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Assay Detail

CHEMBL1008020

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

Functional
Antileishmanial activity against Leishmania donovani MHOM/ET/67/L82
15
Total Activities
15
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

In pursuit of natural product leads: synthesis and biological evaluation of 2-[3-hydroxy-2-[(3-hydroxypyridine-2-carbonyl)amino]phenyl]benzoxazole-4-carboxylic acid (A-33853) and its analogues: discovery of N-(2-benzoxazol-2-ylphenyl)benzamides as novel antileishmanial chemotypes.
Tipparaju SK, Joyasawal S, Pieroni M, Kaiser M, Brun R, Kozikowski AP.
J Med Chem (2008) 51 : 7344 -7347
PubMed 18989953 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 6.07 7.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL463985 1 7.10
CHEMBL125 MILTEFOSINE 4.0 1 6.58
CHEMBL463392 1 6.51
CHEMBL516329 1 6.29
CHEMBL518535 1 6.28
CHEMBL458800 1 6.17
CHEMBL463589 1 6.07
CHEMBL519040 1 6.03
CHEMBL458799 1 6.02
CHEMBL485748 1 5.93
CHEMBL458801 1 5.76
CHEMBL457699 1 5.72
CHEMBL514269 1 5.71
CHEMBL516007 1 5.51
CHEMBL457971 1 5.36

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL463985 IC50 = 80.0 nM 7.10
CHEMBL125 MILTEFOSINE IC50 = 260.0 nM 6.58
CHEMBL463392 IC50 = 310.0 nM 6.51
CHEMBL516329 IC50 = 510.0 nM 6.29
CHEMBL518535 IC50 = 520.0 nM 6.28
CHEMBL458800 IC50 = 680.0 nM 6.17
CHEMBL463589 IC50 = 850.0 nM 6.07
CHEMBL519040 IC50 = 930.0 nM 6.03
CHEMBL458799 IC50 = 960.0 nM 6.02
CHEMBL485748 IC50 = 1170.0 nM 5.93
CHEMBL458801 IC50 = 1730.0 nM 5.76
CHEMBL457699 IC50 = 1900.0 nM 5.72
CHEMBL514269 IC50 = 1930.0 nM 5.71
CHEMBL516007 IC50 = 3070.0 nM 5.51
CHEMBL457971 IC50 = 4360.0 nM 5.36