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Synthesis of N3-substituted uridine and related pyrimidine nucleosides and their antinociceptive effects in mice.

作者信息

Shimizu Tomomi, Kimura Toshiyuki, Funahashi Tatsuya, Watanabe Kazuhito, Ho Ing Kang, Yamamoto Ikuo

机构信息

Faculty of Pharmaceutical Sciences, Hokuriku University, Kanagawa-machi, Kanazawa, Japan.

出版信息

Chem Pharm Bull (Tokyo). 2005 Mar;53(3):313-8. doi: 10.1248/cpb.53.313.

Abstract

Seventy eight N(3)-substituted derivatives of uridine (1), thymidine (2), 2'-deoxyuridine (3), 6-azauridine (4), 2',3'-O-isopropylideneuridine (5), and arabinofuranosyluracil (6) were synthesized and their antinociceptive effects were evaluated. N(3)-(2',4'-Dimethoxyphenacyl)uridine (1l), N(3)-(2',4'-dimethoxyphenacyl)2'-deoxyuridine (3l), and N(3)-(2',5'-dimethoxyphenacyl)arabinofuranosyluracil (6m) possessed 93, 86, and 82% of the antinociceptive effects tested by hot plate, respectively. The antinociceptive effects of three derivatives were 5.8, 5.4, and 5.1-folds of the effect of N(3)-phenacyluridine (1h) (16%), respectively. The structure-activity relationship of N(3)-substituted pyrimidine nucleosides was also discussed.

摘要

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