Key result
Thiosemicarbazide scaffolds demonstrate translational suitability as antiviral agents based on decades of structure-activity relationships.
Why the study?
Viral infection challenges have risen due to resistance and drying antiviral drug discovery, necessitating continuous therapy development and systematic review of the thiosemicarbazide antiviral scaffold.
Systematic Review
Thiosemicarbazides remain a relevant scaffold for antiviral drug discovery, with various chemical modifications enhancing their potential safety and efficacy.
Thiosemicarbazide scaffolds merit further antiviral optimization; extends three decades of SAR data to guide translational safety and efficacy.
The challenges of viral infection have increased in recent decades due to the emergence of resistance, cross-resistance and drying up of antiviral drug discovery. Many neglected tropical viruses including the chikungunya virus, dengue virus & Japanese encephalitis virus have gradually become global pathogens. This has further increased the burden of viral infection which necessitates the continuous development of antiviral therapy. The antiviral chemistry began with the development of thiosemicarbazide derived thiosemicarbazones as antiviral. Although very few thiosemicarbazides have progressed into clinical application, it still inspires antiviral development. During last 3 decades (1990- 2020), several efforts have been made to develop suitable antiviral by using thiosemicarbazide scaffold. Its hybridization with other pharmacophores has been used as a strategy to enhance safety and efficacy. Cyclization and substitution of thiosemicarbazides have also been used to develop potent antiviral. With the ability to form coordinate bonds, thiosemicarbazides have been used either as metal complex or chelator against viruses. This work is an attempt to systematically review the research on the use of thiosemicarbazides as an antiviral scaffold. It also reviews the structure-activity relationship and translational suitability of thiosemicarbazide derived compounds.
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Moharana et al. (2020) conducted a systematic review in Viral infection. Thiosemicarbazides was evaluated. This systematic review highlights the development, structure-activity relationships, and translational suitability of thiosemicarbazide scaffolds as antiviral agents over the last three decades.
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