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Assay Detail

CHEMBL874430

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

Binding
Inhibition of HER2 kinase in intact CSH12 cells; Range = 25-50 nM
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type CSH12
Confidence 9 — Direct single protein target
Curated By Expert

Target

Receptor tyrosine-protein kinase erbB-2 (CHEMBL1824)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

High-affinity epidermal growth factor receptor (EGFR) irreversible inhibitors with diminished chemical reactivities as positron emission tomography (PET)-imaging agent candidates of EGFR overexpressing tumors.
Mishani E, Abourbeh G, Jacobson O, Dissoki S, Ben Daniel R, Rozen Y, Shaul M, Levitzki A.
J Med Chem (2005) 48 : 5337 -5348
PubMed 16078851 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 7.30 7.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL275762 1 7.30
CHEMBL190094 1 7.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL275762 IC50 = 50.0 nM 7.30
CHEMBL190094 IC50 = 50.0 nM 7.30