Pyrimidine acyclonucleosides, inhibitors of uridine phosphorylase
- 1 August 1981
- journal article
- research article
- Published by Elsevier in Biochemical Pharmacology
- Vol. 30 (15) , 2097-2101
- https://doi.org/10.1016/0006-2952(81)90228-8
Abstract
No abstract availableFunding Information
- American Cancer Society (CA-13943, CA-20892)
- National Cancer Institute
This publication has 19 references indexed in Scilit:
- A simple radioisotopic assay for nucleoside kinases employing alumina for separation of nucleosides and nucleotidesAnalytical Biochemistry, 1981
- Inhibition of nucleoside phosphorylase cleavage of 5-fluoro-2'-deoxyuridine by 2,4- pyrimidinedione derivativesBiochemical Pharmacology, 1980
- THYMIDINE SENSITIVITY OF CULTURED LEUKqMIC LYMPHOCYTESThe Lancet, 1979
- Thymidine kinase, DNA synthesis and cancerMolecular and Cellular Biochemistry, 1976
- Irreversible enzyme inhibitors. CLXXI. Inhibition of FUDR [5-fluoro-2'-deoxyuridine] phosphorylase from Walker 256 rat tumor by 5-substituted uracilsJournal of Medicinal Chemistry, 1970
- Inhibition of thymidine phosphorylase by 6-aminothymine and derivatives of 6-aminouracilBiochemical Pharmacology, 1967
- Selective inhibition by deoxyglucosyl thymine of thymidine phosphorylases not catalyzing deoxyribosyl transferBiochemical and Biophysical Research Communications, 1964
- Thymidine Catabolism by Normal and Leukemic Human Leukocytes*Journal of Clinical Investigation, 1964
- Studies of Fluorinated Pyrimidines. XVIII. The Degradation of 5-Fluoro-2'-deoxyuridine and Related Compounds by Nucleoside Phosphorylase*Biochemistry, 1963
- Uridine and deoxyuridine phosphorylases from Ehrlich ascites tumorBiochimica et Biophysica Acta, 1961