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Assay Detail

CHEMBL5503068

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Binding
Inhibition of AXL (unknown origin)
17
Total Activities
17
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

Tyrosine-protein kinase receptor UFO (CHEMBL4895)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Recent discovery and development of AXL inhibitors as antitumor agents.
Liu Z, Chen L, Zhang J, Yang J, Xiao X, Shan L, Mao W.
Eur J Med Chem (2024) 272 : 116475 -116475
PubMed 38714043 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 7.87 9.14

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3301622 GILTERITINIB 4.0 1 9.14
CHEMBL5558637 1 8.92
CHEMBL3545307 MERESTINIB 2.0 1 8.70
CHEMBL5558810 1 8.46
CHEMBL5523430 1 8.40
CHEMBL5555517 1 8.26
CHEMBL5557693 1 8.23
CHEMBL2105717 CABOZANTINIB 4.0 1 8.15
CHEMBL5414779 1 8.05
CHEMBL1230609 FORETINIB 2.0 1 7.96
CHEMBL3809489 BEMCENTINIB 2.0 1 7.85
CHEMBL5558728 1 7.72
CHEMBL2022968 DUBERMATINIB 2.0 1 7.57
CHEMBL5557653 1 7.36
CHEMBL3809908 1 7.24
CHEMBL288441 BOSUTINIB 4.0 1 6.25
CHEMBL5189859 1 5.58

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3301622 GILTERITINIB IC50 = 0.73 nM 9.14
CHEMBL5558637 IC50 = 1.2 nM 8.92
CHEMBL3545307 MERESTINIB IC50 = 2.0 nM 8.70
CHEMBL5558810 IC50 = 3.5 nM 8.46
CHEMBL5523430 IC50 = 4.0 nM 8.40
CHEMBL5555517 IC50 = 5.5 nM 8.26
CHEMBL5557693 IC50 = 5.9 nM 8.23
CHEMBL2105717 CABOZANTINIB IC50 = 7.0 nM 8.15
CHEMBL5414779 IC50 = 9.0 nM 8.05
CHEMBL1230609 FORETINIB IC50 = 11.0 nM 7.96
CHEMBL3809489 BEMCENTINIB IC50 = 14.0 nM 7.85
CHEMBL5558728 IC50 = 19.0 nM 7.72
CHEMBL2022968 DUBERMATINIB IC50 = 27.0 nM 7.57
CHEMBL5557653 IC50 = 43.9 nM 7.36
CHEMBL3809908 IC50 = 58.0 nM 7.24
CHEMBL288441 BOSUTINIB IC50 = 560.0 nM 6.25
CHEMBL5189859 IC50 = 2600.0 nM 5.58