Abstract
New N¹-benzyl esters of N¹-oxide analogues of 5'-noraristeromycin were synthesized and tested as potential inhibitors of S-adenosyl-L-homocysteine hydrolase in Vaccinia virus infected cell systems.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Adenosine / analogs & derivatives*
-
Adenosine / chemical synthesis
-
Adenosine / chemistry
-
Adenosine / pharmacology
-
Animals
-
Antiviral Agents / chemical synthesis*
-
Antiviral Agents / chemistry
-
Antiviral Agents / pharmacology*
-
Chlorocebus aethiops
-
Drug Evaluation, Preclinical
-
Humans
-
Vaccinia / drug therapy*
-
Vaccinia virus*
-
Vero Cells
Substances
-
Antiviral Agents
-
5'-noraristeromycin
-
Adenosine