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Assay Detail

CHEMBL5731335

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Binding
Radioligand Competition Binding Assay: The binding affinities of certain compounds of the present invention were evaluated using radioligand binding assays in membranes prepared from CHO-K1 cells expressing recombinant human kappa (KOR) or mu (MOR) opioid receptors.Competition binding experiments were conducted by incubating membrane protein to equilibrium in triplicate in the presence of a fixed concentration of radioligand and increasing concentrations of test compound for evaluation of binding to KOR or single concentration (10 μM) of test compound for evaluation of binding to MOR in 101 μL final volume. The radioligands used were specific for each receptor type, and the assay conditions are described in Table 1. Following incubations, the membranes were rapidly filtered through GF/B filter plate (presoaked with 0.5% polyethyleneimine), washed five times with cold 50 mM Tris-HCl, pH 7.5, and the bound radioactivity was then measured by liquid scintillation counting. Non-specific binding was measured in the presence of excess ligand; this value was subtracted from the total binding to yield the specific binding at each test concentration.
57
Total Activities
12
Compounds Tested
4
Activity Types
0
Assay Parameters

Assay Information

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

Target

Kappa-type opioid receptor (CHEMBL237)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Opioid agonists and uses thereof
(2018)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
kon 19 - -
k_off 19 - -
Ki 12 6.72 8.89
IC50 7 5.87 8.25

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2107292 KETAZOCINE 2.0 6 8.89
CHEMBL6058797 3 8.54
CHEMBL6060876 3 8.30
CHEMBL5910909 6 6.69
CHEMBL5775609 3 6.31
CHEMBL5852665 6 6.26
CHEMBL6052078 6 6.21
CHEMBL5787972 6 6.11
CHEMBL5874561 3 6.02
CHEMBL6060565 3 5.98
CHEMBL5896197 6 5.85
CHEMBL5822795 6 5.53

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2107292 KETAZOCINE Ki = 1.3 nM 8.89
CHEMBL6058797 Ki = 2.86 nM 8.54
CHEMBL6060876 Ki = 5.0 nM 8.30
CHEMBL2107292 KETAZOCINE IC50 = 5.6 nM 8.25
CHEMBL5910909 Ki = 203.0 nM 6.69
CHEMBL5775609 Ki = 494.0 nM 6.31
CHEMBL5852665 Ki = 549.0 nM 6.26
CHEMBL6052078 Ki = 619.0 nM 6.21
CHEMBL5787972 Ki = 769.0 nM 6.11
CHEMBL5910909 IC50 = 879.0 nM 6.06
CHEMBL5874561 Ki = 955.0 nM 6.02
CHEMBL6060565 Ki = 1055.0 nM 5.98
CHEMBL5896197 Ki = 1403.0 nM 5.85
CHEMBL5852665 IC50 = 2380.0 nM 5.62
CHEMBL6052078 IC50 = 2682.0 nM 5.57
CHEMBL5822795 Ki = 2959.0 nM 5.53
CHEMBL5787972 IC50 = 3333.0 nM 5.48
CHEMBL5896197 IC50 = 6079.0 nM 5.22
CHEMBL5822795 IC50 = 12820.0 nM 4.89
CHEMBL5910909 k_off = - s-1 -
CHEMBL5910909 kon = - -
CHEMBL5787972 k_off = - s-1 -
CHEMBL5896197 kon = - -
CHEMBL5787972 k_off = - s-1 -
CHEMBL5787972 kon = - -
CHEMBL5852665 k_off = - s-1 -
CHEMBL5852665 kon = - -
CHEMBL5852665 k_off = - s-1 -
CHEMBL5852665 kon = - -
CHEMBL6052078 k_off = - s-1 -
CHEMBL6052078 kon = - -
CHEMBL6052078 k_off = - s-1 -
CHEMBL6052078 kon = - -
CHEMBL5787972 kon = - -
CHEMBL2107292 KETAZOCINE k_off = - s-1 -
CHEMBL2107292 KETAZOCINE kon = - -
CHEMBL2107292 KETAZOCINE k_off = - s-1 -
CHEMBL2107292 KETAZOCINE kon = - -
CHEMBL5874561 k_off = - s-1 -
CHEMBL5874561 kon = - -
CHEMBL5775609 k_off = - s-1 -
CHEMBL5775609 kon = - -
CHEMBL6060565 k_off = - s-1 -
CHEMBL6060565 kon = - -
CHEMBL6058797 k_off = - s-1 -
CHEMBL5896197 k_off = - s-1 -
CHEMBL5822795 kon = - -
CHEMBL6060876 kon = - -
CHEMBL6058797 kon = - -
CHEMBL6060876 k_off = - s-1 -