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Author

Stephen J. Cutler

Bio: Stephen J. Cutler is an academic researcher from University of Georgia. The author has contributed to research in topics: Amidine. The author has an hindex of 1, co-authored 1 publications receiving 266 citations.
Topics: Amidine

Papers
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Journal ArticleDOI
TL;DR: In this paper, a synthese sur les acyclonucleosides derives de purine ou de pyrimidine and les acYclo-C-nucleoside.

269 citations


Cited by
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Patent
04 Aug 1993
TL;DR: Resolved enantiomers of formulae (IA) and (IB) wherein B is a purine or pyrimidine base or aza and/or deaza analogs thereof are useful in antiviral pharmaceutical compositions to treat retroviral infections as mentioned in this paper.
Abstract: Resolved enantiomers of formulae (IA) and (IB) wherein B is a purine or pyrimidine base or aza and/or deaza analogs thereof are useful in antiviral pharmaceutical compositions to treat retroviral infections.

83 citations

Journal ArticleDOI
TL;DR: Preparation of some novel substituted pyrazole and pyrazolo[3,4-d]pyrimidine derivatives revealed promising antiviral activity against herpes simplex virus type-1 in comparison to Acyclovir as a control.

79 citations

Journal ArticleDOI
TL;DR: A number of new N‐arylaminomethyl‐1,3,4‐oxadiazole derivatives 2, 3a,b, and 9–12a, b showed higher antiviral activity compared to the other hydrazones and their acetylated derivatives.
Abstract: A number of new N -arylaminomethyl-1,3,4 -oxadiazole derivatives 2, 3a,b, and 9-12a,b were prepared. Sugar (5-N-arylaminomethyl-l,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.

79 citations