Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL747707

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

Binding
Displacement of [3H]naloxone from human mu opioid receptor
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Expert

Target

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

Publication

8-acenaphthen-1-yl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one derivatives as orphanin FQ receptor agonists.
Wichmann J, Adam G, Röver S, Cesura AM, Dautzenberg FM, Jenck F.
Bioorg Med Chem Lett (1999) 9 : 2343 -2348
PubMed 10476866 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 14 7.75 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL78156 1 8.40
CHEMBL355202 1 8.40
CHEMBL281274 1 8.20
CHEMBL77877 1 8.10
CHEMBL308522 1 8.00
CHEMBL1907858 1 7.90
CHEMBL419272 1 7.90
CHEMBL312021 1 7.70
CHEMBL78163 1 7.70
CHEMBL306150 1 7.60
CHEMBL77324 1 7.50
CHEMBL311185 1 7.40
CHEMBL75676 1 7.30
CHEMBL431002 1 6.40

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL78156 Ki = 3.981 nM 8.40
CHEMBL355202 Ki = 3.981 nM 8.40
CHEMBL281274 Ki = 6.31 nM 8.20
CHEMBL77877 Ki = 7.943 nM 8.10
CHEMBL308522 Ki = 10.0 nM 8.00
CHEMBL1907858 Ki = 12.59 nM 7.90
CHEMBL419272 Ki = 12.59 nM 7.90
CHEMBL312021 Ki = 19.95 nM 7.70
CHEMBL78163 Ki = 19.95 nM 7.70
CHEMBL306150 Ki = 25.12 nM 7.60
CHEMBL77324 Ki = 31.62 nM 7.50
CHEMBL311185 Ki = 39.81 nM 7.40
CHEMBL75676 Ki = 50.12 nM 7.30
CHEMBL431002 Ki = 398.11 nM 6.40