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Assay Detail

CHEMBL3887795

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

Functional
Functional Assay: Functional [35S]GTPgammaS binding assays were conducted as follows. Delta opioid receptor membrane solution was prepared by sequentially adding final concentrations of 0.026 ug/ul delta membrane protein (Perkin Elmer, Shelton, Conn.), 10 ug/mL saponin, 3 uM GDP and 0.20 nM [35S]GTPgammaS to binding buffer (100 mM NaCl, 10 mM MgCl2, 20 mM HEPES, pH 7.4) on ice. The prepared membrane solution (190 ul/well) was transferred to 96-shallow well polypropylene plates containing 10 ul of 20x concentrated stock solutions of agonist prepared in DMSO. Plates were incubated for 30 min at a temperature of about 25° C. with shaking. Reactions were terminated by rapid filtration onto 96-well Unifilter GF/B filter plates (Perkin Elmer, Shelton, Conn.) using a 96-well tissue harvester (Packard) and followed by three filtration washes with 200 ul ice-cold binding buffer (10 mM NaH2PO4, 10 mM Na2HPO4, pH 7.4). Filter plates were subsequently dried at 50° C. for 1-2 hours.
38
Total Activities
38
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Delta-type opioid receptor (CHEMBL236)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Buprenorphine analogs
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 38 6.78 9.09

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4115222 1 9.09
CHEMBL3916122 1 7.83
CHEMBL4111231 1 7.76
CHEMBL4111717 1 7.66
CHEMBL4111224 1 7.65
CHEMBL4107681 1 7.34
CHEMBL4111124 1 7.24
CHEMBL4107627 1 7.24
CHEMBL4109061 1 7.18
CHEMBL4108017 1 7.18
CHEMBL4107906 1 7.17
CHEMBL4115091 1 7.12
CHEMBL4114477 1 7.07
CHEMBL4110312 1 7.06
CHEMBL4112771 1 6.89
CHEMBL4107821 1 6.89
CHEMBL4109652 1 6.87
CHEMBL4112051 1 6.82
CHEMBL4109220 1 6.78
CHEMBL4112656 1 6.75
CHEMBL4107918 1 6.75
CHEMBL4115338 1 6.72
CHEMBL4106544 1 6.67
CHEMBL4108066 1 6.64
CHEMBL4112472 1 6.64
CHEMBL4107680 1 6.56
CHEMBL4111244 1 6.40
CHEMBL4109142 1 6.39
CHEMBL4112358 1 6.37
CHEMBL4111233 1 6.32

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4115222 EC50 = 0.82 nM 9.09
CHEMBL3916122 EC50 = 14.69 nM 7.83
CHEMBL4111231 EC50 = 17.32 nM 7.76
CHEMBL4111717 EC50 = 22.0 nM 7.66
CHEMBL4111224 EC50 = 22.25 nM 7.65
CHEMBL4107681 EC50 = 45.67 nM 7.34
CHEMBL4111124 EC50 = 57.22 nM 7.24
CHEMBL4107627 EC50 = 57.56 nM 7.24
CHEMBL4109061 EC50 = 66.23 nM 7.18
CHEMBL4108017 EC50 = 66.45 nM 7.18
CHEMBL4107906 EC50 = 67.82 nM 7.17
CHEMBL4115091 EC50 = 75.3 nM 7.12
CHEMBL4114477 EC50 = 86.0 nM 7.07
CHEMBL4110312 EC50 = 87.47 nM 7.06
CHEMBL4107821 EC50 = 128.96 nM 6.89
CHEMBL4112771 EC50 = 128.05 nM 6.89
CHEMBL4109652 EC50 = 135.49 nM 6.87
CHEMBL4112051 EC50 = 151.21 nM 6.82
CHEMBL4109220 EC50 = 164.73 nM 6.78
CHEMBL4112656 EC50 = 175.81 nM 6.75
CHEMBL4107918 EC50 = 175.75 nM 6.75
CHEMBL4115338 EC50 = 188.68 nM 6.72
CHEMBL4106544 EC50 = 211.43 nM 6.67
CHEMBL4108066 EC50 = 231.32 nM 6.64
CHEMBL4112472 EC50 = 229.26 nM 6.64
CHEMBL4107680 EC50 = 272.8 nM 6.56
CHEMBL4111244 EC50 = 399.74 nM 6.40
CHEMBL4109142 EC50 = 409.6 nM 6.39
CHEMBL4112358 EC50 = 430.63 nM 6.37
CHEMBL4111233 EC50 = 482.06 nM 6.32
CHEMBL4113058 EC50 = 526.04 nM 6.28
CHEMBL4107470 EC50 = 555.58 nM 6.25
CHEMBL4111378 EC50 = 640.21 nM 6.19
CHEMBL4111803 EC50 = 778.12 nM 6.11
CHEMBL4114002 EC50 = 841.4 nM 6.08
CHEMBL4113804 EC50 = 5622.35 nM 5.25
CHEMBL4110639 EC50 = 6061.62 nM 5.22
CHEMBL4106985 EC50 = 8113.67 nM 5.09