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Recent advances on 3-hydroxyflavone derivatives: Structures and properties

  • Burcu Butun
  • , Gulacti Topcu
  • , Turan Ozturk*
  • *Bu çalışma için yazışmadan sorumlu yazar
  • Istanbul Technical University
  • Bezmialem Vakif University
  • Scientific and Technological Research Council of Turkey

Araştırma sonucu: Dergiye katkıİnceleme makalesibilirkişi

34 Atıf (Scopus)

Özet

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.

Orijinal dilİngilizce
Sayfa (başlangıç-bitiş)98-103
Sayfa sayısı6
DergiMini-Reviews in Medicinal Chemistry
Hacim18
Basın numarası2
DOI'lar
Yayın durumuYayınlandı - 2018

Bibliyografik not

Publisher Copyright:
© 2018 Bentham Science Publishers.

Finansman

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

Finansörler
Istanbul Technical
Istanbul Teknik Üniversitesi

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