{"id":6855,"date":"2024-07-04T08:45:47","date_gmt":"2024-07-04T08:45:47","guid":{"rendered":"https:\/\/en.copharm.uobaghdad.edu.iq\/?p=6855"},"modified":"2024-07-04T08:45:47","modified_gmt":"2024-07-04T08:45:47","slug":"new-indole-6-carboxylic-acid-derivatives-as-antiproliferative-agents-synthesis-in-silico-studies-and-cytotoxicity-evaluation","status":"publish","type":"post","link":"https:\/\/en.copharm.uobaghdad.edu.iq\/?p=6855","title":{"rendered":"New Indole-6-Carboxylic acid derivatives as Antiproliferative Agents:-Synthesis, in silico Studies and Cytotoxicity Evaluation"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row][vc_column][vc_column_text]<\/p>\n<p style=\"text-align: justify;\"><span style=\"font-size: 19px;\">The College of Pharmacy discussed the PhD dissertation entitled \u201cNew Indole-6-Carboxylic acid derivatives as Antiproliferative Agents:- Synthesis, In silico Studies and Cytotoxicity Evaluation\u201d<em>, <\/em>by the student Mustafa Mahir Allawi and the supervisor, Professor Dr. Ammar A. Razzak Mahmood, at the Pharmaceutical chemistry Department. The study aimed to synthesize eleven new hydrazine-1-carbothioamide derivatives of indole-6-carboxylic acid and methyl-1-methyl-1H-indole-6-carboxylate that act as EGFR tyrosine kinase inhibitors, and ten new oxadiazole derivatives of indole-6-carboxylic acid and methyl-1-methyl-1H-indole-6-carboxylate that act as VEGFR tyrosine kinase inhibitors, The study included Synthesis indole derivatives and are deduced through molecular docking studies. These derivatives were characterized by different chemical and spectroscopic methods (IR, <sup>1<\/sup>HNMR, <sup>13<\/sup>CNMR and HRMS), and evaluated in vitro for their antiproliferative activities against A549, HeLa, HepG2, HT-29, and HCT-116 cancer cell lines. The results showed that according to in silico studies, compounds 3b and 9a showed good binding energy to EGFR and the best docking scores among the hydrazine-1-carbothioamide derivatives, and its TD50 value was comparable to that of Erlotinib.\u00a0While, <em>in vitro<\/em> studies showed that compounds 3b and 6e were the most cytotoxic among the two groups of derivatives. Compounds (3b,9a) and (6e,11c) are cancer-selective agents based on their selectivity (SI). Compounds (3b,9a) and (6e,11c) targeted EGFR and VEGFR, respectively, inhibiting their kinas activity. The study recommended that the kinetics and the stability of the intended compounds in biological fluids and Conducting ADMET analysis in vitro and compare the findings with <em>in silico<\/em> results.<\/span><\/p>\n<p>[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column]<div id=\"cz_20473\" class=\"cz_grid_p cz_20473\"><div class=\"cz_grid cz_grid_1 clr cz_grid_c2 cz_grid_l2 cz_grid_1_no_title cz_grid_1_mid tac cz_tooltip cz_grid_1_no_title\"><div class=\"cz_grid_item cz_grid_first\"><\/div><div class=\"cz_grid_item \"><div data-title=\"Picture1\"><a class=\"cz_grid_link \" href=\"https:\/\/en.copharm.uobaghdad.edu.iq\/wp-content\/uploads\/sites\/80\/2024\/07\/Picture1.jpg\" data-xtra-lightbox><img loading=\"lazy\" decoding=\"async\" width=\"624\" height=\"468\" src=\"https:\/\/en.copharm.uobaghdad.edu.iq\/wp-content\/uploads\/sites\/80\/2024\/07\/Picture1.jpg\" class=\"attachment-codevz_1200_500\" alt=\"\" title=\"Picture1\" srcset=\"https:\/\/en.copharm.uobaghdad.edu.iq\/wp-content\/uploads\/sites\/80\/2024\/07\/Picture1.jpg 624w, https:\/\/en.copharm.uobaghdad.edu.iq\/wp-content\/uploads\/sites\/80\/2024\/07\/Picture1-300x225.jpg 300w, https:\/\/en.copharm.uobaghdad.edu.iq\/wp-content\/uploads\/sites\/80\/2024\/07\/Picture1-600x450.jpg 600w\" sizes=\"auto, (max-width: 624px) 100vw, 624px\" \/><div class=\"cz_grid_details\"><i class=\"fa fa-search cz_grid_icon\"><\/i><\/div><\/a><\/div><\/div><div class=\"cz_grid_item \"><div data-title=\"Picture2\"><a class=\"cz_grid_link \" href=\"https:\/\/en.copharm.uobaghdad.edu.iq\/wp-content\/uploads\/sites\/80\/2024\/07\/Picture2.jpg\" data-xtra-lightbox><img loading=\"lazy\" decoding=\"async\" width=\"399\" height=\"500\" src=\"https:\/\/en.copharm.uobaghdad.edu.iq\/wp-content\/uploads\/sites\/80\/2024\/07\/Picture2-399x500.jpg\" class=\"attachment-codevz_1200_500\" alt=\"\" title=\"Picture2\" \/><div class=\"cz_grid_details\"><i class=\"fa fa-search cz_grid_icon\"><\/i><\/div><\/a><\/div><\/div><\/div><\/div>[\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column][vc_column_text] The College of Pharmacy discussed the PhD dissertation entitled \u201cNew Indole-6-Carboxylic acid derivatives as Antiproliferative Agents:- Synthesis, In silico &#8230; <a class=\"cz_readmore\" href=\"https:\/\/en.copharm.uobaghdad.edu.iq\/?p=6855\"><i class=\"fa czico-132-arrows-8\" aria-hidden=\"true\"><\/i><span>more<\/span><\/a><\/p>\n","protected":false},"author":9,"featured_media":6856,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[3,7],"tags":[],"class_list":["post-6855","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-latest-news","category-dissuasion"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.8 - 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