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Assay Detail

CHEMBL2014102

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

Binding
Inhibition of Staphylococcus aureus peptide deformylase using N-formylmethionine-alanine-serine as substrate by spectrophotometry
5
Total Activities
3
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Staphylococcus aureus
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Peptide deformylase (CHEMBL2010635)
Type SINGLE PROTEIN
Organism Staphylococcus aureus

Publication

Flavimycins A and B, dimeric 1,3-dihydroisobenzofurans with peptide deformylase inhibitory activity from Aspergillus flavipes.
Kwon YJ, Sohn MJ, Kim CJ, Koshino H, Kim WG.
J Nat Prod (2012) 75 : 271 -274
PubMed 22329646 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 6.08 7.70
Inhibition 2 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL308333 ACTINONIN 1 7.70
CHEMBL2012550 FLAVIMYCIN A 2 4.45
CHEMBL2012551 FLAVIMYCIN B 2 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL308333 ACTINONIN IC50 = 20.0 nM 7.70
CHEMBL2012550 FLAVIMYCIN A IC50 = 35800.0 nM 4.45
CHEMBL2012550 FLAVIMYCIN A Inhibition - % -
CHEMBL2012551 FLAVIMYCIN B Inhibition - % -
CHEMBL2012551 FLAVIMYCIN B IC50 = 100100.0 nM -