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Assay Detail

CHEMBL1961096

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

Binding
Inhibition of Plasmodium falciparum C-terminal hexa-His tagged DHODH expressed in Escherichia coli by DCIP reduction assay
83
Total Activities
83
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Plasmodium falciparum
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Dihydroorotate dehydrogenase (CHEMBL3486)
Type SINGLE PROTEIN
Organism Plasmodium falciparum

Publication

Structure-guided lead optimization of triazolopyrimidine-ring substituents identifies potent Plasmodium falciparum dihydroorotate dehydrogenase inhibitors with clinical candidate potential.
Coteron JM, Marco M, Esquivias J, Deng X, White KL, White J, Koltun M, El Mazouni F, Kokkonda S, Katneni K, Bhamidipati R, Shackleford DM, Angulo-Barturen I, Ferrer SB, Jiménez-Díaz MB, Gamo FJ, Goldsmith EJ, Charman WN, Bathurst I, Floyd D, Matthews D, Burrows JN, Rathod PK, Charman SA, Phillips MA.
J Med Chem (2011) 54 : 5540 -5561
PubMed 21696174 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 83 6.62 7.72

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1956288 1 7.72
CHEMBL1956301 1 7.58
CHEMBL1956291 1 7.52
CHEMBL1956303 1 7.52
CHEMBL1956300 1 7.52
CHEMBL1956287 1 7.52
CHEMBL1956285 DSM-265 2.0 1 7.48
CHEMBL1956286 1 7.47
CHEMBL1956290 1 7.46
CHEMBL1956302 1 7.44
CHEMBL1738786 1 7.42
CHEMBL1956283 1 7.42
CHEMBL1956304 1 7.35
CHEMBL1956284 1 7.27
CHEMBL1956472 1 7.25
CHEMBL1956473 1 7.24
CHEMBL1956289 1 7.12
CHEMBL1956264 1 7.06
CHEMBL1956466 1 7.05
CHEMBL1956279 1 7.03
CHEMBL1956269 1 7.00
CHEMBL1956467 1 6.96
CHEMBL1956268 1 6.96
CHEMBL1956267 1 6.92
CHEMBL1956278 1 6.85
CHEMBL1956265 1 6.82
CHEMBL1956305 1 6.80
CHEMBL1956263 1 6.62
CHEMBL1956471 1 6.57
CHEMBL1956262 1 6.55

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1956288 IC50 = 19.0 nM 7.72
CHEMBL1956301 IC50 = 26.0 nM 7.58
CHEMBL1956303 IC50 = 30.0 nM 7.52
CHEMBL1956300 IC50 = 30.0 nM 7.52
CHEMBL1956287 IC50 = 30.0 nM 7.52
CHEMBL1956291 IC50 = 30.0 nM 7.52
CHEMBL1956285 DSM-265 IC50 = 33.0 nM 7.48
CHEMBL1956286 IC50 = 34.0 nM 7.47
CHEMBL1956290 IC50 = 35.0 nM 7.46
CHEMBL1956302 IC50 = 36.0 nM 7.44
CHEMBL1738786 IC50 = 38.0 nM 7.42
CHEMBL1956283 IC50 = 38.0 nM 7.42
CHEMBL1956304 IC50 = 45.0 nM 7.35
CHEMBL1956284 IC50 = 54.0 nM 7.27
CHEMBL1956472 IC50 = 56.0 nM 7.25
CHEMBL1956473 IC50 = 57.0 nM 7.24
CHEMBL1956289 IC50 = 75.0 nM 7.12
CHEMBL1956264 IC50 = 87.0 nM 7.06
CHEMBL1956466 IC50 = 90.0 nM 7.05
CHEMBL1956279 IC50 = 93.0 nM 7.03
CHEMBL1956269 IC50 = 100.0 nM 7.00
CHEMBL1956467 IC50 = 110.0 nM 6.96
CHEMBL1956268 IC50 = 110.0 nM 6.96
CHEMBL1956267 IC50 = 120.0 nM 6.92
CHEMBL1956278 IC50 = 140.0 nM 6.85
CHEMBL1956265 IC50 = 150.0 nM 6.82
CHEMBL1956305 IC50 = 160.0 nM 6.80
CHEMBL1956263 IC50 = 240.0 nM 6.62
CHEMBL1956471 IC50 = 270.0 nM 6.57
CHEMBL1956262 IC50 = 280.0 nM 6.55
CHEMBL1956266 IC50 = 330.0 nM 6.48
CHEMBL1956275 IC50 = 330.0 nM 6.48
CHEMBL1956274 IC50 = 380.0 nM 6.42
CHEMBL1956295 IC50 = 390.0 nM 6.41
CHEMBL1956470 IC50 = 400.0 nM 6.40
CHEMBL1956294 IC50 = 410.0 nM 6.39
CHEMBL1956469 IC50 = 460.0 nM 6.34
CHEMBL1956272 IC50 = 460.0 nM 6.34
CHEMBL1956468 IC50 = 500.0 nM 6.30
CHEMBL1956273 IC50 = 550.0 nM 6.26
CHEMBL1956277 IC50 = 820.0 nM 6.09
CHEMBL1956276 IC50 = 880.0 nM 6.06
CHEMBL1956499 IC50 = 930.0 nM 6.03
CHEMBL1956281 IC50 = 1700.0 nM 5.77
CHEMBL1956293 IC50 = 1700.0 nM 5.77
CHEMBL1956270 IC50 = 2000.0 nM 5.70
CHEMBL1956292 IC50 = 2200.0 nM 5.66
CHEMBL1956299 IC50 = 2500.0 nM 5.60
CHEMBL1956298 IC50 = 2500.0 nM 5.60
CHEMBL1956475 IC50 = 4900.0 nM 5.31