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Literature summary extracted from

  • Ganesan, M.; Madhukarrao, R.V.; Ramesh, N.G.
    Design and synthesis of new amino-modified iminocyclitols: selective inhibitors of alpha-galactosidase (2010), Org. Biomol. Chem., 8, 1527-1530.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.2.1.22 (2S,3R,4R,5S)-2-(hydroxymethyl)-5-[(methylamino)methyl]pyrrolidine-3,4-diol
-
 Coffea arabica
3.2.1.22 (2S,3R,4R,5S)-2-[(ethylamino)methyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol
-
 Coffea arabica

Organism

EC Number Organism UniProt Comment Textmining
3.2.1.22 Coffea arabica
-
-
-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
3.2.1.22 seed
-
 Coffea arabica
-

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
3.2.1.22 6.9
-
-
 Coffea arabica (2S,3R,4R,5S)-2-(hydroxymethyl)-5-[(methylamino)methyl]pyrrolidine-3,4-diol
3.2.1.22 8.1
-
-
 Coffea arabica (2S,3R,4R,5S)-2-[(ethylamino)methyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol