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Assay Detail

CHEMBL828872

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

Binding
Inhibition of [3H]MRE3008-F20 binding to human adenosine A3 receptor expressed in CHO cells; range is 77 to 129
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type CHO
Confidence 9 — Direct single protein target
Curated By Expert

Target

Adenosine receptor A3 (CHEMBL256)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

New pyrrolo[2,1-f]purine-2,4-dione and imidazo[2,1-f]purine-2,4-dione derivatives as potent and selective human A3 adenosine receptor antagonists.
Baraldi PG, Preti D, Tabrizi MA, Fruttarolo F, Romagnoli R, Zaid NA, Moorman AR, Merighi S, Varani K, Borea PA.
J Med Chem (2005) 48 : 4697 -4701
PubMed 16000006 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 1 7.00 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL191421 1 7.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL191421 Ki = 99.0 nM 7.00