Literature DB >> 4004890

5-Substituted-2,2'-anhydrouridines, potent inhibitors of uridine phosphorylase.

Z Veres, A Szabolcs, I Szinai, G Dénes, M Kajtár-Peredy, L Otvös.   

Abstract

5-Substituted-2,2'-anhydrouridines are a new class of competitive inhibitors of uridine phosphorylase. The most potent member of the series is 2,2'-anhydro-5-ethyluridine with an apparent Ki value of 25 nM. These compounds are selective inhibitors of uridine phosphorylase and have no effect on thymidine phosphorylase. 5-Substituted-2,2'-anhydrouridines are no substrates of either uridine phosphorylase or thymidine phosphorylase.

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Year:  1985        PMID: 4004890     DOI: 10.1016/0006-2952(85)90643-4

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  2 in total

1.  Modification of uridine phosphorylase from Escherichia coli by diethyl pyrocarbonate. Evidence for a histidine residue in the active site of the enzyme.

Authors:  A K Drabikowska; G Woźniak
Journal:  Biochem J       Date:  1990-09-01       Impact factor: 3.857

2.  Cytokines induce uridine phosphorylase in mouse colon 26 carcinoma cells and make the cells more susceptible to 5'-deoxy-5-fluorouridine.

Authors:  H Eda; K Fujimoto; S Watanabe; T Ishikawa; T Ohiwa; K Tatsuno; Y Tanaka; H Ishitsuka
Journal:  Jpn J Cancer Res       Date:  1993-03
  2 in total

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