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Assay Detail

CHEMBL4812658

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

Functional
Antimalarial activity against drug-resistant Plasmodium falciparum 3D7 infected in human erythrocytes assessed as reduction in parasite growth measured after 72 hrs by SYBR Green method
163
Total Activities
107
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

Potent Antimalarials with Development Potential Identified by Structure-Guided Computational Optimization of a Pyrrole-Based Dihydroorotate Dehydrogenase Inhibitor Series.
Palmer MJ, Deng X, Watts S, Krilov G, Gerasyuto A, Kokkonda S, El Mazouni F, White J, White KL, Striepen J, Bath J, Schindler KA, Yeo T, Shackleford DM, Mok S, Deni I, Lawong A, Huang A, Chen G, Wang W, Jayaseelan J, Katneni K, Patil R, Saunders J, Shahi SP, Chittimalla R, Angulo-Barturen I, Jiménez-Díaz MB, Wittlin S, Tumwebaze PK, Rosenthal PJ, Cooper RA, Aguiar ACC, Guido RVC, Pereira DB, Mittal N, Winzeler EA, Tomchick DR, Laleu B, Burrows JN, Rathod PK, Fidock DA, Charman SA, Phillips MA.
J Med Chem (2021) 64 : 6085 -6136
PubMed 33876936 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 163 6.86 9.04

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4847032 1 9.04
CHEMBL4854927 2 8.92
CHEMBL4846297 2 8.92
CHEMBL4855439 1 8.77
CHEMBL4850366 1 8.70
CHEMBL4856991 1 8.66
CHEMBL4850950 1 8.66
CHEMBL4878940 1 8.59
CHEMBL4849154 1 8.52
CHEMBL4855152 1 8.51
CHEMBL4847652 1 8.47
CHEMBL4857890 1 8.43
CHEMBL4855268 1 8.42
CHEMBL4846204 2 8.40
CHEMBL4850116 3 8.35
CHEMBL4871281 2 8.33
CHEMBL4857082 2 8.31
CHEMBL4864218 2 8.28
CHEMBL4876457 3 8.28
CHEMBL4850393 3 8.26
CHEMBL1956291 1 8.22
CHEMBL4856887 2 8.22
CHEMBL4858336 3 8.05
CHEMBL4846174 3 8.03
CHEMBL4861785 1 8.02
CHEMBL4851506 2 8.02
CHEMBL4848632 2 7.92
CHEMBL4847990 2 7.92
CHEMBL4869576 1 7.89
CHEMBL4633246 1 7.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4847032 EC50 = 0.92 nM 9.04
CHEMBL4846297 EC50 = 1.2 nM 8.92
CHEMBL4854927 EC50 = 1.2 nM 8.92
CHEMBL4855439 EC50 = 1.7 nM 8.77
CHEMBL4850366 EC50 = 2.0 nM 8.70
CHEMBL4856991 EC50 = 2.2 nM 8.66
CHEMBL4850950 EC50 = 2.2 nM 8.66
CHEMBL4878940 EC50 = 2.6 nM 8.59
CHEMBL4849154 EC50 = 3.0 nM 8.52
CHEMBL4855152 EC50 = 3.1 nM 8.51
CHEMBL4847652 EC50 = 3.4 nM 8.47
CHEMBL4857890 EC50 = 3.7 nM 8.43
CHEMBL4855268 EC50 = 3.8 nM 8.42
CHEMBL4846204 EC50 = 4.0 nM 8.40
CHEMBL4850116 EC50 = 4.5 nM 8.35
CHEMBL4871281 EC50 = 4.7 nM 8.33
CHEMBL4857082 EC50 = 4.9 nM 8.31
CHEMBL4876457 EC50 = 5.3 nM 8.28
CHEMBL4864218 EC50 = 5.2 nM 8.28
CHEMBL4850393 EC50 = 5.5 nM 8.26
CHEMBL1956291 EC50 = 6.0 nM 8.22
CHEMBL4856887 EC50 = 6.0 nM 8.22
CHEMBL4850393 EC50 = 8.2 nM 8.09
CHEMBL4858336 EC50 = 9.0 nM 8.05
CHEMBL4850116 EC50 = 9.0 nM 8.05
CHEMBL4846174 EC50 = 9.4 nM 8.03
CHEMBL4858336 EC50 = 9.3 nM 8.03
CHEMBL4861785 EC50 = 9.6 nM 8.02
CHEMBL4851506 EC50 = 9.5 nM 8.02
CHEMBL4876457 EC50 = 11.0 nM 7.96
CHEMBL4854927 EC50 = 11.0 nM 7.96
CHEMBL4847990 EC50 = 12.0 nM 7.92
CHEMBL4848632 EC50 = 12.0 nM 7.92
CHEMBL4869576 EC50 = 13.0 nM 7.89
CHEMBL4633246 EC50 = 14.0 nM 7.85
CHEMBL4635646 EC50 = 16.0 nM 7.80
CHEMBL4869753 EC50 = 17.0 nM 7.77
CHEMBL4860884 EC50 = 17.0 nM 7.77
CHEMBL4878579 EC50 = 20.0 nM 7.70
CHEMBL4858790 EC50 = 20.0 nM 7.70
CHEMBL4875526 EC50 = 21.0 nM 7.68
CHEMBL4851471 EC50 = 22.0 nM 7.66
CHEMBL4873337 EC50 = 22.0 nM 7.66
CHEMBL4863410 EC50 = 24.0 nM 7.62
CHEMBL4850090 EC50 = 24.0 nM 7.62
CHEMBL4877462 EC50 = 24.0 nM 7.62
CHEMBL4855411 EC50 = 29.0 nM 7.54
CHEMBL4874425 EC50 = 32.0 nM 7.50
CHEMBL4878824 EC50 = 32.0 nM 7.50
CHEMBL4862161 EC50 = 40.0 nM 7.40