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Assay Detail

CHEMBL5356777

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Binding
Inhibition of MET (unknown origin)
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Hepatocyte growth factor receptor (CHEMBL3717)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Targeting MET: Discovery of Small Molecule Inhibitors as Non-Small Cell Lung Cancer Therapy.
Wang C, Lu X.
J Med Chem (2023) 66 : 7670 -7697
PubMed 37262349 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 8.60 9.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3188267 CAPMATINIB 4.0 1 9.89
CHEMBL5095061 ELZOVANTINIB 2.0 1 9.85
CHEMBL1230609 FORETINIB 2.0 1 9.40
CHEMBL4594400 GUMARONTINIB 2.0 1 9.30
CHEMBL2376648 1 9.16
CHEMBL5408530 1 8.96
CHEMBL2105717 CABOZANTINIB 4.0 1 8.89
CHEMBL2133806 JNJ-38877605 1.0 1 8.77
CHEMBL460472 1 8.70
CHEMBL5275126 1 8.59
CHEMBL460702 BMS-777607 2.0 1 8.41
CHEMBL3545307 MERESTINIB 2.0 1 8.33
CHEMBL5419352 1 8.26
CHEMBL5428302 1 8.00
CHEMBL3039525 GOLVATINIB 2.0 1 7.85
CHEMBL3989914 GLESATINIB 2.0 1 7.72
CHEMBL1615181 1 7.55
CHEMBL3984441 NINGETINIB 2.0 1 7.17

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3188267 CAPMATINIB IC50 = 0.13 nM 9.89
CHEMBL5095061 ELZOVANTINIB IC50 = 0.14 nM 9.85
CHEMBL1230609 FORETINIB IC50 = 0.4 nM 9.40
CHEMBL4594400 GUMARONTINIB IC50 = 0.5 nM 9.30
CHEMBL2376648 IC50 = 0.69 nM 9.16
CHEMBL5408530 IC50 = 1.09 nM 8.96
CHEMBL2105717 CABOZANTINIB IC50 = 1.3 nM 8.89
CHEMBL2133806 JNJ-38877605 IC50 = 1.7 nM 8.77
CHEMBL460472 IC50 = 2.0 nM 8.70
CHEMBL5275126 IC50 = 2.6 nM 8.59
CHEMBL460702 BMS-777607 IC50 = 3.9 nM 8.41
CHEMBL3545307 MERESTINIB IC50 = 4.7 nM 8.33
CHEMBL5419352 IC50 = 5.51 nM 8.26
CHEMBL5428302 IC50 = 10.0 nM 8.00
CHEMBL3039525 GOLVATINIB IC50 = 14.0 nM 7.85
CHEMBL3989914 GLESATINIB IC50 = 19.0 nM 7.72
CHEMBL1615181 IC50 = 28.0 nM 7.55
CHEMBL3984441 NINGETINIB IC50 = 68.0 nM 7.17