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Literature summary for 2.5.1.9 extracted from

  • Zhang, Y.; Illarionov, B.; Morgunova, E.; Jin, G.; Bacher, A.; Fischer, M.; Ladenstein, R.; Cushman, M.
    A new series of N-[2,4-dioxo-6-d-ribitylamino-1,2,3,4-tetrahydropyrimidin-5-yl]oxalamic acid derivatives as inhibitors of lumazine synthase and riboflavin synthase: design, synthesis, biochemical evaluation, crystallography, and mechanistic implications (2008), J. Org. Chem., 73, 2715-2724.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
N-6-(ribitylamino)pyrimidine-2,4(1H,3H)-dion-5-ylpropionamide uncompetitive Escherichia coli
N-6-(ribitylamino)pyrimidine-2,4(1H,3H)-dione-5-ylisobutyramide uncompetitive Escherichia coli
N-[2,4-dioxo-6-(ribitylamino)-1,2,3,4-tetrahydropyrimidin-5-yl]oxalamic acid ethyl ester mixed type inhibition Escherichia coli

Organism

Organism UniProt Comment Textmining
Escherichia coli
-
-
-

IC50 Value

IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
0.0000013
-
pH 7.0, 27°C Escherichia coli N-[2,4-dioxo-6-(ribitylamino)-1,2,3,4-tetrahydropyrimidin-5-yl]oxalamic acid ethyl ester