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Literature summary for 2.4.2.3 extracted from

  • Niedzwicki, J.G.; El Kouni, M.H.; Chu, S.H.; Cha, S.
    Pyrimidine acyclonucleosides, inhibitors of uridine phosphorylase (1981), Biochem. Pharmacol., 30, 2097-2101.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
2'-deoxyglycosylthymine
-
Homo sapiens
2-deoxyglycosylthymine
-
Homo sapiens
5-bromoacyclouridine
-
Homo sapiens
5-fluoro-2'-deoxyuridine
-
Homo sapiens
5-fluoroacyclouridine
-
Homo sapiens
5-iodoacyclouridine
-
Homo sapiens
Acyclothymidine competitive Homo sapiens
acyclouridine competitive Homo sapiens
Pyrimidine acyclonucleosides competitive Homo sapiens

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.13
-
phosphate
-
Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
uridine + phosphate
-
Homo sapiens uracil + alpha-D-ribose 1-phosphate
-
r

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
0.003
-
Acyclothymidine
-
Homo sapiens
0.005
-
2-deoxyglycosylthymine
-
Homo sapiens
0.013
-
5-bromoacyclouridine
-
Homo sapiens
0.014
-
5-fluoroacyclouridine
-
Homo sapiens
0.015
-
acyclouridine
-
Homo sapiens
0.03
-
5-iodoacyclouridine
-
Homo sapiens