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                <text>&lt;strong&gt;Synthesis, solid-state characterization and solution studies of new phytate compounds with Cu(II) and 1,10-phenanthroline: progress in the structural elucidation of phytate coordinating ability&lt;/strong&gt;</text>
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                <text>Within all the eukaryotic cells there is an important group of biomolecules that has been potentially related to signalling functions: myo-inositol phosphates (InsPs). In nature, the most abundant member of this family is the so called phytate (InsP6, L12&amp;minus;). The importance of the interaction of InsP6 with cations has been recognized during the last few years, and any attempt to know the function of this molecule in eukaryotic cells must include the fact that InsP6 will be strongly associated with simple inorganic or organic ammonium cations. In this work we expand on our earlier findings by studying the systems phen&amp;ndash;phytate (phen = 1,10-phenanthroline) and Cu(II)&amp;ndash;phen&amp;ndash;phytate. The structures of (Hphen)4(H8L)&amp;middot;7.5H2O and [Cu5(H7L)2(H2O)2(phen)5]&amp;middot;23H2O are presented. Solution studies of the binary and ternary systems were also performed by means of potentiometric titrations at 37.0 &amp;deg;C and 0.15 M ionic strength. The work was completed with a molecular modelling study. All this information is essential in the process of gaining reliable structural knowledge about the most important InsP6 species in the in vitro and in vivo experiments, and how these features modulate their probable biological functions.</text>
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                <text>Dalton Transactions v. 45, no. 30, 2016. -- p. 12156-12166</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt; La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Synthesis, spectroscopic characterization and crystal structure of [ReV(O)2(pyz)4][ReII(NO)Br4(pyz)] (pyz = pyrazine)&lt;/strong&gt;</text>
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                <text>A novel Re(V)-Re(II) nitrosyl complex, [Re(O)2(pyz)4][Re(NO)Br4(pyz)] (pyz = pyrazine) was prepared and characterized by X-ray diffraction, elemental analysis, infrared and ultraviolet-visible absorption spectra. This product is obtained in the initial steps of the reaction of (NBu4)[Re(NO)Br4(EtOH)] with pyrazine. Both, the cation and the anion are mononuclear complexes. The Re(V) atom in the cation is six-coordinate with four nitrogen atoms from pyrazine ligands, and two oxo ligands. The Re(II) anion is also six-coordinate, with four bromide ligands, a linear nitrosyl group and one nitrogen from pyrazine. The spectroscopic studies are discussed and compared with those already reported separately for the cation and the anion.</text>
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                <text>&lt;strong&gt;Pacheco, Mario&lt;/strong&gt;</text>
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                <text>Communication in Inorganic Synthesis v. 2, no. 2, 2014. -- p. 20-24</text>
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                <text>LatinAmerican Research Group</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Synthesis, spectroscopic characterization and structural study of 2- isopropenyl-3-methylphenol, carquejiphenol, a carquejol derivative with potential medicinal use&lt;/strong&gt;</text>
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                <text>In this work, 2-isopropenyl-3-methylphenol, hereafter referred to as carquejiphenol (CARP), a minor component of &amp;ldquo;carqueja&amp;rdquo; essential oil, was synthesized starting from carquejol and characterized by using Fourier Transform infrared (FT-IR) and Raman (FT-Raman) spectroscopies, Ultraviolet&amp;ndash;Visible (UV&amp;ndash;Visible) spectroscopy, Electron Impact Mass spectrometry (EI-MS), Hydrogen and Carbon Nuclear Magnetic Resonance (1H- and 13C-NMR) and 2D 1H1H gCOSY, 1H13C gHSQC, 1H13C gHMBC experiments. A very good correlation between the predicted FTIR, FTRaman, UV&amp;ndash;visible and 1H13C-NMR spectra for monomer and dimer of CARP by using theoretical B3LYP/6-31G* and 6-311++G** calculations with the corresponding experimental ones was observed. The solvation energies for CARP were predicted by using both levels of calculations and considering the solvent effects with the polarised continuum and solvation models. The increase in volume in solution supports the H bonds formation due to the presence in its structure of an OH group, as revealed by atoms in molecules (AIM) analysis. A high stability for CARP was found by using natural bond orbital (NBO) and AIM studies, while the investigation of the frontier orbitals reveals that CARP is more reactive than carquejol and N-(3,4-dimethoxybenzyl)-hexadecanamide but less reactive than the sesquiterpene lactone cnicin. The proximity of both the electrophilicy and nucleophilicity index of CARP with those obtained respectively for carquejol and for N-(3,4-dimethoxybenzyl)-hexadecanamide, suggests that CARP could probably present pharmacological properties. The scaled quantum mechanical force field (SQMFF) methodology was used to compute the harmonic force fields and to perform the complete vibrational analysis. In this way, 63 normal modes of vibration were assigned and compared with other terpene substances.</text>
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                <text>&lt;strong&gt;Minteguiaga, Manue&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Brand&amp;aacute;n, Silvia Antonia&lt;/strong&gt;</text>
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                <text>&lt;p&gt;Journal of Molecular Structure |g v. 1165, 2018. --&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; p. 332-343&lt;/p&gt;</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt; La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt; ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>DOI: 10.1016/j.molstruc.2018.04.001</text>
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                <text>&lt;strong&gt;Synthesis, structural and magnetic characterizations of new complexes of di-2,6-(2-pyridylcarbonyl)pyridine (pyCOpyCOpy) ligand&lt;/strong&gt;</text>
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                <text>QUIMICA INORGANICA</text>
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                <text>COMPUESTOS DE COORDINACION</text>
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                <text>Using the di-2,6-(2-pyridylcarbonyl)pyridine ligand (L1) as starting framework, five new mononuclear complexes were obtained: [Cu(L1)(MeCN)(ClO4)2] (1) [Co(L1)(MeCN)(Br)2]�MeCN (2), [Fe(L1)2](BF4)2� MeOH�H2O (3), [Cr(L2a)Cl2]�2MeOH (where HL2a is (6-(hydroxyl(methoxy)(pyridin-2-yl)methyl) pyridin-2-yl)(pyridin-2-yl)methanone) (4) and one trinuclear [NiII 3] complex, [Ni3(L2b)2(Bz)2(EtOH)2] (ClO4)2�2EtOH (where HL2b is (6-(hydroxyl(ethoxy)(pyridin-2-yl)methyl)pyridin-2-yl)(pyridin-2-yl) methanone; Bz = benzoato) (5). Their structural and magnetic characterizations are herein reported. All the metal ions show octahedral coordination geometry, which is slightly unusual for the L1-based Cu(II) complex 1. Formation of complexes 4 and 5 is accompanied by the metal-assisted solvent addition to one carbonyl group of the L1 ligand with methanol or ethanol leading to the deprotonated mono-hemiacetals L2a and L2b ligands respectively. The trinuclear [NiII 3] compound 5 shows two different bridging units: two L2b units and two benzoato (Bz) ligands. 5 represents the smallest polynuclear compound in the known {NiII(L1-based)}n (n = 5,6) series. The magnetic properties of the five complexes have been investigated. While compounds 1&amp;ndash;4 show the expected magnetic behavior for mononuclear species, 5 exhibits intramolecular ferromagnetic interactions between the NiII (S = 1) ions stabilizing an ST = 3 ground state.</text>
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                <text>&lt;strong&gt;Calancea, Sergiu&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Pi&amp;ntilde;ero, Dalice&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Poirot, David&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Mathoni&amp;egrave;re, Corine&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Rosa, Patrick&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Cl&amp;eacute;rac, Rodolphe&lt;/strong&gt;</text>
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                <text>Polyhedron v. 64, 2013. -- p. 294-303</text>
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                <text>2013</text>
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            <description>Information about rights held in and over the resource</description>
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              <elementText elementTextId="248145">
                <text>&lt;p&gt;&amp;nbsp;&lt;/p&gt;&#13;
&lt;p align="LEFT"&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
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&lt;p style="margin-bottom: 0cm;"&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Copper coordination complexes are increasingly recognized as potential drugs for therapeutic use in various diseases, especially in cancer. In an attempt to find new leaders for the development of antitumor Cu compounds, heteroleptic Cu(I) complexes with triphenylphosphine (PPh3) and dimethylbipyridine (dmbpy), phenanthroline (phen) or neocuproine (neo) were prepared and characterized. The compounds [CuCl(dmbpy)(PPh3)] (1), [CuCl(phen)(PPh3)]&amp;sdot;0,25H2O (2) and [CuCl(neo)(PPh3)] (3) were obtained. The crystal structures of compounds 2 and 3 were determined. In both complexes, the Cu(I) centre presents distorted tetrahedral coordination. All complexes present cytotoxic activity, against tumor cell lines, being more active than Cisplatin, with IC50 in the low micromolar range. This activity augments in the order 1 &amp;lt; 2 &amp;lt; 3, following the same order as the lipophilicity.</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt; La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Synthesis, structural characterization and cytotoxic activity of ternary copper(II) &amp;ndash; dipeptide &amp;ndash; phenanthroline complexes. A step towards the development of new copper compounds for the treatment of cancer&lt;/strong&gt;</text>
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                <text>In the search for new compounds with antitumor activity, coordination complexes with different metals are being studied by our group. This work presents the synthesis and characterization of six copper complexes with general stoichiometry [Cu(L-dipeptide)(phen)]&amp;middot;nH2O (were phen= 1,10-phenanthroline) and their cytotoxic activities against tumor cell lines. To characterize these systems, analytical and spectroscopic studies were performed in solid state (by UV&amp;ndash;visible, IR, X-ray diffraction) including the crystal structure of four new complexes (of the six complexes studied): [Cu(Ala-Phe)(phen)]&amp;middot;4H2O, [Cu(Phe-Ala)(phen)]&amp;middot;4H2O, [Cu(Phe-Val)(phen)]&amp;middot;4.5H2O and [Cu(Phe-Phe)(phen)]&amp;middot;3H2O. In all of them, the copper ion is situated in a distorted squared pyramidal environment. The phen ligand is perpendicular to the dipeptide, therefore exposed and potentially available for interaction with biological molecules. In addition, for all the studied complexes, structural information in solution using EPR andUV&amp;ndash; visible spectroscopieswere obtained, showing that the coordination observed in solid state ismaintained. The lipophilicity, DNA binding and albumin interaction were also studied. Biological experiments showed that all the complexes induce cell death in the cell lines: HeLa (human cervical adenocarcinoma),MCF-7 (human metastatic breast adenocarcinoma) and A549 (human lung epithelial carcinoma). Among the six complexes, [Cu(Ala-Phe)(phen)] presents the lowest IC50 values. Taken together all these data we hypothesize that [Cu(Ala-Phe)(phen)] may be a good candidate for further studies in vivo.</text>
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                <text>As a part of our studies of copper(II) complexes with possible antitumor activity, the synthesis and structural characterization of two new copper terpyridine (terpy) complexes: [Cu(terpy)(SO4)(H2O)]&amp;middot;2H2O and [Cu2(terpy)2(SO4)2]&amp;middot;4H2O are presented. The crystal structures show that the copper ion in both complexes is in a square pyramidal environment, coordinated equatorially to the terpy N atoms and completing the coordination with O atoms from the sulfate or water molecules. The second compound is a sulfate bridged dinuclear complex. In aqueous solution the coordination scheme is modified. Taking the crystal structure as a starting point the geometries of the complexes were optimized and vibrational spectroscopy calculations were performed allowing an assignation of the experimental IR spectra. Finally, the interaction of the complexes with DNA was studied, by UV titration and docking studies of the complexes. The results suggest that the interaction occur by minor groove interaction and partial insertion of the terpy into the DNA bases and that terpy interaction with DNA is strongly influenced by the Cu-coordination process.</text>
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                <text>The synthesis and spectroscopic characterization (UV&amp;ndash;Vis, IR, EPR) of a new copper complex with a betablocker propranolol (1-(isopropylamino)-3-(1-naphthyloxy)-2-propanol) are presented. Besides, the Xray crystal structure of [Cu(propranolol)2]�2H2O is determined, showing two different copper ions, one coordinated through two S propranolol isomers and the other through two R isomers. The effect on the heart contraction force and on the heart rate plus the block of response to adrenaline of the complex and the free ligand, were studied. The effect of [Cu(propranolol)2]�2H2O on contractility was very similar to that of the free propranolol while the reduction on the heart rate is approximately 30% of the reduction obtained with the free ligand. This is an encouraging result since the search of new beta-blocker drugs that have lesser effect on heart rate is one of the important topics in cardiac pharmacology. The block of the response to adrenaline is at least similar for both ligand and complex.</text>
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                <text>Zinc borates are very important industrial materials with applications that include fire retardants and preservatives in wood. In this work, we report the preparation of three novel zinc borates: [Zn(NH3)3B4O5(OH)4]&amp;middot;H2O (ZB1), Zn3(H2B3O7)2&amp;middot;2NH3&amp;middot;4H2O (ZB2), and [Zn(NH3)4][B4O5(OH)4]&amp;middot;4H2O (ZB3). The solid phases were characterized by elemental analysis, X-ray diffraction, infrared and Raman spectroscopy, scanning electron microscopy and thermal analysis. The crystal structures of ZB1 (monoclinic, Cc, a = 12.1972(8), b = 7.8314(5), c = 12.1441(8) &amp;Aring; and &amp;beta; = 107.404(5)&amp;deg;) and ZB3 (orthorhombic, Pbca, a = 15.0796(9), b = 11.8853(5) and c = 16.7606(8) &amp;Aring;) were determined. They are novel neutral Zn-polyborate complexes [Zn(NH3)3B4O5(OH)4] hydrate and [Zn(NH3)4][B4O5(OH)4] tetrahydrate salt, respectively. The complete assignment of infrared and Raman spectra was performed theoretically using DFT calculations. For ZB2 (obtained as a polycrystalline phase), powder X-ray diffraction confirmed a single phase and allowed the determination of the unit cell parameters and lattice type (rhombohedral, a = 36.78076 (6), c = 12.20052 (3) &amp;Aring;) with an expected formula Zn3(H2B3O7)2&amp;middot;2NH3&amp;middot;4H2O suggesting that this compound is a complex triborate. Furthermore, a low-cost scalable synthetic procedure for ZB1 starting from zinc oxide and boric acid in ammonia solution with a high yield is also reported.</text>
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                <text>&lt;strong&gt;Imer, M. R.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Gonz&amp;aacute;lez, M.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Veiga, Nicolas&lt;/strong&gt;</text>
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                <text>Dalton Transactions&amp;nbsp; v. 46, no. 45, 2017. -- p. 15736-15745</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Synthesis, Structural Characterization, and Pro-apoptotic Activity of 1-Indanone Thiosemicarbazone Platinum(II) and Palladium(II) Complexes: Potential as Antileukemic Agents&lt;/strong&gt;</text>
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                <text>In the search for alternative chemotherapeutic strategies against leukemia, various 1-indanone thiosemicarbazones, as well as eight novel platinum(II) and palladium(II) complexes, with the formula [MCl2(HL)] and [M(HL)(L)]Cl, derived from two 1-indanone thiosemicarbazones were synthesized and tested for antiproliferative activity against the human leukemia U937 cell line. The crystal structure of [Pt(HL1)(L1)]Cl.2MeOH, where L1=1-indanone thiosemicarbazone, was solved by X-ray diffraction. Free thiosemicarbazone ligands showed no antiproliferative effect, but the corresponding platinum(II) and palladium( II) complexes inhibited cell proliferation and induced apoptosis. Platinum(II) complexes also displayed selective apoptotic activity in U937 cells but not in peripheral blood monocytes or the human hepatocellular carcinoma HepG2 cell line used to screen for potential hepatotoxicity. Present findings show that, in U937 cells, 1-indanone thiosemicarbazones coordinated to palladium(II) were more cytotoxic than those complexed with platinum(II), although the latter were found to be more selective for leukemic cells suggesting that they are promising compounds with potential therapeutic application against hematological malignancies.</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Chagas&amp;rsquo; disease, or American trypanosomosiasis, has been the most relevant illness produced by protozoa in Latin America. Synthetic medicinal chemistry efforts have provided an extensive number of chemodiverse hits at the &amp;ldquo;active-to-hit&amp;rdquo; stage. However, only a more limited number of these have been studied in vivo in models of Chagas&amp;rsquo; disease. Herein, we survey some of the cantidates able to surpass the &amp;ldquo;hit-to-lead&amp;rdquo; stage discussing their limitations or merit to enter in clinical trials in the short term.</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>An organocatalyzed asymmetric [4+2]‐cycloaddition between tropolones and electron‐deficient dienophiles is presented. Complex and biologically interesting dihydrohomobarrelenone scaffolds are formed through a Diels‐Alder reaction utilizing bifunctional Br&amp;oslash;nsted‐base catalysis, affording the corresponding bridged bicyclic cycloadducts in up to quantitative yields with good enantio‐ (up to 92% ee) and diastereoselectivity (up to &amp;gt;20:1 d.r.). The synthetic value of the obtained products are explored by downstream transformations, including photoisomerizations, and biological relevancy by in‐vivo testing in MCF‐7 cancer cells.</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Syringic and cinnamic acids antiradical/antioxidant activities as R. ferruginea extract components and membrane physico-chemica&lt;/strong&gt;</text>
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                <text>ACIDO SIRINGICO&#13;
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                <text>RAPANEA FERRUGINEA&#13;
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA&#13;
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                <text>&lt;p&gt;Syringic and cinnamic acids were previously identified as the major components on Rapanea ferruginea0s leaf extract. In this work, these phenolic acids were investigated and correlated in two aspects. The first one was referred to their role against DPPH and hydroxyl radicals, considering the concentration detected in R. ferruginea extract. The second one considered their effects on the physico-chemical properties of soy asolectin liposomes, such as hydration degree, trans-gauche isomerization, vibrational, rotational and translational motions, state-of-phase, size and surface charge. The half-maximum inhibitory concentration (IC50) related to syringic acid in DPPH assays was detected as 7.36 � 10�3 mM.&lt;br /&gt;At the cinnamic acid highest tested concentration (8.23 � 10�3 mM), the activity against DPPH was&lt;br /&gt;around 4.6%. Regarding hydroxyl radical-induced lipid peroxidation, the IC50 detected for syringic acid free in solution (free-form) was equivalent to 0.082 � 10�3 mM, a value 3.6 times lower than the detected for its liposome-loaded form. At the highest tested concentration (0.24 � 10�3 mM), the free-form cinnamic acid inhibited lipid peroxidation by 4 times the observed to its liposome-loaded form. Results showed that hydrogen donation is not the preferential mechanism in which the tested phenolic acids inhibit hydroxyl radical-induced lipid peroxidation. Syringic acid showed higher antioxidant potential than cinnamic acid, probably having a primordial role in the properties related to R. ferruginea. Liposomes&amp;rsquo; physico-chemical data provided correlations between the phenolic acids&amp;rsquo; antioxidant potential and their influence in the mobility of specific lipid groups. The findings of this work will contribute to the design and development of phenolic acids-based and plant extract-based pharmacological systems.&lt;/p&gt;&#13;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&#13;
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                <text>&lt;strong&gt;Magalh&amp;atilde;es dos Santos, Desir&amp;eacute;e&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Paludetto Sanches, Mariele&lt;/strong&gt;&#13;
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                <text>&lt;strong&gt;Sagrera Darelli, Gabriel Jorge&lt;/strong&gt;&#13;
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                <text>&lt;strong&gt;Rodrigues de Lima,&amp;nbsp;&lt;span class="st"&gt;V&amp;acirc;nia&lt;/span&gt;&lt;/strong&gt;&#13;
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                <text>Journal of Molecular Structure v. 1220, 2020. -- p.1-10.--e128749&#13;
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt; (Por favor lea este aviso antes de abrir los documentos u objetos)&lt;strong&gt; La legislaci&amp;oacute;n uruguaya protege el derecho de autor &lt;/strong&gt;sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;&#13;
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                <text>&lt;strong&gt;Systematic Coupled Cluster, Brueckner Coupled Cluster, G3, CBS-QB3, and DFT Investigation of SX Diatomics; X ) First- or Second-Row Atom.&lt;/strong&gt;</text>
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                <text>The SX diatomics, X = first- or second-row atom, have been studied employing coupled cluster theory and the aug-cc-pV(X+d)Z basis sets. To estimate &amp;Delta;fH&amp;deg;298, we have included a correction for core&amp;minus;valence (CV) correlation, spin&amp;minus;orbit splitting, and scalar-relativistic (SR) effects. For SO and SC, the estimated &amp;Delta;fH&amp;deg;298 values are 0.5 kcal/mol within the experiment. However, for the remaining molecules, a revision of their &amp;Delta;H&amp;deg;f,298 are required. Deviations as large as 10 kcal/mol have been found between our best estimates and the values adopted by the NIST-JANAF tables. The proposed &amp;Delta;fH&amp;deg;298 (&amp;plusmn;0.5kcal/mol) are 67.6 (SB), 66.7 (SN), 0.8 (SF), 47.4 (SAl), 27.9 (SSi), 38.1 (SP), 29.4 (S2), and 27.1 (SCl) kcal/mol. For comparative purposes we performed BD(T), G3, CBS-QB3, B3LYP, and B3PW91 calculations. The mean absolute error (MAE) of the G3 and CBS-QB3 &amp;Delta;fH&amp;deg;298 with respect to our best results is 1.0 kcal/mol for both methodologies, whereas for B3LYP/6-311+G(3df) and B3PW91/6-311+G(3df), the MAE is 1.6 and 2.0 kcal/mol, respectively. At the coupled cluster level of theory, with respect to the experiment, the MAE of the equilibrium bond lengths is 0.0013 and 0.0012 &amp;Aring; for the first- and second-row SX, respectively. This result involves extrapolation to the CBS limit, a correction for CV and SR effects, and also a correction for complete triple excitations. Two molecules presented an unstable HF wave function, SN and SP. In both cases, the use of the CCSDT and BD(T) methods outperformed CCSD(T). Our spin&amp;minus;orbit corrected coupled cluster adiabatic electron affinities (EAad) are &amp;plusmn;0.7 kcal/mol within the experiment for SN, SO, SF, and S2. However, some discrepancies were found for SC and SAl. Our best estimates are EAad(SC) = 2.3 kcal/mol and EAad(SAl) = 62.5 kcal/mol, 2.4 and 1.6 kcal/mol larger than the experimental EAad, respectively. For SB, SSi, SP, and SCl, we propose new EAad of 53.7, 12.4, 36.5, and 59.0 kcal/mol, respectively. The MAE of the CBS-QB3 and G3 EAad with respect to our estimated EAad is 0.9 kcal/mol for both methodologies, whereas for B3LYP/6-311+G(3df) and B3PW91/6-311+G(3df), the MAE are 1.9 and 2.7 kcal/mol, respectively, but 50% of the error is provided only by SC and SN. Systematic Coupled Cluster, Brueckner Coupled Cluster, G3, CBS-QB3, and DFT Investigation of SX Diatomics; X = First- or Second-Row Atom - ResearchGate. Available from: http://www.researchgate.net/publication/231639185_Systematic_Coupled_Cluster_Brueckner_Coupled_Cluster_G3_CBS-QB3_and_DFT_Investigation_of_SX_Diatomics_X__First-_or_Second-Row_Atom [accessed Apr 16, 2015].</text>
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                <text>Journal of Physical Chemistry v. 108, 2004. -- p. 11092-11100</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;&#13;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;</text>
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                  <text>Contiene la producción científica nacional de los profesionales químicos e investigadores, durante el período 1929 hasta la fecha.</text>
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          <description>If the image is of an object, state the type of object, such as painting, sculpture, paper, photo, and additional data</description>
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                <text>&lt;strong&gt;T- and pH-Dependent Kinetics of the Reactions of &amp;middot;OH(aq) with Glutaric and Adipic Acid for Atmospheric Aqueous-Phase Chemistry&lt;/strong&gt;</text>
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                <text>ACIDO ADIPICO</text>
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                <text>ACIDO GLUTARICO</text>
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                <text>DFT</text>
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                <text>CINETICA DE COMPETENCIA</text>
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA</text>
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                <text>2021</text>
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                <text>&lt;p&gt;Glutaric acid and adipic acid are dicarboxylic acids (DCAs) that are commonly found in atmospheric aerosols and cloud droplets. Within this study, the temperature- and pH-dependent rate constants of aqueous-phase OH radical reactions&lt;br /&gt;of these two DCAs were determined through the competition kinetics method. The following Arrhenius expressions were derived for the temperature dependency of the OH radical reaction with glutaric acid: k(T, H2A) = (3.9 &amp;plusmn; 0.1) &amp;times; 1010 &amp;times; exp[(&amp;minus;1270 &amp;plusmn; 200 K)/T], k(T, HA&amp;minus;) = (2.3 &amp;plusmn; 0.1) &amp;times; 1011 &amp;times; exp[(&amp;minus;1660 &amp;plusmn; 190 K)/T], k(T, A2&amp;minus;) = (1.4 &amp;plusmn; 0.1) &amp;times; 1011 &amp;times; exp[(&amp;minus;1400 &amp;plusmn; 170 K)/T]. Similarly, for adipic acid: k(T, H2A)&lt;br /&gt;= (7.5 &amp;plusmn; 0.2) &amp;times; 1010 &amp;times; exp[(&amp;minus;1210 &amp;plusmn; 170 K)/T], k(T, HA&amp;minus;) = (9.5 &amp;plusmn; 0.3) &amp;times; 1010 &amp;times; exp[(&amp;minus;1200 &amp;plusmn; 200 K)/T], k(T, A2&amp;minus;) = (8.7 &amp;plusmn; 0.2) &amp;times; 1010 &amp;times; exp[(&amp;minus;1100 &amp;plusmn; 170 K)/T] (in units of L mol&amp;minus;1 s&amp;minus;1). Density functional theory (DFT) calculations were performed to calculate the energy barrier of the H atom abstraction. The calculation results show that the energy barriers at the C&amp;beta;-atoms of the two DCAs are much lower than those at the C&amp;alpha;-atoms, indicating that the H atom abstractions predominantly occur at the C&amp;beta;-atoms. The increased &amp;middot;OH rate constant in the case of the deprotonated form can be explained by the reduction of energy barrier, which is predominately caused by the variation of the inductive effect of the carboxyl group. As an important sink in the atmosphere, the degradation of glutaric acid and adipic acid by &amp;middot;OH under atmospheric conditions can be accurately described by the Arrhenius expressions obtained.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Wen, Liang&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Schaefer, Thomas&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;He, Lin&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Zhang, Yimu&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Sun, Xiaomin&lt;/strong&gt;</text>
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                <text>&lt;a href="https://exportcvuy.anii.org.uy/cv/?a7868d1a46654e7a04ba7167141502086fa0cfad8b13463f75d90af715685994bc8f3eafaad6f6d2f6647277c9782143df93695c8a7d8e14295323ca2e2847d3" target="_blank"&gt;&lt;strong&gt;Ventura, Oscar N.&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Herrmann, Hartmut&lt;/strong&gt;</text>
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                <text>ACS Earth and Space Chemistry,&amp;nbsp;v. 5, n&amp;deg; 8, 2021. -- pp. 1854-1864.</text>
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                <text>ACS Publications</text>
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                <text>2021</text>
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                <text>&lt;p dir="ltr"&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p dir="ltr"&gt;&lt;span&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/span&gt;&lt;/p&gt;&#13;
&lt;p dir="ltr"&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derechode autor&lt;/strong&gt;&lt;span&gt;&amp;nbsp;sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/span&gt;&lt;/p&gt;&#13;
&lt;span id="docs-internal-guid-9d2103f7-7fff-c813-00c7-2528fd4891ff"&gt;&lt;strong&gt;ADVERTENCIA:&lt;/strong&gt;&lt;span&gt;&amp;nbsp;La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/span&gt;&lt;/span&gt;</text>
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                <text>Ingl&amp;eacute;s</text>
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                <text>&lt;p align="JUSTIFY"&gt;&lt;span style="color: #000000;"&gt;&lt;span style="font-family: Arial, sans-serif;"&gt;&lt;span style="font-size: small;"&gt;&lt;span&gt;10.1021/acsearthspacechem.1c00163&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;</text>
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        <name>Ácido adípico</name>
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        <name>Ácido glutárico</name>
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        <name>Cinética de competencia</name>
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        <name>DFT</name>
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      <description>A resource containing textual data.  Note that facsimiles or images of texts are still of the genre text.</description>
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          <name>Original Format</name>
          <description>If the image is of an object, state the type of object, such as painting, sculpture, paper, photo, and additional data</description>
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                <text>&lt;strong&gt;T&amp;eacute;cnias anal&amp;iacute;ticas de ketoprofeno materia prima, comprimidos, gel, supositorios e injectables&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;KETOPROFENO&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;MATERIA PRIMA&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;FORMAS GALENICAS&lt;/strong&gt;</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho de autor&lt;/strong&gt; sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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&lt;p class="western" lang="es-ES"&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p class="western" lang="es-ES"&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p class="western" lang="es-ES"&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p class="western" style="margin-bottom: 0cm;" lang="es-ES"&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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