Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL3398941

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

Binding
Inhibition of Trypanosoma cruzi trypanothione reductase assessed as reduction of trypanothione disulfide by spectrophotometrically
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Trypanosoma cruzi
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Trypanothione reductase (CHEMBL5131)
Type SINGLE PROTEIN
Organism Trypanosoma cruzi

Publication

Dibenzosuberyl substituted polyamines and analogs of clomipramine as effective inhibitors of trypanothione reductase; molecular docking, and assessment of trypanocidal activities.
O'Sullivan MC, Durham TB, Valdes HE, Dauer KL, Karney NJ, Forrestel AC, Bacchi CJ, Baker JF.
Bioorg Med Chem (2015) 23 : 996 -1010
PubMed 25661449 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 7 5.16 6.59

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3398189 1 6.59
CHEMBL378650 1 5.40
CHEMBL415 CLOMIPRAMINE 4.0 1 5.19
CHEMBL3398188 1 5.12
CHEMBL3398187 1 4.55
CHEMBL3398186 1 4.09
CHEMBL332939 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3398189 Ki = 255.0 nM 6.59
CHEMBL378650 Ki = 4000.0 nM 5.40
CHEMBL415 CLOMIPRAMINE Ki = 6500.0 nM 5.19
CHEMBL3398188 Ki = 7620.0 nM 5.12
CHEMBL3398187 Ki = 27900.0 nM 4.55
CHEMBL3398186 Ki = 81600.0 nM 4.09
CHEMBL332939 Ki = 136000.0 nM -