{"id":1364,"date":"2018-03-13T21:23:01","date_gmt":"2018-03-13T21:23:01","guid":{"rendered":"http:\/\/qfm.uc.pt\/?page_id=1364"},"modified":"2018-03-13T21:23:01","modified_gmt":"2018-03-13T21:23:01","slug":"desenvolvimento-de-novos-agentes-anticancerigenos-derivados-fenolicos-de-origem-natural-ou-sintetica-relacoes-estrutura-actividade","status":"publish","type":"page","link":"https:\/\/qfm.uc.pt\/index.html\/language\/en\/projects\/desenvolvimento-de-novos-agentes-anticancerigenos-derivados-fenolicos-de-origem-natural-ou-sintetica-relacoes-estrutura-actividade\/","title":{"rendered":"Desenvolvimento de Novos Agentes Anticancer\u00edgenos: Derivados Fen\u00f3licos de Origem Natural ou Sint\u00e9tica \u2013 Rela\u00e7\u00f5es Estrutura-Actividade"},"content":{"rendered":"<p>A determina\u00e7\u00e3o da actividade antioxidante\u00a0<i>vs<\/i>\u00a0anticancer\u00edgena de compostos fen\u00f3licos de origem natural ou sint\u00e9tica \u00e9 actualmente um importante tema de investiga\u00e7\u00e3o na \u00e1rea das Ci\u00eancias Biol\u00f3gica e Bioqu\u00edmica.<br \/>\nDe facto, t\u00eam sido levados a cabo v\u00e1rios estudos com vista \u00e0 obten\u00e7\u00e3o de novos compostos para a preven\u00e7\u00e3o, tanto\u00a0<i>in vitro<\/i>\u00a0como\u00a0<i>in vivo<\/i>, de processos oxidativos prejudiciais. Os derivados fen\u00f3licos, como os \u00e1cidos benz\u00f3ico e cin\u00e2mico ou flavon\u00f3ides, t\u00eam sido frequentemente usados como modelos para o desenvolvimento deste tipo de compostos. Estudos recentes sobre a actividade biol\u00f3gica de \u00e1cidos fen\u00f3licos de origem natural permitiram concluir que os \u00e1cidos sin\u00e1pico, fer\u00falico e cafeico, tal como os seus an\u00e1logos (presentes na dieta em grandes quantidades) s\u00e3o agentes antioxidantes\/anticancer\u00edgenos muito promissores.<br \/>\nO presente projecto visa a s\u00edntese de v\u00e1rios \u00e1cidos cin\u00e2micos, e derivados, do baseados em modelos naturais, e a determina\u00e7\u00e3o das suas propriedades antioxidantes\u00a0<i>vs<\/i>\u00a0anticancer\u00edgenas. A estrat\u00e9gia ser\u00e1 guiada atrav\u00e9s de um estudo, qualitativo e quantitativo, de Rela\u00e7\u00e3o Estrutura-Actividade (REA). Para os compostos mais promissores, pretendem-se ainda investigar os respectivos mecanismos de ac\u00e7\u00e3o.<\/p>\n<p><b>State<\/b><br \/>\nFinished<br \/>\n<b>Period<\/b><br \/>\n2005 to 2008<br \/>\n<b>Funding<\/b><br \/>\n63.500,00 euros<br \/>\n<b>Project code<\/b><br \/>\nPOCI\/QUI\/55631\/2004<br \/>\n<b>Funding Entity<\/b><br \/>\nPortuguese Foundation for Science and Technology (FCT), Portugal<\/p>\n<p><b>Members<\/b><br \/>\n<a href=\"http:\/\/qfm.uc.pt\/maria-paula-marques-2\/\">Maria Paula Matos Marques Catarro<\/a>\u00a0(Principal Investigator)<br \/>\nMaria Fernanda Martins Borges<br \/>\n<a href=\"http:\/\/qfm.uc.pt\/luis-batista-de-carvalho-2\/\">Lu\u00eds Alberto Esteves Batista de Carvalho<\/a><br \/>\n<a href=\"http:\/\/qfm.uc.pt\/ana-margarida-amado-2\/\">Ana Margarida Amado Roque Batista<\/a><br \/>\nRita Figueiredo Moutinho Calheiros Cruz<br \/>\nFrancisco Paulo S\u00e1 de Campos Gil<br \/>\nNuno Jorge da Silva Pereira Milhazes<br \/>\nAna Maria Matos Beja<br \/>\nNuno Miguel Penacho Pereira<br \/>\nPaulo Jorge Oliveira<br \/>\nAna Maria Brett<br \/>\nMaria Jo\u00e3o Sottomayor<br \/>\nElisi\u00e1rio Jose Tavares Silva<br \/>\nFernanda Maria Fernandes Roleira<br \/>\nJorge Manuel Pinto Jesus Garrido<br \/>\nErmelinda Manuela Pinto Jesus Garrido<br \/>\nCarmen Diniz Pereira<br \/>\nPaula Maria Fa\u00e7anha Cruz Fresco<br \/>\nMaria Nat\u00e1lia Dias Soeiro Cordeiro<\/p>\n<p><b>Publications<\/b><br \/>\n<a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxak1vZkU3MGpDWlE\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Antioxidant Phenolic Esters with Potential Anticancer Activity: A Raman Spectroscopy Study<\/a><br \/>\nR. Calheiros, N.F.L. Machado, S.M. Fiuza, A. Gaspar, J. Garrido, N. Milhazes, F. Borges, M.P.M. Marques<br \/>\nJournal of Raman Spectroscopy\u00a0<b>39<\/b>, 95-107 (2008)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxYVdERkY4STZQc2M\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Phenolic Esters with Potential Anticancer Activity &#8211; The Structural Variable<\/a><br \/>\nN.F.L. Machado, R. Calheiros, S.M. Fiuza, F. Borges, A. Gaspar, J. Garrido, M.P.M Marques<br \/>\nJournal of Molecular Modeling\u00a0<b>13<\/b>, 865-877 (2007)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxdjN4QXMxNUU5V28\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\"><em>Ab Initio<\/em> and Density Functional Study of a Caffeic Acid Amide\u00a0<\/a><br \/>\nDavid A. Rinc\u00f3n D, E.E. Daza C, M.N.D.S. Cordeiro<br \/>\nJournal of Molecular Structure (THEOCHEM)\u00a0<b>804<\/b>, 57-63 (2007)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxSlhuYm5BeWxybjQ\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">New Insights on the Anticancer Properties of Dietary Polyphenols<\/a><br \/>\nP. Fresco, F. Borges, C. Diniz, M.P.M. Marques<br \/>\nMedicinal Research Reviews\u00a0<b>26<\/b>, 747-766 (2006)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxVE16ZUZRc05zbzQ\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Cytotoxic and COX-2 Inhibition Properties of Hydroxycinnamic Derivatives<\/a><br \/>\nM.P.M. Marques, F. Borges, J. Sousa, R. Calheiros, J. Garrido, A. Gaspar, F. Antunes, C. Diniz, P. Fresco<br \/>\nLetters in Drugs Design &amp; Discovery\u00a0<b>3<\/b>, 316-320 (2006)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxOERpc1dGbXBvNWM\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">\u03b2-Nitrostyrene Derivatives as Potential Antibacterial Agents: A Structure-Property-Activity Relationship Study<\/a><br \/>\nN. Milhazes, R. Calheiros, M.P.M. Marques, J. Garrido, M.N.D.S. Cordeiro, C. Rodrigues, S. Quinteira, C. Novais, L. Peixe, F. Borges<br \/>\nBioorganic &amp; Medicinal Chemistry\u00a0<b>14<\/b>, 4078-4088 (2006)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxSm9RM3lIU0k5ZzQ\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Conformational Analysis of the Potential Anticancer Agent Ethyl Trihydroxycinnamate \u2013 A Combined Raman Spectroscopy and Ab Initio Study<\/a><br \/>\nJ.B. Sousa, R. Calheiros, V. Rio, F. Borges, M.P.M. Marques<br \/>\nJournal of Molecular Structure\u00a0<b>783<\/b>, 122-135 (2006)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxa0oyZXZZei14b2M\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Potentiometric studies on the complexation of copper (II) by phenolic acids as ligand models of humic substances<\/a><br \/>\nF. Borges, C. Guimar\u00e3es, J.L.F.C. Lima, I. Pinto, S. Reis<br \/>\nTalanta\u00a0<b>66<\/b>, 670-673 (2005)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxd2EzajVJTk44UkE\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Simple Coumarins and Analogues in Medicinal Chemistry. Ocurrence, Synthesis, and Biological Activity<\/a><br \/>\nF. Roleira, N. Milhazes, F. Borges, L. Santana,\u00a0 E. Uriarte<br \/>\nCurrent Medicinal Chemistry\u00a0<b>12\u00a0<\/b>, 887-916 (2005)<\/p>\n<p>Correlation between the antioxidant activity against lipoperoxidation of polyphenolic compounds and their partition coefficients in a liposome\/buffer media<br \/>\nS. Reis, C. Siquet, V. Rio, F. Borges, J.L.F.C. Lima<br \/>\nRevista Portuguesa de Farm\u00e1cia\u00a0<b>LII(2)<\/b>, 13-14 (2005)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxYXhxMGF2NkJkT3M\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Structure-Property Studies on the Antioxidant Activity of Flavonoids Present in the Diet<\/a><br \/>\nS. Teixeira, C. Siquet, C. Alves, I. Boal, M.P.M. Marques, F. Borges, J.L.F.C. Lima, S. Reis<br \/>\nFree Radicals in Biology &amp; Medicine\u00a0<b>39<\/b>, 1099-1108 (2005)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxbUdhNkZYdEJWQUE\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Phenolic Acid Derivatives with Potential Anticancer Properties \u2013 A Structure-Activity Relationship Study. Part 1: Methyl, Propyl and Octyl Esters of Caffeic and Gallic Acids<\/a><br \/>\nS.M. Fiuza, C.A. Gomes, L.J. Teixeira, T. Gir\u00e3o da Cruz, M.N. Cordeiro, N. Milhazes, F. Borges, M.P.M. Marques<br \/>\nBioorganic &amp; Medicinal Chemistry\u00a0<b>12<\/b>, 3581-3589 (2004)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxNnFpcDZSRW11MDg\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Identification of Synthetic Precursors of Amphetamine-like Drugs based on Raman Spectroscopy and ab Initio Calculations: \u03b2-Methyl-\u03b2-nitrostyrene Derivatives<\/a><br \/>\nN. Milhazes, F. Borges, R. Calheiros\u00a0 M.P.M. Marques<br \/>\nThe Analyst\u00a0<b>129<\/b>, 1106-1117 (2004)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxN3J0bktueTRMVU0\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Conformational Analysis of a Trihydroxylated Derivative of Cinnamic Acid \u2013 A Combined Raman Spectroscopy and Ab Initio Study<\/a><br \/>\nS.M. Fiuza, E. Van Besien, N. Milhazes, F. Borges and M.P.M. Marques<br \/>\nJournal of Molecular Structure\u00a0<b>693<\/b>, 103-118 (2004)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxZ3J2dHJyOTgtMEk\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">\u03b2-Nitrostyrene Derivatives &#8211; A Conformational Study by Combined Raman Spectroscopy and Ab Initio MO Calculations<\/a><br \/>\nR. Calheiros, N. Milhazes, F. Borges, M.P.M. Marques<br \/>\nJournal of Molecular Structure\u00a0<b>692<\/b>, 91-106 (2004)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxbDhkS2tDb2dWMFU\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\">Anticancer Activity of Phenolic Acids of Natural or Synthetic Origin: a Structure-Activity Study<\/a><br \/>\nC.A. Gomes, T. Gir\u00e3o da Cruz, J.L. Andrade, N. Milhazes, F. Borges, M.P.M. Marques<br \/>\nJournal of Medicinal Chemistry\u00a0<b>46<\/b>, 5395-5401 (2003)<\/p>\n<p><a href=\"https:\/\/drive.google.com\/file\/d\/0B_btGj75B4fxRXN3NUU5N2JsdGM\/view?usp=sharing\" target=\"_blank\" rel=\"noopener\"><em>Ab Initio<\/em> Conformational Study of Caffeic Acid\u00a0<\/a><br \/>\nE. Van Besien, M.P.M. Marques<br \/>\nJournal of Molecular Structure (THEOCHEM)\u00a0<b>625<\/b>, 265-275 (2003)<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A determina\u00e7\u00e3o da actividade antioxidante\u00a0vs\u00a0anticancer\u00edgena de compostos fen\u00f3licos de origem natural ou sint\u00e9tica \u00e9 actualmente um importante tema de investiga\u00e7\u00e3o na \u00e1rea das Ci\u00eancias Biol\u00f3gica e Bioqu\u00edmica. De facto, t\u00eam sido levados a cabo v\u00e1rios estudos com vista \u00e0 obten\u00e7\u00e3o de novos compostos para a preven\u00e7\u00e3o, tanto\u00a0in vitro\u00a0como\u00a0in vivo, de processos oxidativos prejudiciais. Os derivados [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":596,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-1364","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/qfm.uc.pt\/index.html\/wp-json\/wp\/v2\/pages\/1364","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/qfm.uc.pt\/index.html\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/qfm.uc.pt\/index.html\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/qfm.uc.pt\/index.html\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/qfm.uc.pt\/index.html\/wp-json\/wp\/v2\/comments?post=1364"}],"version-history":[{"count":0,"href":"https:\/\/qfm.uc.pt\/index.html\/wp-json\/wp\/v2\/pages\/1364\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/qfm.uc.pt\/index.html\/wp-json\/wp\/v2\/pages\/596"}],"wp:attachment":[{"href":"https:\/\/qfm.uc.pt\/index.html\/wp-json\/wp\/v2\/media?parent=1364"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}