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Literature summary for 2.3.1.230 extracted from

  • Allegretta, G.; Weidel, E.; Empting, M.; Hartmann, R.W.
    Catechol-based substrates of chalcone synthase as a scaffold for novel inhibitors of PqsD (2015), Eur. J. Med. Chem., 90, 351-359.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
3-(3,4-dihydroxyphenyl)-N-methylpropanamide potent inhibitor, completely inactive in the cell-based assay Pseudomonas aeruginosa
benzyl 3-(3,4-dihydroxyphenyl)propanoate
-
Pseudomonas aeruginosa
methyl 3-(3,4-dihydroxyphenyl)propanoate potent inhibitor Pseudomonas aeruginosa
additional information evaluation of selected substrates of the Medicago sativa chalcone synthase CHS2 as potential inhibitors of PqsD. Catechol derivatives possessing an ester moiety are able to reduce the production of 2-heptyl-4(1H)-quinolone in the bacterial cultures without affecting cellular growth Pseudomonas aeruginosa

Organism

Organism UniProt Comment Textmining
Pseudomonas aeruginosa P20582
-
-

IC50 Value

IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
0.0059
-
pH not specified in the publication, temperature not specified in the publication Pseudomonas aeruginosa benzyl 3-(3,4-dihydroxyphenyl)propanoate
0.02
-
pH not specified in the publication, temperature not specified in the publication Pseudomonas aeruginosa methyl 3-(3,4-dihydroxyphenyl)propanoate
0.023
-
pH not specified in the publication, temperature not specified in the publication Pseudomonas aeruginosa 3-(3,4-dihydroxyphenyl)-N-methylpropanamide