140 lines
12 KiB
XML
140 lines
12 KiB
XML
<document id="7EE7E719C1FB8BD2EA66037D62C4F8E3" ID-DOI="10.1016/j.phytochem.2018.10.021" ID-ISSN="1873-3700" ID-Zenodo-Dep="10481450" IM.bibliography_approvedBy="karina" IM.illustrations_approvedBy="karina" IM.materialsCitations_approvedBy="felipe" IM.metadata_approvedBy="felipe" IM.tables_approvedBy="karina" IM.taxonomicNames_approvedBy="karina" IM.treatments_approvedBy="karina" checkinTime="1704926402680" checkinUser="felipe" docAuthor="Gousiadou, Chryssoula, Kokubun, Tetsuo, Albach, Dirk C., Gotfredsen, Charlotte H. & Jensen, Søren Rosendal" docDate="2019" docId="03DB683CFFEEFFB7FC97FA8BFBE3F970" docLanguage="en" docName="Phytochemistry.158.149-155.pdf" docOrigin="Phytochemistry 158" docSource="http://dx.doi.org/10.1016/j.phytochem.2018.10.021" docStyle="DocumentStyle:9E596C34F4E94307D29315B03ACE1007.6:Phytochemistry.2014-2019.journal_article" docStyleId="9E596C34F4E94307D29315B03ACE1007" docStyleName="Phytochemistry.2014-2019.journal_article" docStyleVersion="6" docTitle="Sutera cordata" docType="treatment" docVersion="3" lastPageNumber="153" masterDocId="FFE21044FFEAFFB3FFA5FFB9FF9DFFDF" masterDocTitle="Iridoid glucosides in the genus Sutera (Scrophulariaceae) as chemotaxonomic markers in tribe Limoselleae" masterLastPageNumber="155" masterPageNumber="149" pageNumber="153" updateTime="1706741795039" updateUser="karina">
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<mods:mods id="9025A4482A224FEA44B775E3963D0877" xmlns:mods="http://www.loc.gov/mods/v3">
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<mods:titleInfo id="4CB5CB324EFB2E1EEA97EBFE6B6D5F74">
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<mods:title id="623465020D82EE86ACD497E954797049">Iridoid glucosides in the genus Sutera (Scrophulariaceae) as chemotaxonomic markers in tribe Limoselleae</mods:title>
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</mods:titleInfo>
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<mods:name id="F93C674E0AE90AF47596D0FCBAB2A4ED" type="personal">
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<mods:roleTerm id="82AF61AD8733A24AAFC34A513EBC3271">Author</mods:roleTerm>
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<mods:namePart id="B912F0D58D36AAB3FEE08700E06329A1">Gousiadou, Chryssoula</mods:namePart>
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<mods:affiliation id="52C04B975CC5542F9EADD0E0A9FDAC57">∗ & Department of Chemistry, The Technical University of Denmark, Build. 207, DK- 2800 Lyngby, Denmark</mods:affiliation>
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</mods:name>
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<mods:name id="B57477642E91CDBFD627E4E6952E2C9F" type="personal">
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<mods:roleTerm id="CB6239B9E4FC6E1FD1EF43931138411C">Author</mods:roleTerm>
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<mods:namePart id="0CC8945868F4679DDB981D7CC2FFE338">Kokubun, Tetsuo</mods:namePart>
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<mods:roleTerm id="B65F36D7BB99C3ED3978EE75AE92E683">Author</mods:roleTerm>
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<mods:namePart id="0E20D32A8ACC5DCA4BFAC4E4EC843B57">Albach, Dirk C.</mods:namePart>
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<mods:name id="988855024AE5CFE180DE408447932E84" type="personal">
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<mods:roleTerm id="6F8B2674D25AF6A6CD59991A4CA3D9FD">Author</mods:roleTerm>
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</mods:role>
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<mods:namePart id="AB97FD03FF7A3EED78E553BAF5C9950A">Gotfredsen, Charlotte H.</mods:namePart>
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</mods:name>
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<mods:name id="C4FAAF48BB6E91D8352FF59410BC34B3" type="personal">
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<mods:roleTerm id="6606E9DB63AFE732CE4A3625B2F978AB">Author</mods:roleTerm>
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</mods:role>
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<mods:namePart id="61989961B6DEFF23D5848CF6537F050E">Jensen, Søren Rosendal</mods:namePart>
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</mods:name>
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<mods:typeOfResource id="2174BB06BD5A67854926DE071B47ED32">text</mods:typeOfResource>
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<mods:titleInfo id="34DD9E467AD0E8D16B4A96F0CC401E3E">
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<mods:title id="BEB6CE763D721FA880D2CEB485CF0F5E">Phytochemistry</mods:title>
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</mods:titleInfo>
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<mods:part id="C22BEED745F2C8635242ACB31B27E923">
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<mods:date id="E78ED602F9A82EF6AFC8D6BC2569099E">2019</mods:date>
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<mods:detail id="E65FF2C9C45F2216A818F6159F065B95" type="pubDate">
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<mods:number id="FF42CA4E3F29750FC84BA3FBA7585712">2019-02-28</mods:number>
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</mods:detail>
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<mods:detail id="4A9B0D036999899D325ADFD9E7F2A206" type="volume">
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<mods:number id="7CB367FA1F935E43260AE14305E3DB25">158</mods:number>
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<mods:extent id="486BBB3C580AF2E3649D8EFBCF778253" unit="page">
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<mods:start id="D9DB08FD23539283EB9F0385A5374335">149</mods:start>
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<mods:end id="FA5B44EAD1EFB686DF8A4F26F31F1FCA">155</mods:end>
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<mods:url id="D1C54024FB2ADF5D0567C25A2A26057D">http://dx.doi.org/10.1016/j.phytochem.2018.10.021</mods:url>
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</mods:location>
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<mods:classification id="FCFFF7C6417E59F9A160BB8EA00118A2">journal article</mods:classification>
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<mods:identifier id="8AEF5172ECF32E170D2B86C3074CB3EE" type="DOI">10.1016/j.phytochem.2018.10.021</mods:identifier>
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<mods:identifier id="6CFA3EFED5F8F484327DB5209A718F90" type="ISSN">1873-3700</mods:identifier>
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<mods:identifier id="9865CB9E5C6D7FEC3D1347CCB7CB2F10" type="Zenodo-Dep">10481450</mods:identifier>
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</mods:mods>
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<treatment id="03DB683CFFEEFFB7FC97FA8BFBE3F970" ID-DOI="http://doi.org/10.5281/zenodo.10576587" ID-Zenodo-Dep="10576587" LSID="urn:lsid:plazi:treatment:03DB683CFFEEFFB7FC97FA8BFBE3F970" httpUri="http://treatment.plazi.org/id/03DB683CFFEEFFB7FC97FA8BFBE3F970" lastPageNumber="153" pageId="4" pageNumber="153">
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<subSubSection id="C3688AA1FFEEFFB7FC97FA8BFC79FA9B" box="[818,996,1329,1349]" pageId="4" pageNumber="153" type="nomenclature">
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<paragraph id="8BCDD92AFFEEFFB7FC97FA8BFC79FA9B" blockId="4.[818,996,1329,1349]" box="[818,996,1329,1349]" pageId="4" pageNumber="153">
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<heading id="D0856E46FFEEFFB7FC97FA8BFC79FA9B" bold="true" box="[818,996,1329,1349]" fontSize="36" level="1" pageId="4" pageNumber="153" reason="1">
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<emphasis id="B9060538FFEEFFB7FC97FA8BFC79FA9B" bold="true" box="[818,996,1329,1349]" italics="true" pageId="4" pageNumber="153">
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3.5.
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<taxonomicName id="4C72A2A9FFEEFFB7FCC5FA8BFC79FA9B" ID-CoL="53HNQ" authority="(Thunb.) Kuntze" box="[864,996,1329,1349]" class="Magnoliopsida" family="Scrophulariaceae" genus="Sutera" kingdom="Plantae" order="Lamiales" pageId="4" pageNumber="153" phylum="Tracheophyta" rank="species" species="cordata">Sutera cordata</taxonomicName>
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</emphasis>
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</heading>
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</paragraph>
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</subSubSection>
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<subSubSection id="C3688AA1FFEEFFB7FCF6FAD0FBE3F970" pageId="4" pageNumber="153" type="description">
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<paragraph id="8BCDD92AFFEEFFB7FCF6FAD0FBE3F970" blockId="4.[818,1488,1385,1712]" pageId="4" pageNumber="153">
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Fresh plants (
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<quantity id="4C8A74CFFFEEFFB7FC74FAD3FC67FAA2" box="[977,1018,1386,1405]" metricMagnitude="-2" metricUnit="kg" metricValue="4.3" pageId="4" pageNumber="153" unit="g" value="43.0">43 g</quantity>
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) were blended with EtOH (200 ml) and treated as above to give after concentration
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<quantity id="4C8A74CFFFEEFFB7FBCEFA3CFB38FA46" box="[1131,1189,1413,1433]" metricMagnitude="-3" metricUnit="kg" metricValue="1.57" pageId="4" pageNumber="153" unit="g" value="1.57">1.57 g</quantity>
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residue. Chromatography gave: a fraction containing mainly secologanoside (
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<quantity id="4C8A74CFFFEEFFB7FB48FA18FAC3FA6B" box="[1261,1374,1441,1461]" metricMagnitude="-2" metricUnit="kg" metricValue="1.452" pageId="4" pageNumber="153" unit="mg" value="14520.0">
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<emphasis id="B9060538FFEEFFB7FB48FA18FA9BFA6B" bold="true" box="[1261,1286,1441,1460]" pageId="4" pageNumber="153">14</emphasis>
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, 520 mg
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</quantity>
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), a fraction with mainly secologanic acid (
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<emphasis id="B9060538FFEEFFB7FBF7FA04FBF6FA0F" bold="true" box="[1106,1131,1469,1488]" pageId="4" pageNumber="153">13</emphasis>
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,
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<quantity id="4C8A74CFFFEEFFB7FBD2FA04FB29FA0F" box="[1143,1204,1469,1488]" metricMagnitude="-5" metricUnit="kg" metricValue="7.0" pageId="4" pageNumber="153" unit="mg" value="70.0">70 mg</quantity>
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), a mixture (1:1) of sweroside (
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<emphasis id="B9060538FFEEFFB7FC9FFA60FCCEFA33" bold="true" box="[826,851,1497,1516]" pageId="4" pageNumber="153">12</emphasis>
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) and villoside (
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<emphasis id="B9060538FFEEFFB7FC4DFA60FB9CFA33" bold="true" box="[1000,1025,1497,1516]" pageId="4" pageNumber="153">11</emphasis>
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) (
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<quantity id="4C8A74CFFFEEFFB7FBB2FA60FBC8FA33" box="[1047,1109,1497,1516]" metricMagnitude="-5" metricUnit="kg" metricValue="3.3" pageId="4" pageNumber="153" unit="mg" value="33.0">33 mg</quantity>
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), echinacoside (
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<emphasis id="B9060538FFEEFFB7FB48FA60FA9BFA33" bold="true" box="[1261,1286,1497,1516]" pageId="4" pageNumber="153">16</emphasis>
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,
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<quantity id="4C8A74CFFFEEFFB7FAB7FA60FAD2FA33" box="[1298,1359,1497,1516]" metricMagnitude="-5" metricUnit="kg" metricValue="2.2" pageId="4" pageNumber="153" unit="mg" value="22.0">22 mg</quantity>
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), followed by fractions (total
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<quantity id="4C8A74CFFFEEFFB7FC60FA4CFB91F9D7" box="[965,1036,1525,1544]" metricMagnitude="-4" metricUnit="kg" metricValue="3.0" pageId="4" pageNumber="153" unit="mg" value="300.0">300 mg</quantity>
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) which were repeatedly chromatographed over C
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<subScript id="17F6DB6FFFEEFFB7FC9AF9A3FCCCF9F9" attach="left" box="[831,849,1562,1574]" fontSize="5" pageId="4" pageNumber="153">18</subScript>
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HPLC (MeCN-H
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<subScript id="17F6DB6FFFEEFFB7FC4BF9A3FC6AF9F9" attach="both" box="[1006,1015,1562,1574]" fontSize="5" pageId="4" pageNumber="153">2</subScript>
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O) to yield: tubuloside A (
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<emphasis id="B9060538FFEEFFB7FB52F9A8FA8DF9FB" bold="true" box="[1271,1296,1553,1572]" pageId="4" pageNumber="153">18</emphasis>
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, MeCN–H
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<subScript id="17F6DB6FFFEEFFB7FAD6F9A3FAE1F9F9" attach="both" box="[1395,1404,1562,1574]" fontSize="5" pageId="4" pageNumber="153">2</subScript>
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O 15:85,
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<quantity id="4C8A74CFFFEEFFB7FC97F994FCFCF99F" box="[818,865,1581,1600]" metricMagnitude="-6" metricUnit="kg" metricValue="2.0" pageId="4" pageNumber="153" unit="mg" value="2.0">2 mg</quantity>
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) and 2′′′′-acetyl angoroside A (
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<emphasis id="B9060538FFEEFFB7FB2DF994FB3CF99F" bold="true" box="[1160,1185,1581,1600]" pageId="4" pageNumber="153">19</emphasis>
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, MeCN–H
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<subScript id="17F6DB6FFFEEFFB7FAA4F98FFA97F99D" attach="both" box="[1281,1290,1590,1602]" fontSize="5" pageId="4" pageNumber="153">2</subScript>
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O 21:79,
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<quantity id="4C8A74CFFFEEFFB7FAC7F994FA09F99F" box="[1378,1428,1581,1600]" metricMagnitude="-6" metricUnit="kg" metricValue="6.0" pageId="4" pageNumber="153" unit="mg" value="6.0">6 mg</quantity>
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), both in a semi-pure state. Villoside (
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<emphasis id="B9060538FFEEFFB7FBFFF9F1FBEEF984" bold="true" box="[1114,1139,1608,1627]" pageId="4" pageNumber="153">11</emphasis>
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,
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<quantity id="4C8A74CFFFEEFFB7FBDAF9F1FB5DF983" box="[1151,1216,1608,1628]" metricMagnitude="-6" metricUnit="kg" metricValue="5.9" pageId="4" pageNumber="153" unit="mg" value="5.9">5.9 mg</quantity>
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) and sweroside (
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<emphasis id="B9060538FFEEFFB7FAC7F9F1FAE6F984" bold="true" box="[1378,1403,1608,1627]" pageId="4" pageNumber="153">12</emphasis>
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, 6.0 mg) were separated by HPLC with MeCN-H
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<subScript id="17F6DB6FFFEEFFB7FB3BF9D7FB3AF9A5" attach="both" box="[1182,1191,1646,1658]" fontSize="5" pageId="4" pageNumber="153">2</subScript>
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O (20:80). Pure samples of (
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<emphasis id="B9060538FFEEFFB7FA15F9DDFA54F9A8" bold="true" box="[1456,1481,1636,1655]" pageId="4" pageNumber="153">13</emphasis>
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,
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<quantity id="4C8A74CFFFEEFFB7FC97F939FCE2F94C" box="[818,895,1664,1683]" metricMagnitude="-5" metricUnit="kg" metricValue="2.08" pageId="4" pageNumber="153" unit="mg" value="20.8">20.8 mg</quantity>
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) and (
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<emphasis id="B9060538FFEEFFB7FC1EF939FC49F94C" bold="true" box="[955,980,1664,1683]" pageId="4" pageNumber="153">14</emphasis>
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,
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<quantity id="4C8A74CFFFEEFFB7FC7AF939FBBDF94C" box="[991,1056,1664,1683]" metricMagnitude="-6" metricUnit="kg" metricValue="5.2" pageId="4" pageNumber="153" unit="mg" value="5.2">5.2 mg</quantity>
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) were also obtained with MeCN-H
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<subScript id="17F6DB6FFFEEFFB7FAC6F930FAF1F94A" attach="right" box="[1379,1388,1673,1685]" fontSize="5" pageId="4" pageNumber="153">2</subScript>
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O gradient (17:83 → 85:15, v/v, over 15 min).
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</paragraph>
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</subSubSection>
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</treatment>
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</document> |