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Literature summary for 3.1.3.11 extracted from

  • von Geldern, T.W.; Lai, C.; Gum, R.J.; Daly, M.; Sun, C.; Fry, E.H.; Abad-Zapatero, C.
    Benzoxazole benzenesulfonamides are novel allosteric inhibitors of fructose-1,6-bisphosphatase with a distinct binding mode (2006), Bioorg. Med. Chem. Lett., 16, 1811-1815.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
2,5-dichloro-N-(5-chloro-1,3-benzoxazol-2-yl)benzenesulfonamide 50% inhibition at 0.0034 mM Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
0.0011
-
2,5-dichloro-N-(5-chloro-1,3-benzoxazol-2-yl)benzenesulfonamide
-
Homo sapiens