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Assay Detail

CHEMBL2039587

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

Binding
Inhibition of TrxR in human U87MG cells after 12 hrs by insulin-reducing method
6
Total Activities
5
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type U-87MG ATCC
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Thioredoxin reductase (CHEMBL2096978)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

Inhibition of thioredoxin reductase by a novel series of bis-1,2-benzisoselenazol-3(2H)-ones: Organoselenium compounds for cancer therapy.
He J, Li D, Xiong K, Ge Y, Jin H, Zhang G, Hong M, Tian Y, Yin J, Zeng H.
Bioorg Med Chem (2012) 20 : 3816 -3827
PubMed 22579620 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Inhibition 4 - -
IC50 2 5.50 5.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2035489 1 5.70
CHEMBL2035460 ETHASELEN 1.0 2 5.30
CHEMBL2035470 1 -
CHEMBL2035482 1 -
CHEMBL2035484 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2035489 IC50 = 2000.0 nM 5.70
CHEMBL2035460 ETHASELEN IC50 = 5000.0 nM 5.30
CHEMBL2035460 ETHASELEN Inhibition - % -
CHEMBL2035470 Inhibition - % -
CHEMBL2035482 Inhibition - % -
CHEMBL2035484 Inhibition - % -