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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Cytotoxic Stilbenes and Canthinone Alkaloids from <italic>Brucea antidysenterica</italic> (Simaroubaceae)</title><author><name sortKey="Makong, Yves Salomon" sort="Makong, Yves Salomon" uniqKey="Makong Y" first="Yves Salomon" last="Makong">Yves Salomon Makong</name><affiliation><nlm:aff id="af1-molecules-24-04412">Department of Chemistry, Faculty of Science, University of Douala, P.O. Box 24157 Douala, Cameroon;<email>y.makong@yahoo.com</email> (Y.S.M.);<email>dbjl19@yahoo.fr</email> (J.L.D.B.);<email>akamdemfr@yahoo.fr</email> (A.F.K.W.)</nlm:aff></affiliation></author><author><name sortKey="Mouthe Happi, Gervais" sort="Mouthe Happi, Gervais" uniqKey="Mouthe Happi G" first="Gervais" last="Mouthé Happi">Gervais Mouthé Happi</name><affiliation><nlm:aff id="af2-molecules-24-04412">Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, 33501 Bielefeld, Germany;<email>gervais20022003@yahoo.fr</email></nlm:aff></affiliation></author><author><name sortKey="Djouaka Bavoua, Judith Liliane" sort="Djouaka Bavoua, Judith Liliane" uniqKey="Djouaka Bavoua J" first="Judith Liliane" last="Djouaka Bavoua">Judith Liliane Djouaka Bavoua</name><affiliation><nlm:aff id="af1-molecules-24-04412">Department of Chemistry, Faculty of Science, University of Douala, P.O. Box 24157 Douala, Cameroon;<email>y.makong@yahoo.com</email> (Y.S.M.);<email>dbjl19@yahoo.fr</email> (J.L.D.B.);<email>akamdemfr@yahoo.fr</email> (A.F.K.W.)</nlm:aff></affiliation></author><author><name sortKey="Wansi, Jean Duplex" sort="Wansi, Jean Duplex" uniqKey="Wansi J" first="Jean Duplex" last="Wansi">Jean Duplex Wansi</name><affiliation><nlm:aff id="af1-molecules-24-04412">Department of Chemistry, Faculty of Science, University of Douala, P.O. Box 24157 Douala, Cameroon;<email>y.makong@yahoo.com</email> (Y.S.M.);<email>dbjl19@yahoo.fr</email> (J.L.D.B.);<email>akamdemfr@yahoo.fr</email> (A.F.K.W.)</nlm:aff></affiliation><affiliation><nlm:aff id="af2-molecules-24-04412">Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, 33501 Bielefeld, Germany;<email>gervais20022003@yahoo.fr</email></nlm:aff></affiliation></author><author><name sortKey="Nahar, Lutfun" sort="Nahar, Lutfun" uniqKey="Nahar L" first="Lutfun" last="Nahar">Lutfun Nahar</name><affiliation><nlm:aff id="af3-molecules-24-04412">Laboratory of Growth Regulators, Institute of Experimental Botany ASCR & Palacký University, Šlechtitelů 27, 78371 Olomouc, Czech Republic;<email>L.Nahar@ljmu.ac.uk</email></nlm:aff></affiliation><affiliation><nlm:aff id="af4-molecules-24-04412">Centre for Natural Products Discovery (CNPD), School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK;<email>S.Sarker@ljmu.ac.uk</email></nlm:aff></affiliation></author><author><name sortKey="Kamdem Waffo, Alain Francois" sort="Kamdem Waffo, Alain Francois" uniqKey="Kamdem Waffo A" first="Alain François" last="Kamdem Waffo">Alain François Kamdem Waffo</name><affiliation><nlm:aff id="af1-molecules-24-04412">Department of Chemistry, Faculty of Science, University of Douala, P.O. Box 24157 Douala, Cameroon;<email>y.makong@yahoo.com</email> (Y.S.M.);<email>dbjl19@yahoo.fr</email> (J.L.D.B.);<email>akamdemfr@yahoo.fr</email> (A.F.K.W.)</nlm:aff></affiliation></author><author><name sortKey="Martin, Claire" sort="Martin, Claire" uniqKey="Martin C" first="Claire" last="Martin">Claire Martin</name><affiliation><nlm:aff id="af5-molecules-24-04412">Department of Biological Sciences, School of Science and the Environment, University of Worcester, Henwick Grove, Worcester WR2 6AJ, UK;<email>c.martin@worc.ac.uk</email></nlm:aff></affiliation></author><author><name sortKey="Sewald, Norbert" sort="Sewald, Norbert" uniqKey="Sewald N" first="Norbert" last="Sewald">Norbert Sewald</name><affiliation><nlm:aff id="af2-molecules-24-04412">Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, 33501 Bielefeld, Germany;<email>gervais20022003@yahoo.fr</email></nlm:aff></affiliation></author><author><name sortKey="Sarker, Satyajit Dey" sort="Sarker, Satyajit Dey" uniqKey="Sarker S" first="Satyajit Dey" last="Sarker">Satyajit Dey Sarker</name><affiliation><nlm:aff id="af4-molecules-24-04412">Centre for Natural Products Discovery (CNPD), School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK;<email>S.Sarker@ljmu.ac.uk</email></nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">31816856</idno><idno type="pmc">6930556</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930556</idno><idno type="RBID">PMC:6930556</idno><idno type="doi">10.3390/molecules24234412</idno><date when="2019">2019</date><idno type="wicri:Area/Pmc/Corpus">000724</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000724</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Cytotoxic Stilbenes and Canthinone Alkaloids from <italic>Brucea antidysenterica</italic> (Simaroubaceae)</title><author><name sortKey="Makong, Yves Salomon" sort="Makong, Yves Salomon" uniqKey="Makong Y" first="Yves Salomon" last="Makong">Yves Salomon Makong</name><affiliation><nlm:aff id="af1-molecules-24-04412">Department of Chemistry, Faculty of Science, University of Douala, P.O. Box 24157 Douala, Cameroon;<email>y.makong@yahoo.com</email> (Y.S.M.);<email>dbjl19@yahoo.fr</email> (J.L.D.B.);<email>akamdemfr@yahoo.fr</email> (A.F.K.W.)</nlm:aff></affiliation></author><author><name sortKey="Mouthe Happi, Gervais" sort="Mouthe Happi, Gervais" uniqKey="Mouthe Happi G" first="Gervais" last="Mouthé Happi">Gervais Mouthé Happi</name><affiliation><nlm:aff id="af2-molecules-24-04412">Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, 33501 Bielefeld, Germany;<email>gervais20022003@yahoo.fr</email></nlm:aff></affiliation></author><author><name sortKey="Djouaka Bavoua, Judith Liliane" sort="Djouaka Bavoua, Judith Liliane" uniqKey="Djouaka Bavoua J" first="Judith Liliane" last="Djouaka Bavoua">Judith Liliane Djouaka Bavoua</name><affiliation><nlm:aff id="af1-molecules-24-04412">Department of Chemistry, Faculty of Science, University of Douala, P.O. Box 24157 Douala, Cameroon;<email>y.makong@yahoo.com</email> (Y.S.M.);<email>dbjl19@yahoo.fr</email> (J.L.D.B.);<email>akamdemfr@yahoo.fr</email> (A.F.K.W.)</nlm:aff></affiliation></author><author><name sortKey="Wansi, Jean Duplex" sort="Wansi, Jean Duplex" uniqKey="Wansi J" first="Jean Duplex" last="Wansi">Jean Duplex Wansi</name><affiliation><nlm:aff id="af1-molecules-24-04412">Department of Chemistry, Faculty of Science, University of Douala, P.O. Box 24157 Douala, Cameroon;<email>y.makong@yahoo.com</email> (Y.S.M.);<email>dbjl19@yahoo.fr</email> (J.L.D.B.);<email>akamdemfr@yahoo.fr</email> (A.F.K.W.)</nlm:aff></affiliation><affiliation><nlm:aff id="af2-molecules-24-04412">Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, 33501 Bielefeld, Germany;<email>gervais20022003@yahoo.fr</email></nlm:aff></affiliation></author><author><name sortKey="Nahar, Lutfun" sort="Nahar, Lutfun" uniqKey="Nahar L" first="Lutfun" last="Nahar">Lutfun Nahar</name><affiliation><nlm:aff id="af3-molecules-24-04412">Laboratory of Growth Regulators, Institute of Experimental Botany ASCR & Palacký University, Šlechtitelů 27, 78371 Olomouc, Czech Republic;<email>L.Nahar@ljmu.ac.uk</email></nlm:aff></affiliation><affiliation><nlm:aff id="af4-molecules-24-04412">Centre for Natural Products Discovery (CNPD), School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK;<email>S.Sarker@ljmu.ac.uk</email></nlm:aff></affiliation></author><author><name sortKey="Kamdem Waffo, Alain Francois" sort="Kamdem Waffo, Alain Francois" uniqKey="Kamdem Waffo A" first="Alain François" last="Kamdem Waffo">Alain François Kamdem Waffo</name><affiliation><nlm:aff id="af1-molecules-24-04412">Department of Chemistry, Faculty of Science, University of Douala, P.O. Box 24157 Douala, Cameroon;<email>y.makong@yahoo.com</email> (Y.S.M.);<email>dbjl19@yahoo.fr</email> (J.L.D.B.);<email>akamdemfr@yahoo.fr</email> (A.F.K.W.)</nlm:aff></affiliation></author><author><name sortKey="Martin, Claire" sort="Martin, Claire" uniqKey="Martin C" first="Claire" last="Martin">Claire Martin</name><affiliation><nlm:aff id="af5-molecules-24-04412">Department of Biological Sciences, School of Science and the Environment, University of Worcester, Henwick Grove, Worcester WR2 6AJ, UK;<email>c.martin@worc.ac.uk</email></nlm:aff></affiliation></author><author><name sortKey="Sewald, Norbert" sort="Sewald, Norbert" uniqKey="Sewald N" first="Norbert" last="Sewald">Norbert Sewald</name><affiliation><nlm:aff id="af2-molecules-24-04412">Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, 33501 Bielefeld, Germany;<email>gervais20022003@yahoo.fr</email></nlm:aff></affiliation></author><author><name sortKey="Sarker, Satyajit Dey" sort="Sarker, Satyajit Dey" uniqKey="Sarker S" first="Satyajit Dey" last="Sarker">Satyajit Dey Sarker</name><affiliation><nlm:aff id="af4-molecules-24-04412">Centre for Natural Products Discovery (CNPD), School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK;<email>S.Sarker@ljmu.ac.uk</email></nlm:aff></affiliation></author></analytic><series><title level="j">Molecules</title><idno type="eISSN">1420-3049</idno><imprint><date when="2019">2019</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>A phytochemical study of the root and bark of <italic>Brucea antidysenterica</italic> J. F. Mill. (Simaroubaceae) afforded three new compounds, including a stilbene glycoside bruceanoside A (<bold>1</bold>), and two canthinone alkaloids bruceacanthinones A (<bold>3</bold>) and B (<bold>4</bold>), along with ten known secondary metabolites, rhaponticin (<bold>2</bold>), 1,11-dimethoxycanthin-6-one (<bold>5</bold>), canthin-6-one (<bold>6</bold>), 1-methoxycanthin-6-one (<bold>7</bold>), 2-methoxycanthin-6-one (<bold>8</bold>), 2-hydroxy-1,11-dimethoxycanthin-6-one (<bold>9</bold>), <italic>β</italic>-carboline-1-propionic acid (<bold>10</bold>), cleomiscosin C (<bold>11</bold>), cleomiscosin A (<bold>12</bold>), and hydnocarpin (<bold>13</bold>). The structures of all the compounds were determined using spectrometric and spectroscopic methods including 1D and 2D NMR, and HRSEIMS. The identities of the known compounds were further confirmed by comparison of their data with those reported in the literature. The root and bark methanolic extracts, the dichloromethane and ethyl acetate soluble fractions, and the isolated compounds (<bold>3</bold>–<bold>13</bold>), were assessed for their cytotoxicity against the cancer cell lines A-549, MCF-7, and PC-3. The results suggested that compounds in the extracts might possess a synergic action in their cytotoxicity.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Liu, J H" uniqKey="Liu J">J.-H. Liu</name></author><author><name sortKey="Jin, H Z" uniqKey="Jin H">H.-Z. Jin</name></author><author><name sortKey="Zhang, W D" uniqKey="Zhang W">W.-D. Zhang</name></author><author><name sortKey="Yan, S K" uniqKey="Yan S">S.-K. Yan</name></author><author><name sortKey="Shen, Y H" uniqKey="Shen Y">Y.-H. Shen</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wright, C W" uniqKey="Wright C">C.W. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Molecules</journal-id><journal-id journal-id-type="iso-abbrev">Molecules</journal-id><journal-id journal-id-type="publisher-id">molecules</journal-id><journal-title-group><journal-title>Molecules</journal-title></journal-title-group><issn pub-type="epub">1420-3049</issn><publisher><publisher-name>MDPI</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">31816856</article-id><article-id pub-id-type="pmc">6930556</article-id><article-id pub-id-type="doi">10.3390/molecules24234412</article-id><article-id pub-id-type="publisher-id">molecules-24-04412</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Cytotoxic Stilbenes and Canthinone Alkaloids from <italic>Brucea antidysenterica</italic> (Simaroubaceae)</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Makong</surname><given-names>Yves Salomon</given-names></name><xref ref-type="aff" rid="af1-molecules-24-04412">1</xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid" authenticated="true">https://orcid.org/0000-0001-9659-6125</contrib-id><name><surname>Mouthé Happi</surname><given-names>Gervais</given-names></name><xref ref-type="aff" rid="af2-molecules-24-04412">2</xref></contrib><contrib contrib-type="author"><name><surname>Djouaka Bavoua</surname><given-names>Judith Liliane</given-names></name><xref ref-type="aff" rid="af1-molecules-24-04412">1</xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid" authenticated="true">https://orcid.org/0000-0002-5111-4361</contrib-id><name><surname>Wansi</surname><given-names>Jean Duplex</given-names></name><xref ref-type="aff" rid="af1-molecules-24-04412">1</xref><xref ref-type="aff" rid="af2-molecules-24-04412">2</xref><xref rid="c1-molecules-24-04412" ref-type="corresp">*</xref></contrib><contrib contrib-type="author"><name><surname>Nahar</surname><given-names>Lutfun</given-names></name><xref ref-type="aff" rid="af3-molecules-24-04412">3</xref><xref ref-type="aff" rid="af4-molecules-24-04412">4</xref></contrib><contrib contrib-type="author"><name><surname>Kamdem Waffo</surname><given-names>Alain François</given-names></name><xref ref-type="aff" rid="af1-molecules-24-04412">1</xref></contrib><contrib contrib-type="author"><name><surname>Martin</surname><given-names>Claire</given-names></name><xref ref-type="aff" rid="af5-molecules-24-04412">5</xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid" authenticated="true">https://orcid.org/0000-0002-0309-2655</contrib-id><name><surname>Sewald</surname><given-names>Norbert</given-names></name><xref ref-type="aff" rid="af2-molecules-24-04412">2</xref><xref rid="c1-molecules-24-04412" ref-type="corresp">*</xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid" authenticated="true">https://orcid.org/0000-0003-4038-0514</contrib-id><name><surname>Sarker</surname><given-names>Satyajit Dey</given-names></name><xref ref-type="aff" rid="af4-molecules-24-04412">4</xref></contrib></contrib-group><aff id="af1-molecules-24-04412"><label>1</label>Department of Chemistry, Faculty of Science, University of Douala, P.O. Box 24157 Douala, Cameroon;<email>y.makong@yahoo.com</email> (Y.S.M.);<email>dbjl19@yahoo.fr</email> (J.L.D.B.);<email>akamdemfr@yahoo.fr</email> (A.F.K.W.)</aff><aff id="af2-molecules-24-04412"><label>2</label>Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, 33501 Bielefeld, Germany;<email>gervais20022003@yahoo.fr</email></aff><aff id="af3-molecules-24-04412"><label>3</label>Laboratory of Growth Regulators, Institute of Experimental Botany ASCR & Palacký University, Šlechtitelů 27, 78371 Olomouc, Czech Republic;<email>L.Nahar@ljmu.ac.uk</email></aff><aff id="af4-molecules-24-04412"><label>4</label>Centre for Natural Products Discovery (CNPD), School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK;<email>S.Sarker@ljmu.ac.uk</email></aff><aff id="af5-molecules-24-04412"><label>5</label>Department of Biological Sciences, School of Science and the Environment, University of Worcester, Henwick Grove, Worcester WR2 6AJ, UK;<email>c.martin@worc.ac.uk</email></aff><author-notes><corresp id="c1-molecules-24-04412"><label>*</label>Correspondence: <email>jean.wansi@uni-bielefeld.de</email> or <email>jdwansi@yahoo.fr</email> (J.D.W.); <email>norbert.sewald@uni-bielefeld.de</email> (N.S.); Tel.: +49-1521-690-4218 (J.D.W.)</corresp></author-notes><pub-date pub-type="epub"><day>03</day><month>12</month><year>2019</year></pub-date><pub-date pub-type="collection"><month>12</month><year>2019</year></pub-date><volume>24</volume><issue>23</issue><elocation-id>4412</elocation-id><history><date date-type="received"><day>21</day><month>11</month><year>2019</year></date><date date-type="accepted"><day>29</day><month>11</month><year>2019</year></date></history><permissions><copyright-statement>© 2019 by the authors.</copyright-statement><copyright-year>2019</copyright-year><license license-type="open-access"><license-p>Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>).</license-p></license></permissions><abstract><p>A phytochemical study of the root and bark of <italic>Brucea antidysenterica</italic> J. F. Mill. (Simaroubaceae) afforded three new compounds, including a stilbene glycoside bruceanoside A (<bold>1</bold>), and two canthinone alkaloids bruceacanthinones A (<bold>3</bold>) and B (<bold>4</bold>), along with ten known secondary metabolites, rhaponticin (<bold>2</bold>), 1,11-dimethoxycanthin-6-one (<bold>5</bold>), canthin-6-one (<bold>6</bold>), 1-methoxycanthin-6-one (<bold>7</bold>), 2-methoxycanthin-6-one (<bold>8</bold>), 2-hydroxy-1,11-dimethoxycanthin-6-one (<bold>9</bold>), <italic>β</italic>-carboline-1-propionic acid (<bold>10</bold>), cleomiscosin C (<bold>11</bold>), cleomiscosin A (<bold>12</bold>), and hydnocarpin (<bold>13</bold>). The structures of all the compounds were determined using spectrometric and spectroscopic methods including 1D and 2D NMR, and HRSEIMS. The identities of the known compounds were further confirmed by comparison of their data with those reported in the literature. The root and bark methanolic extracts, the dichloromethane and ethyl acetate soluble fractions, and the isolated compounds (<bold>3</bold>–<bold>13</bold>), were assessed for their cytotoxicity against the cancer cell lines A-549, MCF-7, and PC-3. The results suggested that compounds in the extracts might possess a synergic action in their cytotoxicity.</p></abstract><kwd-group><kwd><italic>Brucea antidysenterica</italic></kwd><kwd>Simaroubaceae</kwd><kwd>bruceanoside A</kwd><kwd>bruceacanthinones A–B</kwd><kwd>cytotoxicity</kwd></kwd-group></article-meta></front><body><sec sec-type="intro" id="sec1-molecules-24-04412"><title>1. Introduction</title><p>Plants from the <italic>Brucea</italic> genus (Simaroubaceae) have been extensively investigated for their chemical constituents and pharmacological properties since 1900 [<xref rid="B1-molecules-24-04412" ref-type="bibr">1</xref>]. Among the numerous metabolites reported so far, quassinoids, also called nigakilactones and canthinone alkaloids, are the most important class of compounds [<xref rid="B1-molecules-24-04412" ref-type="bibr">1</xref>], with demonstrable biological activities, including anti-amoebic [<xref rid="B2-molecules-24-04412" ref-type="bibr">2</xref>], antitumour [<xref rid="B3-molecules-24-04412" ref-type="bibr">3</xref>,<xref rid="B4-molecules-24-04412" ref-type="bibr">4</xref>,<xref rid="B5-molecules-24-04412" ref-type="bibr">5</xref>], antiplasmodial [<xref rid="B6-molecules-24-04412" ref-type="bibr">6</xref>,<xref rid="B7-molecules-24-04412" ref-type="bibr">7</xref>], and antituberculosis [<xref rid="B8-molecules-24-04412" ref-type="bibr">8</xref>] effects. As the name indicates, <italic>Brucea antidysenterica</italic> J. F. Mill. is used in traditional medicine for the treatment of dysentery and also against malaria, diarrhoea, and stomach aches [<xref rid="B9-molecules-24-04412" ref-type="bibr">9</xref>,<xref rid="B10-molecules-24-04412" ref-type="bibr">10</xref>]. In Ethiopia, the plant is also used for the treatment of tumors, and a follow-up investigation revealed that the compound has promising activity in vitro against several lymphoma, leukemia, and myeloma cell lines [<xref rid="B11-molecules-24-04412" ref-type="bibr">11</xref>]. In addition, the 80% methanolic extract from the leaf was assayed for antioxidant activity, showing significant inhibition of 87.57% for the water soluble fraction as measured by DPPH assay, and 72.57 mg AAE/g as measured by FRAP assay [<xref rid="B12-molecules-24-04412" ref-type="bibr">12</xref>]. Moreover, 50 mg/mL of the aqueous leaf extract gave a better wound healing effect than the control group when applied topically on a mouse model [<xref rid="B13-molecules-24-04412" ref-type="bibr">13</xref>]. The aqueous, methanolic, and chloroform crude extracts of the seeds delivered significant <italic>Plasmodium berghei</italic> suppression in 6–8 week old Swiss albino mice of both sexes when given at 600 mg/kg body weight, while the acute toxicity test at a single dose of 2000 mg/kg body weight led to the death of all mice within 24 h for each of above extracts [<xref rid="B14-molecules-24-04412" ref-type="bibr">14</xref>]. It should be noted that the first pure compound reported from the plant, the triterpene quassinoid bruceantin, was already isolated in 1973 from the alcoholic stem bark extract and shown in the follow-up to possess activities related to cell apoptosis and proliferation, angiogenesis, inflammation, and metabolic diseases [<xref rid="B11-molecules-24-04412" ref-type="bibr">11</xref>,<xref rid="B15-molecules-24-04412" ref-type="bibr">15</xref>,<xref rid="B16-molecules-24-04412" ref-type="bibr">16</xref>]. Recently, we identified bruceadysentoside A, a pregnane glycoside, from the leaves of <italic>B. antidysenterica</italic>, in addition to seventeen other compounds, including hydnocarpin, which exhibited the strongest antiproliferative activity with IC<sub>50</sub> values of ≈100 µM and ≈200 µM against PC-3 and HT-29, respectively [<xref rid="B17-molecules-24-04412" ref-type="bibr">17</xref>]. In continuation of our program to explore the phytochemicals of <italic>B. antidysenterica</italic> and their cytotoxicity, we investigated the bark and root of this plant. In this report, we describe the isolation and structural elucidation of one new stilbene (<bold>1</bold>) and two new canthinone alkaloids (<bold>3</bold> and <bold>4</bold>) and their cytotoxic activities.</p></sec><sec sec-type="results" id="sec2-molecules-24-04412"><title>2. Results</title><p>The bark and root of <italic>B. antidysenterica</italic> were separately extracted with MeOH. A small amount of each extract was stored for their in vitro-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) cytotoxicity/viability assay on A-549, MCF-7, and PC-3 cell lines. Based on their similar Thin-Layer Chromatography (TLC) profiles both bark and root extracts were combined and partitioned with dichloromethane and ethyl acetate to afford two major fractions. Subsequent purification of these fractions led to the isolation of three new compounds, including one new stilbene glycoside (<bold>1</bold>) and two new canthinone alkaloids (<bold>3</bold> and <bold>4</bold>). The comparison of our data with those reported in the literature allowed identification of the known compounds, such as rhaponticin (<bold>2</bold>) [<xref rid="B18-molecules-24-04412" ref-type="bibr">18</xref>], 1,11-dimethoxycanthin-6-one (<bold>5</bold>) [<xref rid="B19-molecules-24-04412" ref-type="bibr">19</xref>], canthin-6-one (<bold>6</bold>) [<xref rid="B19-molecules-24-04412" ref-type="bibr">19</xref>], 1-methoxycanthin-6-one (<bold>7</bold>) [<xref rid="B20-molecules-24-04412" ref-type="bibr">20</xref>], 2-methoxycanthin-6-one (<bold>8</bold>) [<xref rid="B21-molecules-24-04412" ref-type="bibr">21</xref>], 2-hydroxy-1,11-diméthoxycanthin-6-one (<bold>9</bold>) [<xref rid="B22-molecules-24-04412" ref-type="bibr">22</xref>], <italic>β</italic>-carboline-1-propionic acid (<bold>10</bold>) [<xref rid="B23-molecules-24-04412" ref-type="bibr">23</xref>], cleomiscosin C (<bold>11</bold>) [<xref rid="B24-molecules-24-04412" ref-type="bibr">24</xref>], cleomiscosin A (<bold>12</bold>) [<xref rid="B25-molecules-24-04412" ref-type="bibr">25</xref>], and hydnocarpin (<bold>13</bold>) [<xref rid="B26-molecules-24-04412" ref-type="bibr">26</xref>] (<xref ref-type="fig" rid="molecules-24-04412-f001">Figure 1</xref>).</p><p>Compound <bold>1</bold> was obtained as a white amorphous powder. Its molecular formula C<sub>29</sub>H<sub>39</sub>O<sub>11</sub> was deduced from the ESIMS (<xref ref-type="app" rid="app1-molecules-24-04412">Figures S1 and S2</xref>) and from the (+)-HR-ESIMS showing the pseudo-molecular ion peak at <italic>m</italic>/<italic>z</italic> 563.2488 [M + H]<sup>+</sup> (calculated for C<sub>29</sub>H<sub>39</sub>O<sub>11</sub>, 563.2492). The <sup>1</sup>H NMR spectrum (<xref rid="molecules-24-04412-t001" ref-type="table">Table 1</xref>, <xref ref-type="app" rid="app1-molecules-24-04412">Figure S3</xref>) showed characteristic signals of two aromatic methoxyl (<italic>δ</italic> 3.80, 6H), two <italic>trans</italic>-olefinic protons (<italic>δ</italic> 6.99 and 7.20, d, <italic>J =</italic> 16.4 Hz, 1H each), and the occurrence of two independent aromatic rings, each carrying three protons organized in two different spin systems: The first ring (A) showed the AMX-type signals (<italic>δ</italic> 6.78 and 6.82, brs, 1H each; 6.52, t, <italic>J</italic> = 2.2 Hz, 1H) and were attributed to the protons of a 1,3,5-trisubstituted aromatic ring, while the second ring (B) exhibited <sup>1</sup>H signals of an A<sub>2</sub>B<sub>2</sub>-coupled spin system (<italic>δ</italic> 6.95 and 7.58, d, <italic>J</italic> = 8.8 Hz, 2H each) which were assignable to the protons of a 1,4-disubstituted aromatic ring. Furthermore, the presence of two anomeric proton signals was depicted at <italic>δ</italic> 4.89 (1H, d, <italic>J</italic> = 7.6 Hz) and 4.56 (1H, d, <italic>J</italic> = 1.7 Hz), and a methyl doublet of rhamnose was at <italic>δ</italic> 1.11 (3H, d, <italic>J</italic> = 6.1 Hz). These three <sup>1</sup>H signals coupled to the HSQC and DEPT experiments allowed us to assign their <sup>13</sup>C resonances at <italic>δ</italic> 101.0, 101.0, and 18.3, respectively (<xref ref-type="app" rid="app1-molecules-24-04412">Figures S4–S6</xref>). All these findings indicated that compound <bold>1</bold> was a stilbene glycoside with two sugar moieties; one of them might be rhamnose [<xref rid="B27-molecules-24-04412" ref-type="bibr">27</xref>]. Careful analysis of the HMBC spectrum (<xref ref-type="fig" rid="molecules-24-04412-f002">Figure 2</xref> and <xref ref-type="app" rid="app1-molecules-24-04412">Figure S7</xref>) of compound <bold>1</bold> showed cross-peak correlations between the proton signal at <italic>δ</italic> 6.99 (H-<italic>α</italic>) and the carbon signals of the ring A appearing at <italic>δ</italic> 129.9 (C-1), 107.6 (C-6), and 105 (C-2), while the proton signal at <italic>δ</italic> 7.20 (H-<italic>β</italic>) showed correlations with the carbon signals involved in the ring B and appearing at <italic>δ</italic> 139.7 (C-1′) and 128.4 (C-2′/C-6′), confirming that rings A and B are linked through the <italic>trans</italic>-orientated bond C<italic><sub>α</sub></italic>–C<italic><sub>β</sub></italic> characteristic of stilbene. Furthermore, the two methoxy groups were connected at C-3 and C-5 in ring A according to the correlations observed between the proton signals at <italic>δ</italic> (3.80, s, 6H) and the carbon signals at <italic>δ</italic> 159.3 (C-3) and 160.2 (C-5). Therefore, the aglycone was characterized to be pterostilbene, and the two remaining sugar moieties might be connected at the only position C-4′ (<italic>δ</italic><sub>C</sub>159.8) in cycle B suggesting that <bold>1</bold> is a pterostilbene glycoside [<xref rid="B28-molecules-24-04412" ref-type="bibr">28</xref>]. This partial conclusion was further supported by the mass spectra in positive and negative ionization mode (<xref ref-type="app" rid="app1-molecules-24-04412">Figures S1 and S2</xref>). Briefly, the (–)-HR-ESIMS showed a peak at 255.106 corresponding to the fragment [M − rha − glc]<sup>−</sup>; while the (+)-HR-ESIMS exhibited signal at 441.156 attributed to the fragment [M + Na − rha]<sup>+</sup>. Both observations indicated that the two sugar units are linked to each other and connected to the aglycone pterostilbene via the glucose subunit. Further proof was obtained from the long-range correlation between the anomeric proton of glc at <italic>δ</italic> 4.89 (d, <italic>J</italic> = 7.6 Hz, glc H-1) and the carbon signal at <italic>δ</italic> 159.8 (C-4′). The linkage of the two sugar moieties was established from the HMBC correlations between <italic>δ</italic> 4.56 (1H, d, <italic>J</italic> = 1.6 Hz, ara H-1) and <italic>δ</italic> 66.8 (glc C-6) (<xref ref-type="fig" rid="molecules-24-04412-f002">Figure 2</xref>). The anomeric proton of the glucose was assigned with <italic>β</italic>-configuration based on its <sup>3</sup><italic>J</italic><sub>H-1,H-2</sub> coupling constant of 7.6 Hz (<xref rid="molecules-24-04412-t001" ref-type="table">Table 1</xref>), while the anomeric proton of rhamnose was assigned with <italic>α</italic>-configuration due to the characteristic <sup>13</sup>C chemical shift of C-5 (rha) at <italic>δ</italic> 68.8 (<xref rid="molecules-24-04412-t001" ref-type="table">Table 1</xref>) [<xref rid="B29-molecules-24-04412" ref-type="bibr">29</xref>]. Based on all these above evidence, the structure of compound <bold>1</bold> was assigned to be pterostilbene 3-<italic>O</italic>-<italic>α</italic>-rhamnopyranosyl(1→6)-<italic>β</italic>-glucopyranoside and given the trivial name, bruceanoside A.</p><p>Compound <bold>3</bold>, named bruceacanthinone A, was obtained as an amorphous yellow solid. Its molecular formula was assigned as C<sub>15</sub>H<sub>10</sub>N<sub>2</sub>O<sub>3</sub> with help of the ESIMS (<xref ref-type="app" rid="app1-molecules-24-04412">Figure S10</xref>) and the (+)-HR-ESIMS (<italic>m</italic>/<italic>z</italic> 289.0570 [M + Na]<sup>+</sup>, calculated for C<sub>15</sub>H<sub>10</sub>N<sub>2</sub>O<sub>3</sub>Na, 289.0589) counting for 12 double-bond equivalents. The Dragendorff’s test was positive, suggesting that <bold>3</bold> was an alkaloid. On its <sup>1</sup>H NMR spectrum (<xref rid="molecules-24-04412-t002" ref-type="table">Table 2</xref>, <xref ref-type="app" rid="app1-molecules-24-04412">Figure S11</xref>), the signals of two <italic>cis</italic>-coupled protons [<italic>δ</italic> 8.08 and 6.90 (d, <italic>J</italic> = 9.7 Hz, 1H each)] were observed, which are characteristic of the lactam ring of canthin-6-one [<xref rid="B30-molecules-24-04412" ref-type="bibr">30</xref>]. Furthermore, there were signals corresponding to one methoxyl at <italic>δ</italic> 4.29 (3H, s), one hydroxyl at <italic>δ</italic> 8.52 (1H, s), and signals of a four-spin ABMX-type system supported by the COSY correlations (<xref ref-type="fig" rid="molecules-24-04412-f003">Figure 3</xref>) observed between the four proton signals at <italic>δ</italic> 8.70 (1H, dd, <italic>J</italic> = 1.2 and 7.8 Hz), 8.26 (1H, dd, <italic>J</italic> = 1.0 and 7.6 Hz), 7.70 (1H, td, <italic>J</italic> = 1.0, 7.6, and 7.8 Hz), and 7.58 (1H, td, <italic>J</italic> = 1.2, 7.6, and 7.8 Hz). The <sup>13</sup>C NMR spectrum for <bold>3</bold> (<xref rid="molecules-24-04412-t002" ref-type="table">Table 2</xref>, <xref ref-type="app" rid="app1-molecules-24-04412">Figure S12</xref>)) confirmed 16 carbon signals which were clearly sorted by and HSQC (<xref ref-type="app" rid="app1-molecules-24-04412">Figure S13</xref>) experiments into one methoxyl (<italic>δ</italic> 57.2), one ketone carbonyl characteristic of conjugated lactam (<italic>δ</italic> 159.6), six methines, and seven quaternary carbons. All these data were similar to those of huberine, a canthin-6-one alkaloid recently reported from the stem bark of <italic>Picrolemma huberi</italic> [<xref rid="B31-molecules-24-04412" ref-type="bibr">31</xref>]. The comparison of their NMR data suggested that, besides some changes in chemical shifts, which could be explained by the solvent effect during the analysis, the main and more relevant change is the presence of <sup>1</sup>H and <sup>13</sup>C signals of two methoxyl groups in huberine rather than one in compound <bold>3</bold>. This partial conclusion could be further confirmed by the difference of 14 mass units between the two compounds. The HMBC spectrum of <bold>3</bold> (<xref ref-type="fig" rid="molecules-24-04412-f003">Figure 3</xref> and <xref ref-type="app" rid="app1-molecules-24-04412">Figure S14</xref>) showed the same cross-peaks observed in huberine, indicating that the two compounds share the same core structure [<xref rid="B31-molecules-24-04412" ref-type="bibr">31</xref>]. Furthermore, the HMBC experiment allowed the assignment of the methoxyl unit in C-2 and the hydroxyl group in C-1 according to the cross-peaks observed between <italic>δ</italic> 4.29 (OCH<sub>3</sub>) and <italic>δ</italic> 159.6 (C-2), and between <italic>δ</italic> 8.52 (OH) and <italic>δ</italic> 159.6 (C-2), 140.0 (C-1), and 119.2 (C-14). On the basis of all the evidence obtained, the structure of <bold>3</bold> was deduced as 1-hydroxy-2-methoxycanthin-6-one.</p><p>Compound <bold>4</bold> was isolated as an amorphous yellow solid and its molecular formula was deduced from its ESIMS (<xref ref-type="app" rid="app1-molecules-24-04412">Figure S16</xref>) and HR-ESIMS as C<sub>16</sub>H<sub>12</sub>N<sub>2</sub>O<sub>4</sub> (<italic>m</italic>/<italic>z</italic> 297.0855, calculated for C<sub>16</sub>H<sub>13</sub>N<sub>2</sub>O<sub>4</sub>, 298.0875), exhibiting 30 amu more than that of <bold>3</bold>. We found that compounds <bold>3</bold> and <bold>4</bold> are structurally related according to their close <sup>1</sup>H and <sup>13</sup>C NMR data (<xref rid="molecules-24-04412-t002" ref-type="table">Table 2</xref>, <xref ref-type="app" rid="app1-molecules-24-04412">Figures S17 and S18</xref>). The two main differences were the presence of an additional methoxyl group in compound <bold>3</bold> (<italic>δ</italic> 4.28, 57.8) and the occurrence of a three-spin ABC-system rather of the four-spin ABMX-system previously observed in <bold>3</bold>. All these findings suggested that compound <bold>4</bold> is a derivative of <bold>3</bold> in which a methoxyl group is attached as substituent on the ring A. Therefore, the placement of this additional methoxyl group was easily done with the HMBC experiment (<xref ref-type="fig" rid="molecules-24-04412-f003">Figure 3</xref> and <xref ref-type="app" rid="app1-molecules-24-04412">Figure S19</xref>) which exhibited a cross-peak of correlation between <italic>δ</italic> 4.28 (3H, s) and <italic>δ</italic> 160.0 (C-11). The structure of bruceacanthinone B (<bold>4</bold>) was finally determined as 2,11-dimethoxy-1-hydroxycanthin-6-one.</p><p>The root and bark crude extracts, their dichloromethane and ethyl acetate soluble main fractions, and the compounds <bold>3</bold>–<bold>13</bold>, were assessed for their cytotoxic potency by MTT assay against three human cancer cell lines A-549, MCF-7, and PC-3 using etoposide as the positive control (3.5 ± 0.5, 10.2 ± 1.2, and 7.9 ± 1.1 µg/mL, respectively for A-549, MCF-7, and PC-3 see <xref rid="molecules-24-04412-t003" ref-type="table">Table 3</xref>). The crude extracts and the fractions displayed cytotoxicity with IC<sub>50</sub> values ranging from 50.0 ± 5.2 to 80.5 ± 1.8 µg/mL. However, the potencies of isolated compounds <bold>3</bold>–<bold>13</bold> were indicated by IC<sub>50</sub> values more than the double of those of crude extracts (<xref rid="molecules-24-04412-t003" ref-type="table">Table 3</xref>). This observation supported that the isolated compounds were less cytotoxic in single assay compared to the crude extracts and fractions. The results suggested that compounds from <italic>B. antidysenterica</italic> root and bark extracts might have a synergic effect in cytotoxicity assay.</p></sec><sec id="sec3-molecules-24-04412"><title>3. Materials and Methods</title><sec id="sec3dot1-molecules-24-04412" sec-type="methods"><title>3.1. General Experimental Procedures</title><p>Chromatographic solvents were purchased from Fisher Scientific, UK, and used without further purification. Optical rotations were measured in methanol on a JASCO DIP-360 digital polarimeter using a 10 cm cell. Ultraviolet spectra were recorded on a Hitachi UV 3200 spectrophotometer in MeOH. Infrared spectra were recorded on a JASCO 302-A spectrophotometer. ESIMS was recorded on a Finnigan LCQ with a Rheos 4000 quaternary pump (Flux Instrument). EIMS were recorded on a Varian MAT 311A spectrometer (70 eV). EIMS was performed on a JEOL HX 110 mass spectrometer. The <sup>1</sup>H and <sup>13</sup>C NMR spectra were recorded at 600 and 150 MHz, respectively, on a Bruker AMX 600 NMR spectrometer. Chemical shifts are reported in <italic>δ</italic> (ppm). Column chromatography was carried out on silica gel (70–230 mesh, Merck) and flash silica gel (230–400 mesh, Merck). TLC was performed on Merck precoated silica gel 60 F<sub>254</sub> aluminum foil, using ceric sulfate spray reagent for visualization. The purity of compounds was investigated by HPLC. The degree of purity of the positive control compound was ≥98%, while that of the isolated compounds was ≥95%. All reagents used were analytical grade.</p></sec><sec id="sec3dot2-molecules-24-04412"><title>3.2. Plant Material</title><p>The bark and root of <italic>B. antidysenterica</italic> J. F. Mill. were collected in June 2013 at Bakouok (Bamenda) in the Northwest Region of Cameroon and were authenticated by Nana Victor, a botanist at the National Herbarium of Cameroon where a voucher specimen was deposited under the registration number 54,605 HNC.</p></sec><sec id="sec3dot3-molecules-24-04412"><title>3.3. Extraction and Isolation</title><p>The air-dried and powdered bark (2.5 kg) and root (1.2 kg) of <italic>B. antidysenterica</italic> were separately extracted twice at room temperature with MeOH for 48 h and 24 h, respectively. The solvent was removed by evaporation under reduced pressure to obtain the crude extracts from bark (85.6 g) and root (38.7 g). A small amount (≈5 g) of each extract was kept for cytotoxicity assay against three human cancer cell lines A-549, MCF-7, and PC-3. The two crude extracts were combined according to their very similar compositions observed on a TLC plate. The mixed crude extract (114.3 g) was dissolved in water and partitioned with <italic>n</italic>-hexane, dichloromethane (DCM), and ethyl acetate (EtOAc) to afford three main fractions A (12.2 g), B (23.6 g), and C (41.7 g), respectively. Fraction A was mainly oils and fats; the remaining water-soluble fraction was dried and kept for further analysis while the fractions B and C were purified to yield the thirteen compounds identified in this report. More closely, the DCM soluble fraction B was subjected to silica gel column chromatography using a gradient of EtOAc in <italic>n</italic>-hexane to obtain a total of 73 fractions which were combined based on their TLC profiles into four main subfractions B1–B4. Repeated silica gel column chromatography of the subfractions B1 (7.3 g) and B2 (5.8 g) separately eluted with a gradient of DCM in <italic>n</italic>-hexane yielded compounds <bold>6</bold> (10.5 mg) and <bold>7</bold> (15.5 mg) from B1, while compound <bold>8</bold> (8.7 mg) was obtained from B2. Similarly, the subfractions B3 (6.2 g) was further purified on silica gel column chromatography with DCM-EtOAc gradient to give compounds <bold>3</bold> (9.3 mg), <bold>4</bold> (6.4 mg), and <bold>5</bold> (4.2 mg). Additionally, the EtOAc soluble fraction C was chromatographed on silica gel with a DCM-EtOAc gradient followed by a gradient of MeOH in EtOAc. As a result, 72 fractions of ca. 100 mL each were collected and combined into the subfractions C1–C3 on the basis of TLC. Purification of C1 (10.8 g) over a silica gel column chromatography with the isocratic system DCM-EtOAc (1:2) gave compounds <bold>9</bold> (12.0 mg), <bold>10</bold> (14.0 mg), and <bold>12</bold> (11.8 mg). In the same way, the subfractions C2 (12.4 g) and C3 (14.3 g) were separately chromatographed on silica gel eluted with the isocratic system of 25% DCM in EtOAc to yield compounds <bold>11</bold> (12.3 mg) and <bold>13</bold> (8.7 mg) from C2, and compounds <bold>1</bold> (9.6 mg) and <bold>2</bold> (5.6 mg) from C2.</p><sec id="sec3dot3dot1-molecules-24-04412"><title>3.3.1. Bruceanoside A (<bold>1</bold>)</title><p>White amorphous powder; mp −80.2° (ca. 0.4 acetone); R<sub>f</sub> = 0.25 (CHCl<sub>3</sub>/MeOH, 4/1); IR (KBr) ν<sub>max</sub> 3348, 2940, 2892, 1615, 1593, 1350, 1265, 1255, 890, 750 cm<sup>−1</sup>; UV (MeOH) λ<sub>max</sub> (log ε): 290 (4.25), 265 (4.15) nm; <sup>1</sup>H NMR (600 MHz, DMSO-<italic>d<sub>6</sub></italic>) and <sup>13</sup>C NMR (150 MHz, DMSO-<italic>d<sub>6</sub></italic>) data, see <xref rid="molecules-24-04412-t001" ref-type="table">Table 1</xref>; HRESIMS <italic>m</italic>/<italic>z</italic> 563.2488 [M + H]<sup>+</sup> (calculated for C<sub>29</sub>H<sub>39</sub>O<sub>12</sub>, 563.2492).</p></sec><sec id="sec3dot3dot2-molecules-24-04412"><title>3.3.2. Bruceacanthinone A (<bold>3</bold>)</title><p>Yellowish powder; R<sub>f</sub> = 0.45 (CHCl<sub>3</sub>/MeOH, 9.5/0.5); IR (KBr) ν<sub>max</sub> 3375, 2950, 2350, 1690, 1600, 1435, 1142, 865, 765, 720 cm<sup>−1</sup>; UV (MeOH) λ<sub>max</sub> (log ε): 398 (3.95), 380 (3.90), 365 (3.60), 329 (4.10), 250 (4.70); <sup>1</sup>H NMR (600 MHz, DMSO-<italic>d<sub>6</sub></italic>) and <sup>13</sup>C NMR (150 MHz, DMSO-<italic>d<sub>6</sub></italic>) data, see <xref rid="molecules-24-04412-t002" ref-type="table">Table 2</xref>; HRESIMS <italic>m</italic>/<italic>z</italic> 289.0589 [M + Na]<sup>+</sup> (calculated for C<sub>15</sub>H<sub>10</sub>N<sub>2</sub>O<sub>3</sub>Na, 289.0570).</p></sec><sec id="sec3dot3dot3-molecules-24-04412"><title>3.3.3. Bruceacanthinone B (<bold>4</bold>)</title><p>Yellowish powder; R<sub>f</sub> = 0.40 (CHCl<sub>3</sub>/MeOH, 9.5/0.5); IR (KBr) ν<sub>max</sub> 3370, 2945, 2350, 1700, 1650, 1440, 1143, 870, 766, 722 cm<sup>−1</sup>; UV (MeOH) λ<sub>max</sub> (log ε): 395 (3.90), 376 (3.92), 367 (3.61), 329 (4.15), 255 (4.65); <sup>1</sup>H NMR (600 MHz, DMSO-<italic>d<sub>6</sub></italic>) and <sup>13</sup>C NMR (150 MHz, DMSO-<italic>d<sub>6</sub></italic>) data, see <xref rid="molecules-24-04412-t002" ref-type="table">Table 2</xref>; HRESIMS <italic>m</italic>/<italic>z</italic> 297.0855 [M + H]+ (calculated for C<sub>16</sub>H<sub>13</sub>N<sub>2</sub>O<sub>4</sub>, 298.0875).</p></sec></sec><sec id="sec3dot4-molecules-24-04412"><title>3.4. Cell Lines, Cell Cultures, and the MTT Assay</title><p>The potential cytotoxicity of <italic>Brucea antidysenterica</italic> bark and root extracts, their VLC fractions, and some isolated compounds (<bold>3</bold>–<bold>10</bold>) were studied against cancer cell lines A-549 (human lung adenocarcinoma), MCF-7 (human breast adenocarcinoma), and PC-3 (human prostate adenocarcinoma) using the MTT assay [<xref rid="B32-molecules-24-04412" ref-type="bibr">32</xref>,<xref rid="B33-molecules-24-04412" ref-type="bibr">33</xref>]. Methods used for toxicity assays have been reported by us previously in detail [<xref rid="B34-molecules-24-04412" ref-type="bibr">34</xref>] and are presented here again. All cell lines were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum and 1% antibiotic-antimycotic solution (100×). The cells were cultured at 37 °C in 95% humidity and 5% CO<sub>2</sub>. For the MTT assays, the cells were washed using phosphate-buffered saline and harvested by trypsinization. Cells were then seeded into 24 well plates at a density of 1.2 × 10<sup>4</sup> cells/well in a working volume of 1 mL/well and allowed to grow for 24 h before the commencement of each experiment. The cells were then treated for 24 h with different concentrations of test samples (crude extracts and fractions at 0, 0.8, 4, 20, 100, and 500 μg/mL and the compounds at 0, 0.4, 2, 10, 50, 75, and 100 μg/mL). Dilutions of stock solutions were made in culture media, yielding final sample concentrations and a final dimethyl sulfoxide (DMSO) concentration of 0.1%, including the control. Each sample concentration was used to treat four wells of cells in each 24 well plate. After the 24 h treatment period, the toxicity of the samples on each cell line was quantified. To achieve this, the medium in each well was replaced by MTT solution (500 μg/mL in medium) and incubated for 2 h. Viability of cells was assessed by their ability to reduce the yellow dye MTT to a blue formazan product [<xref rid="B35-molecules-24-04412" ref-type="bibr">35</xref>]. The MTT reagent was removed, the formazan crystals were dissolved in isopropanol, and the absorbance at 560 nm determined using a microplate reader (CLARIO Star Microplate Reader, BMG Labtech, UK). The average absorbance value obtained from zero treatment control (0.1% DMSO) wells was arbitrarily set at 100% for each plate, and the absorbance value for the average of wells of cells treated with each test sample concentration was expressed as a percentage of this control. Each assay was performed on a minimum of three separate occasions, and the IC<sub>50</sub> values for each sample on each cell line were calculated using Microsoft Excel version 2013. The anti-lung cancer semisynthetic glycoside drug etoposide was used as a positive control.</p></sec><sec id="sec3dot5-molecules-24-04412"><title>3.5. Statistical Analysis</title><p>All experiments were carried out in triplicate on separate occasions. Data were expressed as means ± standard errors of the means. The graphs were plotted using nonlinear regression with the use of Microsoft Excel version 2013.</p></sec></sec><sec sec-type="conclusions" id="sec4-molecules-24-04412"><title>4. Conclusions</title><p>The chemical investigation of the root and bark of <italic>Brucea antidysenterica</italic> afforded three new compounds, including one stilbene glycoside bruceanoside A (<bold>1</bold>), and two canthinone alkaloids bruceacanthinones, A (<bold>3</bold>) and B (<bold>4</bold>), along with ten known secondary metabolites sorted into six canthinone alkaloid derivatives (<bold>5</bold>–<bold>10</bold>), two coumarin derivatives (<bold>11</bold> and <bold>12</bold>), one stilbene (<bold>2</bold>), and one flavonoid (<bold>13</bold>). As expected from the genus <italic>Brucea</italic>, canthinone alkaloids were the most abundant class of metabolites isolated during this study and might be classified as chemo markers of <italic>Brucea</italic> genus. Furthermore, the cytotoxicity of the root and bark methanolic extracts, the dichloromethane and ethyl acetate soluble fractions, and the isolated compounds (<bold>3</bold>–<bold>13</bold>), were assessed against the cancer cell lines A-549, MCF-7, and PC-3. The results displayed decreasing of IC<sub>50</sub> values from crude extracts to the isolated compounds, and might suggest a synergistic action of compounds in their cytotoxicity. Since the plant is used in traditional medicine, its extract might be considered an important reservoir of cytotoxic compounds for the treatment of tumors. However, additional in vivo toxicity evaluation of extracts, antiplasmodial or antibacterial activities of extracts and compounds, and chemical investigation of other parts of the plants—leaves and fruits for instance—in addition to supporting the use of this plant in folk medicine, will help to obtain further information to enrich the pharmacology and chemistry of the genus <italic>Brucea</italic>.</p></sec></body><back><fn-group><fn><p><bold>Sample Availability:</bold> Samples of the compounds <bold>1</bold>–<bold>13</bold> are available from the authors.</p></fn></fn-group><app-group><app id="app1-molecules-24-04412"><title>Supplementary Materials</title><p>The spectra of compounds (<bold>1</bold>, <bold>3</bold>, and <bold>4</bold>) are available online.</p><supplementary-material content-type="local-data" id="molecules-24-04412-s001"><media xlink:href="molecules-24-04412-s001.pdf"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material></app></app-group><notes><title>Author Contributions</title><p>Conceptualization and methodology, Y.S.M., G.M.H., J.L.D.B., and J.D.W.; validation, L.N., A.F.K.W., and C.M.; investigation, Y.S.M., G.M.H., J.L.D.B., and J.D.W.; writing of the original draft, G.M.H., A.F.K.W., and J.D.W.; writing of review and editing, J.D.W., C.M., L.N., N.S., and S.D.S.; supervision, N.S. and S.D.S.</p></notes><notes><title>Funding</title><p>One of the authors (J.D.W.) wishes to thank the European Commission, Belgium, for awarding a Marie Curie postdoctoral fellowship (FP7-PEOPLE-2013-IIF, Grant Agreement Number 629482). The Alexander von Humboldt Foundation, Germany, is also acknowledged for the Research Group Linkage funding 2015/2018 to the Sewald/Wansi research group cooperation and for the generous support with laboratory equipment. L. 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<bold>4</bold>.</p></caption><graphic xlink:href="molecules-24-04412-g003"></graphic></fig><table-wrap id="molecules-24-04412-t001" orientation="portrait" position="float"><object-id pub-id-type="pii">molecules-24-04412-t001_Table 1</object-id><label>Table 1</label><caption><p><sup>1</sup>H (600 MHz) and <sup>13</sup>C (150 MHz) NMR assignments of <bold>1</bold> in DMSO-<italic>d<sub>6</sub></italic>.</p></caption><table frame="hsides" rules="groups"><thead><tr><th rowspan="2" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" colspan="1">No</th><th colspan="2" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1">1</th></tr><tr><th align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"><italic>δ</italic><sub>C</sub></th><th align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"><italic>δ</italic><sub>H</sub> (mult., <italic>J</italic> in Hz)</th></tr></thead><tbody><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold><italic>α</italic></bold></td><td align="center" valign="middle" rowspan="1" colspan="1">126.4</td><td align="center" valign="middle" rowspan="1" colspan="1">6.99 (1H, d, 16.4)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold><italic>β</italic></bold></td><td align="center" valign="middle" rowspan="1" colspan="1">129.1</td><td align="center" valign="middle" rowspan="1" colspan="1">7.20 (1H, d, 16.4)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>1</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">129.9</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>2</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">105.6</td><td align="center" valign="middle" rowspan="1" colspan="1">6.82 (1H, brs)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>3</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">159.3</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>4</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">101.9</td><td align="center" valign="middle" rowspan="1" colspan="1">6.52 (1H, t, 2.2)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>5</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">160.2</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>6</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">107.6</td><td align="center" valign="middle" rowspan="1" colspan="1">6.78 (1H, brs)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>1′</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">139.7</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>2′/6′</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">128.4</td><td align="center" valign="middle" rowspan="1" colspan="1">7.58 (2H, d, 8.8)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>3′/5′</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">114.6</td><td align="center" valign="middle" rowspan="1" colspan="1">6.95 (2H, d, 8.8)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>4′</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">159.8</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>OCH<sub>3</sub>-3/5</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">55.6</td><td align="center" valign="middle" rowspan="1" colspan="1">3.80 (6H, s)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1">sugar moieties</td><td align="center" valign="middle" rowspan="1" colspan="1"></td><td align="center" valign="middle" rowspan="1" colspan="1"></td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>glc-1</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">101.0</td><td align="center" valign="middle" rowspan="1" colspan="1">4.89 (1H, d, 7.6)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>2</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">73.7</td><td align="center" valign="middle" rowspan="1" colspan="1">3.19 (1H, m)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>3</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">75.8</td><td align="center" valign="middle" rowspan="1" colspan="1">3.52 (1H. m)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>4</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">70.8</td><td align="center" valign="middle" rowspan="1" colspan="1">3.65 (1H, m)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>5</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">76.9</td><td align="center" valign="middle" rowspan="1" colspan="1">3.30 (1H, m)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>6</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">66.8</td><td align="center" valign="middle" rowspan="1" colspan="1">3.41 (1H, m)<break></break>3.87 (1H, m)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>rha-1</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">101.0</td><td align="center" valign="middle" rowspan="1" colspan="1">4.56 (1H, d, 1.6)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>2</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">71.2</td><td align="center" valign="middle" rowspan="1" colspan="1">3.42 (1H, m)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>3</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">70.3</td><td align="center" valign="middle" rowspan="1" colspan="1">3.46 (1H, m)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>4</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">72.5</td><td align="center" valign="middle" rowspan="1" colspan="1">3.18 (1H, m)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>5</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">68.8</td><td align="center" valign="middle" rowspan="1" colspan="1">3.43 (1H, m)</td></tr><tr><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"><bold>6</bold></td><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">18.3</td><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">1.11 (3H, d, 6.1)</td></tr></tbody></table></table-wrap><table-wrap id="molecules-24-04412-t002" orientation="portrait" position="float"><object-id pub-id-type="pii">molecules-24-04412-t002_Table 2</object-id><label>Table 2</label><caption><p><sup>1</sup>H (600 MHz) and <sup>13</sup>C (150 MHz) NMR assignments of <bold>3</bold> and <bold>4</bold> in DMSO-<italic>d<sub>6</sub></italic>.</p></caption><table frame="hsides" rules="groups"><thead><tr><th rowspan="2" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" colspan="1">No</th><th colspan="2" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1">3</th><th colspan="2" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1">4</th></tr><tr><th align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"><italic>δ</italic><sub>C</sub></th><th align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"><italic>δ</italic><sub>H</sub> (mult., <italic>J</italic> in Hz)</th><th align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"><italic>δ</italic><sub>C</sub></th><th align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"><italic>δ</italic><sub>H</sub> (mult., <italic>J</italic> in Hz)</th></tr></thead><tbody><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>1</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">140.0</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">140.4</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>2</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">152.6</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">151.5</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>4</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">139.0</td><td align="center" valign="middle" rowspan="1" colspan="1">8.08 (1H, d, 9.7)</td><td align="center" valign="middle" rowspan="1" colspan="1">139.9</td><td align="center" valign="middle" rowspan="1" colspan="1">8.04 (1H, d, 9.8)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>5</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">127.3</td><td align="center" valign="middle" rowspan="1" colspan="1">6.90 (1H, d, 9.7)</td><td align="center" valign="middle" rowspan="1" colspan="1">125.9</td><td align="center" valign="middle" rowspan="1" colspan="1">6.90 (1H, d, 9.8)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>6</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">159.6</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">160.0</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>8</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">117.1</td><td align="center" valign="middle" rowspan="1" colspan="1">8.70 (1H, dd, 1.2, 7.8)</td><td align="center" valign="middle" rowspan="1" colspan="1">112.9</td><td align="center" valign="middle" rowspan="1" colspan="1">8.40 (1H, dd, 0.8, 8.2)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>9</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">130.7</td><td align="center" valign="middle" rowspan="1" colspan="1">7.70 (1H, td, 1.0, 7.6, 7.8)</td><td align="center" valign="middle" rowspan="1" colspan="1">132.3</td><td align="center" valign="middle" rowspan="1" colspan="1">7.65 (1H, t, 8.2)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>10</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">127.5</td><td align="center" valign="middle" rowspan="1" colspan="1">7.58 (1H, td, 1.2, 7.6, 7.8)</td><td align="center" valign="middle" rowspan="1" colspan="1">108.0</td><td align="center" valign="middle" rowspan="1" colspan="1">7.01 (1H, dd, 0.8, 8.2)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>11</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">125.0</td><td align="center" valign="middle" rowspan="1" colspan="1">8.26 (1H, dd, 1.0, 7.6)</td><td align="center" valign="middle" rowspan="1" colspan="1">156.1</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>12</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">123.1</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">126.8</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>13</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">136.4</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">139.9</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>14</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">130.7</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">132.9</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>15</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">128.7</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">132.3</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>16</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">126.1</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">126.8</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>OMe-2</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">57.2</td><td align="center" valign="middle" rowspan="1" colspan="1">4.29 (3H, s)</td><td align="center" valign="middle" rowspan="1" colspan="1">56.3</td><td align="center" valign="middle" rowspan="1" colspan="1">4.09 (3H, s)</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>OMe-11</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">–</td><td align="center" valign="middle" rowspan="1" colspan="1">57.8</td><td align="center" valign="middle" rowspan="1" colspan="1">4.28 (3H, s)</td></tr><tr><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"><bold>OH-1</bold></td><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">–</td><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">8.52 (1H, s)</td><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">–</td><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">8.50 (1H, s)</td></tr></tbody></table></table-wrap><table-wrap id="molecules-24-04412-t003" orientation="portrait" position="float"><object-id pub-id-type="pii">molecules-24-04412-t003_Table 3</object-id><label>Table 3</label><caption><p>Cytotoxicity of extracts, fractions, and isolated compounds from <italic>Brucea antidysenterica.</italic></p></caption><table frame="hsides" rules="groups"><thead><tr><th rowspan="2" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" colspan="1">Samples</th><th colspan="3" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1">IC<sub>50</sub> in μg/mL</th></tr><tr><th align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">A-549</th><th align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">MCF-7</th><th align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">PC-3</th></tr></thead><tbody><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>Root extract</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">75.2 ± 3.2</td><td align="center" valign="middle" rowspan="1" colspan="1">80.5 ± 1.8</td><td align="center" valign="middle" rowspan="1" colspan="1">77.7 ± 2.5</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>Bark extract</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">65.1 ± 1.5</td><td align="center" valign="middle" rowspan="1" colspan="1">72.3 ± 3.5</td><td align="center" valign="middle" rowspan="1" colspan="1">70.2 ± 4.2</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>DCM</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">50.0 ± 5.2</td><td align="center" valign="middle" rowspan="1" colspan="1">55.1 ± 4.2</td><td align="center" valign="middle" rowspan="1" colspan="1">57.0 ± 5.3</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>EA</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">61.5 ± 3.2</td><td align="center" valign="middle" rowspan="1" colspan="1">58.1 ± 1.9</td><td align="center" valign="middle" rowspan="1" colspan="1">55.8 ± 2.4</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>3</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">195.5 ± 9.5</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>4</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">150.3 ± 8.5</td><td align="center" valign="middle" rowspan="1" colspan="1">157.5 ± 7.5</td><td align="center" valign="middle" rowspan="1" colspan="1">160.5 ± 5.5</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>5</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>6</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">175.6 ± 6.1</td><td align="center" valign="middle" rowspan="1" colspan="1">170.3 ± 5.8</td><td align="center" valign="middle" rowspan="1" colspan="1">177.3 ± 5.9</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>7</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">125.8 ± 7.2</td><td align="center" valign="middle" rowspan="1" colspan="1">152.1 ± 11.2</td><td align="center" valign="middle" rowspan="1" colspan="1">155.1 ± 5.3</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>8</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">121.5 ± 8.2</td><td align="center" valign="middle" rowspan="1" colspan="1">126.2 ± 5.5</td><td align="center" valign="middle" rowspan="1" colspan="1">130.9 ± 7.4</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>9</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">138.1 ± 9.7</td><td align="center" valign="middle" rowspan="1" colspan="1">145.2 ± 9.9</td><td align="center" valign="middle" rowspan="1" colspan="1">151.5 ± 8.3</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>10</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>11</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>12</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">130.8 ± 7.4</td><td align="center" valign="middle" rowspan="1" colspan="1">132.1 ± 11.2</td><td align="center" valign="middle" rowspan="1" colspan="1">130.1 ± 5.3</td></tr><tr><td align="center" valign="middle" rowspan="1" colspan="1"><bold>13</bold></td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td><td align="center" valign="middle" rowspan="1" colspan="1">>250</td></tr><tr><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"><bold>Etoposide</bold></td><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">3.5 ± 0.5</td><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">10.2 ± 1.2</td><td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">7.9 ± 1.1</td></tr></tbody></table></table-wrap></floats-group></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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