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Assay Detail

CHEMBL5579294

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

Functional
Antiplasmodial activity against asexual Plasmodium falciparum 3D7 incubated for 72 hrs by LDH assay
61
Total Activities
61
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

Property and Activity Refinement of Dihydroquinazolinone-3-carboxamides as Orally Efficacious Antimalarials that Target PfATP4.
Ashton TD, Calic PPS, Dans MG, Ooi ZK, Zhou Q, Palandri J, Loi K, Jarman KE, Qiu D, Lehane AM, Maity BC, De N, Giannangelo C, MacRaild CA, Creek DJ, Mao EY, Gancheva MR, Wilson DW, Chowdury M, de Koning-Ward TF, Famodimu MT, Delves MJ, Pollard H, Sutherland CJ, Baud D, Brand S, Jackson PF, Cowman AF, Sleebs BE.
J Med Chem (2024) 67 : 14493 -14523
PubMed 39134060 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 61 7.11 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5595794 1 8.40
CHEMBL5583869 1 8.15
CHEMBL5594154 1 8.10
CHEMBL5407464 1 8.10
CHEMBL5592834 1 8.10
CHEMBL5592756 1 8.00
CHEMBL5429894 1 8.00
CHEMBL5592695 1 7.96
CHEMBL5592130 1 7.85
CHEMBL5436150 1 7.85
CHEMBL5595902 1 7.80
CHEMBL5593596 1 7.80
CHEMBL5584047 1 7.80
CHEMBL5416425 1 7.77
CHEMBL5427940 1 7.72
CHEMBL5591827 1 7.64
CHEMBL5591057 1 7.60
CHEMBL5595345 1 7.52
CHEMBL5590696 1 7.51
CHEMBL5590156 1 7.43
CHEMBL5593217 1 7.43
CHEMBL5590101 1 7.42
CHEMBL5594930 1 7.33
CHEMBL5583549 1 7.32
CHEMBL5593566 1 7.32
CHEMBL5595740 1 7.29
CHEMBL5594200 1 7.21
CHEMBL5584115 1 7.19
CHEMBL5595251 1 7.17
CHEMBL5591562 1 7.16

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5595794 EC50 = 4.0 nM 8.40
CHEMBL5583869 EC50 = 7.0 nM 8.15
CHEMBL5407464 EC50 = 8.0 nM 8.10
CHEMBL5592834 EC50 = 8.0 nM 8.10
CHEMBL5594154 EC50 = 8.0 nM 8.10
CHEMBL5592756 EC50 = 10.0 nM 8.00
CHEMBL5429894 EC50 = 10.0 nM 8.00
CHEMBL5592695 EC50 = 11.0 nM 7.96
CHEMBL5592130 EC50 = 14.0 nM 7.85
CHEMBL5436150 EC50 = 14.0 nM 7.85
CHEMBL5595902 EC50 = 16.0 nM 7.80
CHEMBL5593596 EC50 = 16.0 nM 7.80
CHEMBL5584047 EC50 = 16.0 nM 7.80
CHEMBL5416425 EC50 = 17.0 nM 7.77
CHEMBL5427940 EC50 = 19.0 nM 7.72
CHEMBL5591827 EC50 = 23.0 nM 7.64
CHEMBL5591057 EC50 = 25.0 nM 7.60
CHEMBL5595345 EC50 = 30.0 nM 7.52
CHEMBL5590696 EC50 = 31.0 nM 7.51
CHEMBL5590156 EC50 = 37.0 nM 7.43
CHEMBL5593217 EC50 = 37.0 nM 7.43
CHEMBL5590101 EC50 = 38.0 nM 7.42
CHEMBL5594930 EC50 = 47.0 nM 7.33
CHEMBL5583549 EC50 = 48.0 nM 7.32
CHEMBL5593566 EC50 = 48.0 nM 7.32
CHEMBL5595740 EC50 = 51.0 nM 7.29
CHEMBL5594200 EC50 = 62.0 nM 7.21
CHEMBL5584115 EC50 = 64.0 nM 7.19
CHEMBL5595251 EC50 = 67.0 nM 7.17
CHEMBL5591562 EC50 = 69.0 nM 7.16
CHEMBL5579745 EC50 = 82.0 nM 7.09
CHEMBL5592041 EC50 = 86.0 nM 7.07
CHEMBL5591680 EC50 = 90.0 nM 7.05
CHEMBL5583998 EC50 = 115.0 nM 6.94
CHEMBL5593293 EC50 = 130.0 nM 6.89
CHEMBL5592811 EC50 = 180.0 nM 6.75
CHEMBL5591833 EC50 = 177.0 nM 6.75
CHEMBL5593134 EC50 = 230.0 nM 6.64
CHEMBL5409773 EC50 = 230.0 nM 6.64
CHEMBL5583852 EC50 = 243.0 nM 6.61
CHEMBL5592741 EC50 = 395.0 nM 6.40
CHEMBL5591693 EC50 = 430.0 nM 6.37
CHEMBL5590644 EC50 = 502.0 nM 6.30
CHEMBL5593597 EC50 = 510.0 nM 6.29
CHEMBL5591440 EC50 = 577.0 nM 6.24
CHEMBL5592989 EC50 = 630.0 nM 6.20
CHEMBL5592803 EC50 = 632.0 nM 6.20
CHEMBL5592131 EC50 = 660.0 nM 6.18
CHEMBL5591064 EC50 = 660.0 nM 6.18
CHEMBL5596015 EC50 = 822.0 nM 6.08