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Assay Detail

CHEMBL3423533

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

Binding
Inhibition of human recombinant FAAH using AMC arachidonoyl amide as substrate preincubated with protein for 30 mins followed by substrate addition by fluorescence assay
3
Total Activities
3
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

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

Publication

Pyrazole phenylcyclohexylcarbamates as inhibitors of human fatty acid amide hydrolases (FAAH).
Aghazadeh Tabrizi M, Baraldi PG, Ruggiero E, Saponaro G, Baraldi S, Romagnoli R, Martinelli A, Tuccinardi T.
Eur J Med Chem (2015) 97 : 289 -305
PubMed 26002335 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 8.04 8.46

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL570812 1 8.46
CHEMBL184238 URB-597 1.0 1 7.89
CHEMBL3422944 1 7.77

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL570812 IC50 = 3.5 nM 8.46
CHEMBL184238 URB-597 IC50 = 13.0 nM 7.89
CHEMBL3422944 IC50 = 17.0 nM 7.77