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Assay Detail

CHEMBL5733240

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

Binding
EGFR Exon 21 L858R and Exon 20 T790M Concurrent Mutations: A compound's ability in selectively inhibiting EGFR L858R and T790M concurrent mutations can be assessed using Ba/F3 cells, a murine pro-B cell line, which have been transduced with EGFR L858R and T790M double mutations. An expression vector, pLVX-IRES puro (Clontech) coding for human EGFR L858R and T790M double mutation, was transfected into HEK293 cells by the Trans-Lentiviral ORF Packaging System (Thermo Scientific), to produce virus encoding EGFR L858R and T790M double mutations. Ba/F3 (DSMZ) cells maintained in RPMI 1640 medium supplemented with 10% fetal bovine serum, 200 μM L-glutamine/200 μg/mL penicillin/200 μg/mL streptomycin (Life Technology) and 10 ng/mL IL-3 (R&D system), were infected by EGFR L858R and T790M double mutation virus and subsequently selected by puromycin (Life Technology) selection and IL-3 depletion. Ba/F3 cells expressing EGFR L858R and T790M double mutation (named Ba/F3-EGFR L858R/T790M) can proliferate in the absence of IL-3. The anti-proliferative activity of compounds was determined as follows: BaF3-EGFR L858R/T790M cells seeded in 96 well plates (2500 cells/well) were treated with test compound (dissolved in DMSO) at a series of concentrations (4-fold dilution, top concentration: 10,000 nM). The plates were incubated for 72 h in a 37° C. incubator with 5% CO2, and the number of viable cells in each well were measured indirectly by CellTiter 96® Aqueous One Solution Cell Proliferation Assay (Promega; this assay is a colorimetric method for determining the number of viable cells through measurement of their metabolic activity by detection of enzymatic conversion of tetrazolium salts into blue formazan derivatives). Reagent (20 μL) was added into each well, and the plates were returned to the incubator for 2 h. The absorbance in each well was then measured at 490 nm using an Envision plate reader (Perkin Elmer). IC50 values were calculated by determining the concentration of compound required to decrease the MTS signal by 50% comparing to the DMSO control in best-fit curves using Microsoft XLfit software or Accelrys Pipeline Pilot.
108
Total Activities
36
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

Epidermal growth factor receptor (CHEMBL203)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Heteroaryl compounds for kinase inhibition
(2019)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 36 6.44 6.52
kon 36 - -
k_off 36 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5946842 3 6.52
CHEMBL5853466 3 6.52
CHEMBL5960275 3 6.52
CHEMBL6009791 3 6.52
CHEMBL5848181 3 6.12
CHEMBL5838931 3 -
CHEMBL3353404 3 -
CHEMBL5290929 3 -
CHEMBL5773016 3 -
CHEMBL5268143 3 -
CHEMBL4650319 MOBOCERTINIB 4.0 3 -
CHEMBL5928706 3 -
CHEMBL3353410 OSIMERTINIB 4.0 3 -
CHEMBL5961813 3 -
CHEMBL5900701 3 -
CHEMBL5270335 3 -
CHEMBL5880754 3 -
CHEMBL5741017 3 -
CHEMBL5938217 3 -
CHEMBL5780612 3 -
CHEMBL5821080 3 -
CHEMBL5938417 3 -
CHEMBL5870116 3 -
CHEMBL5892565 3 -
CHEMBL5978253 3 -
CHEMBL5942093 3 -
CHEMBL5978450 3 -
CHEMBL5266798 3 -
CHEMBL5894504 3 -
CHEMBL6007834 3 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5946842 IC50 = 300.0 nM 6.52
CHEMBL5853466 IC50 = 300.0 nM 6.52
CHEMBL5960275 IC50 = 300.0 nM 6.52
CHEMBL6009791 IC50 = 300.0 nM 6.52
CHEMBL5848181 IC50 = 750.0 nM 6.12
CHEMBL5870116 IC50 < 100.0 nM -
CHEMBL5780612 k_off = - s-1 -
CHEMBL5938217 IC50 < 100.0 nM -
CHEMBL5838931 k_off = - s-1 -
CHEMBL5838931 kon = - -
CHEMBL5838931 IC50 > 1000.0 nM -
CHEMBL5946842 k_off = - s-1 -
CHEMBL5946842 kon = - -
CHEMBL5741017 k_off = - s-1 -
CHEMBL5741017 kon = - -
CHEMBL5741017 IC50 < 100.0 nM -
CHEMBL5848181 k_off = - s-1 -
CHEMBL5848181 kon = - -
CHEMBL5938217 k_off = - s-1 -
CHEMBL5938217 kon = - -
CHEMBL5821080 k_off = - s-1 -
CHEMBL5870116 k_off = - s-1 -
CHEMBL5938417 IC50 < 100.0 nM -
CHEMBL6007834 kon = - -
CHEMBL6007834 k_off = - s-1 -
CHEMBL5821080 IC50 < 100.0 nM -
CHEMBL5821080 kon = - -
CHEMBL5978450 IC50 < 100.0 nM -
CHEMBL6007834 IC50 < 100.0 nM -
CHEMBL5938417 kon = - -
CHEMBL5938417 k_off = - s-1 -
CHEMBL5894504 IC50 < 100.0 nM -
CHEMBL5894504 kon = - -
CHEMBL5894504 k_off = - s-1 -
CHEMBL5853466 kon = - -
CHEMBL5853466 k_off = - s-1 -
CHEMBL5266798 IC50 < 100.0 nM -
CHEMBL5266798 kon = - -
CHEMBL5266798 k_off = - s-1 -
CHEMBL5892565 k_off = - s-1 -
CHEMBL5978450 kon = - -
CHEMBL5978450 k_off = - s-1 -
CHEMBL5942093 IC50 < 100.0 nM -
CHEMBL5942093 kon = - -
CHEMBL5942093 k_off = - s-1 -
CHEMBL5978253 IC50 < 100.0 nM -
CHEMBL5978253 kon = - -
CHEMBL5978253 k_off = - s-1 -
CHEMBL5892565 IC50 < 100.0 nM -
CHEMBL5892565 kon = - -