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

CHEMBL968941

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

Functional
Antimalarial activity after 48 hrs against chloroquine-sensitive Plasmodium falciparum 3D7 by [3H]hypoxanthine uptake
64
Total Activities
64
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 structure-activity relationship of 3-phenylquinoxaline 1,4-di-N-oxide derivatives as antimalarial agents.
Vicente E, Lima LM, Bongard E, Charnaud S, Villar R, Solano B, Burguete A, Perez-Silanes S, Aldana I, Vivas L, Monge A.
Eur J Med Chem (2008) 43 : 1903 -1910
PubMed 18215443 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 64 5.84 7.87

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL76 CHLOROQUINE 4.0 1 7.87
CHEMBL490288 1 6.48
CHEMBL472909 1 6.32
CHEMBL490289 1 6.18
CHEMBL490074 1 6.15
CHEMBL489880 1 6.14
CHEMBL514296 1 6.14
CHEMBL490075 1 6.12
CHEMBL473109 1 6.09
CHEMBL514456 1 6.06
CHEMBL472720 1 6.06
CHEMBL490076 1 6.03
CHEMBL512752 1 6.00
CHEMBL454945 1 5.93
CHEMBL473520 1 5.90
CHEMBL451452 1 5.90
CHEMBL516030 1 5.89
CHEMBL460705 1 5.83
CHEMBL460704 1 5.81
CHEMBL523962 1 5.81
CHEMBL521926 1 5.77
CHEMBL454151 1 5.71
CHEMBL454152 1 5.69
CHEMBL475143 1 5.67
CHEMBL475131 1 5.64
CHEMBL460703 1 5.63
CHEMBL510626 1 5.61
CHEMBL445501 1 5.56
CHEMBL445089 1 5.52
CHEMBL473324 1 5.50

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL76 CHLOROQUINE IC50 = 13.5 nM 7.87
CHEMBL490288 IC50 = 330.0 nM 6.48
CHEMBL472909 IC50 = 480.0 nM 6.32
CHEMBL490289 IC50 = 660.0 nM 6.18
CHEMBL490074 IC50 = 710.0 nM 6.15
CHEMBL489880 IC50 = 720.0 nM 6.14
CHEMBL514296 IC50 = 730.0 nM 6.14
CHEMBL490075 IC50 = 750.0 nM 6.12
CHEMBL473109 IC50 = 810.0 nM 6.09
CHEMBL514456 IC50 = 870.0 nM 6.06
CHEMBL472720 IC50 = 880.0 nM 6.06
CHEMBL490076 IC50 = 930.0 nM 6.03
CHEMBL512752 IC50 = 1010.0 nM 6.00
CHEMBL454945 IC50 = 1180.0 nM 5.93
CHEMBL451452 IC50 = 1260.0 nM 5.90
CHEMBL473520 IC50 = 1270.0 nM 5.90
CHEMBL516030 IC50 = 1300.0 nM 5.89
CHEMBL460705 IC50 = 1470.0 nM 5.83
CHEMBL460704 IC50 = 1550.0 nM 5.81
CHEMBL523962 IC50 = 1560.0 nM 5.81
CHEMBL521926 IC50 = 1700.0 nM 5.77
CHEMBL454151 IC50 = 1930.0 nM 5.71
CHEMBL454152 IC50 = 2030.0 nM 5.69
CHEMBL475143 IC50 = 2150.0 nM 5.67
CHEMBL475131 IC50 = 2290.0 nM 5.64
CHEMBL460703 IC50 = 2350.0 nM 5.63
CHEMBL510626 IC50 = 2440.0 nM 5.61
CHEMBL445501 IC50 = 2770.0 nM 5.56
CHEMBL445089 IC50 = 3020.0 nM 5.52
CHEMBL473324 IC50 = 3140.0 nM 5.50
CHEMBL475144 IC50 = 3160.0 nM 5.50
CHEMBL453122 IC50 = 3220.0 nM 5.49
CHEMBL472910 IC50 = 3460.0 nM 5.46
CHEMBL475290 IC50 = 3910.0 nM 5.41
CHEMBL489291 IC50 = 4210.0 nM 5.38
CHEMBL489290 IC50 = 5780.0 nM 5.24
CHEMBL472719 IC50 = 5830.0 nM 5.23
CHEMBL449174 IC50 = 6540.0 nM 5.18
CHEMBL454153 IC50 - -
CHEMBL517414 IC50 > 7000.0 nM -
CHEMBL454944 IC50 > 7000.0 nM -
CHEMBL490275 IC50 > 5000.0 nM -
CHEMBL506804 IC50 > 5000.0 nM -
CHEMBL512751 IC50 > 5000.0 nM -
CHEMBL522442 IC50 > 20000.0 nM -
CHEMBL489882 IC50 > 20000.0 nM -
CHEMBL475132 IC50 > 20000.0 nM -
CHEMBL475142 IC50 > 20000.0 nM -
CHEMBL453121 IC50 - -
CHEMBL460713 IC50 > 10000.0 nM -