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Assay Detail

CHEMBL829699

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Binding
Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from human expressed in COS-7 cells
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type COS-7
Confidence 9 — Direct single protein target
Curated By Expert

Target

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

Publication

Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics.
Boger DL, Miyauchi H, Du W, Hardouin C, Fecik RA, Cheng H, Hwang I, Hedrick MP, Leung D, Acevedo O, Guimarães CR, Jorgensen WL, Cravatt BF.
J Med Chem (2005) 48 : 1849 -1856
PubMed 15771430 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 3 7.80 8.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL177577 1 8.05
CHEMBL426230 1 8.00
CHEMBL39412 1 7.35

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL177577 Ki = 9.0 nM 8.05
CHEMBL426230 Ki = 10.0 nM 8.00
CHEMBL39412 Ki = 45.0 nM 7.35