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Assay Detail

CHEMBL1786446

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

Binding
Displacement of [3H]DPN from human recombinant mu-type opioid receptor expressed in CHO cell membranes
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Mu-type opioid receptor (CHEMBL233)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-activity studies on the nociceptin/orphanin FQ receptor antagonist 1-benzyl-N-{3-[spiroisobenzofuran-1(3H),4'-piperidin-1-yl]propyl} pyrrolidine-2-carboxamide.
Trapella C, Fischetti C, Pela' M, Lazzari I, Guerrini R, Calo' G, Rizzi A, Camarda V, Lambert DG, McDonald J, Regoli D, Salvadori S.
Bioorg Med Chem (2009) 17 : 5080 -5095
PubMed 19527931 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 2 7.99 9.25

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL80 NALOXONE 4.0 1 9.25
CHEMBL1783826 1 6.72

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL80 NALOXONE Ki = 0.5623 nM 9.25
CHEMBL1783826 Ki = 190.55 nM 6.72