<?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>S1870-249X2017000200158</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[A pyrazine amide - 4-aminoquinoline hybrid and its rhodium and iridium pentamethylcyclopentadienyl complexes; evaluation of anti-mycobacterial and anti-plasmodial activities]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ekengard]]></surname>
<given-names><![CDATA[Erik]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bergare]]></surname>
<given-names><![CDATA[Ida]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hansson]]></surname>
<given-names><![CDATA[Josefine]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Doverbratt]]></surname>
<given-names><![CDATA[Isa]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Monari]]></surname>
<given-names><![CDATA[Magda]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gordhan]]></surname>
<given-names><![CDATA[Bhavna]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Kana]]></surname>
<given-names><![CDATA[Bavesh]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Kock]]></surname>
<given-names><![CDATA[Carmen de]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Smith]]></surname>
<given-names><![CDATA[Peter J.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Nordlander]]></surname>
<given-names><![CDATA[Ebbe]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Lund University Department of Chemistry Chemical Physics]]></institution>
<addr-line><![CDATA[Lund ]]></addr-line>
<country>Sweden</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Lund University Department of Chemistry ]]></institution>
<addr-line><![CDATA[Lund ]]></addr-line>
<country>Sweden</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Università di Bologna Dipartimento di Chimica &#8220;G. Ciamician&#8221; ]]></institution>
<addr-line><![CDATA[Bologna ]]></addr-line>
<country>Italy</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,University of the Witwatersrand Faculty of Health Sciences School of Pathology]]></institution>
<addr-line><![CDATA[Johannesburg ]]></addr-line>
<country>South Africa</country>
</aff>
<aff id="Af5">
<institution><![CDATA[,University of Cape Town Department of Medicine Division of Pharmacology]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>South Africa</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2017</year>
</pub-date>
<volume>61</volume>
<numero>2</numero>
<fpage>158</fpage>
<lpage>166</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2017000200158&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2017000200158&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2017000200158&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract. The synthesis and characterization of N-(2-((7-chloroquinolin-4-yl)amino)ethyl)pyrazine-2-carboxamide (L), an aminoquinoline - pyrazinamide hybrid, and the complexes (N-(2-((7-chloroquinolin-4-yl)amino)ethyl)pyrazine-2-carboxamide)(cyclopentadienyl)chlorido-rhodium or iridium hexafluorophosphate ([M(L)(Cp*)Cl]PF6; M = Rh, Ir) and the corresponding chlorido salts ([M(L)(Cp*)Cl]Cl; M = Rh, Ir) are described. The ligand and the hexafluorophosphate salts of the metal complexes have been evaluated for anti-plasmodial and anti-mycobacterial activity. The rhodium and the iridium complexes were significantly more active against M. tuberculosis than the free ligand. The crystallographically determined molecular structures of complexes (N-(2-((7-chloroquinolin-4-yl)amino)ethyl)pyrazine-2-carboxamide)(cyclopentadienyl)chlororhodium hexafluoro-phosphate and (N-(2-((7-chloroquinolin-4-yl)amino)ethyl)pyrazine-2-carboxamide)(cyclopentadienyl)chloro-iridium chloride are presented.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen. La síntesis y caracterización de N-(2-(7-cloroquinolin-4-il) amino)etil)pirazina-2-carboxamida (L), un híbrido de aminoquinolina-pirazinamida, y los complejos hexafluorofosfato de N-(2-cloroquinolin-4-il)amino)etil)pirazina-2-carboxamida)(ciclopentadienil) clorido rodio o iridio ([M(L)(Cp*)Cl] PF6; M = Rh, Ir) También see describen las sales de cloruro ([M(L)(Cp*) Cl] Cl; M = Rh, Ir). Se evaluó las actividades anti-plasmodial y anti-microbacteriana del ligante y de las sales de hexafluorofosfato de los complejos metálicos. Los complejos de rodio y de iridio eran significativamente más activos contra M. tuberculosis que el ligante libre. Las estructuras moleculares de los complejos (hexafluorofosfato de N-(2-((7-cloroquinolin-4-il) amino)etil)pirazina-2-carboxamida)(ciclopentadienil) cloro-rodio y cloruro de (N-(2-cloroquinolin-4-il)amino)etil) pirazina-2-carboxamida)(ciclopentadienil)cloro-iridio se resolvieron cristalográficamente.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Malaria]]></kwd>
<kwd lng="en"><![CDATA[tuberculosis]]></kwd>
<kwd lng="en"><![CDATA[half-sandwich]]></kwd>
<kwd lng="en"><![CDATA[organometallic]]></kwd>
<kwd lng="en"><![CDATA[chloroquine]]></kwd>
<kwd lng="en"><![CDATA[pyrazinamide]]></kwd>
<kwd lng="es"><![CDATA[Malaria]]></kwd>
<kwd lng="es"><![CDATA[tuberculosis]]></kwd>
<kwd lng="es"><![CDATA[medio sándwich]]></kwd>
<kwd lng="es"><![CDATA[organometálico]]></kwd>
<kwd lng="es"><![CDATA[cloroquina]]></kwd>
<kwd lng="es"><![CDATA[pirazinamida]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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