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Assay Detail

CHEMBL4378233

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

Binding
Inhibition of ALK (unknown origin)
17
Total Activities
16
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

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

Target

ALK tyrosine kinase receptor (CHEMBL4247)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Drug Discovery Targeting Anaplastic Lymphoma Kinase (ALK).
Kong X, Pan P, Sun H, Xia H, Wang X, Li Y, Hou T.
J Med Chem (2019) 62 : 10927 -10954
PubMed 31419130 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 8.45 9.30
Ki 2 9.12 9.12

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL464552 1 9.30
CHEMBL4203266 1 9.12
CHEMBL4436406 2 9.00
CHEMBL4298138 REPOTRECTINIB 4.0 1 9.00
CHEMBL2172315 1 9.00
CHEMBL2172308 1 8.92
CHEMBL1779202 1 8.82
CHEMBL1738797 ALECTINIB 4.0 1 8.72
CHEMBL4476742 1 8.70
CHEMBL3735401 1 8.70
CHEMBL1823221 1 8.54
CHEMBL2172323 1 8.52
CHEMBL1779192 1 8.12
CHEMBL2042829 1 7.85
CHEMBL601719 CRIZOTINIB 4.0 1 7.70
CHEMBL1779097 1 5.87

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL464552 IC50 = 0.5 nM 9.30
CHEMBL4203266 Ki = 0.75 nM 9.12
CHEMBL4436406 IC50 = 1.01 nM 9.00
CHEMBL2172315 IC50 = 1.0 nM 9.00
CHEMBL4298138 REPOTRECTINIB IC50 = 1.01 nM 9.00
CHEMBL2172308 IC50 = 1.2 nM 8.92
CHEMBL1779202 IC50 = 1.5 nM 8.82
CHEMBL1738797 ALECTINIB IC50 = 1.9 nM 8.72
CHEMBL4476742 IC50 = 2.0 nM 8.70
CHEMBL3735401 IC50 = 2.0 nM 8.70
CHEMBL1823221 IC50 = 2.9 nM 8.54
CHEMBL2172323 IC50 = 3.0 nM 8.52
CHEMBL1779192 IC50 = 7.6 nM 8.12
CHEMBL2042829 IC50 = 14.0 nM 7.85
CHEMBL601719 CRIZOTINIB IC50 = 20.0 nM 7.70
CHEMBL1779097 IC50 = 1336.0 nM 5.87
CHEMBL4436406 Ki < 0.02 nM -