<?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>0120-2804</journal-id>
<journal-title><![CDATA[Revista Colombiana de Química]]></journal-title>
<abbrev-journal-title><![CDATA[Rev.Colomb.Quim.]]></abbrev-journal-title>
<issn>0120-2804</issn>
<publisher>
<publisher-name><![CDATA[Departamento de Química,  Universidad Nacional de Colombia.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-28042015000200005</article-id>
<article-id pub-id-type="doi">10.15446/rev.colomb.quim.v44n2.55217</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Antioxidant capacity and total phenol content of Hyptis spp., P. heptaphyllum, T.panamensis, T. rhoifolia and Ocotea sp]]></article-title>
<article-title xml:lang="es"><![CDATA[Capacidad antioxidante y contenido de fenoles totales de hyptis spp., P. heptaphyllum, T. panamensis, T. rhoifolia, y Ocotea sp]]></article-title>
<article-title xml:lang="pt"><![CDATA[Capacidade antioxidante e conteúdo de fenóis totais de Hyptis spp., P. heptaphyllum, T. panamensis, T. rhoifolia, e Ocotea sp]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Tafurt-García]]></surname>
<given-names><![CDATA[Geovanna]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Jiménez-Vidal]]></surname>
<given-names><![CDATA[Luisa F]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Calvo-Salamanca]]></surname>
<given-names><![CDATA[Ana M]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Nacional de Colombia  ]]></institution>
<addr-line><![CDATA[Arauca ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>05</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>05</month>
<year>2015</year>
</pub-date>
<volume>44</volume>
<numero>2</numero>
<fpage>28</fpage>
<lpage>33</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-28042015000200005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-28042015000200005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-28042015000200005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[In this work, the possible correlation between the antioxidant activities and the Total Phenolic Content (TPC) and chemical composition of Lamiaceae (H. conferta, H. dilatata, H. mutabilis, H. suaveolens), Burseraceae (P. heptaphyllum, T. rhoifoila, T. panamensis), and Lauraceae (Ocotea sp.) were evaluated. The Trolox Equivalent Antioxidant Capacity or the Total Antioxidant Activity (TAA) was determined by using a colorimetric assay with the ABTS radical cation, Effective Concentration (EC50) was evaluated with the DPPH radical, and the TPC was established by the Folin-Ciocalteu method, for ethanolic extracts obtained by cold maceration and evaporation to dryness. Both the TAA and the EC50 were highly correlated with the TPC. The barks of T. rhoifolia and T. panamensis demonstrated the highest antioxidant capacities. The Burseraceae spp. exhibited the highest TPC, and the Lamiaceae (Hyptis spp.) demonstrated the lowest TPC.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Neste trabalho foi avaliada a possível correlação entre as atividades antioxidantes, o conteúdo de fenóis totais e a composição química de Lamiaceae (H. conferta, H. dilatata, H. mutabilis, H. suaveolens), Burseraceae (P. heptaphyllum, T. rhoifoila, T. panamensis), e Lauraceae (Ocotea sp.). Para os extratos de etanol obtidos por maceração em frio e evaporação até a secura, a Capacidade Antioxidante Equivalente ao Trolox ou à Atividade Antioxidante Total (AAT), foi determinada por meio de um ensaio colorimétrico com o cátion radical ABTS, a concentração eficaz (EC50) foi avaliada com o radical DPPH, e o Conteúdo de Fenóis Totais (CFT) foi estabelecido pelo método do Folin-Ciocalteu. Tanto a AAT quanto a EC50 estiveram altamente relacionadas com a CFT. A casca de T. rhoifolia e T. panamensis apresentaram as maiores capacidades antioxidantes. As Burseraceae spp. apresentaram o CFT mais alto, e as Lamiaceae (Hyptis spp.) apresentaram o CFT mais baixo.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[En este trabajo se evaluó la posible correlación entre las actividades antioxidantes, el contenido de fenoles totales (CFT) y la composición química de Lamiaceae (H. conferta, H. dilatata, H. mutabilis, H. suaveolens), Burseraceae (P. heptaphyllum, T. rhoifoila, T. panamensis) y Lauraceae (Ocotea sp.). Para los extractos etanólicos obtenidos por maceración en frio y evaporación a sequedad, la Capacidad Antioxidante Equivalente al Trolox o la Actividad Antioxidante Total (AAT), fueron determinadas mediante un ensayo colorimétrico con el catión radical ABTS, la Concentración Efectiva (EC50) fue evaluada con el radical DPPH, y el Contenido de Fenoles Totales (CFT), fue establecido mediante el método de Folin-Ciocalteu. Tanto la AAT como la EC50 estuvieron altamente correlacionados con el CFT. Las cortezas de T. rhoifolia y T. panamensis mostraron las capacidades antioxidantes más altas. Las Burseraceae spp. mostraron los TPC más altos y las Lamiaceae (Hyptis spp.) mostraron los TPC más bajos.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[ABTS]]></kwd>
<kwd lng="en"><![CDATA[Folin-Ciocalteu]]></kwd>
<kwd lng="en"><![CDATA[Lamiaceae]]></kwd>
<kwd lng="en"><![CDATA[Burseraceae]]></kwd>
<kwd lng="en"><![CDATA[Lauraceae]]></kwd>
<kwd lng="pt"><![CDATA[ABTS]]></kwd>
<kwd lng="pt"><![CDATA[Folin-Ciocalteu]]></kwd>
<kwd lng="pt"><![CDATA[Lamiaceae]]></kwd>
<kwd lng="pt"><![CDATA[Burseraceae]]></kwd>
<kwd lng="pt"><![CDATA[Lauraceae]]></kwd>
<kwd lng="es"><![CDATA[ABTS]]></kwd>
<kwd lng="es"><![CDATA[Folin-Ciocalteu]]></kwd>
<kwd lng="es"><![CDATA[Lamiaceae]]></kwd>
<kwd lng="es"><![CDATA[Burseraceae]]></kwd>
<kwd lng="es"><![CDATA[Lauraceae]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <font face="Verdana" size="2">     <p>DOI: <a href="http://dx.doi.org/10.15446/rev.colomb.quim.v44n2.55217" target="_blank">http://dx.doi.org/10.15446/rev.colomb.quim.v44n2.55217</a></p>      <p align="center"><font size="4"><b>Antioxidant capacity and total phenol content of <i>Hyptis</i> spp., <i>P. heptaphyllum</i>, <i>T.panamensis</i>, <i>T. rhoifolia</i> and <i>Ocotea</i> sp.</b></font></p>      <p align="center"><font size="3"><b>Capacidad antioxidante y contenido de fenoles totales de <i>hyptis</i> spp., <i>P. </i>heptaphyllum<i>, T. panamensis, T. rhoifolia</i>, y <i>Ocotea</i> sp.</b></font></p>      <p align="center"><font size="3"><b>Capacidade antioxidante e conte&uacute;do de fen&oacute;is totais de <i>Hyptis</i> spp., <i>P. heptaphyllum, T. panamensis, T. rhoifolia,</i> e <i>Ocotea</i> sp.</b></font></p>      <p align="center"><b>Geovanna Tafurt-Garc&iacute;a</b><Sup>1,*</Sup>, <b>Luisa F. Jim&eacute;nez-Vidal</b><Sup>1</Sup>, <b>Ana M. Calvo-Salamanca</b><Sup>1</Sup></p>      <p><Sup>1</Sup> Orinoqu&iacute;a&acute;s Science Research Group, Universidad Nacional de Colombia, sede Orinoquia, km 9, to Ca&ntilde;o Lim&oacute;n, Arauca, Colombia.    <br>  <sup>*</sup> <b>Corresponding author:</b> <a href="mailto:gtafurg@unal.edu.co">gtafurg@unal.edu.co</a>.</p>      <p><b>Article citation:</b>    <br> Tafurt-Garc&iacute;a, G.; Jim&eacute;nez-Vidal, L. F.; Calvo-Salamanca, A. M.  Antioxidant capacity and total phenol content of <i>Hyptis</i> spp., <i>P. heptaphyllum, T. panamensis, T. rhoifolia</i> and <i>Ocotea</i> sp. <i>Rev. Colomb. Quim.</i> <b>2015</b>, <i>44</i>(2), 28-33. DOI: <a href="http://dx.doi.org/10.15446/rev.colomb.quim.v44n2.55217" target="_blank">http://dx.doi.org/10.15446/rev.colomb.quim.v44n2.55217</a></p>      ]]></body>
<body><![CDATA[<p>Recibido: 19 de junio de 2015 Aceptado: 10 de julio de 2015</p> <hr>      <p><b>Abstract</b></p>      <p>In this work, the possible correlation between the antioxidant activities and the Total Phenolic Content (TPC) and chemical composition of Lamiaceae (<i>H. conferta, H. dilatata, H. mutabilis, H. suaveolens</i>), Burseraceae (<i>P. heptaphyllum, T. rhoifoila, T. panamensis</i>),<i> </i>and Lauraceae (<i>Ocotea </i>sp.) were evaluated. The Trolox Equivalent Antioxidant Capacity or the Total Antioxidant Activity (TAA) was determined by using a colorimetric assay with the ABTS radical cation, Effective Concentration (EC<Sub>50</Sub>) was evaluated with the DPPH radical, and the TPC was established by the Folin-Ciocalteu method, for ethanolic extracts obtained by cold maceration and evaporation to dryness. Both the TAA and the EC<Sub>50</Sub> were highly correlated with the TPC. The barks of <i>T. rhoifolia</i> and<i> T. panamensis</i> demonstrated the highest antioxidant capacities. The Burseraceae spp. exhibited the highest TPC, and the Lamiaceae (<i>Hyptis</i> spp.) demonstrated the lowest TPC.</p>      <p><b>Keywords:</b> ABTS, Folin-Ciocalteu, Lamiaceae, Burseraceae, Lauraceae.</p>  <hr>      <p><b>Resumo</b></p>      <p>Neste trabalho foi avaliada a poss&iacute;vel correla&ccedil;&atilde;o entre as atividades antioxidantes, o conte&uacute;do de fen&oacute;is totais e a composi&ccedil;&atilde;o qu&iacute;mica de Lamiaceae (<i>H. conferta, H. dilatata, H. mutabilis, H. suaveolens</i>), Burseraceae (<i>P. heptaphyllum, T. rhoifoila, T. panamensis</i>), e Lauraceae (<i>Ocotea </i>sp.). Para os extratos de etanol obtidos por macera&ccedil;&atilde;o em frio e evapora&ccedil;&atilde;o at&eacute; a secura, a Capacidade Antioxidante Equivalente ao Trolox ou &agrave; Atividade Antioxidante Total (AAT), foi determinada por meio de um ensaio colorim&eacute;trico com o c&aacute;tion radical ABTS, a concentra&ccedil;&atilde;o eficaz (EC<Sub>50</Sub>) foi avaliada com o radical DPPH, e o Conte&uacute;do de Fen&oacute;is Totais (CFT) foi estabelecido pelo m&eacute;todo do Folin-Ciocalteu. Tanto a AAT quanto a EC<Sub>50 </Sub>estiveram altamente relacionadas com a CFT. A casca de <i>T. rhoifolia</i> e<i> T. panamensis </i>apresentaram as maiores capacidades antioxidantes.  As Burseraceae spp. apresentaram o CFT mais alto, e as Lamiaceae (<i>Hyptis </i>spp.) apresentaram o CFT mais baixo.</p>      <p><b>Palavras chave</b>: ABTS, Folin-Ciocalteu, Lamiaceae, Burseraceae, Lauraceae.</p>  <hr>      <p><b>Resumen</b></p>      <p>En este trabajo se evalu&oacute; la posible correlaci&oacute;n entre las actividades antioxidantes, el contenido de fenoles totales (CFT) y la composici&oacute;n qu&iacute;mica de Lamiaceae (<i>H. conferta, H. dilatata, H. mutabilis, H. suaveolens</i>), Burseraceae (<i>P. heptaphyllum, T. rhoifoila, T. panamensis</i>)<i> </i>y Lauraceae (<i>Ocotea </i>sp.). Para los extractos etan&oacute;licos obtenidos por maceraci&oacute;n en frio y evaporaci&oacute;n a sequedad, la Capacidad Antioxidante Equivalente al Trolox o la Actividad Antioxidante Total (AAT), fueron determinadas mediante un ensayo colorim&eacute;trico con el cati&oacute;n radical ABTS, la Concentraci&oacute;n Efectiva (EC<Sub>50</Sub>) fue evaluada con el radical DPPH, y el Contenido de Fenoles Totales (CFT), fue establecido mediante el m&eacute;todo de Folin-Ciocalteu. Tanto la AAT como la EC<Sub>50</Sub> estuvieron altamente correlacionados con el CFT. Las cortezas de <i>T. rhoifolia</i> y<i> T. panamensis</i> mostraron las capacidades antioxidantes m&aacute;s altas.  Las Burseraceae spp. mostraron los TPC m&aacute;s altos y las Lamiaceae (<i>Hyptis</i> spp.) mostraron los TPC m&aacute;s bajos.</p>      <p><b>Palabras clave</b>: ABTS, Folin-Ciocalteu, Lamiaceae, Burseraceae, Lauraceae.</p> <hr>      ]]></body>
<body><![CDATA[<p><font size="3"><b>Introduction</b></font></p>      <p>Lamiaceae are the most widely distributed angiosperms in the world. They comprise approximately 221 genera and 6000 species. In Colombia, 23 genera and over 190 species of Labiatae have been identified <i>(1)</i>. Studies of plants in this family indicate that Lamiaceae have traditionally been used as condiments or drugs because of their antioxidant, insecticidal, antimicrobial (antibacterial, antiherpes), antiinflammatory, antitumor, antihypertensive, and gastroprotective properties <i>(2,3).</i> Additionally, they are used in the perfume, cosmetic, food, and pharmaceutical industries because of the diversity of flavors present in the essential oils of several species <i>(1)</i>.</p>      <p>The content and type of phenolic compounds found in the essential oils and extracts of these species are among the factors that determine their biological activity <i>(4).</i> The species of the <i>Hyptis</i> genera (Lamiaceae) are used in applications such as repellents and insecticides as well as for antinociceptive, antihyperglycemic, antifungal, antibacterial, antiinflammatory, antimalarial, and gastrointestinal purposes <i>(5,6).</i></p>      <p>Burseraceae are a source of exudate and resins with increased aromatic compounds that are used in traditional medicine and perfumery. The Online Collection of the Instituto de Ciencias Naturales of the Universidad Nacional de Colombia (ICN-UN) reported eight genera of Burseraceae: <i>Bursera, Canarium, Crepidospermum, Dacryodes, Hemicrepidospermum, Protium, Tetragastris</i>,<i> </i>and <i>Trattinnickia.</i> The <i>Protium </i>genus contains the largest number of species, followed by <i>Bursera</i> and <i>Trattinickia(7).</i></p>      <p>The resins, essential oils of resins and leaves, and extracts of leaves, barks and stems of the <i>Protium</i> genus have all been evaluated for potential applications. Species of this genus are antiinflammatory, antinociceptive, analgesic, expectorant, antimalarial, repellent, possess antitumor and acaricide activities, and are gastric and liver protectors <i>(8)</i>.</p>      <p>The <i>Tetragastris </i>and <i>Trattinnickia </i>species have been less thoroughly studied. The bark of <i>Tetragastris panamensis</i> has been used for antihemorrhagic, antiviral, leishmanicidal, and antimalarial purposes <i>(9)</i>.</p>      <p>Lauraceae has 55 genera and approximately 3000 species. It is composed of a wide variety of trees and shrubs that grow in moist tropical dry forests. It is distributed throughout America and Asia, with a considerable number of species in Australia and Madagascar and a small number in Africa (<i>10</i>). Genus <i>Ocotea</i> is the most diverse and abundant of the Lauraceae, with approximately 350 species mainly distributed in the Neotropics. They are found from Mexico to Argentina, in Africa, Madagascar, and one species in the Canary Islands (<i>10</i>). Many species of <i>Ocotea</i> have antirheumatic, analgesic, purgative, and tonic properties (<i>11</i>), they have shown analgesic, antiinflammatory, antithrombotic, antiplaquetales, antioxidant, and antimicrobial properties as well <i>(12)</i>. For example <i>Ocotea paulii</i> (<i>O. atirrensis</i>) has antifungal properties <i>(13),</i> and <i>O. bullata </i>has shown antiinflammatory activity <i>(14).</i> Also several species of this genus are important in the field of perfumery such as <i>O. pretiosa, O. sassafras, O. caudate</i>, and<i> O. cymbarum</i> (<i>15).</i></p>      <p>The species of Lamiaceae, Lauraceae, and Burseraceae are culturally important and have the potential to treat different diseases. Studies of antioxidant activities and Total Phenol Content (TPC) can be used to explain the biological activities that have been reported. In this work, the antioxidant capacities of the ethanolic extracts of <i>H. conferta, H. dilatata, H. mutabilis, H. suaveolens, P. heptaphyllum, T. panamensis, T. rhoifolia, </i>and<i> Ocotea </i>sp<i>.</i>, which were collected<i> </i>from areas near Arauca (Orinoco, Colombia) were evaluated. Assays with the DPPH and ABTS radicals were used to evaluate the Total Antioxidant Capacity (TAA), and the Folin-Ciocalteu reagent was used to determine the TPC.</p>      <p><b><font size="3">Materials and methods</font></b></p>     <p><b>Reagents and materials</b></p>      ]]></body>
<body><![CDATA[<p>Vitamin E (97%), DPPH (90%), gallic acid (98%), Folin-Ciocalteu reagent &reg; (2 N), and ethanol (99.8%) were purchased from Sigma-Aldrich&reg; (Saint Louis, MO, USA). Spectrophotometric data were obtained on a Shimadzu model 2401PC&reg; (Columbia, Maryland, USA). Quartz cuvettes (1 cm x 1 cm x 4 cm) were used to determine the absorbance in the visible range.</p>      <p><b>Plant material</b></p>      <p>Images of the samples collected for this study are shown in <a href="#f1">Figure 1</a>.</p>     <p align="center"><a name="f1"></a><img src="img/revistas/rcq/v44n2/v44n2a05f1.jpg"></p>      <p><i>Hyptis conferta</i> was collected at La Saya village (Arauca, Colombia); coordinates: 7&deg;04'N-70&deg;45'W, 206 meters above sea level (m.a.s.l.). <i>Hyptis dilatata</i> was collected at Mata Corozo farm, La Comarca village of Cravo Norte (Arauca, Colombia); coordinates: 6&deg;21&rsaquo;2.75"N-70&deg;14'27.14"W, 102 m.a.s.l. <i>Tetragastris panamensis</i> and <i>Trattinnickia rhoifolia</i> were collected at La Reforma farm, Rinc&oacute;n Hondo village of Tame (Arauca, Colombia); coordinates: 6&deg;28'50.03"N-71&deg;41'15.09"W, 445 m.a.s.l. <i>Hyptis mutabilis</i> and <i>Hyptis suaveolens</i> were collected at Las Mercedes farm, in Mata de Gallina village of Arauca (Arauca, Colombia); coordinates: 6&deg;58'25,45"N-70&deg;42'24.69"W, 127 m.a.s.l. <i>Protium heptaphyllum</i> was collected in La Mancha farm, on Puerto San Salvador, in Tame (Arauca, Colombia); coordinates: 6&deg;27'N-71&deg;44'W, 240 m.a.s.l.</p>      <p>Taxonomic identification of the following species was performed in the Herbario Nacional Colombiano of the ICN-UN, Bogot&aacute;: <i>H. conferta</i> (COL 563485, 2012), <i>H. dilatata</i> (COL 563486, 2012), <i>T. panamensis</i> (2012), <i>T. rhoifolia</i> (COL 566451, 2012), <i>H. mutabilis</i> (COL 553356, 2011), <i>H. suaveolens</i> (COL 553357, 2011) and<i> P.heptaphyllum</i> (COL 557313).</p>      <p><i>Ocotea </i>sp<i>.</i>, was collected on El Porvenir village of Toledo, Norte de Santander (Colombia). Preliminary identification was performed by Venezuelan Forest.</p>      <p><b>Preparation of ethanolic extract</b></p>      <p>Extracts were obtained from dried plant material, crushed, and homogenized by exhaustive extraction with ethanol as the solvent (leaves or bark). The extracts were dried by vacuum distillation. Inflorescences were used for the extractions of <i>H. conferta,</i> including leaves of <i>H. dilatata, H. mutabilis, H. suaveolens</i>, <i>P. heptaphyllum</i>, and <i>Ocotea</i> sp., and the stem barks of <i>T. panamensis </i>and <i>T. rhoifolia</i>.</p>      <p><b>Reactivity to ABTS and DPPH radicals</b></p>      ]]></body>
<body><![CDATA[<p>The assay for ABTS radical was performed according to the method reported by Re<i> et al. (16</i>)<i>. </i>TEAC or TAA values (Trolox Equivalent Antioxidant Capacity or Total Antioxidant Activity) were obtained in this test. ABTS (38.5 mg) was dissolved in distilled water (10 mL) and potassium persulfate was added to the mixture (6.9 mg). The final solution was allowed to stand for 20 h in the dark at room temperature to obtain the ABTS cation radical. An aliquot of the ABTS solution was diluted in ethanol to achieve an absorbance of 0.70 at 734 nm. A calibration curve was performed with the reference antioxidant (trolox). The decrease in absorbance (dA) of the solution of ABTS (3 mL) was plotted for 6 min following the addition of 30 &micro;l trolox standard mixtures (0.2-1.9 mM). Five mixtures of ethanolic extracts were prepared to assess the decrease in absorbance of the ABTS solution with the reference antioxidant (trolox, vitamin E). The TAA of ethanolic extracts was estimated with reference to trolox (mmol trolox/kg extract). The ratio between the slopes of the curves evaluated for the ethanolic extract (dA vs kg/L), and trolox (dA vs mM) were used to estimate TEAC or TAA.</p>      <p>The assay for DPPH radical was performed according to the procedure described by Brand-Williams <i>et al.(17).</i> EC<Sub>50</Sub> values (Equivalent Concentration of antioxidant that reduces the concentration of the DPPH radical by 50%) were obtained using this test. A calibration curve was prepared with DPPH standard solutions in ethanol (514 nm). The steady state (time when the DPPH concentration or the absorbance stops decreasing) was measured after the addition of 0.5 mL of ethanolic extract to 2.5 mL of the DPPH standard solution. The steady state of the DPPH standard solution was evaluated for five solutions of ethanolic extracts of each plant material. Graphs of DPPH remaining (%) vs EC (Effective Concentration: kg extract/mol initial DPPH) were constructed based on the data obtained for each ethanolic extract (DPPH absorbance vs time), and plant material. The EC<Sub>50</Sub> values were interpolated from these graphs.</p>      <p><b>Total Phenolic Content (TPC)</b></p>      <p>The TPC was calculated as gallic acid equivalents (g GA/g extract) according to the procedure described by Dastmalchi <i>et al</i>. (<i>18</i>). An aliquot of ethanolic extract (1 mL) was transferred to a test tube containing distilled water (6 mL). The Folin-Ciocalteu reagent (500 &micro;L) was added to the test tube. After 5 min, Na<Sub>2</Sub>CO<Sub>3</Sub> (1.5 mL, 200 g/L) and water were added to a final volume of 10 mL. When the reaction was complete (2 h at room temperature), the absorbance at 760 nm was determined and compared to a GA calibration curve.</p>      <p><b><font size="3">Results and discussion</font></b></p>      <p>The yields, antioxidant capacities (EC<Sub>50</Sub> and TAA), and TPC evaluated for the ethanolic extracts of Lamiaceae, Burseraceae, and Lauraceae are shown in Table 1. Higher yields were obtained for Lamiaceae and Burseraceae than those for Lauraceae. For Lamiaceae, <i>H. conferta</i>, and <i>H. dilatata</i>, the yields were higher than those obtained for <i>H. mutabilis</i> and <i>H. suaveolens</i>.</p>      <p>The results shown in <a href="#t1">Table 1</a> indicate that the barks of <i>T. rhoifolia </i>and <i>T. panamensis</i> (Burseraceae), had the highest antioxidant capacities (TAA), followed by the <i>Hyptis</i> spp., <i>H. dilatata </i>and <i>H. conferta</i>. <i>P. heptaphyllum</i>, <i>Ocotea</i> sp., <i>H. mutabilis</i>, and <i>H. suaveolens</i> exhibited the lowest values of TAA. The Burseraceae spp. also had the highest TPC, whereas the Lamiaceae had the lowest. Burseraceae exhibited the lowest EC<Sub>50</Sub> values and Lamiaceae exhibited the highest.</p>     <p align="center"><a name="t1"></a><img src="img/revistas/rcq/v44n2/v44n2a05t1.jpg"></p>      <p>For the ethanolic extracts of the <i>Hyptis</i> spp., the <i>H. dilatata</i> and <i>H. conferta</i> demonstrated the best antioxidant capacities. Their TAA values were the highest, which is related to the largest TPC and the lowest EC<Sub>50</Sub> values. Regarding the Burseraceae, the barks of <i>T. rhoifolia</i> and<i> T. panamensis</i> exhibited the best antioxidant capacities compared to the leaves of <i>P. heptaphyllum</i>. The bark of <i>T. panamensis</i> possessed the highest antioxidant capacity and had the highest values for TAA and TPC, and the lowest EC<Sub>50</Sub> value.</p>      <p>The highest antioxidant activities and TPC belonged to the barks of <i>T, rhoifolia </i>and <i>T. panamensis</i>. These values can be attributed to the large number of tannins (hydrolyzable and condensates) present in wood tissues <i>(19,20)</i>. Tannins have demonstrated considerable antimicrobial and antioxidant capacities (<i>19</i>,<i>20)</i>. The leaves of <i>P. heptaphyllum</i> contained a moderate level of antioxidant activity and TPC, lower than <i>T, rhoifolia </i>and <i>T. panamensis</i>. The promising antioxidant activities of <i>T, rhoifolia</i>, <i>T. panamensis</i>, and <i>P. heptaphyllum</i> may be attributed to the high content of triterpenoids in the Burseraceae spp. <i>(21-23)</i>. The pentacyclic triterpenes have demonstrated antitumor, antiinflammatory and antioxidant potential <i>(24).</i></p>      ]]></body>
<body><![CDATA[<p>Resins, essential oils (EO), and extracts of leaves, barks and stems of the <i>Protium</i> species have been evaluated to assess their pharmacological potential <i>(25,26)</i>. They have shown antiinflammatory, antinociceptive, analgesic, expectorant, antitumor, repellent, acaricide, and antimalarial activities, and may be gastric and hepatic protectors <i>(25,26)</i>. Biological activities for <i>T. panamensis</i> and <i>T. rhoifolia </i>were not previously reported. For Burseraceae, this study suggests that the barks of <i>T rhoifolia</i> and <i>T. panamensis</i> possess promising bio-activity compared to the leaves of <i>P. heptaphyllum</i>.</p>      <p>The antioxidant activities of the <i>Hyptis</i> spp., <i>H. dilatata </i>and <i>H. conferta</i>, may be attributed to the content of sesquiterpenoids and/or diterpenoids <i>(27,28).</i> Tricyclic diterpenes have been reported in <i>H. dilatata(29).</i> Less antioxidant activity was found for <i>H. mutabilis </i>and <i>H. suaveolens.</i> The EO of <i>H. mutabilis</i> may consist of a majority of sesquiterpenes <i>(27).</i> Triterpenoids have also been detected for this species <i>(30). </i>Volatile oils, starches, proteins, tannins, saponins, fats, alkaloids and glycosides have been reported for <i>H. suaveolens(31). </i>Additionally, abietane type endoperoxides, diterpenes, and pentacyclic triterpenes have been detected <i>(32,33)</i>.</p>      <p>Cytostatic and cytotoxic activities against tumor cell lines have been reported for <i>H. dilatata(34)</i>. No biological activity was found for <i>H. conferta</i>. Gastrointestinal, antiparasitic (malaria), and repellent activities have been reported for <i>H. mutabilis(5,30).</i> Antihyperglycemic, insecticidal, antifungal, antiinflammatory, antibacterial, antinociceptive, antiplasmodial and antidermatitis activities have been reported for <i>H. suaveolens</i> (<i>6,32,35</i>).</p>      <p>The results obtained in this study suggest that <i>H. conferta </i>and <i>H. dilatata</i> could have promising biological activities.</p>      <p>Monoterpenes, sesquiterpenes, phenylpropanoids, flavonoids, lignans, and alkaloids have been detected in the <i>Ocotea</i> spp. (Lauraceae) <i>(12,36-41)</i>. Analgesic, antiinflammatory, antithrombotic, antiplaquetal, antioxidant and antimicrobial activities are reported for the <i>Ocotea</i> genus <i>(13-15,38,41)</i>.</p>      <p>The low values for TAA and TPC from the extract of <i>Ocotea </i>sp., indicate that the leaves of this species contain a low number of biologically active compounds such as antioxidants. They are less active than the Burseraceae and Lamiaceae that were analyzed.</p>      <p><b><font size="3">Conclusions</font></b></p>      <p>This work determined the possible relation between antioxidant activities and the TPC, and the chemical composition of <i>H. conferta, H. dilatata, H. mutabilis, H. suaveolens</i>, <i>P. heptaphyllum, T. rhoifoila, T. panamensis </i>and <i>Ocotea </i>sp<i>.</i></p>      <p>The barks of <i>T. rhoifolia</i> and<i> T. panamensis</i> showed the highest antioxidant capacities (high TAA and low EC<Sub>50</Sub>), followed by <i>H. dilatata </i>and <i>H. conferta</i>.</p>      <p><i>P. heptaphyllum</i>, <i>Ocotea</i> sp. <i>H. mutabilis </i>and <i>H. suaveolens</i>, exhibited the lowest antioxidant activities.</p>      ]]></body>
<body><![CDATA[<p>Burseraceae spp. also demonstrated the highest TPC, whereas the Lamiaceae (<i>Hyptis</i> spp.) exhibited the lowest TPC.</p>      <p><b>Acknowledgements</b></p>      <p>The authors thank Fernando Caroprese, Francisco Mijares, Jorge Hern&aacute;ndez Siculaba, Gerardo Aymard (Venezuelan forest) and Oscar Suarez. Also to A. Jara, J. L. Fern&aacute;ndez-A and O. Rivera-D&iacute;az from the Herbario Nacional Colombiano of the ICN-UN.</p>      <p>The authors also thank Mr. Luis Ernesto Rodriguez Quenza, owner of the &ldquo;las Mercedes" farm, Mata de Gallina village, in Arauca, for his kindness in everything related to the accessibility of the collection area.</p> <hr>     <p><b><font size="3">References</font></b></p>      <!-- ref --><p>1. Fern&aacute;ndez-Alonso, J.L.; Rivera-Diaz O. Las labiadas. En <i>Libro rojo de plantas de Colombia. Volumen 3: Las bromelias, las labiadas y las pasifloras</i>. Garc&iacute;a, N.; Galeano, G., Eds.; Serie Libros Rojos de Especies Amenazadas de Colombia. Instituto Alexander von Humboldt-Instituto de Ciencias Naturales de la Universidad de Colombia-Ministerio de Ambiente, Vivienda y Desarrollo Territorial: Bogot&aacute;, 2006; pp 385-679.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000068&pid=S0120-2804201500020000500001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>2. Matkowski, A.; Piotrowska, M. Antioxidant and free radical scavenging activities of some medicinal plants from the Lamiaceae. <i>Fitoterapia</i>. <b>2006</b>, <i>77</i>, 346-353. DOI: <a href="http://dx.doi.org/10.1016/j.fitote.2006.04.004" target="_blank">http://dx.doi.org/10.1016/j.fitote.2006.04.004</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000070&pid=S0120-2804201500020000500002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>3. Birkett, M.A.; Bruce, T.J.A.; Pickett, J.A. Repellent activity of <i>Nepeta grandiflora</i> and <i>Nepeta clarkei</i> (Lamiaceae) against the cereal aphid, <i>Sitobion avenae</i> (Homoptera: Aphididae). <i>Phytochem. Lett</i>. <b>2010</b>, <i>3</i>, 139-142. DOI: <a href="http://dx.doi.org/10.1016/j.phytol.2010.05.001" target="_blank">http://dx.doi.org/10.1016/j.phytol.2010.05.001</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000072&pid=S0120-2804201500020000500003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>4. Valant-Vetschera, K.M.; Roitman, J.N.; Wollenweber, E. Chemodiversity of exudate flavonoids in some members of the Lamiaceae. <i>Biochem. Syst. Ecol</i>. <b>2003</b>, <i>31</i>, 1279-1289. DOI: <a href="http://dx.doi.org/10.1016/S0305-1978(03)00037-1" target="_blank">http://dx.doi.org/10.1016/S0305-1978(03)00037-1</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000074&pid=S0120-2804201500020000500004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>5. Gillij, Y.G.; Gleiser, R.M.; Zygadlo, J.A. Mosquito repellent activity of essential oils of aromatic plants growing in Argentina. <i>Bioresour Technol</i>. <b>2008</b>, <i>99</i>, 2507-2515. DOI: <a href="http://dx.doi.org/10.1016/j.biortech.2007.04.066" target="_blank">http://dx.doi.org/10.1016/j.biortech.2007.04.066</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000076&pid=S0120-2804201500020000500005&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>6. Krishnamurthy, Y.L.; Shashikala, J.; Shankar, B. Antifungal potential of some natural products against <i>Aspergillus flavus</i> in soybean seeds during storage. <i>J. Stored Prod. Res</i>. <b>2008</b>, <i>44</i>, 305-309. DOI: <a href="http://dx.doi.org/10.1016/j.jspr.2008.03.001" target="_blank">http://dx.doi.org/10.1016/j.jspr.2008.03.001</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000078&pid=S0120-2804201500020000500006&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>7. Colombian National Herbarium. Institute of Natural Sciences (ICN). <a href="http://www.biovirtual.unal.edu.co/ICN/" target="_blank">http://www.biovirtual.unal.edu.co/ICN/</a> (Updated October 11 of 2013).    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000080&pid=S0120-2804201500020000500007&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>8. Oliveira, F.A.; Vieira-Junior, G.M.; Chaves, M.H.; Almeida, F.R.C.; Santos, K.A.; Martins, F.S. <i>et al</i>. Gastroprotective effect of the mixture of &#945;- and &#946;-amyrin from <i>Protium heptaphyllum</i>: Role of capsaicin-sensitive primary afferent neurons. <i>Planta Med</i>. <b>2004</b>, <i>70</i>, 780-782. DOI: <a href="http://dx.doi.org/10.1055/s-2004-827212" target="_blank">http://dx.doi.org/10.1055/s-2004-827212</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000082&pid=S0120-2804201500020000500008&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>9. Romin, T.L.; Weber, N.D.; Murray, B.K.; North, J.A.; Wood, S.G.; Hughes, B.G. <i>et al</i>. Antiviral activity of panamanian plant extracts. <i>Phytother. Res</i>. <b>1992</b>, <i>6</i>, 38-43. DOI: <a href="http://dx.doi.org/10.1002/ptr.2650060110" target="_blank">http://dx.doi.org/10.1002/ptr.2650060110</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000084&pid=S0120-2804201500020000500009&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>10. Van der Werff, H. A synopsis of <i>Ocotea</i> (Lauraceae) in Central America and southern Mexico. <i>Ann. Missouri Bot. Gard</i>. <b>2002</b>, <i>89</i>, 429-451. DOI: <a href="http://dx.doi.org/10.2307/3298602" target="_blank">http://dx.doi.org/10.2307/3298602</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000086&pid=S0120-2804201500020000500010&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>11. De Camargo, M.J.; Dantas, M.L.; Miyuki, C.; Delphino, E.; Rodrigues, F.; Silva, W. Sesquiterpenos de <i>Ocotea lancifolia</i> (Lauraceae). <i>Quim. Nova</i>. <b>2013</b>, <i>36</i>, 1008-1013. DOI: <a href="http://dx.doi.org/10.1590/s0100-40422013000700015" target="_blank">http://dx.doi.org/10.1590/s0100-40422013000700015</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000088&pid=S0120-2804201500020000500011&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>12. Guerrini, A.; Moreno, G.; Sacchetti, G.; Muzzoli, M.; Medici, A.; Besco, E. <i>et al</i>. Composition of the volatile fraction of <i>Ocotea bofo</i> Kunth (Lauraceae) calyces by GC-MS and NMR fingerprinting and its antimicrobial and antioxidant activity. <i>J. Agric. Food Chem</i>. <b>2006</b>, <i>54</i>, 7778-7788. DOI: <a href="http://dx.doi.org/10.1021/jf0605493" target="_blank">http://dx.doi.org/10.1021/jf0605493</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000090&pid=S0120-2804201500020000500012&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>13. Ni&ntilde;o, J.; Correa, Y.M.; Mosquera, O.M. In vitro evaluation of Colombian plant extracts against Black Sigatoka (<i>Mycosphaerella fijiensis</i> Morelet). <i>Arch. Phytopathol Pfl</i>. <b>2011</b>, 44, 791-803. DOI: <a href="http://dx.doi.org/10.1080/03235401003672939" target="_blank">http://dx.doi.org/10.1080/03235401003672939</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000092&pid=S0120-2804201500020000500013&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>14. Zschocke, S.; Drewes, S.E.; Paulus, K.; Bauer, R.; van Staden, J. Analytical and pharmacological investigation of <i>Ocotea bullata</i> (black stinkwood) bark and leaves. <i>J. Ethnopharmacol</i>. <b>2000</b>, <i>71</i>, 219-230. DOI: <a href="http://dx.doi.org/10.1016/s0378-8741(00)00159-8" target="_blank">http://dx.doi.org/10.1016/s0378-8741(00)00159-8</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000094&pid=S0120-2804201500020000500014&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>15. Ballabeni, V.; Tognolini, M.; Bertoni, S.; Bruni, R.; Guerrini, A.; Rueda, G. <i>et al</i>. Antiplatelet and antithrombotic activities of essential oil from wild <i>Ocotea quixos</i> (Lam.) Kosterm. (Lauraceae) calices from Amazonian Ecuador. <i>Pharmacol. Res</i>. <b>2007</b>, <i>55,</i> 23-30. DOI: <a href="http://dx.doi.org/10.1016/j.phrs.2006.09.009" target="_blank">http://dx.doi.org/10.1016/j.phrs.2006.09.009</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000096&pid=S0120-2804201500020000500015&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>16. Re, R.; Pellegrini, N.; Proteggente, A.; Pannala, A.; Yang, M.; Rice-Evans, C. Antioxidant activity applying an improved ABTS radical cation decolorization assay. <i>Free Radical Biol Med</i>. <b>1999</b>, <i>26</i>, 1231-1237. DOI: <a href="http://dx.doi.org/10.1016/s0891-5849(98)00315-3" target="_blank">http://dx.doi.org/10.1016/s0891-5849(98)00315-3</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000098&pid=S0120-2804201500020000500016&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>17. Brand-Williams, W.; Cuvelier, M.E.; Berset, C. Use of a free radical method to evaluate antioxidant activity. <i>Lebensm Wiss Technol</i>. <b>1995</b>, <i>28</i>, 25-30. DOI: <a href="http://dx.doi.org/10.1016/S0023-6438(95)80008-5" target="_blank">http://dx.doi.org/10.1016/S0023-6438(95)80008-5</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000100&pid=S0120-2804201500020000500017&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>18. Dastmalchi, K.; Dorman, D.; Kosarb, M.; Hiltunen, R. Chemical composition and in vitro antioxidant evaluation of a watersoluble Moldavian balm (<i>Dracocephalum moldavic</i>a L.) extract. <i>LWT</i>. <b>2007</b>, <i>40</i>, 239-248. DOI: <a href="http://dx.doi.org/10.1016/j.lwt.2005.09.019" target="_blank">http://dx.doi.org/10.1016/j.lwt.2005.09.019</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000102&pid=S0120-2804201500020000500018&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>19. Reddy, M.K.; Gupta, S.K.; Jacob, M.R.; Khan, S.I.; Ferreira, D. Antioxidant, antimalarial and antimicrobial activities of tannin-rich fractions, ellagitannins and phenolic acids from <i>Punica granatum</i> L. <i>Planta Med</i>. <b>2007</b>, <i>73</i>, 461-467. DOI: <a href="http://dx.doi.org/10.1055/s-2007-967167" target="_blank">http://dx.doi.org/10.1055/s-2007-967167</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000104&pid=S0120-2804201500020000500019&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>20. Su, J.D.; Osawa, T.; Kawakishi, S.; Namiki, M. Tannin antioxidants from <i>Osbeckia chinensis</i>. <i>Phytochemistry</i>. <b>1988</b>, <i>27</i>, 1315-1319. DOI: <a href="http://dx.doi.org/10.1016/0031-9422(88)80184-5" target="_blank">http://dx.doi.org/10.1016/0031-9422(88)80184-5</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000106&pid=S0120-2804201500020000500020&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>21. Rudiger, A.L.; Veiga, V.F. Chemodiversity of ursane- and oleanane-type triterpenes in Amazonian Burseraceae oleoresins. <i>Chem. Biodivers</i>. <b>2013</b>, <i>10</i>, 1142-1153. DOI: <a href="http://dx.doi.org/10.1002/cbdv.201200315" target="_blank">http://dx.doi.org/10.1002/cbdv.201200315</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000108&pid=S0120-2804201500020000500021&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>22. De Carvalho, L.E.; Pinto, D.D.; Lima, M.D.; Marques, M.O.M.; Facanali, R. The chemistry of essential oils of <i>Crepidospermum rhoifolium, Trattinnickia rhoifolia </i>and <i>Protium elegans</i> of the Amazon region. <i>J. Essent. Oil Bear Pl</i>. <b>2009</b>, <i>12</i>, 92-96. DOI: <a href="http://dx.doi.org/10.1080/0972060x.2009.10643698" target="_blank">http://dx.doi.org/10.1080/0972060x.2009.10643698</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000110&pid=S0120-2804201500020000500022&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>23. Zoghbi, M.G.B.; Andrade, E.H.A.; Santos, A.S.; Luzb, A.I.R.; Maia, JGS. Volatile constituents of the resins from <i>Protium subserratum</i> (Engl.) Engl. and <i>Tetragastris panamensis</i> (Engl.) Kuntz. <i>J Essent Oil Res</i>. <b>1998</b>, <i>10</i>, 325-326. DOI: <a href="http://dx.doi.org/10.1080/10412905.1998.9700910" target="_blank">http://dx.doi.org/10.1080/10412905.1998.9700910</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000112&pid=S0120-2804201500020000500023&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>24. Vechia, L.D.; Gnoatto, S.C.B.; Gosmann, G. Derivados oleananos e ursanos e sua importancia na descoberta de novos f&aacute;rmacos com atividade antitumoral, anti-inflamat&oacute;ria e antioxidante. <i>Quim. Nova</i>. <b>2009</b>, <i>32</i>, 1245-1252. DOI: <a href="http://dx.doi.org/10.1590/s0100-40422009000500031" target="_blank">http://dx.doi.org/10.1590/s0100-40422009000500031</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000114&pid=S0120-2804201500020000500024&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>25. Da Silva, E.R.; Oliveira, D.R.; Leitao, S.G.; Assis, I.M.; Veiga, V.F.; Lourenco, M.C. <i>et al</i>. Essential oils of <i>Protium</i> spp. samples from Amazonian popular markets: Chemical composition, physicochemical parameters and antimicrobial activity. <i>J. Essent. Oil Res</i>. <b>2013</b>, <i>25</i>, 171-178. DOI: <a href="http://dx.doi.org/10.1080/10412905.2012.751055" target="_blank">http://dx.doi.org/10.1080/10412905.2012.751055</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000116&pid=S0120-2804201500020000500025&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>26. Santos, F.A.; Frota, J.T.; Arruda, B.R.; de Melo, T.S.; da Silva, A.A.D.A.; Brito, G.A.D.C. <i>et al</i>. Antihyperglycemic and hypolipidemic effects of &#945;, &#946;-amyrin, a triterpenoid mixture from <i>Protium heptaphyllum</i> in mice. <i>LipidsHealth Dis</i>. <b>2012</b>, <i>11</i>, 98. DOI: <a href="http://dx.doi.org/10.1186/1476-511X-11-98" target="_blank">http://dx.doi.org/10.1186/1476-511X-11-98</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000118&pid=S0120-2804201500020000500026&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>27. Tafurt-Garc&iacute;a, G.; Mu&ntilde;oz-Acevedo, A.; Calvo, A.N.; Jimenez, L.F.; Delgado, W.A. Componentes vol&aacute;tiles de <i>Eriope crassipes, Hyptis conferta, H. dilatata, H. brachiata, H. suaveolens </i>y <i>H. mutabilis</i> (Lamiaceae). <i>Bol. Latinoam. Caribe</i>. <b>2014</b>, <i>13</i>, 254-269.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000120&pid=S0120-2804201500020000500027&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>28. Ferreira, E.C.; Faria, L.C.; Santos, S.C.; Ferri, P.H.; Silva, J.G.; Raula, J.R. Essential oils of <i>Hyptis conferta </i>Pohl e Benth. var.<i> conferta</i> and <i>Hyptis conferta</i> Pohl e Benth var. <i>angustata </i>(Briq.) Pohl ex Harley from Braziliam Cerrado. <i>J. Essent. Oil Res</i>. <b>2005</b>, <i>17</i>, 145-146. DOI: <a href="http://dx.doi.org/10.1080/10412905.2005.9698859" target="_blank">http://dx.doi.org/10.1080/10412905.2005.9698859</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000122&pid=S0120-2804201500020000500028&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>29. Urones, J.G.; Marcos, I.S.; Diez, D.; Cubilla, L.R. Tricyclic diterpenes from <i>Hyptys dilatata</i>. <i>Phytochemistry</i>. <b>1998</b>, <i>48</i>, 1035-1038. DOI: <a href="http://dx.doi.org/10.1016/s0031-9422(97)00997-7" target="_blank">http://dx.doi.org/10.1016/s0031-9422(97)00997-7</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000124&pid=S0120-2804201500020000500029&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>30. Pereda-Miranda, R.; Gasc&oacute;n-Figueroa, M. Chemistry of <i>Hyptis mutabilis</i>: New pentacyclic triterpenoids. <i>J. Nat. Prod</i>. <b>1988</b>, <i>51</i>, 996-998. DOI: <a href="http://dx.doi.org/10.1021/np50059a035" target="_blank">http://dx.doi.org/10.1021/np50059a035</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000126&pid=S0120-2804201500020000500030&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>31. Pachkore, G.L.; Dhale, D.A.; Dharasurkar, A.N. Antimicrobial and phytochemical screening of <i>Hyptis suaveolens</i> (L. Poit) Lamiaceae. <i>Internat Multidiscipl Res J</i>. <b>2011</b>, <i>1/4</i>,1-3.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000128&pid=S0120-2804201500020000500031&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>32. Barbosa, L.C.; Martins, F.; Texeira, R.; Polo, M.; Montanari, R. Chemical variability and biological activities of volatile oils from <i>H suaveolens</i> (L.) Poit. <i>Agric. Conspec. Sci</i>. <b>2013</b>, <i>78</i>, 1-10.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000130&pid=S0120-2804201500020000500032&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>33. Mukherjee, K.S.; Mukherjee, R.K.; Ghosh, P.K. Chemistry of <i>Hyptis suaveolens</i>: a pentacyclic triterpene. <i>J. Nat. Prod</i>. <b>1984</b>, <i>47</i>, 377-378. DOI: <a href="http://dx.doi.org/10.1021/np50032a025" target="_blank">http://dx.doi.org/10.1021/np50032a025</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000132&pid=S0120-2804201500020000500033&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>34. Taylor, P.; Arsenak, M.; Abad, M.J.; Fernandez, A.; Milano, B.; Gonto, R. <i>et al.</i> Screening of Venezuelan medicinal plant extracts for cytostatic and cytotoxic activity against tumor cell lines. <i>Phytother Res</i>. <b>2013</b>, <i>27</i>, 530-539. DOI: <a href="http://dx.doi.org/10.1002/ptr.4752" target="_blank">http://dx.doi.org/10.1002/ptr.4752</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000134&pid=S0120-2804201500020000500034&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>35. Ziegler, H.L.; Jensen, T.H.; Christensen, J.; Staerk, D.; Hagerstrand, H.; Sittic, A.A.; <i>et al</i>. Possible artifacts in the <i>in vitro</i> determination of antimalarial activity of natural products that incorporate into lipid bilayer: apparent antiplasmodial activity of dehydroabietinol, a constituent of <i>Hyptis suaveolens</i>. <i>Planta Med</i>. <b>2002</b>, <i>68</i>, 547-549. DOI: <a href="http://dx.doi.org/10.1055/s-2002-32548" target="_blank">http://dx.doi.org/10.1055/s-2002-32548</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000136&pid=S0120-2804201500020000500035&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>36. Andrei, C.C.; Braz-Filho, R.; Gottlieb, O.R. Allylphenols from <i>Ocotea cymbarum</i>. <i>Phytochemistry</i>. <b>1988</b>, <i>27</i>, 3992-3993. DOI: <a href="http://dx.doi.org/10.1016/0031-9422(88)83069-3" target="_blank">http://dx.doi.org/10.1016/0031-9422(88)83069-3</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000138&pid=S0120-2804201500020000500036&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>37. Brooks, C.J.W.; Campbell, M.M. Caparrapi oxide, a sesquiterpene from caparrapi oil. <i>Phytochemistry</i>. <b>1969</b>, <i>8</i>, 215-218. DOI: <a href="http://dx.doi.org/10.1016/s0031-9422(00)85815-x" target="_blank">http://dx.doi.org/10.1016/s0031-9422(00)85815-x</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000140&pid=S0120-2804201500020000500037&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>38. Castro, R.D.; Lima, E.O. Atividade antif&uacute;ngica dos &oacute;leos essenciais de sassafr&aacute;s (<i>Ocotea odorifera</i> Vell.) e alecrim (<i>Rosmarinus officinalis</i> L.) sobre o g&ecirc;nero <i>Candida</i>. <i>Rev. Bras. Pl. Med</i>. <b>2011</b>, <i>13</i>, 203-208. DOI: <a href="http://dx.doi.org/10.1590/s1516-05722011000200012" target="_blank">http://dx.doi.org/10.1590/s1516-05722011000200012</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000142&pid=S0120-2804201500020000500038&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p>39. Pab&oacute;n, L.C.; Cuca, L.E. Aporphine alkaloids from <i>Ocotea macrophylla</i> (Lauraceae). <i>Quim. Nova</i>. <b>2010</b>, <i>33</i>, 875-879. DOI: <a href="http://dx.doi.org/10.1590/s0100-40422010000400021" target="_blank">http://dx.doi.org/10.1590/s0100-40422010000400021</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000143&pid=S0120-2804201500020000500039&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>40. Garcez, F.R.; da Silva, A.F.G.; Garcez, W.S.; Linck, G.; Matos, M.D.C.; Santos, E.C.S.; <i>et al.</i> Cytotoxic aporphine alkaloids from <i>Ocotea acutifolia</i>. <i>Planta Med</i>. <b>2011</b>, <i>77</i>, 383-387. DOI: <A href="http://dx.doi.org/10.1055/s-0030-1250401" target="_blank"> http://dx.doi.org/10.1055/s-0030-1250401</A>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000145&pid=S0120-2804201500020000500040&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>41. Neto, R.L.M.; Sousa, L.M.A.; Dias, C.S.; Barbosa, J.M.; Oliveira, M.R.; Figueiredo, R.C.B.Q. Morphological and physiological changes in Leishmania promastigotes induced by yangambin, a lignan obtained from <i>Ocotea duckei</i>. <i>Exp. Parasitol</i>. <b>2011</b>, <i>127</i>, 215-221. DOI: <a href="http://dx.doi.org/10.1016/j.exppara.2010.07.020" target="_blank">http://dx.doi.org/10.1016/j.exppara.2010.07.020</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000147&pid=S0120-2804201500020000500041&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>    </font>      ]]></body><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Fernández-Alonso]]></surname>
<given-names><![CDATA[J.L]]></given-names>
</name>
<name>
<surname><![CDATA[Rivera-Diaz]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
</person-group>
<article-title xml:lang="es"><![CDATA[Las labiadas. En Libro rojo de plantas de Colombia. Volumen 3: Las bromelias, las labiadas y las pasifloras]]></article-title>
<person-group person-group-type="editor">
<name>
<surname><![CDATA[García]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Galeano]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
</person-group>
<source><![CDATA[Serie Libros Rojos de Especies Amenazadas de Colombia]]></source>
<year>2006</year>
<page-range>385-679</page-range><publisher-loc><![CDATA[Bogotá ]]></publisher-loc>
<publisher-name><![CDATA[Instituto Alexander von Humboldt-Instituto de Ciencias Naturales de la Universidad de Colombia-Ministerio de Ambiente, Vivienda y Desarrollo Territorial]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Matkowski]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Piotrowska]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antioxidant and free radical scavenging activities of some medicinal plants from the Lamiaceae]]></article-title>
<source><![CDATA[Fitoterapia]]></source>
<year>2006</year>
<numero>77</numero>
<issue>77</issue>
<page-range>346-353</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Birkett]]></surname>
<given-names><![CDATA[M.A]]></given-names>
</name>
<name>
<surname><![CDATA[Bruce]]></surname>
<given-names><![CDATA[T.J.A]]></given-names>
</name>
<name>
<surname><![CDATA[Pickett]]></surname>
<given-names><![CDATA[J.A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Repellent activity of Nepeta grandiflora and Nepeta clarkei (Lamiaceae) against the cereal aphid, Sitobion avenae (Homoptera: Aphididae)]]></article-title>
<source><![CDATA[Phytochem. Lett]]></source>
<year>2010</year>
<volume>3</volume>
<page-range>139-142</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Valant-Vetschera]]></surname>
<given-names><![CDATA[K.M]]></given-names>
</name>
<name>
<surname><![CDATA[Roitman]]></surname>
<given-names><![CDATA[J.N]]></given-names>
</name>
<name>
<surname><![CDATA[Wollenweber]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Chemodiversity of exudate flavonoids in some members of the Lamiaceae]]></article-title>
<source><![CDATA[Biochem. Syst. Ecol]]></source>
<year>2003</year>
<volume>31</volume>
<page-range>1279-1289</page-range></nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Gillij]]></surname>
<given-names><![CDATA[Y.G]]></given-names>
</name>
<name>
<surname><![CDATA[Gleiser]]></surname>
<given-names><![CDATA[R.M]]></given-names>
</name>
<name>
<surname><![CDATA[Zygadlo]]></surname>
<given-names><![CDATA[J.A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Mosquito repellent activity of essential oils of aromatic plants growing in Argentina]]></article-title>
<source><![CDATA[Bioresour Technol]]></source>
<year>2008</year>
<volume>99</volume>
<page-range>2507-2515</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Krishnamurthy]]></surname>
<given-names><![CDATA[Y.L]]></given-names>
</name>
<name>
<surname><![CDATA[Shashikala]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Shankar]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antifungal potential of some natural products against Aspergillus flavus in soybean seeds during storage]]></article-title>
<source><![CDATA[J. Stored Prod. Res]]></source>
<year>2008</year>
<volume>44</volume>
<page-range>305-309</page-range></nlm-citation>
</ref>
<ref id="B7">
<label>7</label><nlm-citation citation-type="">
<collab>Colombian National Herbarium</collab>
<source><![CDATA[Institute of Natural Sciences (ICN)]]></source>
<year></year>
</nlm-citation>
</ref>
<ref id="B8">
<label>8</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Oliveira]]></surname>
<given-names><![CDATA[F.A]]></given-names>
</name>
<name>
<surname><![CDATA[Vieira-Junior]]></surname>
<given-names><![CDATA[G.M]]></given-names>
</name>
<name>
<surname><![CDATA[Chaves]]></surname>
<given-names><![CDATA[M.H]]></given-names>
</name>
<name>
<surname><![CDATA[Almeida]]></surname>
<given-names><![CDATA[F.R.C]]></given-names>
</name>
<name>
<surname><![CDATA[Santos]]></surname>
<given-names><![CDATA[K.A]]></given-names>
</name>
<name>
<surname><![CDATA[Martins]]></surname>
<given-names><![CDATA[F.S]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Gastroprotective effect of the mixture of &#945;- and &#946;-amyrin from Protium heptaphyllum: Role of capsaicin-sensitive primary afferent neurons]]></article-title>
<source><![CDATA[Planta Med]]></source>
<year>2004</year>
<volume>70</volume>
<page-range>780-782</page-range></nlm-citation>
</ref>
<ref id="B9">
<label>9</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Romin]]></surname>
<given-names><![CDATA[T.L]]></given-names>
</name>
<name>
<surname><![CDATA[Weber]]></surname>
<given-names><![CDATA[N.D]]></given-names>
</name>
<name>
<surname><![CDATA[Murray]]></surname>
<given-names><![CDATA[B.K]]></given-names>
</name>
<name>
<surname><![CDATA[North]]></surname>
<given-names><![CDATA[J.A]]></given-names>
</name>
<name>
<surname><![CDATA[Wood]]></surname>
<given-names><![CDATA[S.G]]></given-names>
</name>
<name>
<surname><![CDATA[Hughes]]></surname>
<given-names><![CDATA[B.G]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antiviral activity of panamanian plant extracts]]></article-title>
<source><![CDATA[Phytother. Res]]></source>
<year>1992</year>
<volume>6</volume>
<page-range>38-43</page-range></nlm-citation>
</ref>
<ref id="B10">
<label>10</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Van der Werff]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[A synopsis of Ocotea (Lauraceae) in Central America and southern Mexico]]></article-title>
<source><![CDATA[Ann. Missouri Bot. Gard]]></source>
<year>2002</year>
<volume>89</volume>
<page-range>429-451</page-range></nlm-citation>
</ref>
<ref id="B11">
<label>11</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[De Camargo]]></surname>
<given-names><![CDATA[M.J]]></given-names>
</name>
<name>
<surname><![CDATA[Dantas]]></surname>
<given-names><![CDATA[M.L]]></given-names>
</name>
<name>
<surname><![CDATA[Miyuki]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Delphino]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Rodrigues]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Silva]]></surname>
<given-names><![CDATA[W]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Sesquiterpenos de Ocotea lancifolia (Lauraceae)]]></article-title>
<source><![CDATA[Quim. Nova]]></source>
<year>2013</year>
<volume>36</volume>
<page-range>1008-1013</page-range></nlm-citation>
</ref>
<ref id="B12">
<label>12</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Guerrini]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Moreno]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Sacchetti]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Muzzoli]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Medici]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Besco]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Composition of the volatile fraction of Ocotea bofo Kunth (Lauraceae) calyces by GC-MS and NMR fingerprinting and its antimicrobial and antioxidant activity]]></article-title>
<source><![CDATA[J. Agric. Food Chem]]></source>
<year>2006</year>
<volume>54</volume>
<page-range>7778-7788</page-range></nlm-citation>
</ref>
<ref id="B13">
<label>13</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Niño]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Correa]]></surname>
<given-names><![CDATA[Y.M]]></given-names>
</name>
<name>
<surname><![CDATA[Mosquera]]></surname>
<given-names><![CDATA[O.M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[In vitro evaluation of Colombian plant extracts against Black Sigatoka (Mycosphaerella fijiensis Morelet)]]></article-title>
<source><![CDATA[Arch. Phytopathol Pfl]]></source>
<year>2011</year>
<volume>44</volume>
<page-range>791-803</page-range></nlm-citation>
</ref>
<ref id="B14">
<label>14</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zschocke]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Drewes]]></surname>
<given-names><![CDATA[S.E]]></given-names>
</name>
<name>
<surname><![CDATA[Paulus]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Bauer]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[van Staden]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Analytical and pharmacological investigation of Ocotea bullata (black stinkwood) bark and leaves]]></article-title>
<source><![CDATA[J. Ethnopharmacol]]></source>
<year>2000</year>
<volume>71</volume>
<page-range>219-230</page-range></nlm-citation>
</ref>
<ref id="B15">
<label>15</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ballabeni]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
<name>
<surname><![CDATA[Tognolini]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Bertoni]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Bruni]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Guerrini]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Rueda]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antiplatelet and antithrombotic activities of essential oil from wild Ocotea quixos (Lam.) Kosterm. (Lauraceae) calices from Amazonian Ecuador]]></article-title>
<source><![CDATA[Pharmacol. Res]]></source>
<year>2007</year>
<volume>55</volume>
<page-range>23-30</page-range></nlm-citation>
</ref>
<ref id="B16">
<label>16</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Re]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Pellegrini]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Proteggente]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Pannala]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Yang]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Rice-Evans]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antioxidant activity applying an improved ABTS radical cation decolorization assay]]></article-title>
<source><![CDATA[Free Radical Biol Med]]></source>
<year>1999</year>
<volume>26</volume>
<page-range>1231-1237</page-range></nlm-citation>
</ref>
<ref id="B17">
<label>17</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Brand-Williams]]></surname>
<given-names><![CDATA[W]]></given-names>
</name>
<name>
<surname><![CDATA[Cuvelier]]></surname>
<given-names><![CDATA[M.E]]></given-names>
</name>
<name>
<surname><![CDATA[Berset]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Use of a free radical method to evaluate antioxidant activity]]></article-title>
<source><![CDATA[Lebensm Wiss Technol]]></source>
<year>1995</year>
<volume>28</volume>
<page-range>25-30</page-range></nlm-citation>
</ref>
<ref id="B18">
<label>18</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dastmalchi]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Dorman]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Kosarb]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Hiltunen]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Chemical composition and in vitro antioxidant evaluation of a watersoluble Moldavian balm (Dracocephalum moldavica L.) extract]]></article-title>
<source><![CDATA[LWT]]></source>
<year>2007</year>
<numero>40</numero>
<issue>40</issue>
<page-range>239-248</page-range></nlm-citation>
</ref>
<ref id="B19">
<label>19</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Reddy]]></surname>
<given-names><![CDATA[M.K]]></given-names>
</name>
<name>
<surname><![CDATA[Gupta]]></surname>
<given-names><![CDATA[S.K]]></given-names>
</name>
<name>
<surname><![CDATA[Jacob]]></surname>
<given-names><![CDATA[M.R]]></given-names>
</name>
<name>
<surname><![CDATA[Khan]]></surname>
<given-names><![CDATA[S.I]]></given-names>
</name>
<name>
<surname><![CDATA[Ferreira]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antioxidant, antimalarial and antimicrobial activities of tannin-rich fractions, ellagitannins and phenolic acids from Punica granatum L]]></article-title>
<source><![CDATA[Planta Med]]></source>
<year>2007</year>
<volume>73</volume>
<page-range>461-467</page-range></nlm-citation>
</ref>
<ref id="B20">
<label>20</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Su]]></surname>
<given-names><![CDATA[J.D]]></given-names>
</name>
<name>
<surname><![CDATA[Osawa]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Kawakishi]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Namiki]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Tannin antioxidants from Osbeckia chinensis]]></article-title>
<source><![CDATA[Phytochemistry]]></source>
<year>1988</year>
<numero>27</numero>
<issue>27</issue>
<page-range>1315-1319</page-range></nlm-citation>
</ref>
<ref id="B21">
<label>21</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rudiger]]></surname>
<given-names><![CDATA[A.L]]></given-names>
</name>
<name>
<surname><![CDATA[Veiga]]></surname>
<given-names><![CDATA[V.F]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Chemodiversity of ursane- and oleanane-type triterpenes in Amazonian Burseraceae oleoresins]]></article-title>
<source><![CDATA[Chem. Biodivers]]></source>
<year>2013</year>
<volume>10</volume>
<page-range>1142-1153</page-range></nlm-citation>
</ref>
<ref id="B22">
<label>22</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[De Carvalho]]></surname>
<given-names><![CDATA[L.E]]></given-names>
</name>
<name>
<surname><![CDATA[Pinto]]></surname>
<given-names><![CDATA[D.D]]></given-names>
</name>
<name>
<surname><![CDATA[Lima]]></surname>
<given-names><![CDATA[M.D]]></given-names>
</name>
<name>
<surname><![CDATA[Marques]]></surname>
<given-names><![CDATA[M.O.M]]></given-names>
</name>
<name>
<surname><![CDATA[Facanali]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The chemistry of essential oils of Crepidospermum rhoifolium, Trattinnickia rhoifolia and Protium elegans of the Amazon region]]></article-title>
<source><![CDATA[J. Essent. Oil Bear Pl]]></source>
<year>2009</year>
<volume>12</volume>
<page-range>92-96</page-range></nlm-citation>
</ref>
<ref id="B23">
<label>23</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zoghbi]]></surname>
<given-names><![CDATA[M.G.B]]></given-names>
</name>
<name>
<surname><![CDATA[Andrade]]></surname>
<given-names><![CDATA[E.H.A]]></given-names>
</name>
<name>
<surname><![CDATA[Santos]]></surname>
<given-names><![CDATA[A.S]]></given-names>
</name>
<name>
<surname><![CDATA[Luzb]]></surname>
<given-names><![CDATA[A.I.R]]></given-names>
</name>
<name>
<surname><![CDATA[Maia]]></surname>
<given-names><![CDATA[JGS]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Volatile constituents of the resins from Protium subserratum (Engl.) Engl. and Tetragastris panamensis (Engl.) Kuntz]]></article-title>
<source><![CDATA[J Essent Oil Res]]></source>
<year>1998</year>
<volume>10</volume>
<page-range>325-326</page-range></nlm-citation>
</ref>
<ref id="B24">
<label>24</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Vechia]]></surname>
<given-names><![CDATA[L.D]]></given-names>
</name>
<name>
<surname><![CDATA[Gnoatto]]></surname>
<given-names><![CDATA[S.C.B]]></given-names>
</name>
<name>
<surname><![CDATA[Gosmann]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Derivados oleananos e ursanos e sua importancia na descoberta de novos fármacos com atividade antitumoral, anti-inflamatória e antioxidante]]></article-title>
<source><![CDATA[Quim. Nova]]></source>
<year>2009</year>
<volume>32</volume>
<page-range>1245-1252</page-range></nlm-citation>
</ref>
<ref id="B25">
<label>25</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Da Silva]]></surname>
<given-names><![CDATA[E.R]]></given-names>
</name>
<name>
<surname><![CDATA[Oliveira]]></surname>
<given-names><![CDATA[D.R]]></given-names>
</name>
<name>
<surname><![CDATA[Leitao]]></surname>
<given-names><![CDATA[S.G]]></given-names>
</name>
<name>
<surname><![CDATA[Assis]]></surname>
<given-names><![CDATA[I.M]]></given-names>
</name>
<name>
<surname><![CDATA[Veiga]]></surname>
<given-names><![CDATA[V.F]]></given-names>
</name>
<name>
<surname><![CDATA[Lourenco]]></surname>
<given-names><![CDATA[M.C]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Essential oils of Protium spp. samples from Amazonian popular markets: Chemical composition, physicochemical parameters and antimicrobial activity]]></article-title>
<source><![CDATA[J. Essent. Oil Res]]></source>
<year>2013</year>
<volume>25</volume>
<page-range>171-178</page-range></nlm-citation>
</ref>
<ref id="B26">
<label>26</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Santos]]></surname>
<given-names><![CDATA[F.A]]></given-names>
</name>
<name>
<surname><![CDATA[Frota]]></surname>
<given-names><![CDATA[J.T]]></given-names>
</name>
<name>
<surname><![CDATA[Arruda]]></surname>
<given-names><![CDATA[B.R]]></given-names>
</name>
<name>
<surname><![CDATA[de Melo]]></surname>
<given-names><![CDATA[T.S]]></given-names>
</name>
<name>
<surname><![CDATA[da Silva]]></surname>
<given-names><![CDATA[A.A.D.A]]></given-names>
</name>
<name>
<surname><![CDATA[Brito]]></surname>
<given-names><![CDATA[G.A.D.C]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antihyperglycemic and hypolipidemic effects of &#945;, &#946;-amyrin, a triterpenoid mixture from Protium heptaphyllum in mice]]></article-title>
<source><![CDATA[LipidsHealth Dis]]></source>
<year>2012</year>
<volume>11</volume>
<page-range>98</page-range></nlm-citation>
</ref>
<ref id="B27">
<label>27</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Tafurt-García]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Muñoz-Acevedo]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Calvo]]></surname>
<given-names><![CDATA[A.N]]></given-names>
</name>
<name>
<surname><![CDATA[Jimenez]]></surname>
<given-names><![CDATA[L.F]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[W.A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Componentes volátiles de Eriope crassipes, Hyptis conferta, H. dilatata, H. brachiata, H. suaveolens y H. mutabilis (Lamiaceae)]]></article-title>
<source><![CDATA[Bol. Latinoam. Caribe]]></source>
<year>2014</year>
<volume>13</volume>
<page-range>254-269</page-range></nlm-citation>
</ref>
<ref id="B28">
<label>28</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ferreira]]></surname>
<given-names><![CDATA[E.C]]></given-names>
</name>
<name>
<surname><![CDATA[Faria]]></surname>
<given-names><![CDATA[L.C]]></given-names>
</name>
<name>
<surname><![CDATA[Santos]]></surname>
<given-names><![CDATA[S.C]]></given-names>
</name>
<name>
<surname><![CDATA[Ferri]]></surname>
<given-names><![CDATA[P.H]]></given-names>
</name>
<name>
<surname><![CDATA[Silva]]></surname>
<given-names><![CDATA[J.G]]></given-names>
</name>
<name>
<surname><![CDATA[Raula]]></surname>
<given-names><![CDATA[J.R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Essential oils of Hyptis conferta Pohl e Benth. var. conferta and Hyptis conferta Pohl e Benth var. angustata (Briq.) Pohl ex Harley from Braziliam Cerrado]]></article-title>
<source><![CDATA[J. Essent. Oil Res]]></source>
<year>2005</year>
<volume>17</volume>
<page-range>145-146</page-range></nlm-citation>
</ref>
<ref id="B29">
<label>29</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Urones]]></surname>
<given-names><![CDATA[J.G]]></given-names>
</name>
<name>
<surname><![CDATA[Marcos]]></surname>
<given-names><![CDATA[I.S]]></given-names>
</name>
<name>
<surname><![CDATA[Diez]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Cubilla]]></surname>
<given-names><![CDATA[L.R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Tricyclic diterpenes from Hyptys dilatata]]></article-title>
<source><![CDATA[Phytochemistry]]></source>
<year>1998</year>
<volume>48</volume>
<page-range>1035-1038</page-range></nlm-citation>
</ref>
<ref id="B30">
<label>30</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pereda-Miranda]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Gascón-Figueroa]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Chemistry of Hyptis mutabilis: New pentacyclic triterpenoids]]></article-title>
<source><![CDATA[J. Nat. Prod]]></source>
<year>1988</year>
<volume>51</volume>
<page-range>996-998</page-range></nlm-citation>
</ref>
<ref id="B31">
<label>31</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pachkore]]></surname>
<given-names><![CDATA[G.L]]></given-names>
</name>
<name>
<surname><![CDATA[Dhale]]></surname>
<given-names><![CDATA[D.A]]></given-names>
</name>
<name>
<surname><![CDATA[Dharasurkar]]></surname>
<given-names><![CDATA[A.N]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antimicrobial and phytochemical screening of Hyptis suaveolens (L. Poit) Lamiaceae]]></article-title>
<source><![CDATA[Internat Multidiscipl Res J]]></source>
<year>2011</year>
<volume>1/4</volume>
<page-range>1-3</page-range></nlm-citation>
</ref>
<ref id="B32">
<label>32</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Barbosa]]></surname>
<given-names><![CDATA[L.C]]></given-names>
</name>
<name>
<surname><![CDATA[Martins]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Texeira]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Polo]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Montanari]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Chemical variability and biological activities of volatile oils from H suaveolens (L.) Poit]]></article-title>
<source><![CDATA[Agric. Conspec. Sci]]></source>
<year>2013</year>
<volume>78</volume>
<page-range>1-10</page-range></nlm-citation>
</ref>
<ref id="B33">
<label>33</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Mukherjee]]></surname>
<given-names><![CDATA[K.S]]></given-names>
</name>
<name>
<surname><![CDATA[Mukherjee]]></surname>
<given-names><![CDATA[R.K]]></given-names>
</name>
<name>
<surname><![CDATA[Ghosh]]></surname>
<given-names><![CDATA[P.K]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Chemistry of Hyptis suaveolens: a pentacyclic triterpene]]></article-title>
<source><![CDATA[J. Nat. Prod]]></source>
<year>1984</year>
<volume>47</volume>
<page-range>377-378</page-range></nlm-citation>
</ref>
<ref id="B34">
<label>34</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Taylor]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Arsenak]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Abad]]></surname>
<given-names><![CDATA[M.J]]></given-names>
</name>
<name>
<surname><![CDATA[Fernandez]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Milano]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
<name>
<surname><![CDATA[Gonto]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Screening of Venezuelan medicinal plant extracts for cytostatic and cytotoxic activity against tumor cell lines]]></article-title>
<source><![CDATA[Phytother Res]]></source>
<year>2013</year>
<volume>27</volume>
<page-range>530-539</page-range></nlm-citation>
</ref>
<ref id="B35">
<label>35</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ziegler]]></surname>
<given-names><![CDATA[H.L]]></given-names>
</name>
<name>
<surname><![CDATA[Jensen]]></surname>
<given-names><![CDATA[T.H]]></given-names>
</name>
<name>
<surname><![CDATA[Christensen]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Staerk]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Hagerstrand]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Sittic]]></surname>
<given-names><![CDATA[A.A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Possible artifacts in the in vitro determination of antimalarial activity of natural products that incorporate into lipid bilayer: apparent antiplasmodial activity of dehydroabietinol, a constituent of Hyptis suaveolens]]></article-title>
<source><![CDATA[Planta Med]]></source>
<year>2002</year>
<volume>68</volume>
<page-range>547-549</page-range></nlm-citation>
</ref>
<ref id="B36">
<label>36</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Andrei]]></surname>
<given-names><![CDATA[C.C]]></given-names>
</name>
<name>
<surname><![CDATA[Braz-Filho]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Gottlieb]]></surname>
<given-names><![CDATA[O.R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Allylphenols from Ocotea cymbarum]]></article-title>
<source><![CDATA[Phytochemistry]]></source>
<year>1988</year>
<volume>27</volume>
<page-range>3992-3993</page-range></nlm-citation>
</ref>
<ref id="B37">
<label>37</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Brooks]]></surname>
<given-names><![CDATA[C.J.W]]></given-names>
</name>
<name>
<surname><![CDATA[Campbell]]></surname>
<given-names><![CDATA[M.M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Caparrapi oxide, a sesquiterpene from caparrapi oil]]></article-title>
<source><![CDATA[Phytochemistry]]></source>
<year>1969</year>
<volume>8</volume>
<page-range>215-218</page-range></nlm-citation>
</ref>
<ref id="B38">
<label>38</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Castro]]></surname>
<given-names><![CDATA[R.D]]></given-names>
</name>
<name>
<surname><![CDATA[Lima]]></surname>
<given-names><![CDATA[E.O]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Atividade antifúngica dos óleos essenciais de sassafrás (Ocotea odorifera Vell.) e alecrim (Rosmarinus officinalis L.) sobre o gênero Candida]]></article-title>
<source><![CDATA[Rev. Bras. Pl. Med]]></source>
<year>2011</year>
<volume>13</volume>
<page-range>203-208</page-range></nlm-citation>
</ref>
<ref id="B39">
<label>39</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pabón]]></surname>
<given-names><![CDATA[L.C]]></given-names>
</name>
<name>
<surname><![CDATA[Cuca]]></surname>
<given-names><![CDATA[L.E]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Aporphine alkaloids from Ocotea macrophylla (Lauraceae)]]></article-title>
<source><![CDATA[Quim. Nova]]></source>
<year>2010</year>
<volume>33</volume>
<page-range>875-879</page-range></nlm-citation>
</ref>
<ref id="B40">
<label>40</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Garcez]]></surname>
<given-names><![CDATA[F.R]]></given-names>
</name>
<name>
<surname><![CDATA[da Silva]]></surname>
<given-names><![CDATA[A.F.G]]></given-names>
</name>
<name>
<surname><![CDATA[Garcez]]></surname>
<given-names><![CDATA[W.S]]></given-names>
</name>
<name>
<surname><![CDATA[Linck]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Matos]]></surname>
<given-names><![CDATA[M.D.C]]></given-names>
</name>
<name>
<surname><![CDATA[Santos]]></surname>
<given-names><![CDATA[E.C.S]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Cytotoxic aporphine alkaloids from Ocotea acutifolia]]></article-title>
<source><![CDATA[Planta Med]]></source>
<year>2011</year>
<volume>77</volume>
<page-range>383-387</page-range></nlm-citation>
</ref>
<ref id="B41">
<label>41</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Neto]]></surname>
<given-names><![CDATA[R.L.M]]></given-names>
</name>
<name>
<surname><![CDATA[Sousa]]></surname>
<given-names><![CDATA[L.M.A]]></given-names>
</name>
<name>
<surname><![CDATA[Dias]]></surname>
<given-names><![CDATA[C.S]]></given-names>
</name>
<name>
<surname><![CDATA[Barbosa]]></surname>
<given-names><![CDATA[J.M]]></given-names>
</name>
<name>
<surname><![CDATA[Oliveira]]></surname>
<given-names><![CDATA[M.R]]></given-names>
</name>
<name>
<surname><![CDATA[Figueiredo]]></surname>
<given-names><![CDATA[R.C.B.Q]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Morphological and physiological changes in Leishmania promastigotes induced by yangambin, a lignan obtained from Ocotea duckei. Exp]]></article-title>
<source><![CDATA[Parasitol]]></source>
<year>2011</year>
<volume>127</volume>
<page-range>215-221</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
