Abstract

A set of 13 alkyl derivatives of 3-phenylpiperidine-2,6-dione were synthesized. Newly obtained compounds were investigated in vitro against HIV-1 and other selected viruses. The benzyl 3f and fluorophenyl 3g derivatives showed moderate protection against CVB-2 and the compound 3g also against HSV-1. Derivatives were tested also for their antibacterial and antifungal activity. The molecular structures of 3a and 3d were determined by an X-ray analysis.

Highlights

  • Literature survey shows that phenylpiperazinyl group is a nuclei of antiviral, antibacterial and antifungal [1,2,3] agents

  • Derivatives of diarylpiperidin-4-one were found as the new class of antimicrobial agents with activity against pathogenic bacterial species and fungal

  • There is an increasing concern on substituted 4-arylpiperazines, 4-azatricyclodec-8-ene-3,5-dione derivatives, as some of them have been reported as antiviral agents, e.g. against Yellow Fever Virus (YFV) and Border Disease Virus (CVB-2), as well as antibacterial and antifungal compounds [1, 15]

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Summary

Introduction

Literature survey shows that phenylpiperazinyl group is a nuclei of antiviral, antibacterial and antifungal [1,2,3] agents. There is an increasing concern on substituted 4-arylpiperazines, 4-azatricyclodec-8-ene-3,5-dione derivatives, as some of them have been reported as antiviral agents, e.g. against Yellow Fever Virus (YFV) and Border Disease Virus (CVB-2), as well as antibacterial and antifungal compounds [1, 15]. N-substituted derivatives of 3-phenylpiperidine-2,6-dione, were evaluated in vitro against viruses, bacteria and fungi.

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