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Literature summary extracted from

  • Oh, K.B.; Mar, W.; Kim, S.; Kim, J.Y.; Oh, M.N.; Kim, J.G.; Shin, D.; Sim, C.J.; Shin, J.
    Bis(indole) alkaloids as sortase A inhibitors from the sponge Spongosorites sp (2005), Bioorg. Med. Chem. Lett., 15, 4927-4931.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.4.22.70 (5R)-3,5-bis(6-bromo-1H-indol-3-yl)-5,6-dihydropyrazin-2(1H)-one IC50: 68.98 mg/L Staphylococcus aureus
3.4.22.70 (6-methyl-1H-inden-3-yl)[4-(6-methyl-1H-indol-3-yl)-1H-imidazol-2-yl]methanone IC50: 15.67 mg/Ll Staphylococcus aureus
3.4.22.70 (6R)-3,6-bis(6-bromo-1H-indol-3-yl)-5,6-dihydropyrazin-2(1H)-one IC50: 86.34 mg/L Staphylococcus aureus
3.4.22.70 (6R)-6-(6-bromo-1H-indol-3-yl)-3-(1H-indol-3-yl)-5,6-dihydropyrazin-2(1H)-one IC50: 34.04 mg/L Staphylococcus aureus
3.4.22.70 beta-sitosterol-3-O-glucopyranoside IC50: 18.3 mg/L Staphylococcus aureus
3.4.22.70 additional information no inhibition by (3R,6S)-3,6-bis(6-bromo-1H-indol-3-yl)piperazin-2-one and (3R,6S)-3,6-bis(6-bromo-1H-indol-3-yl)piperazin-2-one Staphylococcus aureus
3.4.22.70 [4-(6-bromo-1H-indol-3-yl)-1H-imidazol-2-yl](1H-indol-3-yl)methanone IC50: 19.44 mg/L Staphylococcus aureus
3.4.22.70 [4-(6-bromo-1H-indol-3-yl)-1H-imidazol-2-yl](6-hydroxy-1H-indol-3-yl)methanone IC50: 16.7 mg/L Staphylococcus aureus

Organism

EC Number Organism UniProt Comment Textmining
3.4.22.70 Staphylococcus aureus
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3.4.22.70 Staphylococcus aureus Newman
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