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

CHEMBL2434278

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

Functional
Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum 3D7 infected in erythrocytes assessed as parasite growth inhibition after 72 hrs by SYBR green 1 dye-based fluorometric analysis
47
Total Activities
47
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

Novel selective and potent inhibitors of malaria parasite dihydroorotate dehydrogenase: discovery and optimization of dihydrothiophenone derivatives.
Xu M, Zhu J, Diao Y, Zhou H, Ren X, Sun D, Huang J, Han D, Zhao Z, Zhu L, Xu Y, Li H.
J Med Chem (2013) 56 : 7911 -7924
PubMed 24073986 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 47 5.89 7.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL76 CHLOROQUINE 4.0 1 7.82
CHEMBL2431496 1 7.82
CHEMBL2431499 1 7.24
CHEMBL2431515 1 7.11
CHEMBL2431513 1 6.77
CHEMBL2431488 1 6.61
CHEMBL2431514 1 6.60
CHEMBL2431504 1 6.51
CHEMBL2431497 1 6.43
CHEMBL2431498 1 6.31
CHEMBL2431500 1 6.30
CHEMBL2431502 1 6.22
CHEMBL2431501 1 6.17
CHEMBL2431517 1 6.16
CHEMBL2431480 1 6.13
CHEMBL2431489 1 6.05
CHEMBL2431503 1 6.02
CHEMBL2431522 1 5.99
CHEMBL2431518 1 5.91
CHEMBL2431516 1 5.85
CHEMBL2431505 1 5.82
CHEMBL2431521 1 5.73
CHEMBL2431519 1 5.72
CHEMBL2431510 1 5.70
CHEMBL2431523 1 5.68
CHEMBL2431506 1 5.66
CHEMBL2431485 1 5.57
CHEMBL2431484 1 5.50
CHEMBL2431487 1 5.48
CHEMBL2431492 1 5.46

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL76 CHLOROQUINE IC50 = 15.0 nM 7.82
CHEMBL2431496 IC50 = 15.0 nM 7.82
CHEMBL2431499 IC50 = 57.0 nM 7.24
CHEMBL2431515 IC50 = 77.0 nM 7.11
CHEMBL2431513 IC50 = 169.0 nM 6.77
CHEMBL2431488 IC50 = 245.0 nM 6.61
CHEMBL2431514 IC50 = 253.0 nM 6.60
CHEMBL2431504 IC50 = 307.0 nM 6.51
CHEMBL2431497 IC50 = 372.0 nM 6.43
CHEMBL2431498 IC50 = 492.0 nM 6.31
CHEMBL2431500 IC50 = 495.0 nM 6.30
CHEMBL2431502 IC50 = 607.0 nM 6.22
CHEMBL2431501 IC50 = 680.0 nM 6.17
CHEMBL2431517 IC50 = 688.0 nM 6.16
CHEMBL2431480 IC50 = 745.0 nM 6.13
CHEMBL2431489 IC50 = 890.0 nM 6.05
CHEMBL2431503 IC50 = 946.0 nM 6.02
CHEMBL2431522 IC50 = 1018.0 nM 5.99
CHEMBL2431518 IC50 = 1233.0 nM 5.91
CHEMBL2431516 IC50 = 1401.0 nM 5.85
CHEMBL2431505 IC50 = 1525.0 nM 5.82
CHEMBL2431521 IC50 = 1860.0 nM 5.73
CHEMBL2431519 IC50 = 1907.0 nM 5.72
CHEMBL2431510 IC50 = 1992.0 nM 5.70
CHEMBL2431523 IC50 = 2107.0 nM 5.68
CHEMBL2431506 IC50 = 2191.0 nM 5.66
CHEMBL2431485 IC50 = 2696.0 nM 5.57
CHEMBL2431484 IC50 = 3173.0 nM 5.50
CHEMBL2431487 IC50 = 3342.0 nM 5.48
CHEMBL2431492 IC50 = 3476.0 nM 5.46
CHEMBL2431481 IC50 = 3534.0 nM 5.45
CHEMBL2431509 IC50 = 4031.0 nM 5.39
CHEMBL2431511 IC50 = 5048.0 nM 5.30
CHEMBL2431507 IC50 = 5614.0 nM 5.25
CHEMBL2431493 IC50 = 5831.0 nM 5.23
CHEMBL1334527 IC50 = 5903.0 nM 5.23
CHEMBL2431486 IC50 = 6618.0 nM 5.18
CHEMBL2431490 IC50 = 8380.0 nM 5.08
CHEMBL2431483 IC50 = 8470.0 nM 5.07
CHEMBL2431494 IC50 = 10233.0 nM 4.99
CHEMBL2431491 IC50 = 11148.0 nM 4.95
CHEMBL2431495 IC50 = 12402.0 nM 4.91
CHEMBL2431508 IC50 = 14351.0 nM 4.84
CHEMBL2431482 IC50 > 20000.0 nM -
CHEMBL2431512 IC50 > 20000.0 nM -
CHEMBL2431520 IC50 > 20000.0 nM -
CHEMBL1732938 IC50 > 20000.0 nM -