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

C-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 f...
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Autor*in:	Peng Zeng [verfasserIn] Yong Zhang [verfasserIn] Chen Pan [verfasserIn] Qi Jia [verfasserIn] Fujiang Guo [verfasserIn] Yiming Li [verfasserIn] Weiliang Zhu [verfasserIn] Kaixian Chen [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2013

Übergeordnetes Werk:	In: Acta Pharmaceutica Sinica B - Elsevier, 2013, 3(2013), 3, Seite 154-162
Übergeordnetes Werk:	volume:3 ; year:2013 ; number:3 ; pages:154-162

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc Journal toc

DOI / URN:	10.1016/j.apsb.2013.04.004

Katalog-ID:	DOAJ052110958

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allfieldsSound	10.1016/j.apsb.2013.04.004 doi (DE-627)DOAJ052110958 (DE-599)DOAJ29049d25a35d459fbd57e7d825f2c60a DE-627 ger DE-627 rakwb eng RM1-950 Peng Zeng verfasserin aut Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier C-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. Therapeutics. Pharmacology Yong Zhang verfasserin aut Chen Pan verfasserin aut Qi Jia verfasserin aut Fujiang Guo verfasserin aut Yiming Li verfasserin aut Weiliang Zhu verfasserin aut Kaixian Chen verfasserin aut In Acta Pharmaceutica Sinica B Elsevier, 2013 3(2013), 3, Seite 154-162 (DE-627)670211095 (DE-600)2631779-5 22113843 nnns volume:3 year:2013 number:3 pages:154-162 https://doi.org/10.1016/j.apsb.2013.04.004 kostenfrei https://doaj.org/article/29049d25a35d459fbd57e7d825f2c60a kostenfrei http://www.sciencedirect.com/science/article/pii/S2211383513000361 kostenfrei https://doaj.org/toc/2211-3835 Journal toc kostenfrei https://doaj.org/toc/2211-3843 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2013 3 154-162
language	English
source	In Acta Pharmaceutica Sinica B 3(2013), 3, Seite 154-162 volume:3 year:2013 number:3 pages:154-162
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callnumber-first	R - Medicine
author	Peng Zeng
spellingShingle	Peng Zeng misc RM1-950 misc Therapeutics. Pharmacology Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids
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topic_title	RM1-950 Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids
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title	Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids
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title_full	Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids
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title_sort	advances in studying of the pharmacological activities and structure–activity relationships of natural c-glycosylflavonoids
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title_auth	Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids
abstract	C-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.
abstractGer	C-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.
abstract_unstemmed	C-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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title_short	Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids
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Advances in studying of the pharmacological activities and structure–activity relationships of natural C-glycosylflavonoids

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Zugang & Verfügbarkeit

Vorhandene Bände

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