5-Substituted-2,2′-anhydrouridines, potent inhibitors of uridine phosphorylase
Author:
Publisher
Elsevier BV
Subject
Pharmacology,Biochemistry
Reference26 articles.
1. Pyrimidine Nucleosidases
2. Thymidine phosphorylase. Substrate specificity for 5-substituted 2'-deoxyuridines
3. Inhibition of thymidine phosphorylase by 6-aminothymine and derivatives of 6-aminouracil
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1. Intramolecular Michael Additions in Uridine Derivatives: Isolation of the Labile 5′O-C6 Cyclonucleoside;ACS Omega;2020-09-15
2. Constrained nucleoside analogues – Crystal and molecular structure of 6,5′-O-anhydrouridines fixed in the anti conformation;Journal of Molecular Structure;2015-10
3. Potential and Perspectives of Cyclonucleosides;Current Medicinal Chemistry;2010-05-01
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5. Induction of thymidine phosphorylase expression and enhancement of efficacy of capecitabine or 5?-deoxy-5-fluorouridine by cyclophosphamide in mammary tumor models;International Journal of Cancer;1999-09-24
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