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<h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">Hyperosid</span></h1>
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<div id="mw-content-text" class="mw-body-content mw-content-ltr" lang="de" dir="ltr"><div class="mw-content-ltr mw-parser-output" lang="de" dir="ltr"><table class="wikitable infobox float-right" id="Vorlage_Infobox_Chemikalie" style="font-size:90%; margin-top:0; width:350px;" summary="Infobox Chemikalie">
<tbody><tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Strukturformel
</th></tr>
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<td colspan="2" class="hintergrundfarbe-basis skin-invert-image" style="text-align:center;"><span typeof="mw:File"></span>
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<th colspan="2" style="background:#FFDEAD; color:#202122;">Allgemeines
</th></tr>
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<td style="width:33%;">Name
</td>
<td>Hyperosid
</td></tr>
<tr>
<td>Andere Namen
</td>
<td>
<ul><li>Quercetin-3-<i>D</i>-galactosid</li>
<li>3,3′,4′,5,7-Pentahydroxyflavon-3-<i>D</i>-galactosid</li>
<li>Hyperin</li>
<li>2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-{[(2<i>S</i>,3<i>R</i>,4<i>S</i>,5<i>R</i>,6<i>R</i>)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4<i>H</i>-1-benzopyran-4-on</li></ul>
</td></tr>
<tr>
<td><a href="Summenformel" title="Summenformel">Summenformel</a>
</td>
<td>C<sub>21</sub>H<sub>20</sub>O<sub>12</sub>
</td></tr>
<tr>
<td>Kurzbeschreibung
</td>
<td>
<p>weißer bis gelblicher Feststoff<sup id="cite_ref-TCI_1-0" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Externe Identifikatoren/Datenbanken
</th></tr>
<tr>
<td colspan="2" style="padding:0;">
<table class="mw-collapsible mw-collapsed wikitable" data-expandtext="+" data-collapsetext="−" style="border-top:none; margin:-1px; width:calc(100% + 2px);">
<tbody><tr>
<td style="width:33%;"><a href="CAS-Nummer" title="CAS-Nummer">CAS-Nummer</a>
</td>
<td><span title="Untervorlage eingebunden: CASRN"></span><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=482-36-0">482-36-0</a><span class="editoronly" style="display:none;"></span>
</td>
<td style="background:#FFDEAD; color:#202122; border-top:1px solid #FFDEAD; padding:0.2em 0; vertical-align:bottom; width:5%;">
</td></tr>
<tr>
<td><a href="EG-Nummer" title="EG-Nummer">EG-Nummer</a>
</td>
<td colspan="2">207-580-6
</td></tr>
<tr>
<td><a href="Europ%C3%A4ische_Chemikalienagentur" title="Europäische Chemikalienagentur">ECHA</a>-InfoCard
</td>
<td colspan="2"><a rel="nofollow" class="external text" href="https://www.echa.europa.eu/de/substance-information/-/substanceinfo/100.006.892">100.006.892</a>
</td></tr>
<tr>
<td><a href="PubChem" title="PubChem">PubChem</a>
</td>
<td colspan="2"><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/5281643">5281643</a>
</td></tr>
<tr>
<td><a href="ChemSpider" title="ChemSpider">ChemSpider</a>
</td>
<td colspan="2"><a rel="nofollow" class="external text" href="https://www.chemspider.com/Chemical-Structure.4444962.html">4444962</a>
</td></tr>
<tr>
<td style="border-right:1px solid #a2a9b1;"><a href="Wikidata" title="Wikidata">Wikidata</a>
</td>
<td colspan="2"><a href="https://www.wikidata.org/wiki/Q5242815" class="extiw external" title="d:Q5242815">Q5242815</a>
</td></tr></tbody></table>
</td></tr>
<tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Eigenschaften
</th></tr>
<tr>
<td><a href="Molare_Masse" title="Molare Masse">Molare Masse</a>
</td>
<td>464,38 g·<a href="Mol" title="Mol">mol</a><sup>−1</sup>
</td></tr>
<tr>
<td><a href="Aggregatzustand" title="Aggregatzustand">Aggregatzustand</a>
</td>
<td>
<p>fest<sup id="cite_ref-TCI_1-1" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="Schmelzpunkt" title="Schmelzpunkt">Schmelzpunkt</a>
</td>
<td>
<p>233 <a href="Grad_Celsius" title="Grad Celsius">°C</a><sup id="cite_ref-TCI_1-2" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<td><a href="L%C3%B6slichkeit" title="Löslichkeit">Löslichkeit</a>
</td>
<td>
<p>löslich in <a href="Methanol" title="Methanol">Methanol</a><sup id="cite_ref-Curt_Hunnius,_Artur_Burger_2-0" class="reference"><a href="#cite_note-Curt_Hunnius,_Artur_Burger-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
</p>
</td></tr>
<tr>
<th colspan="2" style="background:#FFDEAD; color:#202122;">Sicherheitshinweise
</th></tr>
<tr>
<td colspan="2">
<table cellspacing="0" cellpadding="2" style="width:100%;">
<tbody><tr>
<td colspan="2" style="text-align:center"><b><a href="Global_harmonisiertes_System_zur_Einstufung_und_Kennzeichnung_von_Chemikalien" title="Global harmonisiertes System zur Einstufung und Kennzeichnung von Chemikalien">GHS-Gefahrstoffkennzeichnung</a></b><sup id="cite_ref-TCI_1-3" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
<table class="hintergrundfarbe-neutral" style="text-align:center; margin-left:auto; margin-right:auto; display:flex; justify-content:center;">
<tbody><tr>
<td><i>keine GHS-Piktogramme</i>
</td></tr></tbody></table>
<p>
</p>
</td></tr>
<tr>
<td rowspan="2" width="33%" style="border-top:1px #A7A7A7 dashed; border-right:1px #A7A7A7 dashed;"><a href="H-_und_P-S%C3%A4tze" title="H- und P-Sätze">H- und P-Sätze</a>
</td>
<td style="border-top:1px #A7A7A7 dashed;">H: <span title="Untervorlage eingebunden: H-Sätze"></span><i>keine H-Sätze</i>
</td></tr>
<tr>
<td style="border-top:1px #A7A7A7 dashed;">P: <span title="Untervorlage eingebunden: P-Sätze"></span><i>keine P-Sätze</i><sup id="cite_ref-TCI_1-4" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
</td></tr>
</tbody></table>
</td></tr>
<tr>
<td colspan="2" style="background:#FFDEAD; color:#202122; font-size:80%; text-align:center; line-height:150%; padding:.25em;">Wenn nicht anders vermerkt, gelten die angegebenen Daten bei <a href="Standardbedingungen" title="Standardbedingungen">Standardbedingungen</a> (0 °C, 1000 hPa).
</td></tr></tbody></table><p><span class="editoronly" style="display:none;"></span>
</p><p><b>Hyperosid</b> ist eine <a href="Chemische_Verbindung" title="Chemische Verbindung">chemische Verbindung</a> aus der Gruppe der <a href="Flavonole" title="Flavonole">Flavonol</a>-<a href="Glycoside" title="Glycoside">Glycoside</a> und <a href="Flavonoide" title="Flavonoide">Flavonoide</a>.
</p>
<div class="mw-heading mw-heading2"><h2 id="Vorkommen">Vorkommen</h2></div>
<p>Hyperosid kommt als Flavonosidglykosid in vielen Pflanzen zum Beispiel in Birkenblättern (<a href="Betula" class="mw-redirect" title="Betula">Betula</a>), <a href="Wei%C3%9Fdorne" title="Weißdorne">Weißdornarten</a>, <a href="Johanniskraut" class="mw-redirect" title="Johanniskraut">Johanniskraut</a> (<i><a href="Hypericum_perforatum" class="mw-redirect" title="Hypericum perforatum">Hypericum perforatum</a></i>), <a href="Passionsblume" class="mw-redirect" title="Passionsblume">Passionsblumen</a> (<i><a href="Passiflora_incarnata" title="Passiflora incarnata">Passiflora incarnata</a></i>) und <a href="Holunder" title="Holunder">Holunderblüten</a> (<i><a href="Sambucus_nigra" class="mw-redirect" title="Sambucus nigra">Sambucus nigra</a></i>) vor.<sup id="cite_ref-Curt_Hunnius,_Artur_Burger_2-1" class="reference"><a href="#cite_note-Curt_Hunnius,_Artur_Burger-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
</p>
<ul class="gallery mw-gallery-traditional">
<li class="gallerybox" style="width: 155px">
<div class="thumb" style="width: 150px; height: 150px;"><span typeof="mw:File"></span></div>
<div class="gallerytext">Birkenblätter</div>
</li>
<li class="gallerybox" style="width: 155px">
<div class="thumb" style="width: 150px; height: 150px;"><span typeof="mw:File"></span></div>
<div class="gallerytext">Weißdornblätter</div>
</li>
<li class="gallerybox" style="width: 155px">
<div class="thumb" style="width: 150px; height: 150px;"><span typeof="mw:File"></span></div>
<div class="gallerytext">Holunderblüten</div>
</li>
</ul>
<div class="mw-heading mw-heading2"><h2 id="Gewinnung_und_Darstellung">Gewinnung und Darstellung</h2></div>
<p>Hyperosid kann durch eine Drei-<a href="Enzym" title="Enzym">Enzym</a>-Kaskade unter Verwendung eines <a href="UDP-Galactose" title="UDP-Galactose">UDP-Galactose</a>-Regenerationssystems gewonnen werden. In Pflanzen erfolgt die Hyperosidsynthese durch die <a href="Glykosylierung" title="Glykosylierung">Glykosylierung</a> von <a href="Quercetin" title="Quercetin">Quercetin</a> an der 3C-O-Position durch <a href="Glykosyltransferase" class="mw-redirect" title="Glykosyltransferase">Glykosyltransferasen</a>.<sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Eigenschaften">Eigenschaften</h2></div>
<p>Hyperosid ist ein weißer bis gelblicher, kristalliner Feststoff,<sup id="cite_ref-TCI_1-5" class="reference"><a href="#cite_note-TCI-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup> der löslich in <a href="Methanol" title="Methanol">Methanol</a> ist.<sup id="cite_ref-Curt_Hunnius,_Artur_Burger_2-2" class="reference"><a href="#cite_note-Curt_Hunnius,_Artur_Burger-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> Die Verbindung zeigt gefäßerweiternde Wirkung und hat einen positiven intropischen Effekt auf den <a href="Herzmuskel" title="Herzmuskel">Herzmuskel</a>.<sup id="cite_ref-J._Buckingham_4-0" class="reference"><a href="#cite_note-J._Buckingham-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-Guan-Hua_Du_5-0" class="reference"><a href="#cite_note-Guan-Hua_Du-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup> Es ist ein starker Hemmstoff der <a href="Aldosereduktase" title="Aldosereduktase">Aldosereduktase</a> und zeigt antibakterielle Aktivität gegen Pseudomonas maltophilia.<sup id="cite_ref-Basant_Puri,_Anne_Hall_6-0" class="reference"><a href="#cite_note-Basant_Puri,_Anne_Hall-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> Laut Studien reduziert die Verbindung den oxidativen Stress in der <a href="Leber" title="Leber">Leber</a> durch Aktivierung endogener antioxidativer Mechanismen und schützt vor <a href="Leberfibrose" class="mw-redirect" title="Leberfibrose">Leberfibrose</a>.<sup id="cite_ref-7" class="reference"><a href="#cite_note-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-8" class="reference"><a href="#cite_note-8"><span class="cite-bracket">[</span>8<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Verwendung">Verwendung</h2></div>
<p>Hyperosid ist als Wirkstoff in pflanzlichen Arzneimitteln, die <a href="Wei%C3%9Fdorn" class="mw-redirect" title="Weißdorn">Weißdorn</a>-Extrakt enthalten, vorhanden.<sup id="cite_ref-J._Buckingham_4-1" class="reference"><a href="#cite_note-J._Buckingham-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup> Die Verbindung wird auch in der Textilindustrie eingesetzt.<sup id="cite_ref-K._Lacasse,_Werner_Baumann_9-0" class="reference"><a href="#cite_note-K._Lacasse,_Werner_Baumann-9"><span class="cite-bracket">[</span>9<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Einzelnachweise">Einzelnachweise</h2></div>
<ol class="references">
<li id="cite_note-TCI-1"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-TCI_1-0">a</a></sup> <sup><a href="#cite_ref-TCI_1-1">b</a></sup> <sup><a href="#cite_ref-TCI_1-2">c</a></sup> <sup><a href="#cite_ref-TCI_1-3">d</a></sup> <sup><a href="#cite_ref-TCI_1-4">e</a></sup> <sup><a href="#cite_ref-TCI_1-5">f</a></sup></span> <span class="reference-text">Eintrag zu <span style="font-style:italic;"><a rel="nofollow" class="external text" href="https://www.tcichemicals.com/eshop/de/de/commodity/H1869">Hyperoside, >95.0%</a></span> bei TCI Europe, abgerufen am 3. Oktober 2025.<span class="editoronly" style="display:none;"></span></span>
</li>
<li id="cite_note-Curt_Hunnius,_Artur_Burger-2"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-Curt_Hunnius,_Artur_Burger_2-0">a</a></sup> <sup><a href="#cite_ref-Curt_Hunnius,_Artur_Burger_2-1">b</a></sup> <sup><a href="#cite_ref-Curt_Hunnius,_Artur_Burger_2-2">c</a></sup></span> <span class="reference-text">Curt Hunnius, Artur Burger: <cite style="font-style:italic">Hunnius pharmazeutisches Wörterbuch</cite>. De Gruyter, 2020, ISBN 978-3-11-086901-9, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>709</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=SybbDwAAQBAJ&pg=PA709#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:Hyperosid&rft.au=Curt+Hunnius%2C+Artur+Burger&rft.btitle=Hunnius+pharmazeutisches+W%C3%B6rterbuch&rft.date=2020&rft.genre=book&rft.isbn=9783110869019&rft.pages=709&rft.pub=De+Gruyter" style="display:none"> </span></span>
</li>
<li id="cite_note-3"><span class="mw-cite-backlink"><a href="#cite_ref-3">↑</a></span> <span class="reference-text">Jianjun Pei, Anna Chen, Linguo Zhao, Fuliang Cao, Gang Ding, Wei Xiao: <cite style="font-style:italic">One-Pot Synthesis of Hyperoside by a Three-Enzyme Cascade Using a UDP-Galactose Regeneration System</cite>. In: <cite style="font-style:italic">Journal of Agricultural and Food Chemistry</cite>. <span style="white-space:nowrap">Band<span style="display:inline-block;width:.2em"> </span>65</span>, <span style="white-space:nowrap">Nr.<span style="display:inline-block;width:.2em"> </span>29</span>, 2017, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>6042–6048</span>, <a href="Digital_Object_Identifier" title="Digital Object Identifier">doi</a>:<span class="uri-handle" style="white-space:nowrap"><a rel="nofollow" class="external text" href="https://doi.org/10.1021/acs.jafc.7b02320">10.1021/acs.jafc.7b02320</a></span>.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rfr_id=info:sid/de.wikipedia.org:Hyperosid&rft.atitle=One-Pot+Synthesis+of+Hyperoside+by+a+Three-Enzyme+Cascade+Using+a+UDP-Galactose+Regeneration+System&rft.au=Jianjun+Pei%2C+Anna+Chen%2C+Linguo+Zhao%2C+...&rft.date=2017&rft.doi=10.1021%2Facs.jafc.7b02320&rft.genre=journal&rft.issue=29&rft.jtitle=Journal+of+Agricultural+and+Food+Chemistry&rft.pages=6042-6048&rft.volume=65" style="display:none"> </span></span>
</li>
<li id="cite_note-J._Buckingham-4"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-J._Buckingham_4-0">a</a></sup> <sup><a href="#cite_ref-J._Buckingham_4-1">b</a></sup></span> <span class="reference-text">J. Buckingham: <cite style="font-style:italic">Dictionary of Organic Compounds</cite>. Chapman & Hall, 1996, ISBN 0-412-54090-8, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>3857</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=x2Su3GKCvtsC&pg=PA3857#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:Hyperosid&rft.au=J.+Buckingham&rft.btitle=Dictionary+of+Organic+Compounds&rft.date=1996&rft.genre=book&rft.isbn=0412540908&rft.pages=3857&rft.pub=Chapman+%26+Hall" style="display:none"> </span></span>
</li>
<li id="cite_note-Guan-Hua_Du-5"><span class="mw-cite-backlink"><a href="#cite_ref-Guan-Hua_Du_5-0">↑</a></span> <span class="reference-text">Guan-Hua Du: <cite style="font-style:italic">Natural Small Molecule Drugs from Plants</cite>. Springer Nature Singapore, 2018, ISBN 978-981-10-8022-7, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>699</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=bvh6DwAAQBAJ&pg=PA699#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:Hyperosid&rft.au=Guan-Hua+Du&rft.btitle=Natural+Small+Molecule+Drugs+from+Plants&rft.date=2018&rft.genre=book&rft.isbn=9789811080227&rft.pages=699&rft.pub=Springer+Nature+Singapore" style="display:none"> </span></span>
</li>
<li id="cite_note-Basant_Puri,_Anne_Hall-6"><span class="mw-cite-backlink"><a href="#cite_ref-Basant_Puri,_Anne_Hall_6-0">↑</a></span> <span class="reference-text">Basant Puri, Anne Hall: <cite style="font-style:italic">Phytochemical Dictionary</cite>. CRC Press, 1998, ISBN 0-203-48375-8, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>441</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=oT9ZDwAAQBAJ&pg=PA441#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:Hyperosid&rft.au=Basant+Puri%2C+Anne+Hall&rft.btitle=Phytochemical+Dictionary&rft.date=1998&rft.genre=book&rft.isbn=0203483758&rft.pages=441&rft.pub=CRC+Press" style="display:none"> </span></span>
</li>
<li id="cite_note-7"><span class="mw-cite-backlink"><a href="#cite_ref-7">↑</a></span> <span class="reference-text"><cite style="font-style:italic">Network Pharmacology and Traditional Medicine: Setting the New Standards by...</cite> Frontiers Media SA, 2022, ISBN 978-2-8325-0702-5, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>216</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=b8OdEAAAQBAJ&pg=PA216#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:Hyperosid&rft.btitle=Network+Pharmacology+and+Traditional+Medicine%3A+Setting+the+New+Standards+by...&rft.date=2022&rft.genre=book&rft.isbn=9782832507025&rft.pages=216&rft.pub=Frontiers+Media+SA" style="display:none"> </span></span>
</li>
<li id="cite_note-8"><span class="mw-cite-backlink"><a href="#cite_ref-8">↑</a></span> <span class="reference-text">Xiao Guo, Chengzhan Zhu, Xiaojun Liu, Yiping Ge, Xianyan Jiang, Wei Zhao: <cite style="font-style:italic">Hyperoside protects against heart failure-induced liver fibrosis in rats</cite>. In: <cite style="font-style:italic">Acta Histochemica</cite>. <span style="white-space:nowrap">Band<span style="display:inline-block;width:.2em"> </span>121</span>, <span style="white-space:nowrap">Nr.<span style="display:inline-block;width:.2em"> </span>7</span>, 2019, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>804–811</span>, <a href="Digital_Object_Identifier" title="Digital Object Identifier">doi</a>:<span class="uri-handle" style="white-space:nowrap"><a rel="nofollow" class="external text" href="https://doi.org/10.1016/j.acthis.2019.07.005">10.1016/j.acthis.2019.07.005</a></span>.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rfr_id=info:sid/de.wikipedia.org:Hyperosid&rft.atitle=Hyperoside+protects+against+heart+failure-induced+liver+fibrosis+in+rats&rft.au=Xiao+Guo%2C+Chengzhan+Zhu%2C+Xiaojun+Liu%2C+...&rft.date=2019&rft.doi=10.1016%2Fj.acthis.2019.07.005&rft.genre=journal&rft.issue=7&rft.jtitle=Acta+Histochemica&rft.pages=804-811&rft.volume=121" style="display:none"> </span></span>
</li>
<li id="cite_note-K._Lacasse,_Werner_Baumann-9"><span class="mw-cite-backlink"><a href="#cite_ref-K._Lacasse,_Werner_Baumann_9-0">↑</a></span> <span class="reference-text">K. Lacasse, Werner Baumann: <cite style="font-style:italic">Textile Chemicals</cite>. Springer Berlin Heidelberg, 2012, ISBN 978-3-642-18898-5, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>1022</span> (<a rel="nofollow" class="external text" href="https://books.google.de/books?id=7RH2CAAAQBAJ&pg=PA1022#v=onepage">eingeschränkte Vorschau</a> in der Google-Buchsuche).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:Hyperosid&rft.au=K.+Lacasse%2C+Werner+Baumann&rft.btitle=Textile+Chemicals&rft.date=2012&rft.genre=book&rft.isbn=9783642188985&rft.pages=1022&rft.pub=Springer+Berlin+Heidelberg" style="display:none"> </span></span>
</li>
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