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Assay Detail

CHEMBL839160

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

Binding
Binding inhibition constant was determined by inhibition of [125I]iodocyanopindolol binding to Beta-3 adrenergic receptor
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Beta-3 adrenergic receptor (CHEMBL246)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Tryptamine-based human beta3-adrenergic receptor agonists. Part 1: SAR studies of the 7-position of the indole ring.
Mizuno K, Sawa M, Harada H, Tateishi H, Oue M, Tsujiuchi H, Furutani Y, Kato S.
Bioorg Med Chem Lett (2004) 14 : 5959 -5962
PubMed 15546707 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 4 7.89 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL184407 1 8.40
CHEMBL361505 1 7.85
CHEMBL188196 1 7.77
CHEMBL185836 1 7.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL184407 Ki = 4.0 nM 8.40
CHEMBL361505 Ki = 14.0 nM 7.85
CHEMBL188196 Ki = 17.0 nM 7.77
CHEMBL185836 Ki = 30.0 nM 7.52