期刊
JOURNAL OF CARBOHYDRATE CHEMISTRY
卷 27, 期 6, 页码 357-372出版社
TAYLOR & FRANCIS INC
DOI: 10.1080/07328300802262778
关键词
thioglycosides; oxadiazole; S-functionalized-oxadiazole; glycinoyl hydrazine; antiviral activity; herpes simplex virus type 1 (HSV-1); hepatitis A virus (HAV)
N-Arylaminomethyl-3H-1,3,4-oxadiazole-2-thiones 2a,b were prepared from the corresponding N-arylglycinoylhydrazides. A number of their thioglycoside derivatives 4-7a-c and S-functionalized analogs 8-11a,b were synthesized by the reaction with different acetobromosugars and acyclic hydroxyalkylating agents. The antiviral activity of a number of the synthesized compounds against herpes simplex virus type 1 (HSV-1) and hepatitis A virus (HAV) was evaluated. Compounds 5a and 5b showed promising results against HAV.
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