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Assay Detail

CHEMBL5581996

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

Binding
Inhibition of TRKA F589L mutant (unknown origin) using TK as substrate incubated for 30 mins in presence of ATP by HTRF assay
7
Total Activities
7
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

High affinity nerve growth factor receptor (CHEMBL2815)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of novel indazole derivatives as second-generation TRK inhibitors.
Qin Q, Lu S, Guo Z, Li Z, Fu Q, Wang X, Wu T, Sun Y, Liu N, Zhang H, Zhao D, Cheng M.
Eur J Med Chem (2024) 276 : 116640 -116640
PubMed 39033612 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 8.51 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5594048 1 9.00
CHEMBL5592878 1 9.00
CHEMBL5593896 1 8.70
CHEMBL5594742 1 8.52
CHEMBL4297627 SELITRECTINIB 2.0 1 8.22
CHEMBL5594862 1 8.10
CHEMBL5590602 1 8.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5594048 IC50 = 1.0 nM 9.00
CHEMBL5592878 IC50 = 1.0 nM 9.00
CHEMBL5593896 IC50 = 2.0 nM 8.70
CHEMBL5594742 IC50 = 3.0 nM 8.52
CHEMBL4297627 SELITRECTINIB IC50 = 6.0 nM 8.22
CHEMBL5594862 IC50 = 8.0 nM 8.10
CHEMBL5590602 IC50 = 10.0 nM 8.00