Radical-scavenging activities of marine-derived xyloketals and related chromanes

Xyloketals, a new type of antioxidants from a marine mangrove fungus, have potential pharmacological properties. In this paper, the radical-scavenging activities of a series of synthetic xyloketals and related chromanes toward 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiaz...

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Main Authors: Zhongliang Xu, Bingtai Lu, Qi Xiang, Yiying Li, Shichang Li, Yongcheng Lin, Jiyan Pang
Format: Article
Language:English
Published: Elsevier 2013-09-01
Series:Acta Pharmaceutica Sinica B
Subjects:
DFT
Online Access:http://www.sciencedirect.com/science/article/pii/S2211383513000658
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spelling doaj-bdf1e456dc654dcb8752d3323ef719132020-11-24T22:31:50ZengElsevierActa Pharmaceutica Sinica B2211-38352211-38432013-09-013532232710.1016/j.apsb.2013.06.008Radical-scavenging activities of marine-derived xyloketals and related chromanesZhongliang Xu0Bingtai Lu1Qi Xiang2Yiying Li3Shichang Li4Yongcheng Lin5Jiyan Pang6School of Chemistry & Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry & Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, ChinaBiopharmaceutical R&D Center, Jinan University, Guangzhou 510632, ChinaSchool of Chemistry & Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry & Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry & Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry & Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, ChinaXyloketals, a new type of antioxidants from a marine mangrove fungus, have potential pharmacological properties. In this paper, the radical-scavenging activities of a series of synthetic xyloketals and related chromanes toward 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) were evaluated by absorption spectrometry. One of the compounds (compound 10) displayed significant antioxidative action against DPPH and ABTS. A structure-activity analysis showed that the reactive sites on these compounds correlated with a hydroxy-group and also with ketal or aromatic H substituents. Based in part on a density functional theory (DFT) calculation of compound 10, the antioxidant mechanism of this chromane was deduced as a possible radical-scavenging mechanism by a sequential proton loss electron-transfer (SPLET) process.http://www.sciencedirect.com/science/article/pii/S2211383513000658XyloketalsRadical scavenging activitiesDFTSPLET
collection DOAJ
language English
format Article
sources DOAJ
author Zhongliang Xu
Bingtai Lu
Qi Xiang
Yiying Li
Shichang Li
Yongcheng Lin
Jiyan Pang
spellingShingle Zhongliang Xu
Bingtai Lu
Qi Xiang
Yiying Li
Shichang Li
Yongcheng Lin
Jiyan Pang
Radical-scavenging activities of marine-derived xyloketals and related chromanes
Acta Pharmaceutica Sinica B
Xyloketals
Radical scavenging activities
DFT
SPLET
author_facet Zhongliang Xu
Bingtai Lu
Qi Xiang
Yiying Li
Shichang Li
Yongcheng Lin
Jiyan Pang
author_sort Zhongliang Xu
title Radical-scavenging activities of marine-derived xyloketals and related chromanes
title_short Radical-scavenging activities of marine-derived xyloketals and related chromanes
title_full Radical-scavenging activities of marine-derived xyloketals and related chromanes
title_fullStr Radical-scavenging activities of marine-derived xyloketals and related chromanes
title_full_unstemmed Radical-scavenging activities of marine-derived xyloketals and related chromanes
title_sort radical-scavenging activities of marine-derived xyloketals and related chromanes
publisher Elsevier
series Acta Pharmaceutica Sinica B
issn 2211-3835
2211-3843
publishDate 2013-09-01
description Xyloketals, a new type of antioxidants from a marine mangrove fungus, have potential pharmacological properties. In this paper, the radical-scavenging activities of a series of synthetic xyloketals and related chromanes toward 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) were evaluated by absorption spectrometry. One of the compounds (compound 10) displayed significant antioxidative action against DPPH and ABTS. A structure-activity analysis showed that the reactive sites on these compounds correlated with a hydroxy-group and also with ketal or aromatic H substituents. Based in part on a density functional theory (DFT) calculation of compound 10, the antioxidant mechanism of this chromane was deduced as a possible radical-scavenging mechanism by a sequential proton loss electron-transfer (SPLET) process.
topic Xyloketals
Radical scavenging activities
DFT
SPLET
url http://www.sciencedirect.com/science/article/pii/S2211383513000658
work_keys_str_mv AT zhongliangxu radicalscavengingactivitiesofmarinederivedxyloketalsandrelatedchromanes
AT bingtailu radicalscavengingactivitiesofmarinederivedxyloketalsandrelatedchromanes
AT qixiang radicalscavengingactivitiesofmarinederivedxyloketalsandrelatedchromanes
AT yiyingli radicalscavengingactivitiesofmarinederivedxyloketalsandrelatedchromanes
AT shichangli radicalscavengingactivitiesofmarinederivedxyloketalsandrelatedchromanes
AT yongchenglin radicalscavengingactivitiesofmarinederivedxyloketalsandrelatedchromanes
AT jiyanpang radicalscavengingactivitiesofmarinederivedxyloketalsandrelatedchromanes
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