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Assay Detail

CHEMBL786456

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

Functional
Inhibition of [3H]S-(4-Nitrobenzyl)-6-thioinosine binding to adenosine uptake sites in rat brain membranes
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Rattus norvegicus
Tissue Brain
Subcellular Brain membranes
Confidence 9 — Direct single protein target
Curated By Expert

Target

Equilibrative nucleoside transporter 1 (CHEMBL4604)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptors.
Kim HO, Ji XD, Siddiqi SM, Olah ME, Stiles GL, Jacobson KA.
J Med Chem (1994) 37 : 3614 -3621
PubMed 7932588 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 3 5.27 6.69

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL388757 N6-BENZYLADENOSINE 1 6.69
CHEMBL431733 NAMODENOSON 3.0 1 4.82
CHEMBL2113557 1 4.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL388757 N6-BENZYLADENOSINE Ki = 203.0 nM 6.69
CHEMBL431733 NAMODENOSON Ki = 15200.0 nM 4.82
CHEMBL2113557 Ki = 49500.0 nM 4.30