<document tableId="61A46604FFE86562D15DFEC4204DE1E2" sourceDocId="414BFFE2FFE1656BD139FFB9231DE04A" captionStart="Table 2" checkinTime="1693421358179" checkinUser="jonas" pageId="9" pageNumber="10" updateTime="1699623166778" updateUser="plazi"><mods:mods xmlns:mods="http://www.loc.gov/mods/v3">
    <mods:titleInfo>
        <mods:title>Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds</mods:title>
    </mods:titleInfo>
    <mods:name type="personal">
        <mods:role>
            <mods:roleTerm>Author</mods:roleTerm>
        </mods:role>
        <mods:namePart>Vargas, Jorge Andrés Mora</mods:namePart>
        <mods:affiliation>∗ &amp; São Paulo State University (UNESP), Institute of Biosciences, Humanities and Exact Sciences, São Jose do Rio Preto, SP, Brazil</mods:affiliation>
    </mods:name>
    <mods:name type="personal">
        <mods:role>
            <mods:roleTerm>Author</mods:roleTerm>
        </mods:role>
        <mods:namePart>Ortega, Julieth Orduña</mods:namePart>
    </mods:name>
    <mods:name type="personal">
        <mods:role>
            <mods:roleTerm>Author</mods:roleTerm>
        </mods:role>
        <mods:namePart>Metzker, Gustavo</mods:namePart>
    </mods:name>
    <mods:name type="personal">
        <mods:role>
            <mods:roleTerm>Author</mods:roleTerm>
        </mods:role>
        <mods:namePart>Larrahondo, Jesus Eliecer</mods:namePart>
    </mods:name>
    <mods:name type="personal">
        <mods:role>
            <mods:roleTerm>Author</mods:roleTerm>
        </mods:role>
        <mods:namePart>Boscolo, Mauricio</mods:namePart>
    </mods:name>
    <mods:typeOfResource>text</mods:typeOfResource>
    <mods:relatedItem type="host">
        <mods:titleInfo>
            <mods:title>Phytochemistry</mods:title>
        </mods:titleInfo>
        <mods:part>
            <mods:date>2020</mods:date>
            <mods:detail type="series">
                <mods:title>112433</mods:title>
            </mods:detail>
            <mods:detail type="pubDate">
                <mods:number>2020-09-30</mods:number>
            </mods:detail>
            <mods:detail type="volume">
                <mods:number>177</mods:number>
            </mods:detail>
            <mods:extent unit="page">
                <mods:start>1</mods:start>
                <mods:end>21</mods:end>
            </mods:extent>
        </mods:part>
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    <mods:location>
        <mods:url>http://dx.doi.org/10.1016/j.phytochem.2020.112433</mods:url>
    </mods:location>
    <mods:classification>journal article</mods:classification>
    <mods:identifier type="DOI">10.1016/j.phytochem.2020.112433</mods:identifier>
    <mods:identifier type="ISSN">1873-3700</mods:identifier>
    <mods:identifier type="Zenodo-Dep">8296090</mods:identifier>
</mods:mods>
<table id="61A46604FFE86562D15DFEC4204DE1E2"><caption pageId="9" pageNumber="10" startId="9.[100,150,381,398]" targetType="table"><emphasis bold="true" box="[100,168,381,398]" pageId="9" pageNumber="10">Table 2</emphasis> Natural SEs esters with phenylpropanoid substituents and their physiological activities.</caption><thead><tr id="8BEB34CEFFE89A94D14DFE072498E187"><th box="[116,347,446,461]" id="C83A5DB2FFE89A94D14DFE072246E187" pageId="9" pageNumber="10">Botanical Sources of NSEs</th><th box="[380,401,446,461]" id="C83A5DB2FFE89A94D045FE07228CE187" pageId="9" pageNumber="10">No</th><th box="[425,1552,446,461]" id="C83A5DB2FFE89A94D090FE07250DE187" pageId="9" pageNumber="10">NSEs name</th><th box="[1576,1764,446,461]" id="C83A5DB2FFE89A94D711FE0725F9E187" pageId="9" pageNumber="10">Physiological activities</th><th box="[1791,1925,446,461]" id="C83A5DB2FFE89A94D7C6FE072498E187" pageId="9" pageNumber="10">References</th></tr></thead><tfoot><tr><td colspan="5">(<emphasis bold="true" box="[1747,1934,1734,1751]" italics="true" pageId="9" pageNumber="10">continued on next page</emphasis>)</td></tr></tfoot><tbody><tr id="8BEB34CEFFE89A94D14DFE532498E25A"><th box="[116,347,490,528]" id="C83A5DB2FFE89A94D14DFE532246E25A" pageId="9" pageNumber="10"><taxonomicName _authorityPlausibility="0.54095733" _evidence="catalogs" _step="species1" authority="(Compositae)" baseAuthorityName="Compositae" box="[116,345,490,505]" class="Magnoliopsida" family="Asteraceae" genus="Bidens" id="F2DB4D0FFFE86562D14DFE532244E1B3" kingdom="Plantae" order="Asterales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="parviflora"><emphasis bold="true" box="[116,251,490,505]" id="07AFEA9EFFE86562D14DFE5323E6E1B3" italics="true" pageId="9" pageNumber="10">Bidens parviflora (</emphasis> Compositae)</taxonomicName></th><td box="[380,401,490,528]" id="C83A5DB2FFE89A94D045FE53228CE25A" pageId="9" pageNumber="10">38 39</td><td box="[425,1552,490,528]" id="C83A5DB2FFE89A94D090FE53250DE25A" pageId="9" pageNumber="10">6' - <emphasis bold="true" box="[449,461,490,505]" id="07AFEA9EFFE86562D0F8FE5322D0E1B3" italics="true" pageId="9" pageNumber="10">O</emphasis> -Coumaroyl sucrose 6′,6- <emphasis bold="true" box="[459,471,513,528]" id="07AFEA9EFFE86562D0F2FDB822CAE25A" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-Coumaroyl sucrose</td><td box="[1576,1764,490,528]" id="C83A5DB2FFE89A94D711FE5325F9E25A" pageId="9" pageNumber="10">Anti-inflammatory activity</td><td box="[1791,1925,490,528]" id="C83A5DB2FFE89A94D7C6FE532498E25A" pageId="9" pageNumber="10"><bibRefCitation author="Wang, N. &amp; Yao, X. &amp; Ishii, R. &amp; Kitanaka, S." id="514A4B7DFFE86562D7C6FE53242CE25A" pageId="9" pageNumber="10" pagination="741 - 746" refId="ref23874" refString="Wang, N., Yao, X., Ishii, R., Kitanaka, S., 2003. Bioactive sucrose esters from Bidens parviflora. Phytochemistry 62, 741 - 746. https: // doi. org / 10.1016 / S 0031 - 9422 (02) 00454 - 5." type="journal article" year="2003">Wang et al. (2003)</bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFDA12498E26D"><th id="C83A5DB2FFE89A94D14DFDA12246E26D"/><td box="[380,401,536,551]" id="C83A5DB2FFE89A94D045FDA1228CE26D" pageId="9" pageNumber="10"><emphasis bold="true" box="[380,400,536,551]" id="07AFEA9EFFE86562D045FDA1228DE26D" pageId="9" pageNumber="10">40</emphasis></td><td box="[425,1552,536,551]" id="C83A5DB2FFE89A94D090FDA1250DE26D" pageId="9" pageNumber="10">6,6′-sucrose ester of (1α,2α,3β,4β)-3,4-bis(4-hydroxyphenyl)-1,2-cyclobutanedicarboxylic acid</td><td id="C83A5DB2FFE89A94D711FDA125F9E26D"/><td id="C83A5DB2FFE89A94D7C6FDA12498E26D"/></tr><tr id="8BEB34CEFFE89A94D14DFDFC2498E2FA"><th box="[116,347,581,688]" id="C83A5DB2FFE89A94D14DFDFC2246E2FA" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" class="Magnoliopsida" family="Phyllanthaceae" genus="Phyllanthus" id="F2DB4D0FFFE86562D14DFDFF220EE226" kingdom="Plantae" order="Malpighiales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="cochinchinensis"><emphasis bold="true" box="[116,314,582,597]" id="07AFEA9EFFE86562D14DFDFF2227E21F" italics="true" pageId="9" pageNumber="10">Phyllanthus cochinchinensis</emphasis> (Phyllanthaceae)</taxonomicName></th><td box="[380,401,581,688]" id="C83A5DB2FFE89A94D045FDFC228CE2FA" pageId="9" pageNumber="10">41 42 43 44 45</td><td box="[425,1552,581,688]" id="C83A5DB2FFE89A94D090FDFC250DE2FA" pageId="9" pageNumber="10">3′,6-di- <emphasis bold="true" box="[479,491,582,597]" id="07AFEA9EFFE86562D0E6FDFF22F6E21F" italics="true" pageId="9" pageNumber="10">O</emphasis> -benzoyl sucrose 3′,6-di- <emphasis bold="true" box="[479,491,605,620]" id="07AFEA9EFFE86562D0E6FDE422F6E226" italics="true" pageId="9" pageNumber="10">O</emphasis> -benzoyl-2- <emphasis bold="true" box="[576,588,605,620]" id="07AFEA9EFFE86562D379FDE42151E226" italics="true" pageId="9" pageNumber="10">O</emphasis> -acetyl sucrose 3′,6-di- <emphasis bold="true" box="[479,491,627,642]" id="07AFEA9EFFE86562D0E6FDCA22F6E2C8" italics="true" pageId="9" pageNumber="10">O</emphasis> -benzoyl-4- <emphasis bold="true" box="[576,593,627,642]" id="07AFEA9EFFE86562D379FDCA214CE2C8" italics="true" pageId="9" pageNumber="10">O-</emphasis> acetyl sucrose 3′,6-di- <emphasis bold="true" box="[479,491,650,665]" id="07AFEA9EFFE86562D0E6FD3322F6E2D3" italics="true" pageId="9" pageNumber="10">O</emphasis> -benzoyl-3- <emphasis bold="true" box="[576,588,650,665]" id="07AFEA9EFFE86562D379FD332151E2D3" italics="true" pageId="9" pageNumber="10">O</emphasis> -acetyl sucrose 3′- <emphasis bold="true" box="[445,457,673,688]" id="07AFEA9EFFE86562D084FD1822D4E2FA" italics="true" pageId="9" pageNumber="10">O</emphasis> -benzoyl-6- <emphasis bold="true" box="[541,553,673,688]" id="07AFEA9EFFE86562D324FD182134E2FA" italics="true" pageId="9" pageNumber="10">O</emphasis> -(<emphasis bold="true" box="[565,574,673,688]" id="07AFEA9EFFE86562D30CFD182123E2FA" italics="true" pageId="9" pageNumber="10">E</emphasis>)-cinnamoyl sucrose</td><td box="[1576,1764,581,688]" id="C83A5DB2FFE89A94D711FDFC25F9E2FA" pageId="9" pageNumber="10">No physiological activity determined</td><td box="[1791,1925,581,688]" id="C83A5DB2FFE89A94D7C6FDFC2498E2FA" pageId="9" pageNumber="10"><bibRefCitation author="Zhao, J. - Q. &amp; Wang, Y. - M. &amp; Wang, D. &amp; Yang, C. - R. &amp; Xu, M. &amp; Zhang, Y. - J." box="[1791,1925,582,597]" id="514A4B7DFFE86562D7C6FDFF2498E21F" pageId="9" pageNumber="10" pagination="61 - 65" refId="ref24655" refString="Zhao, J. - Q., Wang, Y. - M., Wang, D., Yang, C. - R., Xu, M., Zhang, Y. - J., 2013. Five new sucrose esters from the whole plants of Phyllanthus cochinchinensis. Nat. Products Bioprospect. 3, 61 - 65. https: // doi. org / 10.1007 / s 13659 - 013 - 0026 - 7." type="journal article" year="2013"><emphasis bold="true" box="[1791,1925,582,597]" id="07AFEA9EFFE86562D7C6FDFF2498E21F" pageId="9" pageNumber="10">Zhao et al. (2013)</emphasis></bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFD762498E2BF"><th box="[116,347,719,757]" id="C83A5DB2FFE89A94D14DFD762246E2BF" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" box="[116,206,719,734]" class="Liliopsida" family="Poaceae" genus="Oryza" id="F2DB4D0FFFE86562D14DFD7623D3E294" kingdom="Plantae" order="Poales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="sativa"><emphasis bold="true" box="[116,206,719,734]" id="07AFEA9EFFE86562D14DFD7623D3E294" italics="true" pageId="9" pageNumber="10">Oryza sativa</emphasis></taxonomicName> L. (<taxonomicName _evidence="catalogs" _step="family" authorityName="Barnhart" authorityYear="1895" baseAuthorityName="R.Br." box="[237,301,719,734]" class="Liliopsida" family="Poaceae" id="F2DB4D0FFFE86562D1D4FD762230E294" kingdom="Plantae" order="Poales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="family">Poaceae</taxonomicName>)</th><td box="[380,401,719,757]" id="C83A5DB2FFE89A94D045FD76228CE2BF" pageId="9" pageNumber="10">46 47</td><td box="[425,1552,719,757]" id="C83A5DB2FFE89A94D090FD76250DE2BF" pageId="9" pageNumber="10">6- <emphasis bold="true" box="[440,452,719,734]" id="07AFEA9EFFE86562D081FD7622D9E294" italics="true" pageId="9" pageNumber="10">O</emphasis> -(<emphasis bold="true" box="[464,473,719,734]" id="07AFEA9EFFE86562D0E9FD7622C4E294" italics="true" pageId="9" pageNumber="10">E</emphasis>)-feruloyl sucrose 6- <emphasis bold="true" box="[440,452,742,757]" id="07AFEA9EFFE86562D081FD5F22D9E2BF" italics="true" pageId="9" pageNumber="10">O</emphasis> -(<emphasis bold="true" box="[464,473,742,757]" id="07AFEA9EFFE86562D0E9FD5F22C4E2BF" italics="true" pageId="9" pageNumber="10">E</emphasis>)-sinapoyl sucrose</td><td box="[1576,1764,719,757]" id="C83A5DB2FFE89A94D711FD7625F9E2BF" pageId="9" pageNumber="10">Antioxidant activity</td><td box="[1791,1925,719,757]" id="C83A5DB2FFE89A94D7C6FD762498E2BF" pageId="9" pageNumber="10"><bibRefCitation author="Tian, S. &amp; Nakamura, K. &amp; Kayahara, H. K." box="[1791,1924,719,734]" id="514A4B7DFFE86562D7C6FD762499E294" pageId="9" pageNumber="10" pagination="4808 - 4813" refId="ref23375" refString="Tian, S., Nakamura, K., Kayahara, H. K., 2004. Analysis of phenolic compounds in white rice, brown rice. J. Agric. Food Chem. 52, 4808 - 4813. https: // doi. org / 10.1021 / jf 049446 f." type="journal article" year="2004"><emphasis bold="true" box="[1791,1924,719,734]" id="07AFEA9EFFE86562D7C6FD762499E294" pageId="9" pageNumber="10">Tian et al. (2004)</emphasis></bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFD452498E373"><th id="C83A5DB2FFE89A94D14DFD452246E373"/><td box="[380,401,764,825]" id="C83A5DB2FFE89A94D045FD45228CE373" pageId="9" pageNumber="10">48 49 50</td><td box="[425,1552,764,825]" id="C83A5DB2FFE89A94D090FD45250DE373" pageId="9" pageNumber="10">3′,6′- <emphasis bold="true" box="[463,475,764,779]" id="07AFEA9EFFE86562D0F6FD4522C6E341" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-feruloyl-3,6- <emphasis bold="true" box="[594,606,764,779]" id="07AFEA9EFFE86562D36BFD452143E341" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-acetyl sucrose 3′,6′- <emphasis bold="true" box="[463,475,787,802]" id="07AFEA9EFFE86562D0F6FCAA22C6E368" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-feruloyl-6- <emphasis bold="true" box="[580,592,787,802]" id="07AFEA9EFFE86562D37DFCAA214DE368" italics="true" pageId="9" pageNumber="10">O</emphasis> -acetyl sucrose 3′,6′- <emphasis bold="true" box="[463,475,810,825]" id="07AFEA9EFFE86562D0F6FC9322C6E373" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-feruloyl-6,4- <emphasis bold="true" box="[594,606,810,825]" id="07AFEA9EFFE86562D36BFC932143E373" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-acetyl sucrose</td><td box="[1576,1764,764,825]" id="C83A5DB2FFE89A94D711FD4525F9E373" pageId="9" pageNumber="10">Inhibitory properties against</td><td box="[1791,1925,764,825]" id="C83A5DB2FFE89A94D7C6FD452498E373" pageId="9" pageNumber="10"><bibRefCitation author="Cho, J. G. &amp; Cha, B. J. &amp; Seo, W. D. &amp; Jeong, R. H. &amp; Shrestha, S. &amp; Kim, J. Y. &amp; Kang, H. C. &amp; Baek, N. I." box="[1791,1925,764,779]" id="514A4B7DFFE86562D7C6FD452498E341" pageId="9" pageNumber="10" pagination="1094 - 1098" refId="ref16109" refString="Cho, J. G., Cha, B. J., Seo, W. D., Jeong, R. H., Shrestha, S., Kim, J. Y., Kang, H. C., Baek, N. I., 2015 b. Feruloyl sucrose esters from Oryza sativa roots and their tyrosinase inhibition activity. Chem. Nat. Compd. 51, 1094 - 1098. https: // doi. org / 10.1007 / s 10600 - 015 - 1500 - 8." type="journal article" year="2015"><emphasis bold="true" box="[1791,1925,764,779]" id="07AFEA9EFFE86562D7C6FD452498E341" pageId="9" pageNumber="10">Cho et al. (2015b)</emphasis></bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFCE12498E3E1"><th box="[116,347,856,939]" id="C83A5DB2FFE89A94D14DFCE12246E3E1" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" box="[116,330,856,871]" class="Magnoliopsida" family="Rosaceae" genus="Prunus" id="F2DB4D0FFFE86562D14DFCE12257E32D" kingdom="Plantae" order="Rosales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="tomentosa"><emphasis bold="true" box="[116,243,856,871]" id="07AFEA9EFFE86562D14DFCE123EEE32D" italics="true" pageId="9" pageNumber="10">Prunus tomentosa</emphasis> (Rosaceae)</taxonomicName></th><td box="[380,401,856,939]" id="C83A5DB2FFE89A94D045FCE1228CE3E1" pageId="9" pageNumber="10">51 52 53 54</td><td box="[425,1552,856,939]" id="C83A5DB2FFE89A94D090FCE1250DE3E1" pageId="9" pageNumber="10">3′- <emphasis bold="true" box="[445,470,856,871]" id="07AFEA9EFFE86562D084FCE122CBE32D" italics="true" pageId="9" pageNumber="10">O -p</emphasis> -coumaroyl-1′,4′,6- <emphasis bold="true" box="[613,625,856,871]" id="07AFEA9EFFE86562D35CFCE1216CE32D" italics="true" pageId="9" pageNumber="10">O</emphasis> -triacetyl sucrose 3′- <emphasis bold="true" box="[450,481,879,894]" id="07AFEA9EFFE86562D0FBFCD622FCE334" italics="true" pageId="9" pageNumber="10">O - p</emphasis> -coumaroyl-1′,4,6- <emphasis bold="true" box="[620,632,879,894]" id="07AFEA9EFFE86562D355FCD62165E334" italics="true" pageId="9" pageNumber="10">O</emphasis> -triacetyl sucrose 3′- <emphasis bold="true" box="[450,481,901,916]" id="07AFEA9EFFE86562D0FBFC3C22FCE3DE" italics="true" pageId="9" pageNumber="10">O - p</emphasis> -coumaroyl-3,4,6- <emphasis bold="true" box="[616,628,901,916]" id="07AFEA9EFFE86562D351FC3C2169E3DE" italics="true" pageId="9" pageNumber="10">O</emphasis> -triacetyl sucrose 3′- <emphasis bold="true" box="[445,457,924,939]" id="07AFEA9EFFE86562D084FC2522D4E3E1" italics="true" pageId="9" pageNumber="10">O</emphasis> -feruloyl-1′,2,6- <emphasis bold="true" box="[574,586,924,939]" id="07AFEA9EFFE86562D307FC252157E3E1" italics="true" pageId="9" pageNumber="10">O</emphasis> -triacetyl sucrose</td><td box="[1576,1764,856,939]" id="C83A5DB2FFE89A94D711FCE125F9E3E1" pageId="9" pageNumber="10">Antitumor activity</td><td box="[1791,1925,856,939]" id="C83A5DB2FFE89A94D7C6FCE12498E3E1" pageId="9" pageNumber="10"><bibRefCitation author="Zhao, W. &amp; Huang, X. X. &amp; Yu, L. H. &amp; Liu, Q. B. &amp; Li, L. Z. &amp; Sun, Q. &amp; Song, S. J." box="[1791,1925,856,871]" id="514A4B7DFFE86562D7C6FCE12498E32D" pageId="9" pageNumber="10" pagination="2459 - 2462" refId="ref24802" refString="Zhao, W., Huang, X. X., Yu, L. H., Liu, Q. B., Li, L. Z., Sun, Q., Song, S. J., 2014. Tomensides A-D, new antiproliferative phenylpropanoid sucrose esters from Prunus tomentosa leaves. Bioorg. Med. Chem. Lett 24, 2459 - 2462. https: // doi. org / 10.1016 / j. bmcl. 2014.04. 018." type="journal article" year="2014"><emphasis bold="true" box="[1791,1925,856,871]" id="07AFEA9EFFE86562D7C6FCE12498E32D" pageId="9" pageNumber="10">Zhao et al. (2014)</emphasis></bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFC732498E3BA"><th box="[116,347,970,1008]" id="C83A5DB2FFE89A94D14DFC732246E3BA" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" class="Magnoliopsida" family="Polygonaceae" genus="Polygonum" id="F2DB4D0FFFE86562D14DFC732214E3BA" kingdom="Plantae" order="Caryophyllales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="lapathifolium">Polygonum lapathifolium (Polygonaceae <emphasis bold="true" box="[258,265,993,1008]" id="07AFEA9EFFE86562D03BFC582214E3BA" italics="true" pageId="9" pageNumber="10">)</emphasis></taxonomicName></th><td box="[380,401,970,1008]" id="C83A5DB2FFE89A94D045FC73228CE3BA" pageId="9" pageNumber="10">55 56</td><td box="[425,1552,970,1008]" id="C83A5DB2FFE89A94D090FC73250DE3BA" pageId="9" pageNumber="10">Vanicoside B: 6,1′,3′,6′- <emphasis bold="true" box="[604,616,970,985]" id="07AFEA9EFFE86562D365FC732175E393" italics="true" pageId="9" pageNumber="10">O</emphasis> -tetracoumaroyl sucrose Lapathoside A: 6,1′,3′- <emphasis bold="true" box="[595,607,993,1008]" id="07AFEA9EFFE86562D36AFC582142E3BA" italics="true" pageId="9" pageNumber="10">O</emphasis> -tricoumaroyl-6′- <emphasis bold="true" box="[735,747,993,1008]" id="07AFEA9EFFE86562D3E6FC5821F6E3BA" italics="true" pageId="9" pageNumber="10">O</emphasis> -feruloyl sucrose</td><td box="[1576,1764,970,1008]" id="C83A5DB2FFE89A94D711FC7325F9E3BA" pageId="9" pageNumber="10">Exhibited significant anti-tumor activity</td><td box="[1791,1925,970,1008]" id="C83A5DB2FFE89A94D7C6FC732498E3BA" pageId="9" pageNumber="10"><bibRefCitation author="Takasaki, M. &amp; Konoshima, T. &amp; Kuroki, S. &amp; Tokuda, H. &amp; Nishino, H." id="514A4B7DFFE86562D7C6FC73242FE3BA" pageId="9" pageNumber="10" pagination="133 - 138" refId="ref23161" refString="Takasaki, M., Konoshima, T., Kuroki, S., Tokuda, H., Nishino, H., 2001. Cancer chemopreventive activity of phenylpropanoid esters of sucrose, vanicoside B and lapathoside A, from Polygonum lapathifolium. Canc. Lett. 173, 133 - 138. https: // doi. org / 10. 1016 / S 0304 - 3835 (01) 00670 - X." type="journal article" year="2001"><emphasis bold="true" box="[1791,1902,970,985]" id="07AFEA9EFFE86562D7C6FC732473E393" italics="true" pageId="9" pageNumber="10">Takasaki et al.</emphasis> (2001)</bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFBB72498E428"><th box="[116,347,1038,1122]" id="C83A5DB2FFE89A94D14DFBB72246E428" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" class="Magnoliopsida" family="Polygonaceae" genus="Polygonum" id="F2DB4D0FFFE86562D14DFBB6221AE47E" kingdom="Plantae" order="Caryophyllales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="perfoliatum"><emphasis bold="true" box="[116,281,1039,1054]" id="07AFEA9EFFE86562D14DFBB62204E454" italics="true" pageId="9" pageNumber="10">Polygonum perfoliatum</emphasis> (Polygonaceae)</taxonomicName></th><td box="[380,401,1038,1122]" id="C83A5DB2FFE89A94D045FBB7228CE428" pageId="9" pageNumber="10">57 58 59 60</td><td box="[425,1552,1038,1122]" id="C83A5DB2FFE89A94D090FBB7250DE428" pageId="9" pageNumber="10">3′, 6′- <emphasis bold="true" box="[469,481,1039,1054]" id="07AFEA9EFFE86562D0ECFBB622FCE454" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-feruloyl-1′,2,6- <emphasis bold="true" box="[618,630,1039,1054]" id="07AFEA9EFFE86562D353FBB6216BE454" italics="true" pageId="9" pageNumber="10">O</emphasis> -triacetyl sucrose 3′,6′- <emphasis bold="true" box="[463,475,1061,1076]" id="07AFEA9EFFE86562D0F6FB9C22C6E47E" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-feruloyl-1′,2,4,6- <emphasis bold="true" box="[627,639,1061,1076]" id="07AFEA9EFFE86562D34AFB9C2162E47E" italics="true" pageId="9" pageNumber="10">O</emphasis> -tetraacetyl sucrose 3′,6′- <emphasis bold="true" box="[463,475,1084,1099]" id="07AFEA9EFFE86562D0F6FB8522C6E401" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-feruloyl-2,4,6- <emphasis bold="true" box="[608,620,1084,1099]" id="07AFEA9EFFE86562D359FB852171E401" italics="true" pageId="9" pageNumber="10">O</emphasis> -triacetyl-sucrose 3′,6′- <emphasis bold="true" box="[463,475,1107,1122]" id="07AFEA9EFFE86562D0F6FBEA22C6E428" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-feruloyl-2,6- <emphasis bold="true" box="[594,606,1107,1122]" id="07AFEA9EFFE86562D36BFBEA2143E428" italics="true" pageId="9" pageNumber="10">O</emphasis> -diacetyl sucrose</td><td box="[1576,1764,1038,1122]" id="C83A5DB2FFE89A94D711FBB725F9E428" pageId="9" pageNumber="10">No physiological activity determined</td><td box="[1791,1925,1038,1122]" id="C83A5DB2FFE89A94D7C6FBB72498E428" pageId="9" pageNumber="10"><bibRefCitation author="Sun, X. &amp; Zimmermann, M. L. &amp; Campagne, J. M. &amp; Sneden, A. T." box="[1791,1919,1039,1054]" id="514A4B7DFFE86562D7C6FBB62462E454" pageId="9" pageNumber="10" pagination="1094 - 1097" refId="ref23020" refString="Sun, X., Zimmermann, M. L., Campagne, J. M., Sneden, A. T., 2000. New sucrose phenylpropanoid esters from Polygonum perfoliatum. J. Nat. Prod. 63, 1094 - 1097. https: // doi. org / 10.1021 / np 000055 e." type="journal article" year="2000"><emphasis bold="true" box="[1791,1919,1039,1054]" id="07AFEA9EFFE86562D7C6FBB62462E454" pageId="9" pageNumber="10">Sun et al. (2000)</emphasis></bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFB382498E4ED"><th box="[116,347,1153,1191]" id="C83A5DB2FFE89A94D14DFB382246E4ED" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" class="Magnoliopsida" family="Boraginaceae" genus="Echium" id="F2DB4D0FFFE86562D14DFB38221BE4ED" kingdom="Plantae" order="Boraginales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="angustifolium"><emphasis bold="true" box="[116,269,1153,1168]" id="07AFEA9EFFE86562D14DFB382210E4DA" italics="true" pageId="9" pageNumber="10">Echium angustifolium</emphasis> (Boraginaceae <emphasis bold="true" box="[255,262,1176,1191]" id="07AFEA9EFFE86562D1C6FB21221BE4ED" italics="true" pageId="9" pageNumber="10">)</emphasis></taxonomicName></th><td box="[380,401,1153,1191]" id="C83A5DB2FFE89A94D045FB38228CE4ED" pageId="9" pageNumber="10">61 62</td><td box="[425,1552,1153,1191]" id="C83A5DB2FFE89A94D090FB38250DE4ED" pageId="9" pageNumber="10">3a <emphasis bold="true" box="[444,461,1153,1168]" id="07AFEA9EFFE86562D085FB3822D0E4DA" italics="true" pageId="9" pageNumber="10">→</emphasis> 9’:6a <emphasis bold="true" box="[497,514,1153,1168]" id="07AFEA9EFFE86562D0C8FB38211FE4DA" italics="true" pageId="9" pageNumber="10">→</emphasis> 9-[(7′R,8′R)-4,4′-dihydroxy-3,3′,5-trimethoxy-2,7′-cycloligna-7-en-9,9′-dicarbonyl]-6b-[4''-(1c-α- rhamnopyranosyl- <emphasis bold="true" box="[1377,1385,1153,1168]" id="07AFEA9EFFE86562D458FB382674E4DA" italics="true" pageId="9" pageNumber="10">p</emphasis> -courmaroyl)] sucrose 6a <emphasis bold="true" box="[444,461,1175,1190]" id="07AFEA9EFFE86562D085FB2E22D0E4EC" italics="true" pageId="9" pageNumber="10">→</emphasis> 9-[(7′R,8′R)-4,4′-dihydroxy-3,3′,5-dimethoxy-2,7′-cycloligna-7-en-9′-methoxycarbonyl-9-carbonyl] sucrose</td><td box="[1576,1764,1153,1191]" id="C83A5DB2FFE89A94D711FB3825F9E4ED" pageId="9" pageNumber="10">Antitumor activity</td><td box="[1791,1925,1153,1191]" id="C83A5DB2FFE89A94D7C6FB382498E4ED" pageId="9" pageNumber="10"><bibRefCitation author="El-Rokh, A. R. &amp; Negm, A. &amp; El-Shamy, M. &amp; El-Gindy, M. &amp; Abdel-Mogib, M." id="514A4B7DFFE86562D7C6FB38242CE4ED" pageId="9" pageNumber="10" pagination="155 - 160" refId="ref17161" refString="El-Rokh, A. R., Negm, A., El-Shamy, M., El-Gindy, M., Abdel-Mogib, M., 2018. Sucrose diester of aryldihydronaphthalene-type lignans from Echium angustifolium Mill. and their antitumor activity. Phytochemistry 149, 155 - 160. https: // doi. org / 10.1016 / j. phytochem. 2018.02.014." type="journal article" year="2018"><emphasis bold="true" box="[1791,1895,1153,1168]" id="07AFEA9EFFE86562D7C6FB38247AE4DA" pageId="9" pageNumber="10">El-Rokh et al.</emphasis> (2018)</bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFB7C2498E4A1"><th box="[116,347,1221,1259]" id="C83A5DB2FFE89A94D14DFB7C2246E4A1" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" class="Magnoliopsida" family="Quillajaceae" genus="Quillaja" id="F2DB4D0FFFE86562D14DFB7C23E3E4A1" kingdom="Plantae" order="Fabales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="saponaria"><emphasis bold="true" box="[116,251,1221,1236]" id="07AFEA9EFFE86562D14DFB7C23E6E49E" italics="true" pageId="9" pageNumber="10">Quillaja Saponaria</emphasis> (Quillajaceae <emphasis bold="true" box="[247,254,1244,1259]" id="07AFEA9EFFE86562D1CEFB6523E3E4A1" italics="true" pageId="9" pageNumber="10">)</emphasis></taxonomicName></th><td box="[380,401,1221,1259]" id="C83A5DB2FFE89A94D045FB7C228CE4A1" pageId="9" pageNumber="10">63 64</td><td box="[425,1552,1221,1259]" id="C83A5DB2FFE89A94D090FB7C250DE4A1" pageId="9" pageNumber="10">Quillajaside B: β- D-apiosyl-(1 <emphasis bold="true" box="[654,671,1221,1236]" id="07AFEA9EFFE86562D3B7FB7C2182E49E" italics="true" pageId="9" pageNumber="10">→</emphasis> 4)-α- L-rhamnosyl-(1 <emphasis bold="true" box="[836,853,1221,1236]" id="07AFEA9EFFE86562D27DFB7C2048E49E" italics="true" pageId="9" pageNumber="10">→</emphasis> 4)-α- L-rhamnosyl-(1 <emphasis bold="true" box="[1017,1034,1221,1236]" id="07AFEA9EFFE86562D2C0FB7C2717E49E" italics="true" pageId="9" pageNumber="10">→</emphasis> 3)-(4-O-(E)-p-coumaroyl)-(3-O-(E)-p-coumaroyl) sucrose Quillajaside A: α- L-rhamnosyl-(1 <emphasis bold="true" box="[680,697,1244,1259]" id="07AFEA9EFFE86562D391FB6521A4E4A1" italics="true" pageId="9" pageNumber="10">→</emphasis> 4)-α- L-rhamnosyl-(1 <emphasis bold="true" box="[861,878,1244,1259]" id="07AFEA9EFFE86562D264FB652073E4A1" italics="true" pageId="9" pageNumber="10">→</emphasis> 3)-(4-O-(E)-p-coumaroyl)-(3-O-(E)-p-coumaroyl) sucrose</td><td box="[1576,1764,1221,1259]" id="C83A5DB2FFE89A94D711FB7C25F9E4A1" pageId="9" pageNumber="10">Antioxidant agents</td><td box="[1791,1925,1221,1259]" id="C83A5DB2FFE89A94D7C6FB7C2498E4A1" pageId="9" pageNumber="10"><bibRefCitation author="Maier, C. &amp; Conrad, J. &amp; Steingass, C. B. &amp; Beifuss, U. &amp; Carle, R. &amp; Schweiggert, R. M." id="514A4B7DFFE86562D7C6FB7C242CE4A1" pageId="9" pageNumber="10" pagination="8905 - 8911" refId="ref19724" refString="Maier, C., Conrad, J., Steingass, C. B., Beifuss, U., Carle, R., Schweiggert, R. M., 2015. Quillajasides A and B: new phenylpropanoid sucrose esters from the inner bark of Quillaja saponaria molina. J. Agric. Food Chem. 63, 8905 - 8911. https: // doi. org / 10. 1021 / acs. jafc. 5 b 03532." type="journal article" year="2015"><emphasis bold="true" box="[1791,1879,1221,1236]" id="07AFEA9EFFE86562D7C6FB7C244AE49E" pageId="9" pageNumber="10">Maier et al.</emphasis> (2015)</bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFAB32498E57A"><th box="[116,347,1290,1328]" id="C83A5DB2FFE89A94D14DFAB32246E57A" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" class="Magnoliopsida" family="Phyllanthaceae" genus="Phyllanthus" id="F2DB4D0FFFE86562D14DFAB32209E57A" kingdom="Plantae" order="Malpighiales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="niruri"><emphasis bold="true" box="[116,245,1290,1305]" id="07AFEA9EFFE86562D14DFAB323E8E553" italics="true" pageId="9" pageNumber="10">Phyllanthus niruri</emphasis> (Phyllanthaceae <emphasis bold="true" box="[269,276,1313,1328]" id="07AFEA9EFFE86562D034FA982209E57A" italics="true" pageId="9" pageNumber="10">)</emphasis></taxonomicName></th><td box="[380,401,1290,1328]" id="C83A5DB2FFE89A94D045FAB3228CE57A" pageId="9" pageNumber="10"><emphasis bold="true" box="[380,400,1290,1305]" id="07AFEA9EFFE86562D045FAB3228DE553" pageId="9" pageNumber="10">65</emphasis></td><td box="[425,1552,1290,1328]" id="C83A5DB2FFE89A94D090FAB3250DE57A" pageId="9" pageNumber="10">3′,6′- <emphasis bold="true" box="[463,475,1290,1305]" id="07AFEA9EFFE86562D0F6FAB322C6E553" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-trans-cinnamoyl-1′, 2, 3, 6- <emphasis bold="true" box="[707,719,1290,1305]" id="07AFEA9EFFE86562D3FAFAB321D2E553" italics="true" pageId="9" pageNumber="10">O</emphasis> -tetracetil sucrose</td><td box="[1576,1764,1290,1328]" id="C83A5DB2FFE89A94D711FAB325F9E57A" pageId="9" pageNumber="10">Inhibitory activity of the HIV virus</td><td box="[1791,1925,1290,1328]" id="C83A5DB2FFE89A94D7C6FAB32498E57A" pageId="9" pageNumber="10"><bibRefCitation author="Qian-Cutrone, J. &amp; Huang, S. &amp; Trimble, J. &amp; Li, H. &amp; Lin, P. 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(1996)</bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFAF72498E53E"><th box="[116,347,1358,1396]" id="C83A5DB2FFE89A94D14DFAF72246E53E" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" class="Magnoliopsida" family="Polygonaceae" genus="Fagopyrum" id="F2DB4D0FFFE86562D14DFAF72215E53E" kingdom="Plantae" order="Caryophyllales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="acutatum"><emphasis bold="true" box="[116,267,1358,1373]" id="07AFEA9EFFE86562D14DFAF72216E517" italics="true" pageId="9" pageNumber="10">Fagopyrum acutatum</emphasis> (Polygonaceae <emphasis bold="true" box="[257,264,1381,1396]" id="07AFEA9EFFE86562D038FADC2215E53E" italics="true" pageId="9" pageNumber="10">)</emphasis></taxonomicName></th><td box="[380,401,1358,1396]" id="C83A5DB2FFE89A94D045FAF7228CE53E" pageId="9" pageNumber="10"><emphasis bold="true" box="[380,400,1358,1373]" id="07AFEA9EFFE86562D045FAF7228DE517" pageId="9" pageNumber="10">66</emphasis></td><td box="[425,1552,1358,1396]" id="C83A5DB2FFE89A94D090FAF7250DE53E" pageId="9" pageNumber="10">1′,3′,6- <emphasis bold="true" box="[477,489,1358,1373]" id="07AFEA9EFFE86562D0E4FAF722F4E517" italics="true" pageId="9" pageNumber="10">O</emphasis> -tri- <emphasis bold="true" box="[518,526,1358,1373]" id="07AFEA9EFFE86562D33FFAF72113E517" italics="true" pageId="9" pageNumber="10">p</emphasis> -coumaroyl-6′- <emphasis bold="true" box="[636,648,1358,1373]" id="07AFEA9EFFE86562D345FAF72195E517" italics="true" pageId="9" pageNumber="10">O</emphasis> -feruloyl sucrose</td><td box="[1576,1764,1358,1396]" id="C83A5DB2FFE89A94D711FAF725F9E53E" pageId="9" pageNumber="10">Inhibits α- amylase activity</td><td box="[1791,1925,1358,1396]" id="C83A5DB2FFE89A94D7C6FAF72498E53E" pageId="9" pageNumber="10"><bibRefCitation author="Liu, T. &amp; Yip, Y. M. &amp; Song, L. &amp; Feng, S. &amp; Liu, Y. &amp; Lai, F. &amp; Zhang, D. &amp; Huang, D." box="[1791,1914,1358,1373]" id="514A4B7DFFE86562D7C6FAF72467E517" pageId="9" pageNumber="10" pagination="595 - 600" refId="ref19561" refString="Liu, T., Yip, Y. M., Song, L., Feng, S., Liu, Y., Lai, F., Zhang, D., Huang, D., 2013. Inhibiting enzymatic starch digestion by the phenolic compound diboside A: a mechanistic and in silico study. Food Res. Int. 54, 595 - 600. https: // doi. org / 10.1016 / j. foodres. 2013. 07.062." type="journal article" year="2013">Liu et al. (2013)</bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFA212498E5ED"><th box="[116,347,1432,1447]" id="C83A5DB2FFE89A94D14DFA212246E5ED" pageId="9" pageNumber="10">Botanical Sources of NSEs</th><td id="C83A5DB2FFE89A94D045FA21228CE5ED"/><td box="[425,1552,1432,1447]" id="C83A5DB2FFE89A94D090FA21250DE5ED" pageId="9" pageNumber="10">No. NSEs name Physiological activities</td><td box="[1576,1925,1432,1447]" colspan="2" id="C83A5DB2FFE89A94D711FA212498E5ED" pageId="9" pageNumber="10">References</td></tr><tr id="8BEB34CEFFE89A94D14DFA7D2498E599"><th box="[116,401,1476,1491]" colspan="2" id="C83A5DB2FFE89A94D14DFA7D228CE599" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" box="[116,398,1476,1491]" class="Magnoliopsida" family="Polygonaceae" genus="Bistorta" id="F2DB4D0FFFE86562D14DFA7D2293E599" kingdom="Plantae" order="Caryophyllales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="manshuriensis"><emphasis bold="true" box="[116,276,1476,1491]" id="07AFEA9EFFE86562D14DFA7D2209E599" italics="true" pageId="9" pageNumber="10">Bistorta manshuriensis</emphasis> (Polygonaceae)</taxonomicName></th><td box="[425,1552,1476,1491]" id="C83A5DB2FFE89A94D090FA7D250DE599" pageId="9" pageNumber="10"><emphasis bold="true" box="[471,491,1476,1491]" id="07AFEA9EFFE86562D0EEFA7D22F6E599" pageId="9" pageNumber="10">67</emphasis> Bistoroside A: 3′,6′-di- <emphasis bold="true" box="[727,754,1476,1491]" id="07AFEA9EFFE86562D3EEFA7D21EFE599" italics="true" pageId="9" pageNumber="10">O -Z</emphasis> -feruloyl sucrose No physiological activity determined</td><td box="[1576,1925,1476,1491]" colspan="2" id="C83A5DB2FFE89A94D711FA7D2498E599" pageId="9" pageNumber="10"><bibRefCitation author="Kim, K. H. &amp; Chang, S. W. &amp; Lee, K. R." box="[1718,1849,1476,1491]" id="514A4B7DFFE86562D78FFA7D2424E599" pageId="9" pageNumber="10" pagination="519 - 523" refId="ref19090" refString="Kim, K. H., Chang, S. W., Lee, K. R., 2010. Feruloyl sucrose derivatives from Bistorta manshuriensis. Can. J. Chem. 88, 519 - 523. https: // doi. org / 10.1139 / V 10 - 037." type="journal article" year="2010">Kim et al. (2010)</bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DFA622498E64B"><th id="C83A5DB2FFE89A94D14DFA622246E64B"/><td id="C83A5DB2FFE89A94D045FA62228CE64B"/><td box="[425,1552,1499,1537]" id="C83A5DB2FFE89A94D090FA62250DE64B" pageId="9" pageNumber="10"><emphasis bold="true" box="[471,491,1499,1514]" id="07AFEA9EFFE86562D0EEFA6222F6E5A0" pageId="9" pageNumber="10">68</emphasis> Bistoroside B: 3′,6′-di- <emphasis bold="true" box="[725,753,1499,1514]" id="07AFEA9EFFE86562D3ECFA6221ECE5A0" italics="true" pageId="9" pageNumber="10">O -Z</emphasis> -feruloyl-6- <emphasis bold="true" box="[837,849,1499,1514]" id="07AFEA9EFFE86562D27CFA62204CE5A0" italics="true" pageId="9" pageNumber="10">O</emphasis> -acetyl sucrose <emphasis bold="true" box="[471,491,1522,1537]" id="07AFEA9EFFE86562D0EEFA4B22F6E64B" pageId="9" pageNumber="10">69</emphasis> Helonioside A: 3′,6′-di- <emphasis bold="true" box="[733,759,1522,1537]" id="07AFEA9EFFE86562D3E4FA4B21EAE64B" italics="true" pageId="9" pageNumber="10">O -E</emphasis> -feruloyl sucrose</td><td id="C83A5DB2FFE89A94D711FA6225F9E64B"/><td id="C83A5DB2FFE89A94D7C6FA622498E64B"/></tr><tr id="8BEB34CEFFE89A94D14DF9B12498E65D"><th id="C83A5DB2FFE89A94D14DF9B12246E65D"/><td id="C83A5DB2FFE89A94D045F9B1228CE65D"/><td box="[425,1552,1544,1559]" id="C83A5DB2FFE89A94D090F9B1250DE65D" pageId="9" pageNumber="10"><emphasis bold="true" box="[471,491,1544,1559]" id="07AFEA9EFFE86562D0EEF9B122F6E65D" pageId="9" pageNumber="10">70</emphasis> Helonioside B: 3′,6′-di- <emphasis bold="true" box="[732,758,1544,1559]" id="07AFEA9EFFE86562D3E5F9B121EBE65D" italics="true" pageId="9" pageNumber="10">O -E</emphasis> -feruloyl-6- <emphasis bold="true" box="[843,855,1544,1559]" id="07AFEA9EFFE86562D272F9B1204AE65D" italics="true" pageId="9" pageNumber="10">O</emphasis> -acetyl sucrose</td><td id="C83A5DB2FFE89A94D711F9B125F9E65D"/><td id="C83A5DB2FFE89A94D7C6F9B12498E65D"/></tr><tr id="8BEB34CEFFE89A94D14DF98F2498E60F"><th box="[116,347,1590,1605]" id="C83A5DB2FFE89A94D14DF98F2246E60F" pageId="9" pageNumber="10"><taxonomicName _evidence="catalogs" _step="species1" box="[116,347,1590,1605]" class="Liliopsida" family="Smilacaceae" genus="Smilax" id="F2DB4D0FFFE86562D14DF98F2246E60F" kingdom="Plantae" order="Liliales" pageId="9" pageNumber="10" phylum="Tracheophyta" rank="species" species="bracteata"><emphasis bold="true" box="[116,237,1590,1605]" id="07AFEA9EFFE86562D14DF98F23F0E60F" italics="true" pageId="9" pageNumber="10">Smilax bracteata</emphasis> (Smilacaceae)</taxonomicName></th><td id="C83A5DB2FFE89A94D045F98F228CE60F"/><td box="[425,1552,1590,1605]" id="C83A5DB2FFE89A94D090F98F250DE60F" pageId="9" pageNumber="10"><emphasis bold="true" box="[471,491,1590,1605]" id="07AFEA9EFFE86562D0EEF98F22F6E60F" pageId="9" pageNumber="10">71</emphasis> Smilaside L: 1′,3′,6′- <emphasis bold="true" box="[711,723,1590,1605]" id="07AFEA9EFFE86562D3FEF98F21CEE60F" italics="true" pageId="9" pageNumber="10">O</emphasis> -tri-feruloyl sucrose Antioxidant activity</td><td box="[1576,1925,1590,1605]" colspan="2" id="C83A5DB2FFE89A94D711F98F2498E60F" pageId="9" pageNumber="10"><bibRefCitation author="Zhang, L. &amp; Liao, C. C. &amp; Huang, H. C. &amp; Shen, Y. C. &amp; Yang, L. M. &amp; Kuo, Y. H." box="[1718,1865,1590,1605]" id="514A4B7DFFE86562D78FF98F2454E60F" pageId="9" pageNumber="10" pagination="1398 - 1404" refId="ref24584" refString="Zhang, L., Liao, C. C., Huang, H. C., Shen, Y. C., Yang, L. M., Kuo, Y. H., 2008. Antioxidant phenylpropanoid glycosides from Smilax bracteata. Phytochemistry 69, 1398 - 1404. https: // doi. org / 10.1016 / j. phytochem. 2008.01.002." type="journal article" year="2008">Zhang et al. (2008)</bibRefCitation></td></tr><tr id="8BEB34CEFFE89A94D14DF9F42498E6FD"><th id="C83A5DB2FFE89A94D14DF9F42246E6FD"/><td id="C83A5DB2FFE89A94D045F9F4228CE6FD"/><td box="[425,1552,1613,1719]" id="C83A5DB2FFE89A94D090F9F4250DE6FD" pageId="9" pageNumber="10"><emphasis bold="true" box="[471,491,1613,1628]" id="07AFEA9EFFE86562D0EEF9F422F6E616" pageId="9" pageNumber="10">72</emphasis> Smilaside G: 1′,3′- <emphasis bold="true" box="[696,708,1613,1628]" id="07AFEA9EFFE86562D381F9F421D9E616" italics="true" pageId="9" pageNumber="10">O</emphasis> -di- <emphasis bold="true" box="[733,741,1613,1628]" id="07AFEA9EFFE86562D3E4F9F421F8E616" italics="true" pageId="9" pageNumber="10">p</emphasis> -coumaroyl-6′- <emphasis bold="true" box="[852,864,1613,1628]" id="07AFEA9EFFE86562D26DF9F4207DE616" italics="true" pageId="9" pageNumber="10">O</emphasis> -feruloyl sucrose <emphasis bold="true" box="[471,491,1636,1651]" id="07AFEA9EFFE86562D0EEF9DD22F6E639" pageId="9" pageNumber="10">73</emphasis> Smilaside H: 1′,3′- <emphasis bold="true" box="[696,708,1636,1651]" id="07AFEA9EFFE86562D381F9DD21D9E639" italics="true" pageId="9" pageNumber="10">O</emphasis> -di- <emphasis bold="true" box="[734,742,1636,1651]" id="07AFEA9EFFE86562D3E7F9DD21FBE639" italics="true" pageId="9" pageNumber="10">p</emphasis> -coumaroyl-6′- <emphasis bold="true" box="[853,865,1636,1651]" id="07AFEA9EFFE86562D26CF9DD207CE639" italics="true" pageId="9" pageNumber="10">O</emphasis> -feruloyl-2- <emphasis bold="true" box="[949,961,1636,1651]" id="07AFEA9EFFE86562D28CF9DD20DCE639" italics="true" pageId="9" pageNumber="10">O</emphasis> -acetyl sucrose <emphasis bold="true" box="[471,491,1659,1674]" id="07AFEA9EFFE86562D0EEF9C222F6E6C0" pageId="9" pageNumber="10">74</emphasis> Smilaside I: 1′,3′- <emphasis bold="true" box="[690,702,1659,1674]" id="07AFEA9EFFE86562D38BF9C221A3E6C0" italics="true" pageId="9" pageNumber="10">O</emphasis> -di- <emphasis bold="true" box="[727,735,1659,1674]" id="07AFEA9EFFE86562D3EEF9C221C2E6C0" italics="true" pageId="9" pageNumber="10">p</emphasis> -coumaroyl-6′- <emphasis bold="true" box="[846,858,1659,1674]" id="07AFEA9EFFE86562D277F9C22047E6C0" italics="true" pageId="9" pageNumber="10">O</emphasis> -feruloyl-6- <emphasis bold="true" box="[942,954,1659,1674]" id="07AFEA9EFFE86562D297F9C220A7E6C0" italics="true" pageId="9" pageNumber="10">O</emphasis> -acetyl sucrose <emphasis bold="true" box="[471,491,1682,1697]" id="07AFEA9EFFE86562D0EEF92B22F6E6EB" pageId="9" pageNumber="10">75</emphasis> Smilaside J: 3′- <emphasis bold="true" box="[673,699,1682,1697]" id="07AFEA9EFFE86562D398F92B21A6E6EB" italics="true" pageId="9" pageNumber="10">O -p</emphasis> -coumaroyl-1′,6′- <emphasis bold="true" box="[828,840,1682,1697]" id="07AFEA9EFFE86562D205F92B2055E6EB" italics="true" pageId="9" pageNumber="10">O</emphasis> -di-feruloyl sucrose <emphasis bold="true" box="[471,491,1704,1719]" id="07AFEA9EFFE86562D0EEF91122F6E6FD" pageId="9" pageNumber="10">76</emphasis> Smilaside K: 1′- <emphasis bold="true" box="[676,702,1704,1719]" id="07AFEA9EFFE86562D39DF91121A3E6FD" italics="true" pageId="9" pageNumber="10">O -p</emphasis> -coumaroyl-3′,6′- <emphasis bold="true" box="[831,843,1704,1719]" id="07AFEA9EFFE86562D206F9112056E6FD" italics="true" pageId="9" pageNumber="10">O</emphasis> -diferuloyl-2- <emphasis bold="true" box="[942,954,1704,1719]" id="07AFEA9EFFE86562D297F91120A7E6FD" italics="true" pageId="9" pageNumber="10">O</emphasis> -acetyl sucrose</td><td id="C83A5DB2FFE89A94D711F9F425F9E6FD"/><td id="C83A5DB2FFE89A94D7C6F9F42498E6FD"/></tr></tbody></table></document>