Promising Schiff bases in antiviral drug design and discovery

Abstract Emerging and re-emerging illnesses will probably present a new hazard of infectious diseases and have fostered the urge to research new antiviral agents. Most of the antiviral agents are analogs of nucleosides and only a few are non-nucleoside antiviral agents. There is quite a less percentage of marketed/clinically approved non-nucleoside antiviral medications. Schiff bases are organic compounds that possess a well-demonstrated profile against cancer, viruses, fungus, and bacteria, as well as in the management of diabetes, chemotherapy-resistant cases, and malarial infections. Schiff bases resemble aldehydes or ketones with an imine/azomethine group instead of a carbonyl ring. Schiff bases have a broad application profile not only in therapeutics/medicine but also in industrial applications. Researchers have synthesized and screened various Schiff base analogs for their antiviral potential. Some of the important heterocyclic compounds like istatin, thiosemicarbazide, quinazoline, quinoyl acetohydrazide, etc. have been used to derive novel Schiff base analogs. Keeping in view the outbreak of viral pandemics and epidemics, this manuscript compiles a review of Schiff base analogs concerning their antiviral properties and structural-activity relationship analysis..

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:32

Enthalten in:

Medicinal chemistry research - 32(2023), 6 vom: 10. Mai, Seite 1063-1076

Sprache:

Englisch

Beteiligte Personen:

Kaushik, Shikha [VerfasserIn]
Paliwal, Sarvesh Kumar [VerfasserIn]
Iyer, Malliga R. [VerfasserIn]
Patil, Vaishali M. [VerfasserIn]

Links:

Volltext [lizenzpflichtig]

Themen:

Antiviral agents
COVID-19
Istatin
Quinazoline
Schiff base
Thiosemicarbazide

Anmerkungen:

© The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

doi:

10.1007/s00044-023-03068-0

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

OLC2143774494