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Assay Detail

CHEMBL4841672

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

Binding
Inhibition of N-terminal DYKDDDD-tagged EGFR (669 to 1210 residues) (unknown origin) expressed in Sf21 insect cells using NH2-ETVYSEVRK-biotin as substrate preincubated for 1 hr followed by ATP addition and measured after 2 hrs by ELISA
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type Sf21
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

Discovery of 1-Amino-1<i>H</i>-imidazole-5-carboxamide Derivatives as Highly Selective, Covalent Bruton's Tyrosine Kinase (BTK) Inhibitors.
Ma C, Li Q, Zhao M, Fan G, Zhao J, Zhang D, Yang S, Zhang S, Gao D, Mao L, Zhu L, Li W, Xu G, Jiang Y, Ding Q.
J Med Chem (2021) 64 : 16242 -16270
PubMed 34672559 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 6.60 8.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1873475 IBRUTINIB 4.0 1 8.77
CHEMBL4878626 1 7.90
CHEMBL3936761 ZANUBRUTINIB 4.0 1 7.67
CHEMBL4863836 1 7.10
CHEMBL4863913 1 6.95
CHEMBL4860527 1 6.75
CHEMBL4864983 1 6.36
CHEMBL4874550 1 6.35
CHEMBL4878421 1 6.24
CHEMBL3707348 ACALABRUTINIB 4.0 1 5.45
CHEMBL4847730 1 4.93
CHEMBL4849268 1 4.78
CHEMBL4852748 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1873475 IBRUTINIB IC50 = 1.7 nM 8.77
CHEMBL4878626 IC50 = 12.6 nM 7.90
CHEMBL3936761 ZANUBRUTINIB IC50 = 21.2 nM 7.67
CHEMBL4863836 IC50 = 79.4 nM 7.10
CHEMBL4863913 IC50 = 113.0 nM 6.95
CHEMBL4860527 IC50 = 176.0 nM 6.75
CHEMBL4864983 IC50 = 433.0 nM 6.36
CHEMBL4874550 IC50 = 450.0 nM 6.35
CHEMBL4878421 IC50 = 578.0 nM 6.24
CHEMBL3707348 ACALABRUTINIB IC50 = 3513.0 nM 5.45
CHEMBL4847730 IC50 = 11802.0 nM 4.93
CHEMBL4849268 IC50 = 16807.0 nM 4.78
CHEMBL4852748 IC50 > 30000.0 nM -