{"id":1980,"date":"2024-05-17T10:29:38","date_gmt":"2024-05-17T08:29:38","guid":{"rendered":"https:\/\/portale2.unime.it\/desylab\/?post_type=staffs&#038;p=1980"},"modified":"2024-06-04T16:47:23","modified_gmt":"2024-06-04T14:47:23","slug":"nunzio-iraci","status":"publish","type":"staffs","link":"https:\/\/portale2.unime.it\/desylab\/staffs\/nunzio-iraci\/","title":{"rendered":"Nunzio Iraci"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"1980\" class=\"elementor elementor-1980\">\n\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-0f8795f elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"0f8795f\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t\t<div class=\"elementor-background-overlay\"><\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-ea600af\" data-id=\"ea600af\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-d8411e7 elementor-invisible elementor-widget elementor-widget-heading\" data-id=\"d8411e7\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;_animation&quot;:&quot;fadeInDown&quot;}\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\"><br><br>   PROF. NUNZIO IRACI<br><br><br><\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-acc281b elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"acc281b\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-4a83c03\" data-id=\"4a83c03\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-b14090a elementor-widget elementor-widget-image\" data-id=\"b14090a\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"image.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<img fetchpriority=\"high\" decoding=\"async\" width=\"762\" height=\"917\" src=\"https:\/\/portale2.unime.it\/desylab\/wp-content\/uploads\/sites\/40\/2024\/05\/Nunzio1.jpg\" class=\"attachment-large size-large wp-image-1997\" alt=\"\" srcset=\"https:\/\/portale2.unime.it\/desylab\/wp-content\/uploads\/sites\/40\/2024\/05\/Nunzio1.jpg 762w, https:\/\/portale2.unime.it\/desylab\/wp-content\/uploads\/sites\/40\/2024\/05\/Nunzio1-249x300.jpg 249w\" sizes=\"(max-width: 762px) 100vw, 762px\" style=\"width:100%;height:120.34%;max-width:762px\" \/>\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<section class=\"elementor-section elementor-inner-section elementor-element elementor-element-fb92420 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"fb92420\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-inner-column elementor-element elementor-element-12dc4cb\" data-id=\"12dc4cb\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-419a635 elementor-view-default elementor-widget elementor-widget-icon\" data-id=\"419a635\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"icon.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-icon-wrapper\">\n\t\t\t<div class=\"elementor-icon\">\n\t\t\t<svg aria-hidden=\"true\" class=\"e-font-icon-svg e-far-envelope\" viewBox=\"0 0 512 512\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"><path d=\"M464 64H48C21.49 64 0 85.49 0 112v288c0 26.51 21.49 48 48 48h416c26.51 0 48-21.49 48-48V112c0-26.51-21.49-48-48-48zm0 48v40.805c-22.422 18.259-58.168 46.651-134.587 106.49-16.841 13.247-50.201 45.072-73.413 44.701-23.208.375-56.579-31.459-73.413-44.701C106.18 199.465 70.425 171.067 48 152.805V112h416zM48 400V214.398c22.914 18.251 55.409 43.862 104.938 82.646 21.857 17.205 60.134 55.186 103.062 54.955 42.717.231 80.509-37.199 103.053-54.947 49.528-38.783 82.032-64.401 104.947-82.653V400H48z\"><\/path><\/svg>\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-inner-column elementor-element elementor-element-10f57c8\" data-id=\"10f57c8\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-4d3de23 elementor-widget elementor-widget-heading\" data-id=\"4d3de23\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\"><a href=\"mailto:nunzio.iraci@unime.it\">nunzio.iraci@unime.it<\/a><\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-inner-section elementor-element elementor-element-dde33a5 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"dde33a5\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-inner-column elementor-element elementor-element-4749558\" data-id=\"4749558\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-ed94bd3 elementor-view-default elementor-widget elementor-widget-icon\" data-id=\"ed94bd3\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"icon.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-icon-wrapper\">\n\t\t\t<div class=\"elementor-icon\">\n\t\t\t<svg aria-hidden=\"true\" class=\"e-font-icon-svg e-fas-chart-bar\" viewBox=\"0 0 512 512\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"><path d=\"M332.8 320h38.4c6.4 0 12.8-6.4 12.8-12.8V172.8c0-6.4-6.4-12.8-12.8-12.8h-38.4c-6.4 0-12.8 6.4-12.8 12.8v134.4c0 6.4 6.4 12.8 12.8 12.8zm96 0h38.4c6.4 0 12.8-6.4 12.8-12.8V76.8c0-6.4-6.4-12.8-12.8-12.8h-38.4c-6.4 0-12.8 6.4-12.8 12.8v230.4c0 6.4 6.4 12.8 12.8 12.8zm-288 0h38.4c6.4 0 12.8-6.4 12.8-12.8v-70.4c0-6.4-6.4-12.8-12.8-12.8h-38.4c-6.4 0-12.8 6.4-12.8 12.8v70.4c0 6.4 6.4 12.8 12.8 12.8zm96 0h38.4c6.4 0 12.8-6.4 12.8-12.8V108.8c0-6.4-6.4-12.8-12.8-12.8h-38.4c-6.4 0-12.8 6.4-12.8 12.8v198.4c0 6.4 6.4 12.8 12.8 12.8zM496 384H64V80c0-8.84-7.16-16-16-16H16C7.16 64 0 71.16 0 80v336c0 17.67 14.33 32 32 32h464c8.84 0 16-7.16 16-16v-32c0-8.84-7.16-16-16-16z\"><\/path><\/svg>\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-inner-column elementor-element elementor-element-c68080d\" data-id=\"c68080d\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-444ef8d elementor-widget elementor-widget-heading\" data-id=\"444ef8d\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\"><a href=\"https:\/\/www.scopus.com\/authid\/detail.uri?authorId=14029917100\">ID scopus: 14029917100<\/a><\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-inner-section elementor-element elementor-element-849571b elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"849571b\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-inner-column elementor-element elementor-element-d6eb523\" data-id=\"d6eb523\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-bf6825d elementor-view-default elementor-widget elementor-widget-icon\" data-id=\"bf6825d\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"icon.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-icon-wrapper\">\n\t\t\t<div class=\"elementor-icon\">\n\t\t\t<svg aria-hidden=\"true\" class=\"e-font-icon-svg e-fas-phone\" viewBox=\"0 0 512 512\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"><path d=\"M493.4 24.6l-104-24c-11.3-2.6-22.9 3.3-27.5 13.9l-48 112c-4.2 9.8-1.4 21.3 6.9 28l60.6 49.6c-36 76.7-98.9 140.5-177.2 177.2l-49.6-60.6c-6.8-8.3-18.2-11.1-28-6.9l-112 48C3.9 366.5-2 378.1.6 389.4l24 104C27.1 504.2 36.7 512 48 512c256.1 0 464-207.5 464-464 0-11.2-7.7-20.9-18.6-23.4z\"><\/path><\/svg>\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-inner-column elementor-element elementor-element-e5ee8f1\" data-id=\"e5ee8f1\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-c9c9db2 elementor-widget elementor-widget-heading\" data-id=\"c9c9db2\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\"><a href=\"mailto:zoccali@unime.it\">0906765827<\/a><\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-2563ae1\" data-id=\"2563ae1\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-f9c51c2 elementor-widget elementor-widget-text-editor\" data-id=\"f9c51c2\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-size: 14pt\">Il Dott. <strong>Nunzio Iraci<\/strong> ha conseguito la laurea in Chimica e Tecnologia Farmaceutiche e il titolo di Dottore di Ricerca in Scienze Farmaceutiche presso l\u2019Universit\u00e0 degli Studi di Messina.\u00a0<\/span><\/p><p><span style=\"font-size: 14pt\">Dopo essere stato Visiting Assistant in Research presso la Yale University, assegnista di ricerca e docente a contratto presso l\u2019Universit\u00e0 degli Studi di Perugia, Visiting Scholar presso la Boston University e assegnista di ricerca presso l\u2019Universit\u00e0 degli Studi della Basilicata, \u00e8 oggi ricercatore (SSD CHIM\/08 \u2013 Chimica Farmaceutica) e docente presso il Dipartimento di Scienze Chimiche, Biologiche, Farmaceutiche ed Ambientali dell\u2019Universit\u00e0 degli Studi di Messina.\u00a0<\/span><\/p><p><span style=\"font-size: 14pt\">La sua attivit\u00e0 di ricerca verte principalmente sull\u2019applicazione di metodiche di chimica computazionale allo studio di molecole di interesse biologico e farmaceutico.\u00a0<\/span><\/p><p><span style=\"font-size: 14pt\">Il Dott. Iraci \u00e8, ad oggi (30\/10\/2023), co-autore di 57 pubblicazioni su riviste peer-reviewed a diffusione\u00a0 internazionale (1803 citazioni), e ha un H-index di 31. (Fonte: Scopus)<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-7dfaa38 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"7dfaa38\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-1919920\" data-id=\"1919920\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-61ca840 elementor-widget elementor-widget-heading\" data-id=\"61ca840\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">PUBBLICAZIONI<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-d600186 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"d600186\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-5615800\" data-id=\"5615800\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-59716bb elementor-widget elementor-widget-text-editor\" data-id=\"59716bb\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<ul><li><span style=\"font-size: 14pt\">Rossi, A., Stagno, C., Piperno, A., <strong>Iraci, N.<\/strong>, Panseri, S., Montesi, M., Feizi-Dehnayebi, M., Bassi, G., Di Pietro, M.L., Micale, N. Anticancer activity and morphological analysis of Pt (II) complexes: Their DFT approach, docking simulation, and ADME-Tox profiling. <em>Applied Organometallic Chemistry<\/em>, <strong>2024<\/strong>, <em>38<\/em> (5), art. no. e7403. DOI: 10.1002\/aoc.7403<\/span><\/li><li><span style=\"font-size: 14pt\">Akbari, Z., Stagno, C., <strong>Iraci, N.<\/strong>, Efferth, T., Omer, E.A., Piperno, A., Montazerozohori, M., Feizi-Dehnayebi, M., Micale, N. Biological evaluation, DFT, MEP, HOMO-LUMO analysis and ensemble docking studies of Zn(II) complexes of bidentate and tetradentate Schiff base ligands as antileukemia agents. Journal of Molecular Structure, <strong>2024<\/strong>, 1301, art. no. 137400. DOI: 10.1016\/j.molstruc.2023.137400<\/span><\/li><li><span style=\"font-size: 14pt\">Taghizadeh Shool, M., Amiri Rudbari, H., Cuevas-Vicario, J.V., Rodr\u00edguez-Rubio, A., Stagno, C., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Efferth, T., Omer, E.A., Schirmeister, T., Blacque, O., Moini, N., Sheibani, E., Micale, N. Investigating the Cytotoxicity of Ru(II) Polypyridyl Complexes by Changing the Electronic Structure of Salicylaldehyde Ligands. Inorganic Chemistry, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2024<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">63<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\"> (2), pp. 1083-1101. DOI: 10.1021\/acs.inorgchem.3c03414<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Marsili, G., Acchioni, C., Remoli, A.L., Amatore, D., Sgarbanti, R., De Angelis, M., Orsatti, R., Acchioni, M., Astolfi, A., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Puzelli, S., Facchini, M., Perrotti, E., Cecchetti, V., Sabatini, S., Superti, F., Agamennone, M., Barreca, M.L., Hiscott, J., Nencioni, L., Sgarbanti, M. Identification of Anti-Influenza A Compounds Inhibiting the Viral Non-Structural Protein 1 (NS1) Using a Type I Interferon-Driven Screening Strategy. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">International Journal of Molecular Sciences<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2023<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">24<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\"> (13), art. no. 10495. DOI: 10.3390\/ijms241310495<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Smeriglio, A., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Denaro, M., Mandalari, G., Giofr\u00e8, S.V., Trombetta, D. Synergistic Combination of Citrus Flavanones as Strong Antioxidant and COX-Inhibitor Agent. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Antioxidants<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2023<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\"> 12 (4), art. no. 972. DOI: 10.3390\/antiox12040972<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">De Gaetano, F., Scala, A., Celesti, C., Lambertsen Larsen, K., Genovese, F., Bongiorno, C., Leggio, L., Iraci, N., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Mazzaglia, A., Ventura, C.A. 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New pyrazolobenzothiazine derivatives as hepatitis C virus NS5B polymerase palm site I inhibitors. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Journal of Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 57 <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2014<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, (8), pp. 3247-3262. 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Accounting for target flexibility and water molecules by docking to ensembles of target structures: The HCV NS5B palm site I inhibitors case study. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Journal of Chemical Information and Modeling<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2014<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 54 (2), pp. 481-497. 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Re-evolution of the 2-phenylquinolines: Ligand-based design, synthesis, and biological evaluation of a potent new class of staphylococcus aureus NorA efflux pump inhibitors to combat antimicrobial resistance. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Journal of Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2013<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 56 (12), pp. 4975-4989. 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Structure-based discovery of pyrazolobenzothiazine derivatives as inhibitors of hepatitis C virus replication. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Journal of Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2013<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 56 (6), pp. 2270-2282. 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Computer-aided design, synthesis and validation of 2-phenylquinazolinone fragments as CDK9 inhibitors with anti-HIV-1 tat-mediated transcription activity. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">ChemMedChem<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2013<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 8 (12), pp. 1941-1953. 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A highly intensified ART regimen induces long-term viral suppression and restriction of the viral reservoir in a simian AIDS model. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">PLoS Pathogens<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2012<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 8 (6), art. no. e1002774. 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Pyrazolo[4,3-c ][1,2]benzothiazines 5,5-dioxide: A promising new class of staphylococcus aureus NorA efflux pump inhibitors. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Journal of Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2012<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 55 (7), pp. 3568-3572. 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Pyridobenzothiazole derivatives as new chemotype targeting the HCV NS5B polymerase. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Bioorganic and Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2012<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 20 (2), pp. 866-876. DOI: 10.1016\/j.bmc.2011.11.061<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Barreca, M.L., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Manfroni, G., Cecchetti, V. Allosteric inhibition of the hepatitis C virus NS5B polymerase: In silico strategies for drug discovery and development. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Future Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2011<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 3 (8), pp. 1027-1055. 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Response of a simian immunodeficiency virus (SIVmac251) to raltegravir: A basis for a new treatment for simian AIDS and an animal model for studying lentiviral persistence during antiretroviral therapy. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Retrovirology<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2010<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 7, art. no. 21. DOI: 10.1186\/1742-4690-7-21<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Monforte, A.-M., Logoteta, P., Luca, L.D., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Ferro, S., Maga, G., De Clercq, E., Pannecouque, C., Chimirri, A. Novel 1,3-dihydro-benzimidazol-2-ones and their analogues as potent non-nucleoside HIV-1 reverse transcriptase inhibitors. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Bioorganic and Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2010<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 18 (4), pp. 1702-1710. DOI: 10.1016\/j.bmc.2009.12.059<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Barreca, M.L., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, De Luca, L., Chimirri, A. Induced-fit docking approach provides insight into the binding mode and mechanism of action of HIV-1 integrase inhibitors. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">ChemMedChem<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2009<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 4 (9), pp. 1446-1456. DOI: 10.1002\/cmdc.200900166<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Monforte, A.-M., Logoteta, P., Ferro, S., Luca, L.D., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Maga, G., Clercq, E.D., Pannecouque, C., Chimirri, A. Design, synthesis, and structure-activity relationships of 1,3-dihydrobenzimidazol-2-one analogues as anti-HIV agents. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Bioorganic and Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2009<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 17 (16), pp. 5962-5967. DOI: 10.1016\/j.bmc.2009.06.068<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">De Luca, L., Barreca, M.L., Ferro, S., Christ, F., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Gitto, R., Monforte, A.M., Debyser, Z., Chimirri, A. Pharmacophore-based discovery of small-molecule inhibitors of protein-protein interactions between HIV-1 integrase and cellular cofactor LEDGF\/p75. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">ChemMedChem<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2009<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 4 (8), pp. 1311-1316. DOI: 10.1002\/cmdc.200900070<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Ferro, S., De Luca, L., Barreca, M.L., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, De Grazia, S., Christ, F., Witvrouw, M., Debyser, Z., Chimirri, A. Docking studies on a new human immunodeficiency virus integrase-Mg-DNA complex: phenyl ring exploration and synthesis of 1H-benzylindole derivatives through fluorine substitutions. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Journal of medicinal chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2009<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 52 (2), pp. 569-573. DOI: 10.1021\/jm8009266<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Stancanelli, R., Crupi, V., De Luca, L., Ficarra, P., Ficarra, R., Gitto, R., Guardo, M., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Majolino, D., Tommasini, S., Venuti, V. Improvement of water solubility of non-competitive AMPA receptor antagonists by complexation with \u03b2-cyclodextrin. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Bioorganic and Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2008<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 16 (18), pp. 8706-8712. DOI: 10.1016\/j.bmc.2008.07.085<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Monforte, A.-M., Rao, A., Logoteta, P., Ferro, S., De Luca, L., Barreca, M.L., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Maga, G., De Clercq, E., Pannecouque, C., Chimirri, A. Novel N1-substituted 1,3-dihydro-2H-benzimidazol-2-ones as potent non-nucleoside reverse transcriptase inhibitors. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Bioorganic and Medicinal Chemistry<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2008<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 16 (15), pp. 7429-7435. DOI: 10.1016\/j.bmc.2008.06.012<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">De Luca, L., Barreca, M.L., Ferro, S., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Michiels, M., Christ, F., Debyser, Z., Witvrouw, M., Chimirri, A. A refined pharmacophore model for HIV-1 integrase inhibitors: Optimization of potency in the 1H-benzylindole series. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Bioorganic and Medicinal Chemistry Letters<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2008<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 18 (9), pp. 2891-2895. DOI: 10.1016\/j.bmcl.2008.03.089<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Barreca, M.L., Ortuso, F., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, De Luca, L., Alcaro, S., Chimirri, A. Tn5 transposase as a useful platform to simulate HIV-1 integrase inhibitor binding mode. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Biochemical and Biophysical Research Communications<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2007<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 363 (3), pp. 554-560. DOI: 10.1016\/j.bbrc.2007.08.199<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Barreca, M.L., Rao, A., Luca, L.D., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Monforte, A.-M., Maga, G., Clercq, E.D., Pannecouque, C., Balzarini, J., Chimirri, A. Discovery of novel benzimidazolones as potent non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Bioorganic and Medicinal Chemistry Letters<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2007<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 17 (7), pp. 1956-1960. DOI: 10.1016\/j.bmcl.2007.01.025<\/span><\/span><\/li><li><span style=\"font-size: 14pt\">Barreca, M.L., De Luca, L., <strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Iraci, N.<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, Rao, A., Ferro, S., Maga, G., Chimirri, A. Structure-based pharmacophore identification of new chemical scaffolds as non-nucleoside reverse transcriptase inhibitors. <\/span><em style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">Journal of Chemical Information and Modeling<\/em><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, <\/span><strong style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">2007<\/strong><span style=\"font-family: var(--list--font-family);background-color: var(--global--color-background)\">, 47 (2), pp. 557-562. DOI: 10.1021\/ci600320q<\/span><\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"featured_media":1997,"template":"elementor_header_footer","class_list":["post-1980","staffs","type-staffs","status-publish","has-post-thumbnail","hentry","entry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Nunzio Iraci - Desy Lab<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/portale2.unime.it\/desylab\/staffs\/nunzio-iraci\/\" \/>\n<meta property=\"og:locale\" content=\"it_IT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Nunzio Iraci - Desy Lab\" \/>\n<meta property=\"og:description\" content=\"PROF. 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