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Assay Detail

CHEMBL5739186

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Binding
Binding Affinities to Different Adenosine Receptors: Binding affinity and specificities of the compounds against different subtype of human adenosine receptors (hA1, hA2A, hA2B and hA3) were characterized with cell membrane chromatography binding analysis. The compounds at different concentrations were incubate with hA1 membrane (from PerkinElmer) and [3H]-8-Cyclopentyl-1,3-dipropylxanthine (DPCPX) for 50 min at 25° C., meanwhile 100 μL 0.5% PEI solution was added into UNFILTER-96 GF/B filter plate for 60 min at 4° C., then UNIFILTER-96 GF/B filter plate was washed twice with 50 ml wash buffer, the membrane mix was transferred into UNIFILTER-96 GF/B filter plate, and the filter plate was washed 4 times before incubated at 55° C. for 10 min. At last, 40 μL ULTIMA GOLD was added into each well, and CPM was read by TopCount.The compounds at different concentrations were incubate with hA2a membrane (from PerkinElmer) and [3H]-CGS21680 for 90 min at 25° C., meanwhile 100 μL 0.5% PEI solution was added into UNFILTER-96 GF/B filter plate for 60 min at 4° C., then UNIFILTER-96 GF/B filter plate was washed twice with 50 ml wash buffer, the membrane mix was transferred into UNIFILTER-96 GF/B filter plate, and the filter plate was washed 4 timesbefore incubated at 55° C. for 10 min. At last, 40 μL ULTIMA GOLD was added into each well, and CPM was read by TopCount.
63
Total Activities
21
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

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

Target

Adenosine receptor A2a (CHEMBL251)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Triazolo-pyrimidine compounds and uses thereof
(2023)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 21 8.39 9.05
kon 21 - -
k_off 21 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5827075 3 9.05
CHEMBL5847654 3 8.85
CHEMBL5756623 3 8.68
CHEMBL5993458 3 8.64
CHEMBL5956015 3 8.55
CHEMBL5966778 3 8.55
CHEMBL6063197 3 8.52
CHEMBL5931362 3 8.47
CHEMBL6062538 3 8.46
CHEMBL6030840 3 8.44
CHEMBL5957422 3 8.40
CHEMBL6043653 3 8.39
CHEMBL5988628 3 8.38
CHEMBL6022055 3 8.28
CHEMBL5841873 3 8.26
CHEMBL5795044 3 8.26
CHEMBL5867675 3 8.20
CHEMBL6044836 3 8.14
CHEMBL5810207 3 8.08
CHEMBL5781725 3 7.92
CHEMBL6007073 3 7.70

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5827075 IC50 = 0.9 nM 9.05
CHEMBL5847654 IC50 = 1.4 nM 8.85
CHEMBL5756623 IC50 = 2.1 nM 8.68
CHEMBL5993458 IC50 = 2.3 nM 8.64
CHEMBL5966778 IC50 = 2.8 nM 8.55
CHEMBL5956015 IC50 = 2.8 nM 8.55
CHEMBL6063197 IC50 = 3.0 nM 8.52
CHEMBL5931362 IC50 = 3.4 nM 8.47
CHEMBL6062538 IC50 = 3.5 nM 8.46
CHEMBL6030840 IC50 = 3.6 nM 8.44
CHEMBL5957422 IC50 = 4.0 nM 8.40
CHEMBL6043653 IC50 = 4.1 nM 8.39
CHEMBL5988628 IC50 = 4.2 nM 8.38
CHEMBL6022055 IC50 = 5.2 nM 8.28
CHEMBL5795044 IC50 = 5.5 nM 8.26
CHEMBL5841873 IC50 = 5.5 nM 8.26
CHEMBL5867675 IC50 = 6.3 nM 8.20
CHEMBL6044836 IC50 = 7.2 nM 8.14
CHEMBL5810207 IC50 = 8.3 nM 8.08
CHEMBL5781725 IC50 = 12.0 nM 7.92
CHEMBL6007073 IC50 = 20.0 nM 7.70
CHEMBL6062538 kon = - -
CHEMBL6062538 k_off = - s-1 -
CHEMBL5847654 kon = - -
CHEMBL5993458 kon = - -
CHEMBL5993458 k_off = - s-1 -
CHEMBL5756623 kon = - -
CHEMBL5756623 k_off = - s-1 -
CHEMBL5827075 kon = - -
CHEMBL5827075 k_off = - s-1 -
CHEMBL5956015 kon = - -
CHEMBL5956015 k_off = - s-1 -
CHEMBL6007073 kon = - -
CHEMBL6007073 k_off = - s-1 -
CHEMBL5781725 kon = - -
CHEMBL5810207 k_off = - s-1 -
CHEMBL5810207 kon = - -
CHEMBL5795044 k_off = - s-1 -
CHEMBL5795044 kon = - -
CHEMBL6030840 k_off = - s-1 -
CHEMBL6030840 kon = - -
CHEMBL5867675 kon = - -
CHEMBL6043653 kon = - -
CHEMBL6044836 k_off = - s-1 -
CHEMBL6044836 kon = - -
CHEMBL5988628 kon = - -
CHEMBL5988628 k_off = - s-1 -
CHEMBL6022055 k_off = - s-1 -
CHEMBL6022055 kon = - -
CHEMBL6043653 k_off = - s-1 -