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Literature summary for 1.1.1.267 extracted from

  • Zingle, C.; Tritsch, D.; Grosdemange-Billiard, C.; Rohmer, M.
    Catechol-rhodanine derivatives: Specific and promiscuous inhibitors of Escherichia coli deoxyxylulose phosphate reductoisomerase (DXR) (2014), Bioorg. Med. Chem., 22, 3713-3719.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
2-[(5Z)-5-(3,4-dihydroxybenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]-N-hydroxyacetamide inhibitor keeps its inhibition capacity in the presence of Triton X-100 and shows antimicrobial activity against Escherichia coli Escherichia coli
[(5Z)-5-(3,4-dihydroxybenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]acetic acid inhibitor keeps its inhibition capacity in the presence of Triton X-100 Escherichia coli

Organism

Organism UniProt Comment Textmining
Escherichia coli Q1RG16
-
-
Escherichia coli UPEC Q1RG16
-
-

IC50 Value

IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
0.0031
-
pH 7.5, 37°C Escherichia coli [(5Z)-5-(3,4-dihydroxybenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]acetic acid
0.0038
-
pH 7.5, 37°C Escherichia coli 2-[(5Z)-5-(3,4-dihydroxybenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]-N-hydroxyacetamide
0.0044
-
presence of 0.01% Triton X-100, pH 7.5, 37°C Escherichia coli [(5Z)-5-(3,4-dihydroxybenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]acetic acid
0.0061
-
presence of 0.01% Triton X-100, pH 7.5, 37°C Escherichia coli 2-[(5Z)-5-(3,4-dihydroxybenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]-N-hydroxyacetamide