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Inositol Derivatives and Phenolic Compounds from the Roots of Taraxacum coreanum
In this study, the characterization of chemical constituents and biological activity of the roots of (Asteraceae) was attempted. Phytochemical investigation of the roots of led to the isolation of two new inositol derivatives, taraxinositols A ( ) and B ( ), and a new phenolic compound, taraxinol (...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2017-08, Vol.22 (8), p.1349 |
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description | In this study, the characterization of chemical constituents and biological activity of the roots of
(Asteraceae) was attempted. Phytochemical investigation of the roots of
led to the isolation of two new inositol derivatives, taraxinositols A (
) and B (
), and a new phenolic compound, taraxinol (
), together with twenty known compounds including four inositol derivatives,
-inositol-1,4-bis (4-hydroxybenzeneacetate) (
),
-inositol-1,5-bis(4- hydroxybenzeneacetate) (
),
-inositol-2,3-bis (4-hydroxybenzeneacetate) (
) and
-inositol- 1,2,3-tris (4-hydroxybenzeneacetate) (
), nine phenolic compounds:
-hydroxybenzaldehyde (
), vanillin (
), syringaldehyde (
), vanillic acid (
), 4-methoxyphenylacetic acid (
), 4-hydroxy- phenylacetic acid methyl ester (
), optivanin (
), isoferulic acid (
) and dihydroconiferyl alcohol (
), four coumarins: nodakenetin (
), decursinol (
), prangol (
) and isobyakangelicin (
), and three lignans: syringaresinol-4'-
-β-d-glucoside (
), syringaresinol (
), and pinoresinol (
). The structures of isolated compounds were determined on the basis of spectroscopic analysis. Among the isolated compounds, vanillic acid, isoferulic acid and syringaresinol showed radical scavenging activity with IC
values ranging from 30.4 to 75.2 μM. |
doi_str_mv | 10.3390/molecules22081349 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_1d84b684148e480b84e01c489fe9a331</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_1d84b684148e480b84e01c489fe9a331</doaj_id><sourcerecordid>1939939371</sourcerecordid><originalsourceid>FETCH-LOGICAL-c493t-c63babc47396df37baf06afe6aa8233625022341f83238f510e8987fbf9cf5e53</originalsourceid><addsrcrecordid>eNplkU1v1DAQhiMEoqXwA7ggS1y4LNgeJ7EvSGj5WqkSFSpna-KMu1klmcVOVuXfk7KlakGa0Vjjdx6N_RbFSyXfAjj5buCewtxT1lpaBcY9Kk6V0XIF0rjH984nxbOcd1JqZVT5tDjR1sqyLuVpcbEZOXcT9-Ijpe6AU3egLHBsxcWWRu67INY87Hke2yxi4kFMWxLfmacsOIpLTHiNYR5E4EQ4zsPz4knEPtOL23pW_Pj86XL9dXX-7ctm_eF8FYyDaRUqaLAJpgZXtRHqBqOsMFKFaDVApUupNRgVLWiwsVSSrLN1bKILsaQSzorNkdsy7vw-dQOmX56x838anK48pqkLPXnVWtNU1ihjyVjZWENSBWNdJIcAamG9P7L2czNQG2icEvYPoA9vxm7rr_jgK1Vq7eoF8OYWkPjnTHnyQ5cD9T2OxHP2ymlbW7PkIn39j3THcxqXr1pU4JaA-mYjdVSFxDkninfLKOlvvPf_eb_MvLr_iruJv2bDbyXwrLg</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1939939371</pqid></control><display><type>article</type><title>Inositol Derivatives and Phenolic Compounds from the Roots of Taraxacum coreanum</title><source>PubMed (Medline)</source><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><creator>Mo, Eun Jin ; Ahn, Jong Hoon ; Jo, Yang Hee ; Kim, Seon Beom ; Hwang, Bang Yeon ; Lee, Mi Kyeong</creator><creatorcontrib>Mo, Eun Jin ; Ahn, Jong Hoon ; Jo, Yang Hee ; Kim, Seon Beom ; Hwang, Bang Yeon ; Lee, Mi Kyeong</creatorcontrib><description>In this study, the characterization of chemical constituents and biological activity of the roots of
(Asteraceae) was attempted. Phytochemical investigation of the roots of
led to the isolation of two new inositol derivatives, taraxinositols A (
) and B (
), and a new phenolic compound, taraxinol (
), together with twenty known compounds including four inositol derivatives,
-inositol-1,4-bis (4-hydroxybenzeneacetate) (
),
-inositol-1,5-bis(4- hydroxybenzeneacetate) (
),
-inositol-2,3-bis (4-hydroxybenzeneacetate) (
) and
-inositol- 1,2,3-tris (4-hydroxybenzeneacetate) (
), nine phenolic compounds:
-hydroxybenzaldehyde (
), vanillin (
), syringaldehyde (
), vanillic acid (
), 4-methoxyphenylacetic acid (
), 4-hydroxy- phenylacetic acid methyl ester (
), optivanin (
), isoferulic acid (
) and dihydroconiferyl alcohol (
), four coumarins: nodakenetin (
), decursinol (
), prangol (
) and isobyakangelicin (
), and three lignans: syringaresinol-4'-
-β-d-glucoside (
), syringaresinol (
), and pinoresinol (
). The structures of isolated compounds were determined on the basis of spectroscopic analysis. Among the isolated compounds, vanillic acid, isoferulic acid and syringaresinol showed radical scavenging activity with IC
values ranging from 30.4 to 75.2 μM.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules22081349</identifier><identifier>PMID: 28805750</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Acids ; Alcohols ; antioxidant ; Antioxidants - chemistry ; Antioxidants - pharmacology ; Biological activity ; Chromatography, High Pressure Liquid - methods ; Coumarins - chemistry ; Furans - chemistry ; Glucosides - chemistry ; Humans ; Hydroxybenzaldehydes ; Inhibitory Concentration 50 ; Inositol ; Inositol - chemistry ; Inositol - isolation & purification ; Inositol 1,4,5-trisphosphate receptors ; Lignans ; Lignans - chemistry ; Magnetic Resonance Spectroscopy - methods ; Phenol - chemistry ; Phenol - isolation & purification ; phenolic ; Phenolic compounds ; Phenols ; Phenylacetic acid ; Plant Extracts - chemistry ; Plant Extracts - isolation & purification ; Plant Roots - chemistry ; Receptors, Scavenger - chemistry ; Receptors, Scavenger - metabolism ; Roots ; Syringaldehyde ; Taraxacum - chemistry ; Taraxacum coreanum ; Vanillic acid ; Vanillin</subject><ispartof>Molecules (Basel, Switzerland), 2017-08, Vol.22 (8), p.1349</ispartof><rights>Copyright MDPI AG 2017</rights><rights>2017 by the authors. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-c63babc47396df37baf06afe6aa8233625022341f83238f510e8987fbf9cf5e53</citedby><cites>FETCH-LOGICAL-c493t-c63babc47396df37baf06afe6aa8233625022341f83238f510e8987fbf9cf5e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1939939371/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1939939371?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28805750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mo, Eun Jin</creatorcontrib><creatorcontrib>Ahn, Jong Hoon</creatorcontrib><creatorcontrib>Jo, Yang Hee</creatorcontrib><creatorcontrib>Kim, Seon Beom</creatorcontrib><creatorcontrib>Hwang, Bang Yeon</creatorcontrib><creatorcontrib>Lee, Mi Kyeong</creatorcontrib><title>Inositol Derivatives and Phenolic Compounds from the Roots of Taraxacum coreanum</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>In this study, the characterization of chemical constituents and biological activity of the roots of
(Asteraceae) was attempted. Phytochemical investigation of the roots of
led to the isolation of two new inositol derivatives, taraxinositols A (
) and B (
), and a new phenolic compound, taraxinol (
), together with twenty known compounds including four inositol derivatives,
-inositol-1,4-bis (4-hydroxybenzeneacetate) (
),
-inositol-1,5-bis(4- hydroxybenzeneacetate) (
),
-inositol-2,3-bis (4-hydroxybenzeneacetate) (
) and
-inositol- 1,2,3-tris (4-hydroxybenzeneacetate) (
), nine phenolic compounds:
-hydroxybenzaldehyde (
), vanillin (
), syringaldehyde (
), vanillic acid (
), 4-methoxyphenylacetic acid (
), 4-hydroxy- phenylacetic acid methyl ester (
), optivanin (
), isoferulic acid (
) and dihydroconiferyl alcohol (
), four coumarins: nodakenetin (
), decursinol (
), prangol (
) and isobyakangelicin (
), and three lignans: syringaresinol-4'-
-β-d-glucoside (
), syringaresinol (
), and pinoresinol (
). The structures of isolated compounds were determined on the basis of spectroscopic analysis. Among the isolated compounds, vanillic acid, isoferulic acid and syringaresinol showed radical scavenging activity with IC
values ranging from 30.4 to 75.2 μM.</description><subject>Acids</subject><subject>Alcohols</subject><subject>antioxidant</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - pharmacology</subject><subject>Biological activity</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Coumarins - chemistry</subject><subject>Furans - chemistry</subject><subject>Glucosides - chemistry</subject><subject>Humans</subject><subject>Hydroxybenzaldehydes</subject><subject>Inhibitory Concentration 50</subject><subject>Inositol</subject><subject>Inositol - chemistry</subject><subject>Inositol - isolation & purification</subject><subject>Inositol 1,4,5-trisphosphate receptors</subject><subject>Lignans</subject><subject>Lignans - chemistry</subject><subject>Magnetic Resonance Spectroscopy - methods</subject><subject>Phenol - chemistry</subject><subject>Phenol - isolation & purification</subject><subject>phenolic</subject><subject>Phenolic compounds</subject><subject>Phenols</subject><subject>Phenylacetic acid</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - isolation & purification</subject><subject>Plant Roots - chemistry</subject><subject>Receptors, Scavenger - chemistry</subject><subject>Receptors, Scavenger - metabolism</subject><subject>Roots</subject><subject>Syringaldehyde</subject><subject>Taraxacum - chemistry</subject><subject>Taraxacum coreanum</subject><subject>Vanillic acid</subject><subject>Vanillin</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkU1v1DAQhiMEoqXwA7ggS1y4LNgeJ7EvSGj5WqkSFSpna-KMu1klmcVOVuXfk7KlakGa0Vjjdx6N_RbFSyXfAjj5buCewtxT1lpaBcY9Kk6V0XIF0rjH984nxbOcd1JqZVT5tDjR1sqyLuVpcbEZOXcT9-Ijpe6AU3egLHBsxcWWRu67INY87Hke2yxi4kFMWxLfmacsOIpLTHiNYR5E4EQ4zsPz4knEPtOL23pW_Pj86XL9dXX-7ctm_eF8FYyDaRUqaLAJpgZXtRHqBqOsMFKFaDVApUupNRgVLWiwsVSSrLN1bKILsaQSzorNkdsy7vw-dQOmX56x838anK48pqkLPXnVWtNU1ihjyVjZWENSBWNdJIcAamG9P7L2czNQG2icEvYPoA9vxm7rr_jgK1Vq7eoF8OYWkPjnTHnyQ5cD9T2OxHP2ymlbW7PkIn39j3THcxqXr1pU4JaA-mYjdVSFxDkninfLKOlvvPf_eb_MvLr_iruJv2bDbyXwrLg</recordid><startdate>20170814</startdate><enddate>20170814</enddate><creator>Mo, Eun Jin</creator><creator>Ahn, Jong Hoon</creator><creator>Jo, Yang Hee</creator><creator>Kim, Seon Beom</creator><creator>Hwang, Bang Yeon</creator><creator>Lee, Mi Kyeong</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20170814</creationdate><title>Inositol Derivatives and Phenolic Compounds from the Roots of Taraxacum coreanum</title><author>Mo, Eun Jin ; Ahn, Jong Hoon ; Jo, Yang Hee ; Kim, Seon Beom ; Hwang, Bang Yeon ; Lee, Mi Kyeong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-c63babc47396df37baf06afe6aa8233625022341f83238f510e8987fbf9cf5e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acids</topic><topic>Alcohols</topic><topic>antioxidant</topic><topic>Antioxidants - chemistry</topic><topic>Antioxidants - pharmacology</topic><topic>Biological activity</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Coumarins - chemistry</topic><topic>Furans - chemistry</topic><topic>Glucosides - chemistry</topic><topic>Humans</topic><topic>Hydroxybenzaldehydes</topic><topic>Inhibitory Concentration 50</topic><topic>Inositol</topic><topic>Inositol - chemistry</topic><topic>Inositol - isolation & purification</topic><topic>Inositol 1,4,5-trisphosphate receptors</topic><topic>Lignans</topic><topic>Lignans - chemistry</topic><topic>Magnetic Resonance Spectroscopy - methods</topic><topic>Phenol - chemistry</topic><topic>Phenol - isolation & purification</topic><topic>phenolic</topic><topic>Phenolic compounds</topic><topic>Phenols</topic><topic>Phenylacetic acid</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - isolation & purification</topic><topic>Plant Roots - chemistry</topic><topic>Receptors, Scavenger - chemistry</topic><topic>Receptors, Scavenger - metabolism</topic><topic>Roots</topic><topic>Syringaldehyde</topic><topic>Taraxacum - chemistry</topic><topic>Taraxacum coreanum</topic><topic>Vanillic acid</topic><topic>Vanillin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mo, Eun Jin</creatorcontrib><creatorcontrib>Ahn, Jong Hoon</creatorcontrib><creatorcontrib>Jo, Yang Hee</creatorcontrib><creatorcontrib>Kim, Seon Beom</creatorcontrib><creatorcontrib>Hwang, Bang Yeon</creatorcontrib><creatorcontrib>Lee, Mi Kyeong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mo, Eun Jin</au><au>Ahn, Jong Hoon</au><au>Jo, Yang Hee</au><au>Kim, Seon Beom</au><au>Hwang, Bang Yeon</au><au>Lee, Mi Kyeong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inositol Derivatives and Phenolic Compounds from the Roots of Taraxacum coreanum</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2017-08-14</date><risdate>2017</risdate><volume>22</volume><issue>8</issue><spage>1349</spage><pages>1349-</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>In this study, the characterization of chemical constituents and biological activity of the roots of
(Asteraceae) was attempted. Phytochemical investigation of the roots of
led to the isolation of two new inositol derivatives, taraxinositols A (
) and B (
), and a new phenolic compound, taraxinol (
), together with twenty known compounds including four inositol derivatives,
-inositol-1,4-bis (4-hydroxybenzeneacetate) (
),
-inositol-1,5-bis(4- hydroxybenzeneacetate) (
),
-inositol-2,3-bis (4-hydroxybenzeneacetate) (
) and
-inositol- 1,2,3-tris (4-hydroxybenzeneacetate) (
), nine phenolic compounds:
-hydroxybenzaldehyde (
), vanillin (
), syringaldehyde (
), vanillic acid (
), 4-methoxyphenylacetic acid (
), 4-hydroxy- phenylacetic acid methyl ester (
), optivanin (
), isoferulic acid (
) and dihydroconiferyl alcohol (
), four coumarins: nodakenetin (
), decursinol (
), prangol (
) and isobyakangelicin (
), and three lignans: syringaresinol-4'-
-β-d-glucoside (
), syringaresinol (
), and pinoresinol (
). The structures of isolated compounds were determined on the basis of spectroscopic analysis. Among the isolated compounds, vanillic acid, isoferulic acid and syringaresinol showed radical scavenging activity with IC
values ranging from 30.4 to 75.2 μM.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>28805750</pmid><doi>10.3390/molecules22081349</doi><oa>free_for_read</oa></addata></record> |
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subjects | Acids Alcohols antioxidant Antioxidants - chemistry Antioxidants - pharmacology Biological activity Chromatography, High Pressure Liquid - methods Coumarins - chemistry Furans - chemistry Glucosides - chemistry Humans Hydroxybenzaldehydes Inhibitory Concentration 50 Inositol Inositol - chemistry Inositol - isolation & purification Inositol 1,4,5-trisphosphate receptors Lignans Lignans - chemistry Magnetic Resonance Spectroscopy - methods Phenol - chemistry Phenol - isolation & purification phenolic Phenolic compounds Phenols Phenylacetic acid Plant Extracts - chemistry Plant Extracts - isolation & purification Plant Roots - chemistry Receptors, Scavenger - chemistry Receptors, Scavenger - metabolism Roots Syringaldehyde Taraxacum - chemistry Taraxacum coreanum Vanillic acid Vanillin |
title | Inositol Derivatives and Phenolic Compounds from the Roots of Taraxacum coreanum |
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