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Assay Detail

CHEMBL3398943

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

Functional
Trypanocidal activity against drug-sensitive Trypanosoma brucei brucei Lab 110 EATRO assessed as inhibition of trypanosomes after 48 hrs
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Trypanosoma brucei brucei
Confidence 1 — Organism
Curated By Autocuration

Target

Trypanosoma brucei brucei (CHEMBL612851)
Type ORGANISM
Organism Trypanosoma brucei brucei

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
IC50 6 5.80 6.21

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL378650 1 6.21
CHEMBL3398186 1 5.86
CHEMBL332939 1 5.78
CHEMBL3398189 1 5.59
CHEMBL3398187 1 5.55
CHEMBL3398188 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL378650 IC50 = 620.0 nM 6.21
CHEMBL3398186 IC50 = 1380.0 nM 5.86
CHEMBL332939 IC50 = 1680.0 nM 5.78
CHEMBL3398189 IC50 = 2550.0 nM 5.59
CHEMBL3398187 IC50 = 2800.0 nM 5.55
CHEMBL3398188 IC50 - -