<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1870-249X</journal-id>
<journal-title><![CDATA[Journal of the Mexican Chemical Society]]></journal-title>
<abbrev-journal-title><![CDATA[J. Mex. Chem. Soc]]></abbrev-journal-title>
<issn>1870-249X</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Química de México A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1870-249X2005000300004</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Chemical Constituents of Senecio procumbens]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Arciniegas]]></surname>
<given-names><![CDATA[Amira]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pérez-Castorena]]></surname>
<given-names><![CDATA[Ana L.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Villaseñor]]></surname>
<given-names><![CDATA[José Luis]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Romo de Vivar]]></surname>
<given-names><![CDATA[Alfonso]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Nacional Autónoma de México Instituto de Química ]]></institution>
<addr-line><![CDATA[México Distrito Federal]]></addr-line>
<country>México</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidad Nacional Autónoma de México Instituto de Biología ]]></institution>
<addr-line><![CDATA[México Distrito Federal]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2005</year>
</pub-date>
<volume>49</volume>
<numero>3</numero>
<fpage>284</fpage>
<lpage>286</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2005000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2005000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2005000300004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[A chemical study of Senecio procumbens afforded the 12-membered macrocyclic diester pyrrolizidine alkaloids senecionine (1), senecivernine (2), retrorsine (3) and their N-oxides, together with 13²-hydroxyphaeophytin a (4), caffeic acid methyl ester (5), and cacticin (6). The identification of these compounds was accomplished by comparison of their spectral features with those reported in literature. The structures of compounds 1, and those of the N-oxides of 1 and 3 were confirmed by comparison with authentic samples. In addition, the ¹H and 13C NMR spectroscopies of 2 N-oxide are reported since they were not available in the literature.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[De un estudio químico de Senecio procumbens se aislaron los alcaloides pirrolizidínicos diésteres macrocíclicos de 12 miembros: senecionina (1), senecivernina (2), retrorsina (3) y sus N-óxidos, junto con 13²-hidroxifeofitina a (4), cafeato de metilo (5) y cacticina (6). Estos metabolitos fueron identificados por comparación de sus datos espectroscópicos con los descritos. La estructura de 1, y de los N-óxidos de 1 y 3 fue confirmada por comparación con muestras auténticas. Adicionalmente se incluyen los datos de RMN de ¹H y 13C del N-óxido de 2, los cuales no han sido descritos.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Senecio procumbens]]></kwd>
<kwd lng="en"><![CDATA[Asteraceae]]></kwd>
<kwd lng="en"><![CDATA[Senecioneae]]></kwd>
<kwd lng="en"><![CDATA[Pyrrolizidine alkaloids]]></kwd>
<kwd lng="es"><![CDATA[Senecio procumbens]]></kwd>
<kwd lng="es"><![CDATA[Asteraceae]]></kwd>
<kwd lng="es"><![CDATA[Senecioneae]]></kwd>
<kwd lng="es"><![CDATA[alcaloides pirrolizidínicos]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  	    <p align="justify"><font face="verdana" size="4">Article</font></p>     <p align="justify">&nbsp;</p>     <p align="center"><font face="verdana" size="4"><b>Chemical Constituents of <i>Senecio procumbens</i></b></font></p>     <p align="center">&nbsp;</p>      <p align="center"><font face="verdana" size="2"><b>Amira Arciniegas,<sup>a</sup> Ana L. P&eacute;rez&#45;Castorena,*<sup>a</sup> Jos&eacute; Luis Villase&ntilde;or,<sup>b</sup> Alfonso Romo de Vivar<sup>a</sup></b></font></p>     <p align="center">&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><sup><i>a</i></sup><i> Instituto de Qu&iacute;mica, Universidad Nacional Aut&oacute;noma de M&eacute;xico, Circuito Exterior, Ciudad Universitaria, Coyoac&aacute;n 04510, D.F., M&eacute;xico Tel: +52&#45;55&#45;5622&#45;4412, Fax: +52&#45;55&#45;5622&#45;2217, </i>E&#45;mail: <a href="mailto:alperezc@servidor.unam.mx" target="_blank">alperezc@servidor.unam.mx</a></font></p> 	    <p align="justify"><font face="verdana" size="2"><i><sup>b </sup>Instituto de Biolog&iacute;a, Universidad Nacional Aut&oacute;noma de M&eacute;xico, Circuito Exterior, Ciudad Universitaria, Coyoac&aacute;n 04510, D.F., M&eacute;xico Tel: +52&#45;55&#45;5622&#45;4412, Fax: +52&#45;55&#45;5622&#45;2217.</i></font></p>     <p align="justify">&nbsp;</p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">Recibido el 20 de abril del 2005.    <br> Aceptado el 15 de junio del 2005.</font></p>     <p align="justify">&nbsp;</p>      <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>     <p align="justify"><font face="verdana" size="2"> A chemical study of <i>Senecio procumbens</i> afforded the 12&#45;membered macrocyclic diester pyrrolizidine alkaloids senecionine (<b>1</b>), senecivernine (<b>2</b>), retrorsine (<b>3</b>) and their <i>N</i>&#45;oxides, together with 13<sup>2</sup>&#45;hydroxyphaeophytin a (<b>4</b>), caffeic acid methyl ester (<b>5</b>), and cacticin (<b>6</b>). The identification of these compounds was accomplished by comparison of their spectral features with those reported in literature. The structures of compounds <b>1</b>, and those of the <i>N</i>&#45;oxides of <b>1</b> and <b>3</b> were confirmed by comparison with authentic samples. In addition, the <sup>1</sup>H and <sup>13</sup>C NMR spectroscopies of <b>2 </b><i>N</i>&#45;oxide are reported since they were not available in the literature.</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Keywords:</b> <i>Senecio procumbens,</i> Asteraceae, Senecioneae, Pyrrolizidine alkaloids.</font></p>     <p align="justify">&nbsp;</p>      <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>     <p align="justify"><font face="verdana" size="2"> De un estudio qu&iacute;mico de <i>Senecio procumbens</i> se aislaron los alcaloides pirrolizid&iacute;nicos di&eacute;steres macroc&iacute;clicos de 12 miembros: senecionina (<b>1</b>), senecivernina (<b>2</b>), retrorsina (<b>3</b>) y sus <i>N</i>&#45;&oacute;xidos, junto con 13<sup>2</sup>&#45;hidroxifeofitina a (<b>4</b>), cafeato de metilo (<b>5</b>) y cacticina (<b>6</b>). Estos metabolitos fueron identificados por comparaci&oacute;n de sus datos espectrosc&oacute;picos con los descritos. La estructura de <b>1</b>, y de los <i>N</i>&#45;&oacute;xidos de <b>1</b> y <b>3</b> fue confirmada por comparaci&oacute;n con muestras aut&eacute;nticas. Adicionalmente se incluyen los datos de RMN de <sup>1</sup>H y <sup>13</sup>C del <i>N</i>&#45;&oacute;xido de <b>2</b>, los cuales no han sido descritos. </font></p> 	    <p align="justify"><font face="verdana" size="2"><b>Palabras clave:</b> <i>Senecio procumbens,</i> Asteraceae, Senecioneae, alcaloides pirrolizid&iacute;nicos.</font></p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p> 	    <p><font face="verdana" size="2"><a href="../pdf/jmcs/v49n3/v49n3a4.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p> 	    <p>&nbsp; </p>     <p align="justify"><font face="verdana" size="2"><b>References</b></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">1. Hartmann, T.; Witte, L., in: <i>Alkaloids: Chemical and biology perspectives,</i> Vol. 9, Pelletier, S. W., Ed., Pergamon, Oxford, U.K., <b>1995</b>, 155&#45;233.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4891747&pid=S1870-249X200500030000400001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font>	</p> 	    <!-- ref --><p align="justify"><font face="verdana" size="2">2.&nbsp;Liddell, J. R. <i>Vat. Prod, Rep.</i> <b>2002</b>, <i>20</i>, 773&#45;781.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4891749&pid=S1870-249X200500030000400002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">3.&nbsp;Roeder, E. <i>Pharmazie</i> <b>1995</b>, <i>50</i>, 83&#45;97.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4891751&pid=S1870-249X200500030000400003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	    ]]></body>
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