4.5 Article

Synthesis and antiviral evaluation of novel 5-(N-Arylaminomethyl-1,3,4-oxadiazol-2-yl)hydrazines and their sugars, 1,2,4-triazoles, tetrazolles and pyrazolyl derivatives

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ARCHIV DER PHARMAZIE
卷 341, 期 5, 页码 307-313

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/ardp.200700154

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acyclo-nucleosides; antiviral activity; 1,3,4-oxadiazoles; sugar hydrazones; triazolo-oxadiazoles

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A number of new N-arylaminomethyl-1,3,4-oxadiazole derivatives 2, 3a,b, and 9-12a,b were prepared. Sugar (5-N-arylaminomethyl-1,3,4-oxadiazol-2-yl) hydrazones 4-6a,b were synthesized by the reaction of the hydrazino derivatives 3a,b with the corresponding monosaccharides. The novel acyclo-C-nucleosides 7, 8a,b were prepared by heterocyclization of the sugar hydrazones 4, 5a,b with acetic anhydride. A number of the synthesized compounds were tested for their antiviral activity against herpes simplex virus type-1 (HSV-1) and hepatitis-A virus (HAV, MBBcell culture-adapted strain). The results revealed that the sugar hydrazones 6a,b showed higher antiviral activity compared to the other hydrazones and their acetylated derivatives.

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