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Review of bioactivity and structure-activity relationship on baicalein (5,6,7-trihydroxyflavone) and wogonin (5,7-dihydroxy-8-methoxyflavone) derivatives: Structural modifications inspired from flavonoids in Scutellaria baicalensis.

Authors :
Zhao, Zefeng
Nian, Meng
Qiao, Haifa
Yang, Xiaohang
Wu, Shaoping
Zheng, Xiaohui
Source :
European Journal of Medicinal Chemistry. Dec2022, Vol. 243, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Baicalein (5,6,7-trihydroxyflavone) and wogonin (5,7-dihydroxy-8-methoxyflavone), as typical flavonoids isolated from Scutellaria baicalensis , are well important precursors in drug discovery which produce diverse therapeutically related applications in pharmacological practices. Researches in medicinal chemistry field have synthesized baicalein and wogonin derivatives with multiple medicinal properties including antitumor, central nervous system (CNS), anti-inflammatory, antiviral, antimicrobial and hypoglycemic activities. Simultaneously, SAR (Structure-Activity Relationship) analysis has been gradually possessed, along with a great deal of derivatives have been derived for potential targets. In this article, we comprehensively summarize the biological activities and SAR for baicalein and wogonin derivatives, along with the featuring bioactive molecules reported in patents, wishing to provide an overall retrospect and prospect on baicalein and wogonin analogues. [Display omitted] • Baicalein and wogonin structural motif is a critical element of promising drug candidates aimed at different biological end-points. • Researches on modifications of the baicalein and wogonin analogues have been possessed with broad range of medicinal properties. • This review summarizes the biological activity and SAR for baicalein and wogonin analogues, providing retrospect and prospect on derivatives. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02235234
Volume :
243
Database :
Academic Search Index
Journal :
European Journal of Medicinal Chemistry
Publication Type :
Academic Journal
Accession number :
159858838
Full Text :
https://doi.org/10.1016/j.ejmech.2022.114733