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Literature summary extracted from

  • Furneaux, R.H.; Schramm, V.L.; Tyler, P.C.
    Transition state analogue inhibitors of protozoan nucleoside hydrolases (1999), Bioorg. Med. Chem., 7, 2599-2606.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.2.2.1 (1S)-(1-aminonaphthalen-4-yl)-1,4-dideoxy-1,4-imino-D-ribitol
-
Trypanosoma brucei
3.2.2.1 (1S)-1-(2,3-diamino-5-pyridyl)-1,4-dideoxy-1,4-imino-D-ribitol
-
Trypanosoma brucei
3.2.2.1 (1S)-1-(3,4-diaminophenyl)-1,4-dideoxy-1,4-imino-D-ribitol
-
Trypanosoma brucei
3.2.2.1 (1S)-1-(4-aminomethyl)phenyl-1,4-dideoxy-1,4-imino-D-ribitol
-
Trypanosoma brucei
3.2.2.1 (1S)-1-(4-cyanophenyl)1,4-dideoxy-1,4-imino-D-ribitol
-
Trypanosoma brucei
3.2.2.1 1,2,5-trideoxy-1-(guanin-9-yl)-2,5-imino-D-allitol
-
Trypanosoma brucei
3.2.2.1 1,2,5-trideoxy-1-(hypoxanthin-9-yl)-2,5-imino-D-alitol
-
Trypanosoma brucei
3.2.2.1 1-(5-carboxamido-2-pyridyl)-1,2,5-trideoxy-2,5-imino-D-allitol
-
Trypanosoma brucei
3.2.2.1 1-(adenin-9-yl)-1,2,5-trideoxy-2,5-imino-D-allitol
-
Trypanosoma brucei
3.2.2.1 iminoribitols poorly inhibited by free or substituted iminoribitols Trypanosoma brucei
3.2.2.1 additional information transition state analogue inhibitors of protozoan nucleoside hydrolases Trypanosoma brucei

Organism

EC Number Organism UniProt Comment Textmining
3.2.2.1 Trypanosoma brucei
-
brucei
-