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Assay Detail

CHEMBL5543640

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

Binding
Inhibition of AXL (unknown origin)
3
Total Activities
3
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

Structure-activity relationship study of 1,6-naphthyridinone derivatives as selective type II AXL inhibitors with potent antitumor efficacy.
Zhuo L, Guo M, Zhang S, Wu J, Wang M, Shen Y, Peng X, Wang Z, Jiang W, Huang W.
Eur J Med Chem (2024) 265 : 116090 -116090
PubMed 38169272 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 8.62 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3984441 NINGETINIB 2.0 1 9.00
CHEMBL3545307 MERESTINIB 2.0 1 8.70
CHEMBL4776274 1 8.15

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3984441 NINGETINIB IC50 = 1.0 nM 9.00
CHEMBL3545307 MERESTINIB IC50 = 2.0 nM 8.70
CHEMBL4776274 IC50 = 7.0 nM 8.15