Nucleosides: XI. Synthesis and Antiviral Evaluation of 5'-Alkylthio-5'-deoxy Quinazolinone Nucleoside Derivatives as S-Adenosyl-L-homocysteine Analogs-Reference-Cited by-同舟云学术

Nucleosides: XI. Synthesis and Antiviral Evaluation of 5'-Alkylthio-5'-deoxy Quinazolinone Nucleoside Derivatives as S-Adenosyl-L-homocysteine Analogs

Published:2004 Issue:12 Volume:52 Page:1422-1426
ISSN:0009-2363
Container-title:Chemical and Pharmaceutical Bulletin
language:en
Short-container-title:CHEMICAL & PHARMACEUTICAL BULLETIN

Author:

Chien Tun-Cheng¹,Chen Chien-Shu¹,Yu Fang-Hwa¹,Chern Ji-Wang¹

Affiliation:

1. School of Pharmacy, College of Medicine, National Taiwan University No. 1, Section 1

Publisher

Pharmaceutical Society of Japan

Subject

Drug Discovery,General Chemistry,General Medicine

Link

http://www.jstage.jst.go.jp/article/cpb/52/12/52_12_1422/_pdf

Reference37 articles.

1. A convenient preparation of 1,2,3-tri-O-acetyl-β-d-ribofuranose by enzymatic regioselective 5-O-deacetylation of the peracetylated ribofuranose

2. 2) Present address: Department of Chemistry, The University of Michigan, Ann Arbor, MI 48109, U.S.A.

3. Antiviral potency of adenosine analogues: Correlation with inhibition of S-adenosylhomocysteine hydrolase

4. S-Adenosyl-L-homocysteine hydrolase as a target for antiviral chemotherapy

5. A convenient method for the synthesis of 5′-S-alkylthio-5′-deoxyribonucleosides

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