 -
CHEMBL5804750 3 -
CHEMBL5801339 3 -
CHEMBL5953811 3 -
CHEMBL5916459 3 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1336 SORAFENIB IC50 = 47.0 nM 7.33
CHEMBL4449250 IC50 = 275.0 nM 6.56
CHEMBL6048799 IC50 = 275.0 nM 6.56
CHEMBL4514617 IC50 = 275.0 nM 6.56
CHEMBL4528373 IC50 = 275.0 nM 6.56
CHEMBL5887076 IC50 = 275.0 nM 6.56
CHEMBL4466426 IC50 = 275.0 nM 6.56
CHEMBL6001367 IC50 = 2750.0 nM 5.56
CHEMBL5757962 IC50 = 2750.0 nM 5.56
CHEMBL5967090 IC50 = 2750.0 nM 5.56
CHEMBL5821626 IC50 = 2750.0 nM 5.56
CHEMBL4516513 IC50 = 2750.0 nM 5.56
CHEMBL1336 SORAFENIB k_off = - s-1 -
CHEMBL5930162 k_off = - s-1 -
CHEMBL5967090 kon = - -
CHEMBL6001367 kon = - -
CHEMBL6001367 k_off = - s-1 -
CHEMBL5916459 IC50 > 5000.0 nM -
CHEMBL5916459 kon = - -
CHEMBL5916459 k_off = - s-1 -
CHEMBL4514617 kon = - -
CHEMBL4514617 k_off = - s-1 -
CHEMBL5953811 IC50 < 50.0 nM -
CHEMBL5953811 kon = - -
CHEMBL5953811 k_off = - s-1 -
CHEMBL4466426 kon = - -
CHEMBL4466426 k_off = - s-1 -
CHEMBL5835833 k_off = - s-1 -
CHEMBL5967090 k_off = - s-1 -
CHEMBL5930162 IC50 > 5000.0 nM -
CHEMBL5930162 kon = - -
CHEMBL5801339 k_off = - s-1 -
CHEMBL4449250 k_off = - s-1 -
CHEMBL5804750 kon = - -
CHEMBL5804750 IC50 > 5000.0 nM -
CHEMBL5815669 k_off = - s-1 -
CHEMBL5804750 k_off = - s-1 -
CHEMBL5801339 IC50 > 5000.0 nM -
CHEMBL5815669 kon = - -
CHEMBL5815669 IC50 > 5000.0 nM -
CHEMBL5801339 kon = - -
CHEMBL1336 SORAFENIB kon = - -
CHEMBL4449250 kon = - -
CHEMBL5887076 kon = - -
CHEMBL6048799 kon = - -
CHEMBL6048799 k_off = - s-1 -
CHEMBL4516513 kon = - -
CHEMBL4516513 k_off = - s-1 -
CHEMBL5757962 kon = - -
CHEMBL5757962 k_off = - s-1 -