Identification of Barrenwort flavonoids by high-resolution tandem mass spectrometry
Fragmentation of the main Barrenwort flavonoids—icariin, icaritin, icarisides I and II, and epimedins A and B—is studied by tandem mass spectrometry. High-resolution mass spectra of positively charged ions of these compounds are obtained under the conditions of collision-induced dissociation. Charac...
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Veröffentlicht in: | Journal of analytical chemistry (New York, N.Y.) N.Y.), 2016-08, Vol.71 (8), p.768-776 |
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creator | Shevlyakova, O. A. Vasil’ev, K. Yu Ikhalainen, A. A. Antokhin, A. M. Taranchenko, V. F. Goncharov, V. M. Mitrofanov, D. A. Aksenov, A. V. Rodin, I. A. Shpigun, O. A. |
description | Fragmentation of the main Barrenwort flavonoids—icariin, icaritin, icarisides I and II, and epimedins A and B—is studied by tandem mass spectrometry. High-resolution mass spectra of positively charged ions of these compounds are obtained under the conditions of collision-induced dissociation. Characteristic fragment ions are determined, which ensured the classification of unknown compounds as Barrenwort flavonoids. Epimedin C was isolated from raw plant material by preparative liquid chromatography; its structure was confirmed by
1
H and
13
C NMR spectra. |
doi_str_mv | 10.1134/S106193481608013X |
format | Article |
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1
H and
13
C NMR spectra.</description><identifier>ISSN: 1061-9348</identifier><identifier>EISSN: 1608-3199</identifier><identifier>DOI: 10.1134/S106193481608013X</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Analytical Chemistry ; Chemical properties ; Chemistry ; Chemistry and Materials Science ; Flavonoids ; Mass spectrometry ; Methods</subject><ispartof>Journal of analytical chemistry (New York, N.Y.), 2016-08, Vol.71 (8), p.768-776</ispartof><rights>Pleiades Publishing, Ltd. 2016</rights><rights>COPYRIGHT 2016 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-3649e5a8b362005609e2682f7a13d68f795517f34acbb4a075245ac02fcec3093</citedby><cites>FETCH-LOGICAL-c427t-3649e5a8b362005609e2682f7a13d68f795517f34acbb4a075245ac02fcec3093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S106193481608013X$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S106193481608013X$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,41486,42555,51317</link.rule.ids></links><search><creatorcontrib>Shevlyakova, O. A.</creatorcontrib><creatorcontrib>Vasil’ev, K. Yu</creatorcontrib><creatorcontrib>Ikhalainen, A. A.</creatorcontrib><creatorcontrib>Antokhin, A. M.</creatorcontrib><creatorcontrib>Taranchenko, V. F.</creatorcontrib><creatorcontrib>Goncharov, V. M.</creatorcontrib><creatorcontrib>Mitrofanov, D. A.</creatorcontrib><creatorcontrib>Aksenov, A. V.</creatorcontrib><creatorcontrib>Rodin, I. A.</creatorcontrib><creatorcontrib>Shpigun, O. A.</creatorcontrib><title>Identification of Barrenwort flavonoids by high-resolution tandem mass spectrometry</title><title>Journal of analytical chemistry (New York, N.Y.)</title><addtitle>J Anal Chem</addtitle><description>Fragmentation of the main Barrenwort flavonoids—icariin, icaritin, icarisides I and II, and epimedins A and B—is studied by tandem mass spectrometry. High-resolution mass spectra of positively charged ions of these compounds are obtained under the conditions of collision-induced dissociation. Characteristic fragment ions are determined, which ensured the classification of unknown compounds as Barrenwort flavonoids. Epimedin C was isolated from raw plant material by preparative liquid chromatography; its structure was confirmed by
1
H and
13
C NMR spectra.</description><subject>Analytical Chemistry</subject><subject>Chemical properties</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Flavonoids</subject><subject>Mass spectrometry</subject><subject>Methods</subject><issn>1061-9348</issn><issn>1608-3199</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp90c9LwzAUB_AiCs7pH-Ct4MlDZ9KkaXOc4o_BQHAK3kqavXQZbTKSTN1_b-a8DIfkkEfe5xtIXpJcYjTCmNCbGUYMc0IrzFCFMHk_SgbbMiOY8-NYx3a27Z8mZ94vEUI80kEym8zBBK20FEFbk1qV3grnwHxaF1LViQ9rrJ77tNmkC90uMgfedusfG4SZQ5_2wvvUr0AGZ3sIbnOenCjRebj43YfJ28P9691TNn1-nNyNp5mkeRkywiiHQlQNYTlCBUMcclblqhSYzFmlSl4UuFSECtk0VKCyyGkhJMqVBEkQJ8PkandvKzqotVE2OCF77WU9ppwRyjBCUWUHVAsGnOisAaXj8Z4fHfBxxbdqeTBwvReIJsBXaMXa-3oye9m3eGels947UPXK6V64TY1RvR1k_WeQMZPvMj5a04Krl3btTPzZf0Lfnqudpw</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Shevlyakova, O. A.</creator><creator>Vasil’ev, K. Yu</creator><creator>Ikhalainen, A. A.</creator><creator>Antokhin, A. M.</creator><creator>Taranchenko, V. F.</creator><creator>Goncharov, V. M.</creator><creator>Mitrofanov, D. A.</creator><creator>Aksenov, A. V.</creator><creator>Rodin, I. A.</creator><creator>Shpigun, O. A.</creator><general>Pleiades Publishing</general><general>Springer</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope></search><sort><creationdate>20160801</creationdate><title>Identification of Barrenwort flavonoids by high-resolution tandem mass spectrometry</title><author>Shevlyakova, O. A. ; Vasil’ev, K. Yu ; Ikhalainen, A. A. ; Antokhin, A. M. ; Taranchenko, V. F. ; Goncharov, V. M. ; Mitrofanov, D. A. ; Aksenov, A. V. ; Rodin, I. A. ; Shpigun, O. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-3649e5a8b362005609e2682f7a13d68f795517f34acbb4a075245ac02fcec3093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Analytical Chemistry</topic><topic>Chemical properties</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Flavonoids</topic><topic>Mass spectrometry</topic><topic>Methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shevlyakova, O. A.</creatorcontrib><creatorcontrib>Vasil’ev, K. Yu</creatorcontrib><creatorcontrib>Ikhalainen, A. A.</creatorcontrib><creatorcontrib>Antokhin, A. M.</creatorcontrib><creatorcontrib>Taranchenko, V. F.</creatorcontrib><creatorcontrib>Goncharov, V. M.</creatorcontrib><creatorcontrib>Mitrofanov, D. A.</creatorcontrib><creatorcontrib>Aksenov, A. V.</creatorcontrib><creatorcontrib>Rodin, I. A.</creatorcontrib><creatorcontrib>Shpigun, O. A.</creatorcontrib><collection>CrossRef</collection><collection>Gale In Context: Science</collection><jtitle>Journal of analytical chemistry (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shevlyakova, O. A.</au><au>Vasil’ev, K. Yu</au><au>Ikhalainen, A. A.</au><au>Antokhin, A. M.</au><au>Taranchenko, V. F.</au><au>Goncharov, V. M.</au><au>Mitrofanov, D. A.</au><au>Aksenov, A. V.</au><au>Rodin, I. A.</au><au>Shpigun, O. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of Barrenwort flavonoids by high-resolution tandem mass spectrometry</atitle><jtitle>Journal of analytical chemistry (New York, N.Y.)</jtitle><stitle>J Anal Chem</stitle><date>2016-08-01</date><risdate>2016</risdate><volume>71</volume><issue>8</issue><spage>768</spage><epage>776</epage><pages>768-776</pages><issn>1061-9348</issn><eissn>1608-3199</eissn><abstract>Fragmentation of the main Barrenwort flavonoids—icariin, icaritin, icarisides I and II, and epimedins A and B—is studied by tandem mass spectrometry. High-resolution mass spectra of positively charged ions of these compounds are obtained under the conditions of collision-induced dissociation. Characteristic fragment ions are determined, which ensured the classification of unknown compounds as Barrenwort flavonoids. Epimedin C was isolated from raw plant material by preparative liquid chromatography; its structure was confirmed by
1
H and
13
C NMR spectra.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S106193481608013X</doi><tpages>9</tpages></addata></record> |
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subjects | Analytical Chemistry Chemical properties Chemistry Chemistry and Materials Science Flavonoids Mass spectrometry Methods |
title | Identification of Barrenwort flavonoids by high-resolution tandem mass spectrometry |
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