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Assay Detail

CHEMBL3888044

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Binding
Scintillation Proximity Assay (SPA): Briefly, serial dilutions of the test compounds were placed in a 96-well plate to which were added SPA beads, membrane and radioligand. The assay conditions for each opioid receptor subtype are described in Table 10 below. The plates were incubated for 8 hours-overnight at room temperature, spun at 1000 rpm to pellet the SPA beads, and radioactivity was measured using the TopCount microplate Scintillation counter. Specific binding at each concentration of test compound was calculated by subtracting the non-specific binding measured in the presence of excess cold ligand. IC50 values were obtained by non-linear regression of specific binding versus concentration curves and Ki values were calculated using Kd values that were experimentally pre-determined for each lot of membrane preparations.
27
Total Activities
27
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

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

Publication

Oligomer-opioid agonist conjugates
(2016)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 27 6.30 8.07

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3923831 1 8.07
CHEMBL4110373 1 7.80
CHEMBL4107642 1 7.66
CHEMBL4106506 1 7.64
CHEMBL4108649 1 7.41
CHEMBL4112562 1 7.29
CHEMBL4110642 1 7.25
CHEMBL4112722 1 7.14
CHEMBL4108525 1 6.95
CHEMBL656 OXYCODONE 4.0 1 6.88
CHEMBL4112234 1 6.20
CHEMBL4110656 1 6.18
CHEMBL4111500 1 6.11
CHEMBL4112727 1 6.05
CHEMBL3937789 1 5.86
CHEMBL4114370 1 5.79
CHEMBL3895828 1 5.74
CHEMBL4108425 1 5.73
CHEMBL4109078 1 5.72
CHEMBL2448883 1 5.71
CHEMBL3933053 1 5.62
CHEMBL3967811 1 5.54
CHEMBL4108254 1 5.44
CHEMBL3934684 1 5.37
CHEMBL3984515 1 5.00
CHEMBL3911284 1 5.00
CHEMBL3956767 1 4.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3923831 Ki = 8.44 nM 8.07
CHEMBL4110373 Ki = 15.72 nM 7.80
CHEMBL4107642 Ki = 21.97 nM 7.66
CHEMBL4106506 Ki = 23.11 nM 7.64
CHEMBL4108649 Ki = 39.4 nM 7.41
CHEMBL4112562 Ki = 50.66 nM 7.29
CHEMBL4110642 Ki = 56.86 nM 7.25
CHEMBL4112722 Ki = 72.98 nM 7.14
CHEMBL4108525 Ki = 111.05 nM 6.95
CHEMBL656 OXYCODONE Ki = 133.48 nM 6.88
CHEMBL4112234 Ki = 631.76 nM 6.20
CHEMBL4110656 Ki = 653.9 nM 6.18
CHEMBL4111500 Ki = 775.19 nM 6.11
CHEMBL4112727 Ki = 892.7 nM 6.05
CHEMBL3937789 Ki = 1383.07 nM 5.86
CHEMBL4114370 Ki = 1607.19 nM 5.79
CHEMBL3895828 Ki = 1821.51 nM 5.74
CHEMBL4108425 Ki = 1862.14 nM 5.73
CHEMBL4109078 Ki = 1898.3 nM 5.72
CHEMBL2448883 Ki = 1953.0 nM 5.71
CHEMBL3933053 Ki = 2427.13 nM 5.62
CHEMBL3967811 Ki = 2891.36 nM 5.54
CHEMBL4108254 Ki = 3616.6 nM 5.44
CHEMBL3934684 Ki = 4260.21 nM 5.37
CHEMBL3984515 Ki = 9963.93 nM 5.00
CHEMBL3911284 Ki = 9975.84 nM 5.00
CHEMBL3956767 Ki = 14202.77 nM 4.85