Synthesis of N3-substituted uridine and related pyrimidine nucleosides and their antinociceptive effects in mice. 2005

Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
Faculty of Pharmaceutical Sciences, Hokuriku University, Kanagawa-machi, Kanazawa, Japan.

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.

UI MeSH Term Description Entries
D008297 Male Males
D011741 Pyrimidine Nucleosides Pyrimidines with a RIBOSE attached that can be phosphorylated to PYRIMIDINE NUCLEOTIDES. Nucleosides, Pyrimidine
D000700 Analgesics Compounds capable of relieving pain without the loss of CONSCIOUSNESS. Analgesic,Anodynes,Antinociceptive Agents,Analgesic Agents,Analgesic Drugs,Agents, Analgesic,Agents, Antinociceptive,Drugs, Analgesic
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships
D014529 Uridine A ribonucleoside in which RIBOSE is linked to URACIL. Allo-Uridine,Allouridine,Allo Uridine
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus

Related Publications

Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
May 2005, Proceedings of the National Academy of Sciences of the United States of America,
Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
January 1987, Nucleic acids symposium series,
Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
January 1965, Chemical & pharmaceutical bulletin,
Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
January 1995, Nucleic acids symposium series,
Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
August 1975, Annals of the New York Academy of Sciences,
Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
July 1986, Journal of medicinal chemistry,
Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
March 1954, The Journal of biological chemistry,
Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
January 1989, Archiv der Pharmazie,
Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
June 2019, Current protocols in nucleic acid chemistry,
Tomomi Shimizu, and Toshiyuki Kimura, and Tatsuya Funahashi, and Kazuhito Watanabe, and Ing Kang Ho, and Ikuo Yamamoto
December 2005, Bioorganic & medicinal chemistry,
Copied contents to your clipboard!