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Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids

descriptionPublicationkeyboard_double_arrow_right Article 01 May 2013 English Publisher:Elsevier BVJournal:Acta Pharmaceutica Sinica B, volume 3, pages 154-162 (issn: 2211-3835, Copyright policy )
Authors: Peng Zeng; Yong Zhang; Chen Pan; Qi Jia; Fujiang Guo; Yiming Li; Weiliang Zhu; +1 Authors

doi: 10.1016/j.apsb.2013.04.004

Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids

Abstract

AbstractC-glycosylflavonoids are characterized by a bond between the anomeric carbon of a sugar moiety and the C-6 or C-8 position of a flavonoid A ring. These compounds are widespread in nature and have become the subject of increasing research interest due to their high biological potential. This review focuses on the biological effects of various C-glycosylflavonoids and their structure–activity relationships (SAR) as elucidated over the last 5 years.

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Keywords

Therapeutics. Pharmacology, RM1-950

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
45
Top 10%
Top 10%
Top 10%
gold
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