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Assay Detail

CHEMBL3390205

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

Functional
Antimalarial activity against chloroquine-sensitive Plasmodium falciparum 3D7 infected in human type A-positive red blood cells assessed as growth inhibition after 72 hrs by spectrophotometrically
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Plasmodium falciparum
Confidence 1 — Organism
Curated By Autocuration

Target

Plasmodium falciparum (CHEMBL364)
Type ORGANISM
Organism Plasmodium falciparum

Publication

Synthesis and evaluation of the antiplasmodial activity of novel indeno[2,1-c]quinoline derivatives.
Barteselli A, Parapini S, Basilico N, Mommo D, Sparatore A.
Bioorg Med Chem (2014) 22 : 5757 -5765
PubMed 25311562 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 6.08 7.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL76 CHLOROQUINE 4.0 1 7.92
CHEMBL38827 LUMEFANTRINE 4.0 1 7.92
CHEMBL3344524 1 6.28
CHEMBL3344526 1 6.09
CHEMBL3344523 1 6.07
CHEMBL3344519 1 5.99
CHEMBL3344516 1 5.77
CHEMBL3344517 1 5.63
CHEMBL3344525 1 5.27
CHEMBL3344518 1 5.17
CHEMBL216579 1 4.77

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL76 CHLOROQUINE IC50 = 12.0 nM 7.92
CHEMBL38827 LUMEFANTRINE IC50 = 12.0 nM 7.92
CHEMBL3344524 IC50 = 530.0 nM 6.28
CHEMBL3344526 IC50 = 818.0 nM 6.09
CHEMBL3344523 IC50 = 843.0 nM 6.07
CHEMBL3344519 IC50 = 1031.0 nM 5.99
CHEMBL3344516 IC50 = 1713.0 nM 5.77
CHEMBL3344517 IC50 = 2339.0 nM 5.63
CHEMBL3344525 IC50 = 5390.0 nM 5.27
CHEMBL3344518 IC50 = 6775.0 nM 5.17
CHEMBL216579 IC50 = 16900.0 nM 4.77