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Assay Detail

CHEMBL2329355

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

Binding
Inhibition of Plasmodium falciparum recombinant DXR using DXP as substrate preincubated for 5 mins
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Plasmodium falciparum
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Antimalarial and Structural Studies of Pyridine-containing Inhibitors of 1-Deoxyxylulose-5-phosphate Reductoisomerase.
Xue J, Diao J, Cai G, Deng L, Zheng B, Yao Y, Song Y.
ACS Med Chem Lett (2013) 4 : 278 -282
PubMed 23795240 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 8 7.66 8.72

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2323930 1 8.72
CHEMBL2323929 1 8.05
CHEMBL2323931 1 7.89
CHEMBL2323928 1 7.89
CHEMBL203125 FOSMIDOMYCIN 3.0 1 7.68
CHEMBL205052 1 7.07
CHEMBL2323932 1 6.32
CHEMBL76 CHLOROQUINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2323930 Ki = 1.9 nM 8.72
CHEMBL2323929 Ki = 8.9 nM 8.05
CHEMBL2323931 Ki = 13.0 nM 7.89
CHEMBL2323928 Ki = 13.0 nM 7.89
CHEMBL203125 FOSMIDOMYCIN Ki = 21.0 nM 7.68
CHEMBL205052 Ki = 85.0 nM 7.07
CHEMBL2323932 Ki = 480.0 nM 6.32
CHEMBL76 CHLOROQUINE Ki - -