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Assay Detail

CHEMBL870710

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

Binding
Inhibition of recombinant Escherichia coli DXR
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Escherichia coli
Confidence 8 — Homologous single protein target
Curated By Expert

Target

1-deoxy-D-xylulose 5-phosphate reductoisomerase (CHEMBL4091)
Type SINGLE PROTEIN
Organism Escherichia coli K-12

Publication

Synthesis and biological evaluation of cyclopropyl analogues of fosmidomycin as potent Plasmodium falciparum growth inhibitors.
Devreux V, Wiesner J, Goeman JL, Van der Eycken J, Jomaa H, Van Calenbergh S.
J Med Chem (2006) 49 : 2656 -2660
PubMed 16610809 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 7.03 7.32

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL203125 FOSMIDOMYCIN 3.0 1 7.32
CHEMBL204406 1 7.30
CHEMBL205338 FR-900098 1 7.24
CHEMBL380319 1 6.80
CHEMBL205091 1 6.50
CHEMBL381270 1 -
CHEMBL382795 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL203125 FOSMIDOMYCIN IC50 = 48.0 nM 7.32
CHEMBL204406 IC50 = 50.0 nM 7.30
CHEMBL205338 FR-900098 IC50 = 58.0 nM 7.24
CHEMBL380319 IC50 = 160.0 nM 6.80
CHEMBL205091 IC50 = 313.0 nM 6.50
CHEMBL381270 IC50 > 3000.0 nM -
CHEMBL382795 IC50 > 30000.0 nM -