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Assay Detail

CHEMBL957240

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

Binding
Inhibition of Staphylococcus aureus wild-type topoisomerase 4 decatenation activity assessed as unlinking of DNA microcircles from kinetoplast DNA
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Staphylococcus aureus
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Dual targeting of DNA gyrase and topoisomerase IV: target interactions of heteroaryl isothiazolones in Staphylococcus aureus.
Cheng J, Thanassi JA, Thoma CL, Bradbury BJ, Deshpande M, Pucci MJ.
Antimicrob Agents Chemother (2007) 51 : 2445 -2453
PubMed 17502409 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 6.00 6.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL430 GEMIFLOXACIN 4.0 1 6.40
CHEMBL220656 1 6.10
CHEMBL219534 1 6.00
CHEMBL32 MOXIFLOXACIN 4.0 1 6.00
CHEMBL8 CIPROFLOXACIN 4.0 1 5.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL430 GEMIFLOXACIN IC50 = 400.0 nM 6.40
CHEMBL220656 IC50 = 800.0 nM 6.10
CHEMBL219534 IC50 = 1000.0 nM 6.00
CHEMBL32 MOXIFLOXACIN IC50 = 1000.0 nM 6.00
CHEMBL8 CIPROFLOXACIN IC50 = 3000.0 nM 5.52