4.6 Review

Flavones and Related Compounds: Synthesis and Biological Activity

Journal

MOLECULES
Volume 28, Issue 18, Pages -

Publisher

MDPI
DOI: 10.3390/molecules28186528

Keywords

chalcones; flavones; flavonols; aurones; anticancer activity; antimicrobial activity

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This review discusses the synthesis and biological activity of flavones and related compounds, such as flavonols and aurones. It highlights the anticancer, antioxidant, and antimicrobial properties of natural and synthetic flavones and aurones, and summarizes the most promising methods for their synthesis. The review also focuses on the development of new effective antimicrobial derivatives and identifies the most promising antimicrobial agents. Overall, the review provides valuable insights into the synthesis and biological potential of flavones and related compounds.
This review focuses on the synthesis and biological activity of flavones and their related flavonoidic compounds, namely flavonols and aurones. Among the biological activities of natural and synthetic flavones and aurones, their anticancer, antioxidant, and antimicrobial properties are highlighted and detailed in this review. Starting from the structures of natural flavones acting on multiple anticancer targets (myricetin, genkwanin, and other structurally related compounds), new flavone analogs were recently designed and evaluated for their anticancer activity. The most representative compounds and their anticancer activity are summarized in this review. Natural flavones recognized for their antimicrobial properties (baicalein, luteolin, quercetol, apigenin, kaempferol, tricin) have been recently derivatized or structurally modulated by chemical synthetic methods in order to obtain new effective antimicrobial flavonoidic derivatives with improved biological properties. The most promising antimicrobial agents are systematically highlighted in this review. The most applied method for the synthesis of flavones and aurones is based on the oxidative cyclization of o-hydroxychalcones. Depending on the reaction conditions and the structure of the precursor, in some cases, several cyclization products result simultaneously: flavones, flavanones, flavonols, and aurones. Based on the literature data and the results obtained by our research group, our aim is to highlight the most promising methods for the synthesis of flavones, as well as the synthetic routes for the other structurally related cyclization products, such as hydroxyflavones and aurones, while considering that, in practice, it is difficult to predict which is the main or exclusive cyclization product of o-hydroxychalcones under certain reaction conditions.

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