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Assay Detail

CHEMBL4839494

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

Binding
Inhibition of human recombinant CSF1R using ATP/Ulight-TK peptide incubated for 15 mins
13
Total Activities
13
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

Macrophage colony-stimulating factor 1 receptor (CHEMBL1844)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of Potent Antiallergic Agents Based on an <i>o</i>-Aminopyridinyl Alkynyl Scaffold.
Xie Z, Xiang C, Li X, Fan C, Chen T, Liu M, Ma Y, Bai F, Tang W, Hu Y.
J Med Chem (2021) 64 : 13588 -13603
PubMed 34476950 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 8.17 9.15

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4576115 1 9.15
CHEMBL4438121 1 8.89
CHEMBL4517659 1 8.62
CHEMBL4553298 1 8.59
CHEMBL4589346 1 8.52
CHEMBL4467948 1 8.23
CHEMBL4854948 1 8.10
CHEMBL1171837 PONATINIB 4.0 1 8.07
CHEMBL3813873 PEXIDARTINIB 4.0 1 7.89
CHEMBL4850154 1 7.66
CHEMBL4854116 1 7.62
CHEMBL4869362 1 7.52
CHEMBL4862806 1 7.32

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4576115 IC50 = 0.7 nM 9.15
CHEMBL4438121 IC50 = 1.3 nM 8.89
CHEMBL4517659 IC50 = 2.4 nM 8.62
CHEMBL4553298 IC50 = 2.6 nM 8.59
CHEMBL4589346 IC50 = 3.0 nM 8.52
CHEMBL4467948 IC50 = 5.9 nM 8.23
CHEMBL4854948 IC50 = 8.0 nM 8.10
CHEMBL1171837 PONATINIB IC50 = 8.6 nM 8.07
CHEMBL3813873 PEXIDARTINIB IC50 = 13.0 nM 7.89
CHEMBL4850154 IC50 = 22.0 nM 7.66
CHEMBL4854116 IC50 = 24.0 nM 7.62
CHEMBL4869362 IC50 = 30.0 nM 7.52
CHEMBL4862806 IC50 = 48.0 nM 7.32