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Assay Detail

CHEMBL1961099

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Functional
Antimalarial activity against Plasmodium falciparum 3D7 by [3H]hypoxanthine incorporation assay in presence of human serum
ChEMBL ↗
83
Total Activities
83
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

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
EC50 83 6.46 8.08

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1956302 — — 1 8.08
CHEMBL1738786 — — 1 8.00
CHEMBL1956303 — — 1 7.50
CHEMBL1956288 — — 1 7.35
CHEMBL1956285 DSM-265 2.0 1 7.34
CHEMBL1956283 — — 1 7.30
CHEMBL1956264 — — 1 7.24
CHEMBL1956472 — — 1 7.24
CHEMBL1956290 — — 1 7.14
CHEMBL1956286 — — 1 7.03
CHEMBL1956268 — — 1 7.01
CHEMBL1956265 — — 1 7.00
CHEMBL1956473 — — 1 7.00
CHEMBL1956284 — — 1 6.89
CHEMBL1956291 — — 1 6.85
CHEMBL1956300 — — 1 6.82
CHEMBL1956301 — — 1 6.82
CHEMBL1956278 — — 1 6.82
CHEMBL1956466 — — 1 6.77
CHEMBL1956274 — — 1 6.57
CHEMBL1956272 — — 1 6.54
CHEMBL1956269 — — 1 6.38
CHEMBL1956499 — — 1 6.32
CHEMBL1956279 — — 1 6.30
CHEMBL1956275 — — 1 6.29
CHEMBL1956289 — — 1 6.26
CHEMBL1956469 — — 1 6.23
CHEMBL1956262 — — 1 6.10
CHEMBL1956266 — — 1 6.07
CHEMBL1956468 — — 1 6.01

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1956302 — EC50 = 8.4 nM 8.08
CHEMBL1738786 — EC50 = 10.0 nM 8.00
CHEMBL1956303 — EC50 = 32.0 nM 7.50
CHEMBL1956288 — EC50 = 45.0 nM 7.35
CHEMBL1956285 DSM-265 EC50 = 46.0 nM 7.34
CHEMBL1956283 — EC50 = 50.0 nM 7.30
CHEMBL1956264 — EC50 = 58.0 nM 7.24
CHEMBL1956472 — EC50 = 58.0 nM 7.24
CHEMBL1956290 — EC50 = 73.0 nM 7.14
CHEMBL1956286 — EC50 = 94.0 nM 7.03
CHEMBL1956268 — EC50 = 98.0 nM 7.01
CHEMBL1956265 — EC50 = 100.0 nM 7.00
CHEMBL1956473 — EC50 = 100.0 nM 7.00
CHEMBL1956284 — EC50 = 130.0 nM 6.89
CHEMBL1956291 — EC50 = 140.0 nM 6.85
CHEMBL1956300 — EC50 = 150.0 nM 6.82
CHEMBL1956278 — EC50 = 150.0 nM 6.82
CHEMBL1956301 — EC50 = 150.0 nM 6.82
CHEMBL1956466 — EC50 = 170.0 nM 6.77
CHEMBL1956274 — EC50 = 270.0 nM 6.57
CHEMBL1956272 — EC50 = 290.0 nM 6.54
CHEMBL1956269 — EC50 = 420.0 nM 6.38
CHEMBL1956499 — EC50 = 480.0 nM 6.32
CHEMBL1956279 — EC50 = 500.0 nM 6.30
CHEMBL1956275 — EC50 = 510.0 nM 6.29
CHEMBL1956289 — EC50 = 550.0 nM 6.26
CHEMBL1956469 — EC50 = 590.0 nM 6.23
CHEMBL1956262 — EC50 = 790.0 nM 6.10
CHEMBL1956266 — EC50 = 850.0 nM 6.07
CHEMBL1956468 — EC50 = 980.0 nM 6.01
CHEMBL1956294 — EC50 = 1000.0 nM 6.00
CHEMBL1956267 — EC50 = 1100.0 nM 5.96
CHEMBL1956287 — EC50 = 1200.0 nM 5.92
CHEMBL1956471 — EC50 = 1300.0 nM 5.89
CHEMBL1956304 — EC50 = 1400.0 nM 5.85
CHEMBL1956467 — EC50 = 2000.0 nM 5.70
CHEMBL1956295 — EC50 = 2100.0 nM 5.68
CHEMBL1956273 — EC50 = 2300.0 nM 5.64
CHEMBL1956263 — EC50 = 3300.0 nM 5.48
CHEMBL1956281 — EC50 = 3400.0 nM 5.47
CHEMBL1956298 — EC50 = 4200.0 nM 5.38
CHEMBL1956470 — EC50 = 4400.0 nM 5.36
CHEMBL1956299 — EC50 = 5000.0 nM 5.30
CHEMBL1956276 — EC50 = 6800.0 nM 5.17
CHEMBL1956261 — EC50 - — -
CHEMBL1956486 — EC50 - — -
CHEMBL1956277 — EC50 - — -
CHEMBL1956487 — EC50 - — -
CHEMBL1956488 — EC50 > 2500.0 nM -
CHEMBL1956489 — EC50 - — -