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Literature summary for 3.2.1.22 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
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Inhibitors

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

Organism

Organism UniProt Comment Textmining
Coffea arabica
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
seed
-
 Coffea arabica
-

IC50 Value

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