<?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>S1870-249X2018000400177</article-id>
<article-id pub-id-type="doi">10.29356/jmcs.v62i4.544</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[GC/MS Analysis and Bioactive Properties of Extracts Obtained from Clusia minor L. Leaves]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mangas Marín]]></surname>
<given-names><![CDATA[Raisa]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Montes de Oca Porto]]></surname>
<given-names><![CDATA[Rodny]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Herrera Paredes]]></surname>
<given-names><![CDATA[Maria Elisabeth]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bello Alarcón]]></surname>
<given-names><![CDATA[Adonis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hernández Balmaseda]]></surname>
<given-names><![CDATA[Ivones]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Menéndez Soto del Valle]]></surname>
<given-names><![CDATA[Roberto]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lopes]]></surname>
<given-names><![CDATA[Miriam Teresa Paz]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodeiro Guerra]]></surname>
<given-names><![CDATA[Idania]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,University of Havana Food and Pharmacy Institute ]]></institution>
<addr-line><![CDATA[Havana ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Institute of Sport Medicine Antidoping Laboratory ]]></institution>
<addr-line><![CDATA[Havana ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,University of Guayaquil Faculty of Chemical Sciences ]]></institution>
<addr-line><![CDATA[Guayaquil ]]></addr-line>
<country>Ecuador</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Institute of Marine Sciences Department of Pharmacology ]]></institution>
<addr-line><![CDATA[Havana ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af5">
<institution><![CDATA[,Center of Neurosciences  ]]></institution>
<addr-line><![CDATA[Havana ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af6">
<institution><![CDATA[,Federal University Minas Gerais Biological Science Institute Laboratory of Antitumor Substances]]></institution>
<addr-line><![CDATA[Belo Horizonte ]]></addr-line>
<country>Brazil</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>177</fpage>
<lpage>188</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2018000400177&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2018000400177&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2018000400177&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract. Clusia minor L. is traditionally used to treat many disorders that including pain and inflammation such as sores and warts. Four extracts from the leaves of the plant were prepared: hexane (A), ethyl acetate (B), methanol (C) and ethanol (E). GC/MS analysis of extracts B and C led to the identification of thirty-three and twenty-seven compounds, respectively. The presence of vitamin E and lupeol was relevant in both extracts. All extracts showed effective radical scavenger properties in the 2,2-diphenyl-2-picryl-hydrazyl (DPPH) assay, being extract E the most promissory (IC50 = 10.25 µg/mL). Extracts A, C and E, administered topically (0.5-4 mg per ear), significantly reduced ear edema induced by croton oil at 4 mg per ear, meanwhile, extract B was able to significantly reduce the inflammation at the dose of 2 mg per ear. The cytotoxic activity of the extracts was evaluated against four cell lines. Extract B showed the most cytotoxicity effect, with IC50 values in the range of 32.01-203.5 µg/mL. In addition, no acute oral toxicity after mice exposure to the four extracts was observed. The results suggest Clusia minor L. may be an excellent potential source of new bioactive agents for the development of new medicinal agents.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen. La especie Clusia minor L. se usa tradicionalmente para tratar algunos trastornos que incluyen dolor e inflamación, como son las llagas y verrugas. Se prepararon cuatro extractos a partir de las hojas de la planta: hexano (A), acetato de etilo (B), metanol (C) y etanol (E). El análisis por CG/EM de los extractos B y C permitieron la identificación de 33 y 27 compuestos, respectivamente. La presencia de vitamina E y lupeol fue relevante en ambos extractos. Todos los extractos mostraron capacidad secuestradora del radical 2,2-difenil-2-picril-hidrazilo (DPPH), siendo el extracto E el más prometedor (IC50 = 10,25 &#956;g/ml). Los extractos A, C y E, administrados tópicamente (0,5-4 mg por oreja), redujeron significativamente el edema de oreja inducido por aceite de crotón a 4 mg por oreja; mientras que el extracto B lo logró a la dosis de 2 mg por oreja. También fue evaluada la actividad citotóxica de los extractos contra cuatro líneas celulares. El extracto B mostró el mayor efecto de citotoxicidad, con valores de IC50 en el rango de 32,01-203,5 &#956;g/mL. Además, no se observó toxicidad aguda por vía oral después de la exposición de los ratones a los extractos. Los resultados sugieren que esta especie puede ser una fuente potencial de nuevos agentes bioactivos para desarrollar agentes medicinales.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[GC/MS analysis]]></kwd>
<kwd lng="en"><![CDATA[antioxidant]]></kwd>
<kwd lng="en"><![CDATA[anti-inflammatory]]></kwd>
<kwd lng="en"><![CDATA[cytotoxicity]]></kwd>
<kwd lng="en"><![CDATA[acute oral toxicity]]></kwd>
<kwd lng="es"><![CDATA[CG/EM]]></kwd>
<kwd lng="es"><![CDATA[antioxidante]]></kwd>
<kwd lng="es"><![CDATA[anti-inflamatorio]]></kwd>
<kwd lng="es"><![CDATA[citotoxicidad]]></kwd>
<kwd lng="es"><![CDATA[toxicidad aguda oral]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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