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Assay Detail

CHEMBL651916

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

Binding
Concentration required for 50% inhibition of [125I]eotaxin binding to human CCR1 receptor expressed in CHO cells
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type CHO
Confidence 9 — Direct single protein target
Curated By Expert

Target

C-C chemokine receptor type 1 (CHEMBL2413)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of a novel CCR3 selective antagonist.
Naya A, Kobayashi K, Ishikawa M, Ohwaki K, Saeki T, Noguchi K, Ohtake N.
Bioorg Med Chem Lett (2001) 11 : 1219 -1223
PubMed 11354381 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 6.24 9.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL277930 1 9.05
CHEMBL282285 1 6.58
CHEMBL20532 1 6.35
CHEMBL20921 1 5.72
CHEMBL21143 1 5.44
CHEMBL21199 1 5.38
CHEMBL20539 1 5.15
CHEMBL266181 1 -
CHEMBL20612 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL277930 IC50 = 0.9 nM 9.05
CHEMBL282285 IC50 = 260.0 nM 6.58
CHEMBL20532 IC50 = 450.0 nM 6.35
CHEMBL20921 IC50 = 1900.0 nM 5.72
CHEMBL21143 IC50 = 3600.0 nM 5.44
CHEMBL21199 IC50 = 4200.0 nM 5.38
CHEMBL20539 IC50 = 7100.0 nM 5.15
CHEMBL266181 IC50 > 10000.0 nM -
CHEMBL20612 IC50 > 10000.0 nM -