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Assay Detail

CHEMBL615322

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

Binding
Inhibition of [125I]L-T3 binding to rat hepatic 3,5,3''-triiodo-L-thyronine receptor
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Synthesis and biological activity of phenoxyphenyl oxamic acid derivatives related to L-thyronine.
Stanton JL, Cahill E, Dotson R, Tan J, Tomaselli HC, Wasvary JM, Stephan ZF, Steele RE.
Bioorg Med Chem Lett (2000) 10 : 1661 -1663
PubMed 10937719 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 8.76 9.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL297540 1 9.77
CHEMBL46882 1 9.72
CHEMBL415889 1 9.60
CHEMBL297183 1 9.19
CHEMBL45371 1 9.04
CHEMBL1544 LIOTHYRONINE 4.0 1 8.96
CHEMBL46814 1 8.72
CHEMBL43544 1 8.72
CHEMBL44667 1 8.72
CHEMBL44809 1 8.70
CHEMBL42961 1 8.66
CHEMBL44052 1 8.27
CHEMBL47137 1 8.05
CHEMBL46796 1 7.85
CHEMBL288972 1 7.50

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL297540 IC50 = 0.17 nM 9.77
CHEMBL46882 IC50 = 0.19 nM 9.72
CHEMBL415889 IC50 = 0.25 nM 9.60
CHEMBL297183 IC50 = 0.64 nM 9.19
CHEMBL45371 IC50 = 0.92 nM 9.04
CHEMBL1544 LIOTHYRONINE IC50 = 1.1 nM 8.96
CHEMBL46814 IC50 = 1.9 nM 8.72
CHEMBL43544 IC50 = 1.9 nM 8.72
CHEMBL44667 IC50 = 1.9 nM 8.72
CHEMBL44809 IC50 = 2.0 nM 8.70
CHEMBL42961 IC50 = 2.2 nM 8.66
CHEMBL44052 IC50 = 5.4 nM 8.27
CHEMBL47137 IC50 = 9.0 nM 8.05
CHEMBL46796 IC50 = 14.0 nM 7.85
CHEMBL288972 IC50 = 32.0 nM 7.50