<?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>S1870-249X2006000300014</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Screening of Liver Acetone Powders in the Enantioselective Hydrolysis of Naproxen Esters]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pacheco]]></surname>
<given-names><![CDATA[Ana]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Luna]]></surname>
<given-names><![CDATA[Héctor]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Solís]]></surname>
<given-names><![CDATA[Aida]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pérez]]></surname>
<given-names><![CDATA[Herminia I.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Manjarrez]]></surname>
<given-names><![CDATA[Norberto]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Autónoma Metropolitana Departamento de Sistemas Biológicos ]]></institution>
<addr-line><![CDATA[Xochimilco Distrito Federal]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2006</year>
</pub-date>
<volume>50</volume>
<numero>3</numero>
<fpage>137</fpage>
<lpage>142</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2006000300014&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2006000300014&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2006000300014&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[LAPs from different sources were used to hydrolyze the methyl and butyl esters of naproxen. The results revealed that no generalization can be done about the reaction conditions, since they greatly depend on the LAP source and the substrate. For example, in the hydrolysis of methyl naproxenate by rabbit LAP the conversion was 20% at pH 8, but the ee for the acid produced was 44%, in contrast to 80% ee at pH 7.5 with chicken LAP at the same conversion. In other hand cat LAP gave a conversion of 80% at all pHs and 90% ee at pH 7.5. The results for the butyl naproxenate hydrolysis were different; with pig LAP the conversion was 40% but only 34% ee, turkey LAP gave 12% conversion and 90% ee, and cat provided 17% conversion and 90% ee, all these results at pH 7.5. All LAP tested, except sheep, gave enantiopreference for the hydrolysis of the R-enantiomer.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Polvos acetónicos de hígado de diferentes fuentes fueron aplicados a la hidrólisis de los ésteres metílico y butílico del naproxén. Los resultados muestran que es difícil hacer generalizaciones respecto a las condiciones de reacción, ya que estas dependen significativamente de la fuente del LAP y del sustrato. Por ejemplo, en la hidrólisis del naproxenato de metilo por el LAP de conejo la conversión fue del 20% con un ee en el ácido producido del 44% a pH 8, en contraste a un 80% de ee a pH 7.5 con el LAP de pollo a la misma conversión. El LAP de gato dio una conversión del 80% en todos los pHs con un 90% de ee a pH 7.5. Los resultados para la hidrólisis del naproxenato de butílo fueron diferentes; con el LAP de puerco la conversión fue del 40%, pero solo dio 43% ee, el LAP de guajolote dio solo 12% de conversión y un 90% de ee y el LAP de gato dio 17% de conversión y 90% de ee, todos estos resultados a un pH de 7.5. Todos los LAPs probados, a excepción del de borrego, mostraron una preferencia hacia la hidrólisis del enantiómero R.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Naproxen]]></kwd>
<kwd lng="en"><![CDATA[enzymatic resolution]]></kwd>
<kwd lng="en"><![CDATA[liver acetone powder]]></kwd>
<kwd lng="es"><![CDATA[Naproxen]]></kwd>
<kwd lng="es"><![CDATA[resolución enzimática]]></kwd>
<kwd lng="es"><![CDATA[polvo acetónico de hígado]]></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>Screening of Liver Acetone Powders in the Enantioselective Hydrolysis of Naproxen Esters</b></font></p> 	    <p align="justify">&nbsp;</p> 	    <p align="center"><font face="verdana" size="2"><b>Ana Pacheco, H&eacute;ctor Luna,* Aida Sol&iacute;s, Herminia I. P&eacute;rez, Norberto Manjarrez</b></font></p> 	    <p align="justify">&nbsp;</p> 	    <p align="justify"><font face="verdana" size="2"><i>Departamento de Sistemas Biol&oacute;gicos, Universidad Aut&oacute;noma Metropolitana&#45;Xochimilco, Calzada del Hueso 1100, Col. Villa Quietud, Delg. Coyoacan, M&eacute;xico, D.F. CP 04960, Phone: (55) 5483&#45;7255 Fax: (55) 5483&#45;7237, e&#45;mail:</i> <a href="mailto:lchm1964@correo.xoc.uam.mx">lchm1964@correo.xoc.uam.mx</a></font></p>     <p align="justify">&nbsp;</p> 	    <p align="justify"><font face="verdana" size="2">Recibido el 1 de marzo del 2006.     ]]></body>
<body><![CDATA[<br>     Aceptado el 26 de septiembre del 2006</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"> LAPs from different sources were used to hydrolyze the methyl and butyl esters of naproxen. The results revealed that no generalization can be done about the reaction conditions, since they greatly depend on the LAP source and the substrate. For example, in the hydrolysis of methyl naproxenate by rabbit LAP the conversion was 20% at pH 8, but the ee for the acid produced was 44%, in contrast to 80% ee at pH 7.5 with chicken LAP at the same conversion. In other hand cat LAP gave a conversion of 80% at all pHs and 90% ee at pH 7.5. The results for the butyl naproxenate hydrolysis were different; with pig LAP the conversion was 40% but only 34% ee, turkey LAP gave 12% conversion and 90% ee, and cat provided 17% conversion and 90% ee, all these results at pH 7.5. All LAP tested, except sheep, gave enantiopreference for the hydrolysis of the <i>R</i>-enantiomer</font>.</p>     <p align="justify"><font face="verdana" size="2"><b>Key words:</b> Naproxen, enzymatic resolution, liver acetone powder.</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"> Polvos acet&oacute;nicos de h&iacute;gado de diferentes fuentes fueron aplicados a la hidr&oacute;lisis de los &eacute;steres met&iacute;lico y but&iacute;lico del naprox&eacute;n. Los resultados muestran que es dif&iacute;cil hacer generalizaciones respecto a las condiciones de reacci&oacute;n, ya que estas dependen significativamente de la fuente del LAP y del sustrato. Por ejemplo, en la hidr&oacute;lisis del naproxenato de metilo por el LAP de conejo la conversi&oacute;n fue del 20% con un ee en el &aacute;cido producido del 44% a pH 8, en contraste a un 80% de ee a pH 7.5 con el LAP de pollo a la misma conversi&oacute;n. El LAP de gato dio una conversi&oacute;n del 80% en todos los pHs con un 90% de ee a pH 7.5. Los resultados para la hidr&oacute;lisis del naproxenato de but&iacute;lo fueron diferentes; con el LAP de puerco la conversi&oacute;n fue del 40%, pero solo dio 43% ee, el LAP de guajolote dio solo 12% de conversi&oacute;n y un 90% de ee y el LAP de gato dio 17% de conversi&oacute;n y 90% de ee, todos estos resultados a un pH de 7.5. Todos los LAPs probados, a excepci&oacute;n del de borrego, mostraron una preferencia hacia la hidr&oacute;lisis del enanti&oacute;mero <i>R.</i></font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave:</b> Naproxen, resoluci&oacute;n enzim&aacute;tica, polvo acet&oacute;nico de h&iacute;gado. </font></p>     <p align="justify">&nbsp;</p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><a href="/pdf/jmcs/v50n3/v50n3a14.pdf" target="_blank">DESCARGAR ARCHIVO EN FORMATO PDF</a></font></p>     <p align="justify">&nbsp;</p>     <p align="justify"><font face="verdana" size="2"><b>Acknowledgments</b></font></p>     <p align="justify"><font face="verdana" size="2">We thank the financial support of Consejo Nacional de</font> <font face="verdana" size="2">Ciencia y Tecnolog&iacute;a (CONACyT) Grant num. 37272&#45;N. We</font><font face="verdana" size="2">also thank Julia Cassani Hern&aacute;ndez for the NMR espectra. We thank Dr. Ignacio Regla for the racemic naproxen donation. We thank to the University animal facilities (Unidad de Producci&oacute;n y Experimentaci&oacute;n de Animales de Laboratorio: Bioterio) for providing the rat livers.</font></p>     <p align="justify">&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. Patel, R. N. <i>Stereoselective biocatalysis</i> Marcel Dekker Inc., Ed. New York: 2000.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4894908&pid=S1870-249X200600030001400001&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. a) Patel, R. N. <i>Adv. Synth. 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