{"id":133537,"date":"1997-01-01T00:00:00","date_gmt":"1997-01-01T00:00:00","guid":{"rendered":""},"modified":"1997-01-01T00:00:00","modified_gmt":"1997-01-01T00:00:00","slug":"butirofenonas-conformacionalmente-restringidas-sintesis-y-estudio-de-la-interaccion-frente-a-receptores-dopaminergicos-d2-y-serotoninergicos-5-ht2a-de-series-de-aminoalquiltienocicloalcanonas-com","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/ciencias-medicas\/butirofenonas-conformacionalmente-restringidas-sintesis-y-estudio-de-la-interaccion-frente-a-receptores-dopaminergicos-d2-y-serotoninergicos-5-ht2a-de-series-de-aminoalquiltienocicloalcanonas-com\/","title":{"rendered":"Butirofenonas conformacionalmente restringidas. sintesis y estudio de la interaccion frente a receptores dopaminergicos (d2) y serotoninergicos (5-ht2a) de series de aminoalquiltienocicloalcanonas como derivados con perfil antipsicotico."},"content":{"rendered":"<h2>Tesis doctoral de <strong>  Negreira Del Rio Jes\u00fas <\/strong><\/h2>\n<p>Sintesis de butirofenonas conformacionalmente restringidas, analogos ciclicos del haloperidol, donde se ha realizado la sustitucion bioisosterica del benceno por tiofeno y diversas modificaciones en el fragmento amina, incorporando los restos 4-(p-fluorobenzoil)piperidina 4-(6-fluorobencisoxazol-3-il)piperidina, n-(o-metoxifenil)piperazina, n-(2-piridil)piperazinas, 4(3-p-fluorobenzoilpropil)piperazina, se describe asimismo la resolucion del racemato correspondiente a una de las moleculas sintetizadas utilizando un sistema hplc y una columna quiral. Se ha estudiado la interaccion de todos los compuestos finales frente a receptores dopaminergicos (d2) y serotoninergicos (5-ht2a) obteniendose resultados muy esperanzadores.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Butirofenonas conformacionalmente restringidas. sintesis y estudio de la interaccion frente a receptores dopaminergicos (d2) y serotoninergicos (5-ht2a) de series de aminoalquiltienocicloalcanonas como derivados con perfil antipsicotico.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Butirofenonas conformacionalmente restringidas. sintesis y estudio de la interaccion frente a receptores dopaminergicos (d2) y serotoninergicos (5-ht2a) de series de aminoalquiltienocicloalcanonas como derivados con perfil antipsicotico. <\/li>\n<li><strong>Autor:<\/strong>\u00a0  Negreira Del Rio Jes\u00fas <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Santiago de compostela<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1997<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Enrique Ravi\u00f1a Rubira<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Felipe Alcudia Gonzalez <\/li>\n<li>Antonio Monge Vega (vocal)<\/li>\n<li> Gallo Mezo Miguel Angel (vocal)<\/li>\n<li>Ram\u00f3n Estevez Cabanas (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Negreira Del Rio Jes\u00fas Sintesis de butirofenonas conformacionalmente restringidas, analogos ciclicos del haloperidol, donde se ha realizado [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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