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Assay Detail

CHEMBL3405398

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

Binding
Inhibition of human FAAH using [ethanolamine 1-3H] substrate assessed as radioactivity by liquid scintillation counting analysis
6
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

Loratadine analogues as MAGL inhibitors.
Patel JZ, Ahenkorah S, Vaara M, Staszewski M, Adams Y, Laitinen T, Navia-Paldanius D, Parkkari T, Savinainen JR, Walczyński K, Laitinen JT, Nevalainen TJ.
Bioorg Med Chem Lett (2015) 25 : 1436 -1442
PubMed 25752982 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 5.21 5.32

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3087181 2 5.32
CHEMBL3402827 2 5.16
CHEMBL3401455 2 5.14

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3087181 IC50 = 4786.3 nM 5.32
CHEMBL3087181 IC50 = 4800.0 nM 5.32
CHEMBL3402827 IC50 = 6918.31 nM 5.16
CHEMBL3402827 IC50 = 6910.0 nM 5.16
CHEMBL3401455 IC50 = 7244.36 nM 5.14
CHEMBL3401455 IC50 = 7240.0 nM 5.14