Recent advances on 3-hydroxyflavone derivatives: Structures and properties

Burcu Butun, Gulacti Topcu, Turan Ozturk*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

24 Citations (Scopus)

Abstract

Flavonoids are naturally occurring phenolic compounds named as 2-phenyl-1-benzopyran-4-one and classified into several subclasses according to their basic chemical structures such as flavones, flavonols, flavanones, flavanonols, and flavanols. Among them, flavonols (3-hydroxyflavone), containing a 3-hydroxyl group in association with its 4-keto group and double bond between 2- and 3-carbon atoms, have the best electron conjugated skeleton in flavonoid family, providing several resonance structures and chelating ability, through which various pharmacological activities such as antiviral, anti-tumour, anti-inflammatory, anticholinesterase, cytotoxicity and particularly high antioxidant activity are demonstrated. They prevent generation of free radicals and are used as food preservatives. Their strong electron conjugation provides them with fluorescent property, which make them used as imaging agents for therapeutic purpose.

Original languageEnglish
Pages (from-to)98-103
Number of pages6
JournalMini-Reviews in Medicinal Chemistry
Volume18
Issue number2
DOIs
Publication statusPublished - 2018

Bibliographical note

Publisher Copyright:
© 2018 Bentham Science Publishers.

Funding

We thank Istanbul Technical grant to Burcu Butun (PhD). We thank Istanbul Technical University, Turkey, for grant to Burcu Butun (PhD).

FundersFunder number
Istanbul Technical
Istanbul Teknik Üniversitesi

    Keywords

    • 3-hydroxyflavones
    • Dye
    • Flavonoids
    • Flavonols
    • Fluorescent
    • Pharmacological activities

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