<?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>S1870-249X2018000400135</article-id>
<article-id pub-id-type="doi">10.29356/jmcs.v62i4.472</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Synthesis of Novel Pyridine-connected Piperidine and 2H-thiopyran Derivatives and their Larvicidal, Nematicidal, and Antimicrobial Activities]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ahamed]]></surname>
<given-names><![CDATA[Anis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Arif]]></surname>
<given-names><![CDATA[Ibrahim A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Kumar]]></surname>
<given-names><![CDATA[Radhakrishnan Surendra]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Idhayadhulla]]></surname>
<given-names><![CDATA[Akbar]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Selva raj]]></surname>
<given-names><![CDATA[Keerthana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Manilal]]></surname>
<given-names><![CDATA[Aseer]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,King Saud University College of Sciences Department of Botany &amp; Microbiology]]></institution>
<addr-line><![CDATA[Riyadh ]]></addr-line>
<country>Saudi Arabia</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Nehru Memorial College Research Department of Chemistry ]]></institution>
<addr-line><![CDATA[Puthanampatti Tamil Nadu]]></addr-line>
<country>India</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Arba Minch University College of Medicine and Health Sciences Department of Medical Laboratory Sciences]]></institution>
<addr-line><![CDATA[Arba Minch ]]></addr-line>
<country>Ethiopia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2018</year>
</pub-date>
<volume>62</volume>
<numero>4</numero>
<fpage>135</fpage>
<lpage>147</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2018000400135&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2018000400135&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2018000400135&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract. A series of novel pyridine-connected piperidine derivatives (2a-g) and pyridine-connected 2H-thiopyran derivatives (4a-g) were synthesized and evaluated for larvicidal, nematicidal, and antimicrobial activities. Compound 4e exhibited larvicidal activity against second instar larvae with an LD50 value of 0.8 &#956;g/mL. In addition, 4e was most effective against root knot nematode Meloidogyne javanica , with an LD50 value of 3.2 &#956;g/mL. Compounds 2e (MIC: 4 &#956;g/mL) and 2d (MIC: 4 &#956;g/mL) exhibited high antibacterial activity against Klebsiella pneumonia, and Escherichia coli, respectively. Compounds 4b (MIC: 0.25 &#956;g/mL) and 4f (MIC: 2 &#956;g/mL) showed high antifungal activity against Candida albicans and Microsporum audouinii, respectively. Therefore, overall activity profiles envisages that compounds 2e, 2d, 4e, 4b, and 4f could be employed for the development of new classes of drugs with larvicidal, nematicidal, and antimicrobial activities.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen. Se sintetizaron una serie de nuevos derivados de piperidina conectados con piridina (2a-g) y derivados de 2H-tiopirano conectados con piridina (4a-g) para evaluar las actividades larvicidas, nematicidas y antimicrobianas. El compuesto 4e exhibió actividad larvicida contra larvas de segundo estadio con un valor de LD50 de 0.8 &#956;g / mL. Además, 4e fue más efectivo contra el nematodo de nudo de la raíz Meloidogyne javanica, con un valor de LD50 de 3.2 &#956;g / mL. Los compuestos 2e (MIC: 4 &#956;g / ml) y 2d (MIC: 4 &#956;g / ml) mostraron una alta actividad antibacteriana contra la neumonía de Klebsiella y Escherichia coli, respectivamente. Los compuestos 4b (MIC: 0.25 &#956;g / ml) y 4f (MIC: 2 &#956;g / ml) mostraron una alta actividad antifúngica contra Candida albicans y Microsporum audouinii, respectivamente. Por lo tanto, los perfiles de actividad general prevén que los compuestos 2e, 2d, 4e, 4b y 4f podrían emplearse para el desarrollo de nuevas clases de fármacos con actividades larvicidas, nematicidas y antimicrobianas.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Larvicidal activity]]></kwd>
<kwd lng="en"><![CDATA[Nematicidal activity]]></kwd>
<kwd lng="en"><![CDATA[Antimicrobial activity]]></kwd>
<kwd lng="en"><![CDATA[Piperidine]]></kwd>
<kwd lng="en"><![CDATA[2H-Thiopyran derivatives]]></kwd>
<kwd lng="es"><![CDATA[Actividad larvicida]]></kwd>
<kwd lng="es"><![CDATA[Actividad nematicida]]></kwd>
<kwd lng="es"><![CDATA[Actividad antimicrobiana]]></kwd>
<kwd lng="es"><![CDATA[Piperidina]]></kwd>
<kwd lng="es"><![CDATA[Derivado 2H-Tiopirano]]></kwd>
</kwd-group>
</article-meta>
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