Synthesis and antiviral evaluation against the Vaccinia virus of new N1-oxide analogs of 5′-noraristeromycin

New N 1 -benzyl esters of N 1 -oxide analogues of 5′-noraristeromycin were synthesized and tested as potential inhibitors of S -adenosyl- L -homocysteine hydrolase in Vaccinia virus-infected cell systems.

Saved in:
Bibliographic Details
Published inRussian journal of bioorganic chemistry Vol. 36; no. 6; pp. 730 - 733
Main Authors Matyugina, E. S., Seley-Radtke, K. L., Andronova, V. L., Galegov, G. A., Kochetkov, S. N., Khandazhinskaya, A. L.
Format Journal Article
LanguageEnglish
Published Dordrecht SP MAIK Nauka/Interperiodica 2010
Springer Nature B.V
Subjects
Biochemistry
Biomedical and Life Sciences
Biomedicine
Bioorganic Chemistry
Esters
hydrolase
Life Sciences
Organic Chemistry
Vaccinia
Vaccinia virus
Viruses
Vaccinia virus
inhibitors
oxide-5′-noraristeromycin derivatives
antiviral activity in vitro
S-adenosyl-L-homocysteine hydrolase
N
Online AccessGet full text

Cover

More Information
Summary:New N 1 -benzyl esters of N 1 -oxide analogues of 5′-noraristeromycin were synthesized and tested as potential inhibitors of S -adenosyl- L -homocysteine hydrolase in Vaccinia virus-infected cell systems.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:1068-1620
1608-330X
DOI:10.1134/S1068162010060099