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<document id="65B1811E0BC107D87E3D91E19DE62ACB" ID-DOI="10.1016/j.phytochem.2018.12.022" ID-ISSN="1873-3700" ID-Zenodo-Dep="10481924" IM.bibliography_approvedBy="karina" IM.illustrations_approvedBy="karina" IM.materialsCitations_approvedBy="felipe" IM.metadata_approvedBy="felipe" IM.tables_requiresApprovalFor="GgImagineBatch" IM.taxonomicNames_approvedBy="karina" IM.treatments_approvedBy="karina" checkinTime="1704928502977" checkinUser="felipe" docAuthor="Nawrot, Joanna, Budzianowski, Jaromir &amp; Nowak, Gerard" docDate="2019" docId="038587F2FFB2FFC22933FB4EFC67F9FB" docLanguage="en" docName="Phytochemistry.159.172-178.pdf" docOrigin="Phytochemistry 159" docSource="http://dx.doi.org/10.1016/j.phytochem.2018.12.022" docStyle="DocumentStyle:9E596C34F4E94307D29315B03ACE1007.6:Phytochemistry.2014-2019.journal_article" docStyleId="9E596C34F4E94307D29315B03ACE1007" docStyleName="Phytochemistry.2014-2019.journal_article" docStyleVersion="6" docTitle="Psephellus sibiricus subsp. leaves Wagenitz" docType="treatment" docVersion="4" lastPageNumber="177" masterDocId="FFBCFF8AFFB7FFC72A01FFD8FFA3FFEF" masterDocTitle="Phytochemical profiles of the leaves of Stizolophus balsamita and Psephellus sibiricus and their chemotaxonomic implications" masterLastPageNumber="178" masterPageNumber="172" pageNumber="177" updateTime="1706407054321" updateUser="karina">
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<mods:title id="3ED78663D1ACC7A478BA9B03FFBDDF0D">Phytochemical profiles of the leaves of Stizolophus balsamita and Psephellus sibiricus and their chemotaxonomic implications</mods:title>
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<mods:namePart id="2CC52022EEA5CD6830F733E4FC641204">Nawrot, Joanna</mods:namePart>
<mods:affiliation id="A3C33C011B8682A9B61D6249103BD00E"> &amp; Department of Medicinal and Cosmetic Natural Products, Poznan University of Medical Sciences, Mazowiecka Str. 33, 60 - 623 Poznan, Poland</mods:affiliation>
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<mods:namePart id="CC8A73DF7357F80265F5B863A5E5A4B4">Budzianowski, Jaromir</mods:namePart>
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<mods:namePart id="098C209598005D14DAA0A7CD135204A8">Nowak, Gerard</mods:namePart>
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<mods:title id="1867C28040832116270A48382590F548">Phytochemistry</mods:title>
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<treatment id="038587F2FFB2FFC22933FB4EFC67F9FB" LSID="urn:lsid:plazi:treatment:038587F2FFB2FFC22933FB4EFC67F9FB" httpUri="http://treatment.plazi.org/id/038587F2FFB2FFC22933FB4EFC67F9FB" lastPageNumber="177" pageId="5" pageNumber="177">
<subSubSection id="C336656FFFB2FFC22933FB4EFA2DFB46" box="[818,1422,1174,1193]" pageId="5" pageNumber="177" type="nomenclature">
<paragraph id="8B9336E4FFB2FFC22933FB4EFA2DFB46" blockId="5.[818,1422,1174,1193]" box="[818,1422,1174,1193]" pageId="5" pageNumber="177">
<heading id="D0DB8188FFB2FFC22933FB4EFA2DFB46" bold="true" box="[818,1422,1174,1193]" fontSize="36" level="1" pageId="5" pageNumber="177" reason="1">
<emphasis id="B958EAF6FFB2FFC22933FB4EFA2DFB46" bold="true" box="[818,1422,1174,1193]" italics="true" pageId="5" pageNumber="177">
3.4. Extraction and isolation of compounds from
<taxonomicName id="4C2C4D67FFB2FFC22EF0FB4EFAF1FB46" authority="(L.) Wagenitz" authorityName="Wagenitz" baseAuthorityName="L." box="[1265,1362,1174,1193]" class="Magnoliopsida" family="Asteraceae" genus="Psephellus" kingdom="Plantae" order="Asterales" pageId="5" pageNumber="177" phylum="Tracheophyta" rank="subSpecies" species="sibiricus" subSpecies="leaves">P. sibiricus</taxonomicName>
leaves
</emphasis>
</heading>
</paragraph>
</subSubSection>
<subSubSection id="C336656FFFB2FFC22952FB16FC67F9FB" pageId="5" pageNumber="177" type="description">
<paragraph id="8B9336E4FFB2FFC22952FB16FC67F9FB" blockId="5.[818,1488,1230,1556]" pageId="5" pageNumber="177">
The dried leaves of
<taxonomicName id="4C2C4D67FFB2FFC22E10FB16FBD0FB0E" box="[1041,1139,1230,1249]" class="Magnoliopsida" family="Asteraceae" genus="Psephellus" kingdom="Plantae" order="Asterales" pageId="5" pageNumber="177" phylum="Tracheophyta" rank="species" species="sibiricus">
<emphasis id="B958EAF6FFB2FFC22E10FB16FBD0FB0E" bold="true" box="[1041,1139,1230,1249]" italics="true" pageId="5" pageNumber="177">P. sibiricus</emphasis>
</taxonomicName>
(
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) were crushed and soaked in MeOH. The MeOH extract was evapd, and the residue was dissolved in H
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O. The aq. soln was re-extracted with
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Cl
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. The
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Cl
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extract was dried with Na
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SO
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, filtrated and evapd gave a residue (
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) and chromatographed with CC method on silica gel with a mixtures of
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Cl
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and (
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)
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CO (ratio 45:1, 35:1 and 10:1) as eluent. The result was the isolation of the following compounds: scoparone (
<emphasis id="B958EAF6FFB2FFC22F5AFAADFAC4FA67" bold="true" box="[1371,1383,1397,1416]" pageId="5" pageNumber="177">9</emphasis>
) (
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, amorphous solid), scopoletin (
<emphasis id="B958EAF6FFB2FFC22E52FA49FBCFFA4B" bold="true" box="[1107,1132,1425,1444]" pageId="5" pageNumber="177">10</emphasis>
) (
<quantity id="4CD49B01FFB2FFC22E83FA49FB71FA4A" box="[1154,1234,1425,1445]" metricMagnitude="-5" metricUnit="kg" metricValue="4.54" pageId="5" pageNumber="177" unit="mg" value="45.4">45.4 mg</quantity>
, m.p. 192195 °C), umbelliferone (
<emphasis id="B958EAF6FFB2FFC22988FA75FC01FA2F" bold="true" box="[905,930,1453,1472]" pageId="5" pageNumber="177">11</emphasis>
) (
<quantity id="4CD49B01FFB2FFC229B9FA75FBABFA2E" box="[952,1032,1453,1473]" metricMagnitude="-5" metricUnit="kg" metricValue="6.37" pageId="5" pageNumber="177" unit="mg" value="63.7">63.7 mg</quantity>
, m.p. 230 °C), cynaropicrin (
<emphasis id="B958EAF6FFB2FFC22F1AFA75FA97FA2F" bold="true" box="[1307,1332,1453,1472]" pageId="5" pageNumber="177">12</emphasis>
) (
<quantity id="4CD49B01FFB2FFC22F4BFA75FA2EFA2E" box="[1354,1421,1453,1473]" metricMagnitude="-6" metricUnit="kg" metricValue="6.7" pageId="5" pageNumber="177" unit="mg" value="6.7">6.7 mg</quantity>
, amorphous solid) and desacylcynaropicrin 8α-(
<emphasis id="B958EAF6FFB2FFC22EDEFA11FB48FA33" bold="true" box="[1247,1259,1481,1500]" italics="true" pageId="5" pageNumber="177">Z</emphasis>
)-(4-hydroxy-2-methyl) butenoate (]cebellin F) (
<emphasis id="B958EAF6FFB2FFC22E26FA3DFBE3FA17" bold="true" box="[1063,1088,1509,1528]" pageId="5" pageNumber="177">13</emphasis>
) (
<quantity id="4CD49B01FFB2FFC22E57FA3DFB3AFA17" box="[1110,1177,1509,1528]" metricMagnitude="-6" metricUnit="kg" metricValue="3.9" pageId="5" pageNumber="177" unit="mg" value="3.9">3.9 mg</quantity>
, amorphous solid). NMR data in
<tableCitation id="C6AE035FFFB2FFC22933F9D9FC22F9FB" box="[818,897,1537,1556]" captionStart="Table 7" captionStartId="5.[100,150,897,913]" captionTargetPageId="5" captionText="Table 7 1H and13C NMR data of compounds 9-11." pageId="5" pageNumber="177">Tables 7</tableCitation>
and
<tableCitation id="C6AE035FFFB2FFC229B3F9D9FC1DF9FB" box="[946,958,1537,1556]" captionStart="Table 8" captionStartId="5.[818,868,161,177]" captionTargetPageId="5" captionText="Table 8 1H and13C NMR data of compounds 12 and 13 in DMSO-d6" pageId="5" pageNumber="177">8</tableCitation>
.
</paragraph>
</subSubSection>
</treatment>
</document>