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

CHEMBL4605392

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

Functional
Antimalarial activity against Plasmodium falciparum 3D7 infected in human red blood cells after 72 hrs by SYBR Green 1 dye based fluorescence assay
72
Total Activities
72
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

Lead Optimization of a Pyrrole-Based Dihydroorotate Dehydrogenase Inhibitor Series for the Treatment of Malaria.
Kokkonda S, Deng X, White KL, El Mazouni F, White J, Shackleford DM, Katneni K, Chiu FCK, Barker H, McLaren J, Crighton E, Chen G, Angulo-Barturen I, Jimenez-Diaz MB, Ferrer S, Huertas-Valentin L, Martinez-Martinez MS, Lafuente-Monasterio MJ, Chittimalla R, Shahi SP, Wittlin S, Waterson D, Burrows JN, Matthews D, Tomchick D, Rathod PK, Palmer MJ, Charman SA, Phillips MA.
J Med Chem (2020) 63 : 4929 -4956
PubMed 32248693 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 72 6.81 8.22

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1956285 DSM-265 2.0 1 8.22
CHEMBL1234899 1 8.15
CHEMBL4636879 1 8.04
CHEMBL4639806 1 8.00
CHEMBL4634454 1 7.89
CHEMBL4633246 1 7.85
CHEMBL4635646 1 7.80
CHEMBL4643360 1 7.75
CHEMBL4644619 1 7.70
CHEMBL4639663 1 7.57
CHEMBL4639907 1 7.55
CHEMBL4636553 1 7.54
CHEMBL4633770 1 7.54
CHEMBL4639489 1 7.48
CHEMBL4643370 1 7.44
CHEMBL4649411 1 7.36
CHEMBL4643327 1 7.36
CHEMBL4644974 1 7.33
CHEMBL4641948 1 7.29
CHEMBL4638564 1 7.29
CHEMBL4636157 1 7.29
CHEMBL4645475 1 7.22
CHEMBL4642145 1 7.21
CHEMBL4635012 1 7.19
CHEMBL4645764 1 7.18
CHEMBL4634831 1 7.09
CHEMBL4633356 1 7.00
CHEMBL4646287 1 6.96
CHEMBL4638098 1 6.89
CHEMBL4635607 1 6.77

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1956285 DSM-265 EC50 = 6.0 nM 8.22
CHEMBL1234899 EC50 = 7.0 nM 8.15
CHEMBL4636879 EC50 = 9.2 nM 8.04
CHEMBL4639806 EC50 = 9.9 nM 8.00
CHEMBL4634454 EC50 = 13.0 nM 7.89
CHEMBL4633246 EC50 = 14.0 nM 7.85
CHEMBL4635646 EC50 = 16.0 nM 7.80
CHEMBL4643360 EC50 = 18.0 nM 7.75
CHEMBL4644619 EC50 = 20.0 nM 7.70
CHEMBL4639663 EC50 = 27.0 nM 7.57
CHEMBL4639907 EC50 = 28.0 nM 7.55
CHEMBL4636553 EC50 = 29.0 nM 7.54
CHEMBL4633770 EC50 = 29.0 nM 7.54
CHEMBL4639489 EC50 = 33.0 nM 7.48
CHEMBL4643370 EC50 = 36.0 nM 7.44
CHEMBL4649411 EC50 = 44.0 nM 7.36
CHEMBL4643327 EC50 = 44.0 nM 7.36
CHEMBL4644974 EC50 = 47.0 nM 7.33
CHEMBL4641948 EC50 = 51.0 nM 7.29
CHEMBL4638564 EC50 = 51.0 nM 7.29
CHEMBL4636157 EC50 = 51.0 nM 7.29
CHEMBL4645475 EC50 = 60.0 nM 7.22
CHEMBL4642145 EC50 = 61.0 nM 7.21
CHEMBL4635012 EC50 = 65.0 nM 7.19
CHEMBL4645764 EC50 = 66.0 nM 7.18
CHEMBL4634831 EC50 = 82.0 nM 7.09
CHEMBL4633356 EC50 = 100.0 nM 7.00
CHEMBL4646287 EC50 = 110.0 nM 6.96
CHEMBL4638098 EC50 = 130.0 nM 6.89
CHEMBL4635607 EC50 = 170.0 nM 6.77
CHEMBL4633797 EC50 = 200.0 nM 6.70
CHEMBL600689 EC50 = 230.0 nM 6.64
CHEMBL4646801 EC50 = 240.0 nM 6.62
CHEMBL4642065 EC50 = 260.0 nM 6.58
CHEMBL4634334 EC50 = 290.0 nM 6.54
CHEMBL4636829 EC50 = 340.0 nM 6.47
CHEMBL4636244 EC50 = 390.0 nM 6.41
CHEMBL4636376 EC50 = 420.0 nM 6.38
CHEMBL4646226 EC50 = 470.0 nM 6.33
CHEMBL4633597 EC50 = 470.0 nM 6.33
CHEMBL4633302 EC50 = 500.0 nM 6.30
CHEMBL4646919 EC50 = 530.0 nM 6.28
CHEMBL4649039 EC50 = 590.0 nM 6.23
CHEMBL4641398 EC50 = 710.0 nM 6.15
CHEMBL4645972 EC50 = 770.0 nM 6.11
CHEMBL4643434 EC50 = 810.0 nM 6.09
CHEMBL4634278 EC50 = 1000.0 nM 6.00
CHEMBL4634603 EC50 = 1200.0 nM 5.92
CHEMBL4641890 EC50 = 1300.0 nM 5.89
CHEMBL4633381 EC50 = 1900.0 nM 5.72