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Assay Detail

CHEMBL642156

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

Binding
Inhibition of [3H]DPCPX binding to human Adenosine A1 receptor expressed in CHO cells; Range 256-620
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 A1 (CHEMBL226)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

1,2,4-Triazolo[5,1-i]purine derivatives as highly potent and selective human adenosine A(3) receptor ligands.
Okamura T, Kurogi Y, Nishikawa H, Hashimoto K, Fujiwara H, Nagao Y.
J Med Chem (2002) 45 : 3703 -3708
PubMed 12166943 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 1 6.40 6.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL331111 1 6.40

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL331111 Ki = 398.0 nM 6.40