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Assay Detail

CHEMBL4023889

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

Functional
Antileishmanial activity against sodium stibogluconate resistant Leishmania donovani isolate BHU1 after 3 to 5 days
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Leishmania donovani
Confidence 1 — Organism
Curated By Autocuration

Target

Leishmania donovani (CHEMBL367)
Type ORGANISM
Organism Leishmania donovani

Publication

Development of (6 R)-2-Nitro-6-[4-(trifluoromethoxy)phenoxy]-6,7-dihydro-5 H-imidazo[2,1- b][1,3]oxazine (DNDI-8219): A New Lead for Visceral Leishmaniasis.
Thompson AM, O'Connor PD, Marshall AJ, Blaser A, Yardley V, Maes L, Gupta S, Launay D, Braillard S, Chatelain E, Wan B, Franzblau SG, Ma Z, Cooper CB, Denny WA.
J Med Chem (2018) 61 : 2329 -2352
PubMed 29461823 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 6.00 6.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL267345 AMPHOTERICIN B 4.0 1 6.70
CHEMBL4078293 1 5.87
CHEMBL125 MILTEFOSINE 4.0 1 5.42
CHEMBL4075089 1 -
CHEMBL370143 PAROMOMYCIN 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL267345 AMPHOTERICIN B IC50 = 200.0 nM 6.70
CHEMBL4078293 IC50 = 1340.0 nM 5.87
CHEMBL125 MILTEFOSINE IC50 = 3800.0 nM 5.42
CHEMBL4075089 IC50 > 150000.0 nM -
CHEMBL370143 PAROMOMYCIN IC50 > 30000.0 nM -