Synthesis, biotransformation, pharmacokinetics, and antiviral properties of 5-ethyl-5-halo-6-methoxy-5,6-dihydro-2′-deoxyuridine diastereomers
Author:
Publisher
Elsevier BV
Subject
Pharmacology,Biochemistry
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Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Prodrug Strategies in the Design of Nucleoside and Nucleotide Antiviral Therapeutics;Annual Reports in Medicinal Chemistry;2004
2. 5-Bromo (or chloro)-6-azido-5,6-dihydro-2′-deoxyuridine and -thymidine derivatives with potent antiviral activity;Bioorganic & Medicinal Chemistry Letters;2002-02
3. Synthesis and Antiviral Activity of 5-Ethyl-5-halo-6-alkoxy-(or Azido)-5,6-dihydro-2′-deoxyuridine Diastereomers as Potential Prodrugs to 5-Ethyl-2′-deoxyuridine;Archiv der Pharmazie;1997
4. A Comparative Study of 5-ethyl-2′-Deoxyuridine and Selected Lipophilic 5,6-Dihydro Double/Triple Prodrugs;Antiviral Chemistry and Chemotherapy;1995-12
5. Accumulation of 5-Ethyl-2′-deoxyuridine and its 5,6-Dihydro Prodrugs in Murine Lung and its Potential Clinical Application;Journal of Pharmacy and Pharmacology;1995-07
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