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Assay Detail

CHEMBL5733142

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Binding
Radioligand Binding Assay: Rat and Human Orexin 1 Receptor:Human Embryonic Kidney 293 cells (HEK293) stably expressing rat orexin 1 receptor (Genebank accession number NM_001525) or Chinese ovary cells (CHO) stably expressing human orexin 1 receptor (Genebank accession number NM_001526) were grown to confluency in DMEM (Hyclone, cat # SH30022), 10% FBS, 1× Pen/Strep, 1× sodium pyruvate, 10 mM HEPES, 600 μg/mL G418 and DMEM/F12 (Gibco, Cat #11039), 10% FBS, 1× Pen/Strep, 600 μg/mL G418 media, respectively on 150 cm2 tissue culture plates, washed with 5 mM EDTA in PBS (HyClone Dulbecco's Phosphate Buffered Saline 1× with Calcium and Magnesium, Cat # SH30264.01, hereafter referred to simply as PBS) and scraped into 50 ml tubes. After centrifugation (2K×G, 5 min at 4° C.), the supernatant was aspirated and the pellets frozen and stored at −80° C. Cells were resuspended in PBS in the presence of 1 tablet of protease inhibitor cocktail (Roche, Cat. #11836145001) per 50 mL. Each cell pellet from a 15 cm plate was resuspended in 10 mL, stored on ice, and homogenized for 45 sec prior to addition to the reactions. Competition binding experiments in 96 well polypropylene plates were performed using [3H]-(1-(5-(2-fluoro-phenyl)-2-methyl-thiazol-4-yl)-1-((S)-2-(5-phenyl-(1,3,4)oxadiazol-2-ylmethyl)-pyrrolidin-1-yl)-methanone) (Moraveck Corporation, specific activity=35.3 Ci/mmol), diluted to a 10 nM concentration in PBS (4 nM final). Compounds were solubilized in 100% DMSO (Acros Organics, Cat. #61042-1000) and tested over a range of 7 concentrations (from 0.1 nM to 10 μM). The final concentration of DMSO in the reactions is equal to or less than 0.1%. Total and nonspecific binding was determined in the absence and presence of 10 μM almorexant. The total volume of each reaction is 200 μL (20 μL of diluted compounds, 80 μL of [3H]-(1-(5-(2-fluoro-phenyl)-2-methyl-thiazol-4-yl)-1-((S)-2-(5-phenyl-(1,3,4)oxadiazol-2-ylmethyl)-pyrrolidin-1-yl)-methanone) diluted in PBS and 100 μL of the cell suspension). Reactions were run for 60 min at room temperature and terminated by filtration through GF/C filter plates (PerkinElmer, Cat. #6005174) presoaked in 0.3% polyethylenimine using the cell harvester (PerkinElmer Filtermate). The plates were washed 3 times by aspirating 30 ml PBS through the plates. Plates were dried in 55° C. oven for 60 min, scintillation fluid was added, and the radioactivity was counted on a Topcount (Packard).
171
Total Activities
47
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Orexin/Hypocretin receptor type 1 (CHEMBL1075232)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Substituted 2-azabicycles and their use as orexin receptor modulators
(2017)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 57 7.61 8.52
kon 57 - -
k_off 57 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3691846 3 8.52
CHEMBL3691841 3 8.52
CHEMBL3691829 3 8.52
CHEMBL3691848 3 8.52
CHEMBL3691851 3 8.40
CHEMBL3691814 6 8.40
CHEMBL3691810 6 8.30
CHEMBL3691847 3 8.30
CHEMBL3691852 3 8.22
CHEMBL3691850 3 8.22
CHEMBL3691842 3 8.22
CHEMBL3691843 3 8.15
CHEMBL3691840 3 8.15
CHEMBL3691849 3 8.10
CHEMBL3691833 3 8.10
CHEMBL3691820 3 8.10
CHEMBL3691819 6 8.10
CHEMBL3691821 6 8.00
CHEMBL3691823 6 7.92
CHEMBL3691817 6 7.80
CHEMBL3691811 3 7.80
CHEMBL3691835 3 7.80
CHEMBL3691818 3 7.77
CHEMBL3691825 12 7.77
CHEMBL3691822 3 7.75
CHEMBL3691813 3 7.75
CHEMBL3691827 3 7.72
CHEMBL3691838 3 7.66
CHEMBL3691812 6 7.50
CHEMBL3691815 3 7.36

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3691848 Ki = 3.0 nM 8.52
CHEMBL3691846 Ki = 3.0 nM 8.52
CHEMBL3691841 Ki = 3.0 nM 8.52
CHEMBL3691829 Ki = 3.0 nM 8.52
CHEMBL3691851 Ki = 4.0 nM 8.40
CHEMBL3691814 Ki = 4.0 nM 8.40
CHEMBL3691810 Ki = 5.0 nM 8.30
CHEMBL3691847 Ki = 5.0 nM 8.30
CHEMBL3691852 Ki = 6.0 nM 8.22
CHEMBL3691850 Ki = 6.0 nM 8.22
CHEMBL3691842 Ki = 6.0 nM 8.22
CHEMBL3691843 Ki = 7.0 nM 8.15
CHEMBL3691840 Ki = 7.0 nM 8.15
CHEMBL3691833 Ki = 8.0 nM 8.10
CHEMBL3691819 Ki = 8.0 nM 8.10
CHEMBL3691849 Ki = 8.0 nM 8.10
CHEMBL3691819 Ki = 8.0 nM 8.10
CHEMBL3691820 Ki = 8.0 nM 8.10
CHEMBL3691821 Ki = 10.0 nM 8.00
CHEMBL3691814 Ki = 11.0 nM 7.96
CHEMBL3691823 Ki = 12.0 nM 7.92
CHEMBL3691823 Ki = 15.0 nM 7.82
CHEMBL3691817 Ki = 16.0 nM 7.80
CHEMBL3691817 Ki = 16.0 nM 7.80
CHEMBL3691835 Ki = 16.0 nM 7.80
CHEMBL3691811 Ki = 16.0 nM 7.80
CHEMBL3691825 Ki = 17.0 nM 7.77
CHEMBL3691818 Ki = 17.0 nM 7.77
CHEMBL3691813 Ki = 18.0 nM 7.75
CHEMBL3691822 Ki = 18.0 nM 7.75
CHEMBL3691827 Ki = 19.0 nM 7.72
CHEMBL3691825 Ki = 20.0 nM 7.70
CHEMBL3691810 Ki = 21.0 nM 7.68
CHEMBL3691838 Ki = 22.0 nM 7.66
CHEMBL3691825 Ki = 25.0 nM 7.60
CHEMBL3691821 Ki = 25.0 nM 7.60
CHEMBL3691812 Ki = 32.0 nM 7.50
CHEMBL3691815 Ki = 44.0 nM 7.36
CHEMBL3691816 Ki = 52.0 nM 7.28
CHEMBL3691826 Ki = 55.0 nM 7.26
CHEMBL3691812 Ki = 56.0 nM 7.25
CHEMBL3691839 Ki = 60.0 nM 7.22
CHEMBL3691808 Ki = 63.0 nM 7.20
CHEMBL3691830 Ki = 74.0 nM 7.13
CHEMBL3691806 Ki = 74.0 nM 7.13
CHEMBL3691831 Ki = 117.0 nM 6.93
CHEMBL3691834 Ki = 132.0 nM 6.88
CHEMBL3691832 Ki = 170.0 nM 6.77
CHEMBL3691837 Ki = 184.0 nM 6.74
CHEMBL3691807 Ki = 200.0 nM 6.70