<?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>S1870-249X2010000200002</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Synthesis and Biological Activity of Novel 6-Substituted Purine Derivatives]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Yu Lin]]></surname>
<given-names><![CDATA[Hu]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Xiang]]></surname>
<given-names><![CDATA[Liu]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ming]]></surname>
<given-names><![CDATA[Lu]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Nanjing University of Science and Technology Chemical Engineering College ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>China</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2010</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2010</year>
</pub-date>
<volume>54</volume>
<numero>2</numero>
<fpage>74</fpage>
<lpage>78</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2010000200002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2010000200002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2010000200002&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[A series of 6-substituted purines were synthesized from commercially available 2-amino-6-chloropurine with appropriate reagents, and nine new compounds 7, 8, and 11-17 have been discovered. The compounds synthesized were identified by elemental analysis, ¹H NMR, as well as mass spectral data. All the title compounds were screened for their antifungal activities, under the method of the disc diffusion, using three species of fungi - Bacillus subtillis, Aspergillus niger, and Candida tropicalis- and some of the compounds showed promising activities.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Se preparó una serie de purinas 6-sustituidas a partir de la 2-amino-6-cloropurina, que está disponible comercialmente, y de los reactivos apropiados, de los cuales los derivados 7, 8 y 11-17 no han sido reportados previamente. Los compuestos sintetizados se caracterizaron por análisis elemental, RMN ¹H y espectrometría de masas. Todos los compuestos se evaluaron en su actividad antifúngica, a través del método de difusión de discos, sobre tres especies de hongos - Bacillus subtillis, Aspergillus niger y Candida tropicalis-, mostrando algunos de ellos una actividad promisoria.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[6-Substituted purines]]></kwd>
<kwd lng="en"><![CDATA[2-amino-6-chloropurine]]></kwd>
<kwd lng="en"><![CDATA[Synthesis]]></kwd>
<kwd lng="en"><![CDATA[Antifungal Activity]]></kwd>
<kwd lng="es"><![CDATA[Purinas 6-sustituidas]]></kwd>
<kwd lng="es"><![CDATA[2-amino-6-cloropurina]]></kwd>
<kwd lng="es"><![CDATA[síntesis]]></kwd>
<kwd lng="es"><![CDATA[actividad antifúngica]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="4">Article</font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="4"><b>Synthesis and Biological Activity of Novel 6&#150;Substituted Purine Derivatives</b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>Yu Lin Hu, Xiang Liu, and Ming Lu<sup>*</sup></b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i>Chemical Engineering College, Nanjing University of Science and Technology, Nanjing 210094, PR China, Tel: 86&#150;02584315030, Fax: 86&#150;025&#150;84315030, <sup>*</sup>Responsible author:</i> <a href="mailto:luming1963@163.com">luming1963@163.com</a></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">Received December 9, 2009    <br>   Accepted March 5, 2010</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>     <p align="justify"><font face="verdana" size="2">A series of 6&#150;substituted purines were synthesized from commercially available 2&#150;amino&#150;6&#150;chloropurine with appropriate reagents, and nine new compounds <b>7, 8, </b>and <b>11&#150;17 </b>have been discovered. The compounds synthesized were identified by elemental analysis, <sup>1</sup>H NMR, as well as mass spectral data. All the title compounds were screened for their antifungal activities, under the method of the disc diffusion, using three species of fungi &#151; <i>Bacillus subtillis, Aspergillus niger, </i>and <i>Candida tropicalis</i>&#151; and some of the compounds showed promising activities.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Key words: </b>6&#150;Substituted purines, 2&#150;amino&#150;6&#150;chloropurine, Synthesis, Antifungal Activity.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>     <p align="justify"><font face="verdana" size="2">Se prepar&oacute; una serie de purinas 6&#150;sustituidas a partir de la 2&#150;amino&#150;6&#150;cloropurina, que est&aacute; disponible comercialmente, y de los reactivos apropiados, de los cuales los derivados <b>7, 8 </b>y <b>11&#150;17 </b>no han sido reportados previamente. Los compuestos sintetizados se caracterizaron por an&aacute;lisis elemental, RMN <sup>1</sup>H y espectrometr&iacute;a de masas. Todos los compuestos se evaluaron en su actividad antif&uacute;ngica, a trav&eacute;s del m&eacute;todo de difusi&oacute;n de discos, sobre tres especies de hongos &#151; <i>Bacillus subtillis, Aspergillus niger </i>y <i>Candida tropicalis&#151;, </i>mostrando algunos de ellos una actividad promisoria.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave: </b>Purinas 6&#150;sustituidas, 2&#150;amino&#150;6&#150;cloropurina, s&iacute;ntesis, actividad antif&uacute;ngica.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><a href="/pdf/jmcs/v54n2/v54n2a2.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Acknowledgement</b></font></p>     <p align="justify"><font face="verdana" size="2">We thank the National Basic Research Program (973 Program) of China and Ministry of Education of the Republic of China for support of this research.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>References</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">1. Draanen, N. A. V. G.; Freeman, A.; Short, S. A.; Harvey, R.; Jansen, R.; Szczech, G.; Koszalka, G. W. <i>J. Med. 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