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Assay Detail

CHEMBL1036670

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

Functional
Antiprotozoal activity against chloroquine and pyrimethamine-resistant Plasmodium falciparum K1 after 72 hrs by [3H]hypoxanthine uptake
13
Total Activities
13
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 linear triaryl guanidines, N-substituted guanidines and potential prodrugs as antiprotozoal agents.
Arafa RK, Ismail MA, Munde M, Wilson WD, Wenzler T, Brun R, Boykin DW.
Eur J Med Chem (2008) 43 : 2901 -2908
PubMed 18455271 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 8.01 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL215692 1 9.00
CHEMBL457986 1 8.77
CHEMBL458214 1 8.72
CHEMBL467401 1 8.59
CHEMBL446515 1 8.54
CHEMBL508828 1 8.35
CHEMBL456688 1 8.15
CHEMBL456899 1 8.05
CHEMBL515509 1 7.85
CHEMBL459062 1 7.57
CHEMBL458215 1 7.27
CHEMBL458213 1 6.82
CHEMBL468965 1 6.41

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL215692 IC50 = 1.0 nM 9.00
CHEMBL457986 IC50 = 1.7 nM 8.77
CHEMBL458214 IC50 = 1.9 nM 8.72
CHEMBL467401 IC50 = 2.6 nM 8.59
CHEMBL446515 IC50 = 2.9 nM 8.54
CHEMBL508828 IC50 = 4.5 nM 8.35
CHEMBL456688 IC50 = 7.0 nM 8.15
CHEMBL456899 IC50 = 8.9 nM 8.05
CHEMBL515509 IC50 = 14.0 nM 7.85
CHEMBL459062 IC50 = 27.0 nM 7.57
CHEMBL458215 IC50 = 54.0 nM 7.27
CHEMBL458213 IC50 = 151.0 nM 6.82
CHEMBL468965 IC50 = 393.0 nM 6.41