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Assay Detail

CHEMBL2015571

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

Binding
Inhibition of human recombinant Trx1/TrxR assessed as reduction in number of free thiols from reduced insulin after 30 mins by insulin reduction assay
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Studies toward novel peptidomimetic inhibitors of thioredoxin-thioredoxin reductase system.
Kłossowski S, Muchowicz A, Firczuk M, Swiech M, Redzej A, Golab J, Ostaszewski R.
J Med Chem (2012) 55 : 55 -67
PubMed 22128876 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 5.59 6.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2010865 1 6.70
CHEMBL2010864 1 6.40
CHEMBL1255721 METHYL BROMOMETHYL ACRYLATE 1 6.36
CHEMBL1974159 1 5.92
CHEMBL2010863 1 5.62
CHEMBL2010867 1 5.52
CHEMBL2010866 1 5.48
CHEMBL2010860 1 5.41
CHEMBL2010861 1 5.05
CHEMBL2010859 1 5.00
CHEMBL406050 PX-12 2.0 1 4.91
CHEMBL2010858 1 4.65
CHEMBL2010857 1 -
CHEMBL2010854 1 -
CHEMBL2010804 1 -
CHEMBL2010855 1 -
CHEMBL2010856 1 -
CHEMBL2010862 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2010865 IC50 = 200.0 nM 6.70
CHEMBL2010864 IC50 = 400.0 nM 6.40
CHEMBL1255721 METHYL BROMOMETHYL ACRYLATE IC50 = 440.0 nM 6.36
CHEMBL1974159 IC50 = 1200.0 nM 5.92
CHEMBL2010863 IC50 = 2400.0 nM 5.62
CHEMBL2010867 IC50 = 3000.0 nM 5.52
CHEMBL2010866 IC50 = 3300.0 nM 5.48
CHEMBL2010860 IC50 = 3900.0 nM 5.41
CHEMBL2010861 IC50 = 8900.0 nM 5.05
CHEMBL2010859 IC50 = 10000.0 nM 5.00
CHEMBL406050 PX-12 IC50 = 12300.0 nM 4.91
CHEMBL2010858 IC50 = 22300.0 nM 4.65
CHEMBL2010857 IC50 > 50000.0 nM -
CHEMBL2010854 IC50 > 50000.0 nM -
CHEMBL2010804 IC50 > 50000.0 nM -
CHEMBL2010855 IC50 > 50000.0 nM -
CHEMBL2010856 IC50 > 50000.0 nM -
CHEMBL2010862 IC50 > 50000.0 nM -