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Assay Detail

CHEMBL888482

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

Binding
Inhibition of human FAAH expressed in CHO cells
5
Total Activities
5
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 Intermediate

Target

Fatty-acid amide hydrolase 1 (CHEMBL2243)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-activity relationships of alpha-ketooxazole inhibitors of fatty acid amide hydrolase.
Hardouin C, Kelso MJ, Romero FA, Rayl TJ, Leung D, Hwang I, Cravatt BF, Boger DL.
J Med Chem (2007) 50 : 3359 -3368
PubMed 17559203 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 5 8.87 9.35

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL427424 1 9.35
CHEMBL410598 1 9.22
CHEMBL226883 1 8.92
CHEMBL227046 1 8.54
CHEMBL226938 1 8.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL427424 Ki = 0.45 nM 9.35
CHEMBL410598 Ki = 0.6 nM 9.22
CHEMBL226883 Ki = 1.2 nM 8.92
CHEMBL227046 Ki = 2.9 nM 8.54
CHEMBL226938 Ki = 5.0 nM 8.30