Evolution of uracil based thymidine phosphorylase inhibitors, SAR and electronic correlation: revisit
Author:
Affiliation:
1. Department of Studies in ChemistrySRMPP Govt. First Grade College Huvinahadagali Karnataka India
Publisher
Wiley
Subject
Drug Discovery
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ddr.21592
Reference81 articles.
1. 5-(Phenylthio)acyclouridine: a powerful enhancer of oral uridine bioavailability: relevance to chemotherapy with 5-fluorouracil and other uridine rescue regimens
2. Synthesis and Evaluation of Multisubstrate Bicyclic Pyrimidine Nucleoside Inhibitors of Human Thymidine Phosphorylase
3. Irreversible enzyme inhibitors. CLXVII. Thymidine phosphorylase. 10. On the nature and dimensions of the hydrophobic bonding region. A
4. Irreversible Enzyme Inhibitors. LXXVIII.1,2 Inhibitors of Thymidine Phosphorylase. IV.2 Hydrophobic Bonding by Uracils Substituted at the 5 and 6 Positions
5. Irreversible Enzyme Inhibitors. LXXX.1,2 Inhibitors of Thymidine Phosphorylase. VI.2 Hydrophobic Bonding with 6 Substituents on the Acidic 5-Nitro- and 5-Bromouracils
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1. Dihydropyrimidone Derivatives as Thymidine Phosphorylase Inhibitors: Inhibition Kinetics, Cytotoxicity, and Molecular Docking;Molecules;2023-04-21
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3. Multilevel virtual screening approach for discovery of thymidine phosphorylase inhibitors as potential anticancer agents;Journal of Molecular Structure;2022-02
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