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Assay Detail

CHEMBL1763750

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

Binding
Inhibition of FAAH in human T84 cell assessed as conversion of [3H]AEA to [3H]ethanolamine by scintillation counting
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type T84
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

Identification of potent, noncovalent fatty acid amide hydrolase (FAAH) inhibitors.
Gustin DJ, Ma Z, Min X, Li Y, Hedberg C, Guimaraes C, Porter AC, Lindstrom M, Lester-Zeiner D, Xu G, Carlson TJ, Xiao S, Meleza C, Connors R, Wang Z, Kayser F.
Bioorg Med Chem Lett (2011) 21 : 2492 -2496
PubMed 21392988 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 4 7.85 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1761302 1 8.70
CHEMBL1761301 1 8.52
CHEMBL1761304 1 7.70
CHEMBL1761300 1 6.46

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1761302 EC50 = 2.0 nM 8.70
CHEMBL1761301 EC50 = 3.0 nM 8.52
CHEMBL1761304 EC50 = 20.0 nM 7.70
CHEMBL1761300 EC50 = 350.0 nM 6.46