Abstract

Chalcones belong to the flavonoid class of phenolic compounds. They form one of the largest groups of bioactive natural products. The potential anticancer, anti-inflammatory, antimicrobial, antioxidant, and antiparasitic properties of naturally occurring chalcones, and their unique chemical structural features inspired the synthesis of numerous chalcone derivatives. In fact, structural features of chalcones are easy to construct from simple aromatic compounds, and it is convenient to perform structural modifications to generate functionalized chalcone derivatives. Many of these synthetic analogs were shown to possess similar bioactivities as their natural counterparts, but often with an enhanced potency and reduced toxicity. This review article aims to demonstrate how bioinspired synthesis of chalcone derivatives can potentially introduce a new chemical space for exploitation for new drug discovery, justifying the title of this article. However, the focus remains on critical appraisal of synthesized chalcones and their derivatives for their bioactivities, linking to their interactions at the biomolecular level where appropriate, and revealing their possible mechanisms of action.

Highlights

  • Chalcones are flavonoid-type phenolic phytochemicals, often referred to as ‘openchain flavonoids’, and biosynthesized via the shikimate pathway [1]

  • There are several thousand naturally occurring chalcones reported in the literature [2], and many of those chalcones were shown to interact with various biomolecules and possess cytoprotective and modulatory properties, making them potentially suitable candidates for therapeutic interventions in many human ailments

  • Occurring chalcones are phenolic compounds, and often possess one or more phenolic hydroxyl functionality in their structures, which generally offer them with the inherent free-radical-scavenging properties that can be useful against oxidative stress

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Summary

Introduction

Chalcones are flavonoid-type phenolic phytochemicals, often referred to as ‘openchain flavonoids’, and biosynthesized via the shikimate pathway [1]. Chalcones are considered as the biosynthetic precursors of flavonoids. Among the naturally occurring chalcones, the presence of one or more phenolic hydroxyl functionalities is ubiquitous, and prenyl and geranyl substitutions on the aromatic rings are widely observed. There are several thousand naturally occurring chalcones reported in the literature [2], and many of those chalcones were shown to interact with various biomolecules and possess cytoprotective and modulatory properties, making them potentially suitable candidates for therapeutic interventions in many human ailments. Several patents are available for chalcones and their derivatives for their activities as anticancer, anti-inflammatory, antimitotic, antioxidant, and cytotoxic properties [3].

General
Chalcone Synthesis
Synthesis
Molecular Mechanisms of Chalcone Actions
Effects on the Cell Cycle
B: Chalcones that arrest thecycle cell cycle
Effects on Apoptosis
Bioactivity of Chalcones
Anticancer and Cancer Chemopreventive Activity
Antidiabetic Activity
Anti-Inflammatory Activity
Antimicrobial
Antibacterial Activity
Antifungal
Antiviral Activity
16. Structures
Antioxidant Activity
Antiparasitic Activity
Immunoregulatory
Immunoregulatory Activity
Conclusions
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