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Assay Detail

CHEMBL4624587

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

Binding
Inhibition of FAAH (unknown origin)
1
Total Activities
1
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

The discovery of azetidine-piperazine di-amides as potent, selective and reversible monoacylglycerol lipase (MAGL) inhibitors.
Zhu B, Connolly PJ, Zhang YM, McDonnell ME, Bian H, Lin SC, Liu L, Zhang SP, Chevalier KM, Brandt MR, Milligan CM, Flores CM, Macielag MJ.
Bioorg Med Chem Lett (2020) 30 : 127243 -127243
PubMed 32527545 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 5.40 5.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3658400 1 5.40

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3658400 IC50 = 4000.0 nM 5.40