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Literature summary extracted from

  • Faugeroux, V.; Genisson, Y.; Andrieu-Abadie, N.; Colie, S.; Levade, T.; Baltas, M.
    C-Alkyl 5-membered ring imino sugars as new potent cytotoxic glucosylceramide synthase inhibitors (2006), Org. Biomol. Chem., 4, 4437-4439.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
2.4.1.80 (2S,3R)-2-(hydroxymethyl)pyrrolidin-3-ol 0.05 mM, about 15% inhibition Mus musculus
2.4.1.80 (2S,3R,4S)-2-(hydroxymethyl)-4-octylpyrrolidin-3-ol 0.01 mM, about 70% inhibition Mus musculus
2.4.1.80 (2S,3R,4S)-4-butyl-2-(hydroxymethyl)pyrrolidin-3-ol 0.05 mM, about 30% inhibition Mus musculus
2.4.1.80 N-butyl-1-deoxynojirimycin
-
 Mus musculus

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
2.4.1.80 UDP-glucose + N-acylsphingosine Mus musculus first step in the biosynthesis of glucosylceramide-based glycosphingolipids UDP + D-glucosyl-N-acylsphingosine
-
 ?

Organism

EC Number Organism UniProt Comment Textmining
2.4.1.80 Mus musculus
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2.4.1.80 UDP-glucose + N-acylsphingosine first step in the biosynthesis of glucosylceramide-based glycosphingolipids Mus musculus UDP + D-glucosyl-N-acylsphingosine
-
 ?