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Assay Detail

CHEMBL3101661

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

Binding
Inhibition of Staphylococcus aureus FabI-mediated trans-2-octenoyl N-acetylcysteamine reduction assessed as NADPH level by ELISA
6
Total Activities
4
Compounds Tested
2
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

Verrulactone C with an unprecedented dispiro skeleton, a new inhibitor of Staphylococcus aureus enoyl-ACP reductase, from Penicillium verruculosum F375.
Kim N, Sohn MJ, Koshino H, Kim EH, Kim WG.
Bioorg Med Chem Lett (2014) 24 : 83 -86
PubMed 24332629 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 5.19 6.04
Inhibition 2 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2011360 VERRULACTONE A 1 6.04
CHEMBL2011361 VERRULACTONE B 1 5.85
CHEMBL3098272 2 4.79
CHEMBL593328 2 4.07

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2011360 VERRULACTONE A IC50 = 920.0 nM 6.04
CHEMBL2011361 VERRULACTONE B IC50 = 1410.0 nM 5.85
CHEMBL3098272 IC50 = 16100.0 nM 4.79
CHEMBL593328 IC50 = 85400.0 nM 4.07
CHEMBL593328 Inhibition - % -
CHEMBL3098272 Inhibition - % -