<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-10T14:21:53Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/4929" metadataPrefix="oai_dc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/4929</identifier><datestamp>2022-12-19T12:26:22Z</datestamp><setSpec>com_10259_3593</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>com_10259_3596</setSpec><setSpec>col_10259_3594</setSpec><setSpec>col_10259_3597</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>Revisiting the thiosemicarbazonecopper(II) reaction with glutathione. Activity against colorectal carcinoma cell lines</dc:title>
<dc:creator>García Tojal, Javier</dc:creator>
<dc:creator>Gil García, Rubén</dc:creator>
<dc:creator>Fouz Cuesta, Víctor Ivo</dc:creator>
<dc:creator>Madariaga, Gotzon</dc:creator>
<dc:creator>Lezama, Luis</dc:creator>
<dc:creator>Galletero, María S.</dc:creator>
<dc:creator>Borrás, Joaquín</dc:creator>
<dc:creator>Nollmann, Friederike I.</dc:creator>
<dc:creator>García Girón, Carlos</dc:creator>
<dc:creator>Alcaraz, Raquel</dc:creator>
<dc:creator>Cavia Saiz, Mónica</dc:creator>
<dc:creator>Muñiz Rodríguez, Pilar</dc:creator>
<dc:creator>Palacios, Óscar</dc:creator>
<dc:creator>Samper, Katia G.</dc:creator>
<dc:creator>Rojo, Teófilo</dc:creator>
<dc:subject>Colon carcinoma</dc:subject>
<dc:subject>Copper</dc:subject>
<dc:subject>Molecular magnetism</dc:subject>
<dc:subject>Thiosemicarbazone</dc:subject>
<dc:subject>Química inorgánica</dc:subject>
<dc:subject>Aparato digestivo-Enfermedades</dc:subject>
<dc:subject>Chemistry, Inorganic</dc:subject>
<dc:subject>Digestive organs-Diseases</dc:subject>
<dc:description>Thiosemicarbazones (TSCs), and their copper derivatives, have been extensively studied mainly due to the&#xd;
potential applications as antitumor compounds. A part of the biological activity of the TSC-CuII complexes rests&#xd;
on their reactivity against cell reductants, as glutathione (GSH). The present paper describes the structure of the&#xd;
[Cu(PTSC)(ONO2)]n compound (1) (HPTSC =pyridine-2-carbaldehyde thiosemicarbazone) and its spectroscopic&#xd;
and magnetic properties. ESI studies performed on the reaction of GSH with 1 and the analogous [{Cu&#xd;
(PTSC*)(ONO2)}2] derivative (2, HPTSC* =pyridine-2-carbaldehyde 4N-methylthiosemicarbazone) show the&#xd;
absence of peaks related with TSC-Cu-GSH species. However GSH-Cu ones are detected, in good agreement with&#xd;
the release of CuI ions after reduction in the experimental conditions. The reactivity of 1 and 2 with cytochrome&#xd;
c and myoglobin and their activities against HT-29 and SW-480 colon carcinoma cell lines are compared with&#xd;
those shown by the free HPTSC and HPTSC* ligands.</dc:description>
<dc:description>Obra Social “la&#xd;
Caixa” (OSLC-2012-007), Ministerio de Economía y Competitividad and&#xd;
FEDER funds (CTQ2013-48937-C2-1-P, CTQ2015-70371-REDT,&#xd;
MAT2015-66441-P, BIO2015-67358-C2-2-P), Junta de Castilla y León&#xd;
(BU237U13), Gerencia Regional de Salud, Consejería de Sanidad, Junta&#xd;
de Castilla y León (GRS 1023/A/14), the Basque Government (project&#xd;
IT-779-13)</dc:description>
<dc:date>2018-09-10T08:48:17Z</dc:date>
<dc:date>2018-03</dc:date>
<dc:date>2020-04</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
<dc:identifier>0162-0134</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/4929</dc:identifier>
<dc:identifier>10.1016/j.jinorgbio.2017.12.005</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Journal of Inorganic Biochemistry. 2018, V. 180, p. 69–79</dc:relation>
<dc:relation>https://doi.org/10.1016/j.jinorgbio.2017.12.005</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/FundaciónLaCaixa/ OSLC-2012-007</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/CTQ2013-48937-C2-1-P</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/CTQ2015-70371-REDT</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/MAT2015-66441-P</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/MINECO/BIO2015-67358-C2-2-P</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/BU237U13</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/JCyL/GRS 1023/A/14</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/GV/IT-779-13</dc:relation>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Elsevier</dc:publisher>
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