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Literature summary extracted from

  • Lee, Y.J.; Han, Y.R.; Park, W.; Nam, S.H.; Oh, K.B.; Lee, H.S.
    Synthetic analogs of indole-containing natural products as inhibitors of sortase A and isocitrate lyase (2010), Bioorg. Med. Chem. Lett., 20, 6882-6885.
    View publication on PubMed

Cloned(Commentary)

EC Number Cloned (Comment) Organism
4.1.3.1
-
Candida albicans

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.4.22.70 (2-methyl-1H-indol-3-yl)(oxo)acetic acid
-
Staphylococcus aureus
3.4.22.70 (6-hydroxy-1H-indol-3-yl)(oxo)acetic acid
-
Staphylococcus aureus
3.4.22.70 (6-methoxy-1H-indol-3-yl)(oxo)acetic acid
-
Staphylococcus aureus
3.4.22.70 1,2-bis(5-hydroxy-1H-indol-3-yl)ethane-1,2-dione
-
Staphylococcus aureus
3.4.22.70 1-(3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline
-
Staphylococcus aureus
3.4.22.70 1-(4-methoxyphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline
-
Staphylococcus aureus
3.4.22.70 1-(naphthalen-2-yl)-2,3,4,9-tetrahydro-1H-beta-carboline
-
Staphylococcus aureus
3.4.22.70 1-pentyl-2,3,4,9-tetrahydro-1H-beta-carboline
-
Staphylococcus aureus
3.4.22.70 1-phenyl-2,3,4,9-tetrahydro-1H-beta-carbolin-7-ol
-
Staphylococcus aureus
3.4.22.70 1-phenyl-2,3,4,9-tetrahydro-1H-beta-carboline
-
Staphylococcus aureus
3.4.22.70 1-phenyl-4,9-dihydro-3H-beta-carboline
-
Staphylococcus aureus
3.4.22.70 1H-indol-3-yl(oxo)acetic acid
-
Staphylococcus aureus
3.4.22.70 2,3,4,9-tetrahydro-1H-beta-carboline-1-carboxylic acid
-
Staphylococcus aureus
3.4.22.70 2-(1H-indol-3-yl)-2-oxo-N-phenylacetamide
-
Staphylococcus aureus
3.4.22.70 2-(2-methyl-1H-indol-3-yl)-2-oxo-N-phenylacetamide
-
Staphylococcus aureus
3.4.22.70 2-(6-hydroxy-1H-indol-3-yl)-2-oxo-N-phenylacetamide
-
Staphylococcus aureus
3.4.22.70 2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-phenylacetamide
-
Staphylococcus aureus
3.4.22.70 2-hydroxy-1-(5-hydroxy-1H-indol-3-yl)ethanone
-
Staphylococcus aureus
3.4.22.70 3-(2-aminoethyl)-1H-indol-5-ol
-
Staphylococcus aureus
3.4.22.70 5-hydroxy-1H-indole-3-carbaldehyde
-
Staphylococcus aureus
3.4.22.70 6-hydroxy-2,3,4,9-tetrahydro-1H-beta-carbolin-1-one
-
Staphylococcus aureus
3.4.22.70 6-hydroxydihydro-beta-carboline
-
Staphylococcus aureus
3.4.22.70 7-hydroxy-2,3,4,9-tetrahydro-1H-beta-carboline-1-carboxylic acid
-
Staphylococcus aureus
3.4.22.70 7-methoxy-1-pentyl-2,3,4,9-tetrahydro-1H-beta-carboline
-
Staphylococcus aureus
3.4.22.70 7-methoxy-1-phenyl-2,3,4,9-tetrahydro-1H-beta-carboline
-
Staphylococcus aureus
3.4.22.70 7-methoxy-1-phenyl-4,9-dihydro-3H-beta-carboline
-
Staphylococcus aureus
3.4.22.70 7-methoxy-2,3,4,9-tetrahydro-1H-beta-carboline-1-carboxylic acid
-
Staphylococcus aureus
3.4.22.70 methyl 5-hydroxy-1H-indole-3-carboxylate
-
Staphylococcus aureus
3.4.22.70 additional information not inhibited by 3-nitropropionate Staphylococcus aureus
3.4.22.70 p-hydroxymercuribenzoic acid
-
Staphylococcus aureus
4.1.3.1 1,2-bis(5-hydroxy-1H-indol-3-yl)ethane-1,2-dione
-
Candida albicans
4.1.3.1 1-(2-aminoethyl)-1H-indol-6-ol
-
Candida albicans
4.1.3.1 1-(3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-b-carboline
-
Candida albicans
4.1.3.1 1-(4-methoxyphenyl)-2,3,4,9-tetrahydro-1H-b-carboline
-
Candida albicans
4.1.3.1 1-(naphthalen-2-yl)-2,3,4,9-tetrahydro-1H-b-carboline
-
Candida albicans
4.1.3.1 2-hydroxy-1-(5-hydroxy-1H-indol-3-yl)ethanone
-
Candida albicans
4.1.3.1 3-nitropropionate
-
Candida albicans
4.1.3.1 5-hydroxy-1H-indole-3-carbaldehyde
-
Candida albicans
4.1.3.1 6-hydroxy-4,9-dihydro-3H-beta-carboline-1-carboxylic acid
-
Candida albicans

Organism

EC Number Organism UniProt Comment Textmining
3.4.22.70 Staphylococcus aureus
-
-
-
4.1.3.1 Candida albicans
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
4.1.3.1
-
Candida albicans

Synonyms

EC Number Synonyms Comment Organism
3.4.22.70 SrtA
-
Staphylococcus aureus
4.1.3.1 isocitrate lyase
-
Candida albicans

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
3.4.22.70 0.0106
-
pH and temperature not specified in the publication Staphylococcus aureus 1-phenyl-2,3,4,9-tetrahydro-1H-beta-carbolin-7-ol
3.4.22.70 0.0115
-
pH and temperature not specified in the publication Staphylococcus aureus 7-methoxy-1-phenyl-2,3,4,9-tetrahydro-1H-beta-carboline
3.4.22.70 0.025
-
pH and temperature not specified in the publication Staphylococcus aureus 7-methoxy-1-phenyl-4,9-dihydro-3H-beta-carboline
3.4.22.70 0.042
-
pH and temperature not specified in the publication Staphylococcus aureus p-hydroxymercuribenzoic acid
3.4.22.70 0.061
-
pH and temperature not specified in the publication Staphylococcus aureus 2-(2-methyl-1H-indol-3-yl)-2-oxo-N-phenylacetamide
3.4.22.70 0.067
-
pH and temperature not specified in the publication Staphylococcus aureus 6-hydroxydihydro-beta-carboline
3.4.22.70 0.069
-
pH and temperature not specified in the publication Staphylococcus aureus 1H-indol-3-yl(oxo)acetic acid
3.4.22.70 0.097
-
pH and temperature not specified in the publication Staphylococcus aureus 1-phenyl-4,9-dihydro-3H-beta-carboline
3.4.22.70 0.133
-
pH and temperature not specified in the publication Staphylococcus aureus (2-methyl-1H-indol-3-yl)(oxo)acetic acid
3.4.22.70 0.174
-
pH and temperature not specified in the publication Staphylococcus aureus 2-(1H-indol-3-yl)-2-oxo-N-phenylacetamide
4.1.3.1 0.051
-
pH not specified in the publication, temperature not specified in the publication Candida albicans 3-nitropropionate
4.1.3.1 0.075
-
pH not specified in the publication, temperature not specified in the publication Candida albicans 1-(3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-b-carboline
4.1.3.1 0.089
-
pH not specified in the publication, temperature not specified in the publication Candida albicans 1,2-bis(5-hydroxy-1H-indol-3-yl)ethane-1,2-dione
4.1.3.1 0.137
-
pH not specified in the publication, temperature not specified in the publication Candida albicans 1-(naphthalen-2-yl)-2,3,4,9-tetrahydro-1H-b-carboline
4.1.3.1 0.18
-
pH not specified in the publication, temperature not specified in the publication Candida albicans 1-(4-methoxyphenyl)-2,3,4,9-tetrahydro-1H-b-carboline
4.1.3.1 0.247
-
pH not specified in the publication, temperature not specified in the publication Candida albicans 5-hydroxy-1H-indole-3-carbaldehyde
4.1.3.1 0.301
-
pH not specified in the publication, temperature not specified in the publication Candida albicans 1-(2-aminoethyl)-1H-indol-6-ol
4.1.3.1 0.318
-
pH not specified in the publication, temperature not specified in the publication Candida albicans 2-hydroxy-1-(5-hydroxy-1H-indol-3-yl)ethanone
4.1.3.1 0.38
-
pH not specified in the publication, temperature not specified in the publication Candida albicans 6-hydroxy-4,9-dihydro-3H-beta-carboline-1-carboxylic acid