{"id":9744,"date":"2022-04-20T04:14:58","date_gmt":"2022-04-19T20:14:58","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=9744"},"modified":"2022-04-20T04:14:58","modified_gmt":"2022-04-19T20:14:58","slug":"the-absolute-best-science-experiment-for-22600-77-7","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=9744","title":{"rendered":"The Absolute Best Science Experiment for 22600-77-7"},"content":{"rendered":"<p>The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (1H-Imidazol-2-yl)methanamine dihydrochloride( cas:22600-77-7 ) is researched.<a href=\"https:\/\/www.ambeed.com\/products\/22600-77-7.html\">Computed Properties of  C4H9Cl2N3<\/a>.Casagrande, Manolo; Barteselli, Anna; Basilico, Nicoletta; Parapini, Silvia; Taramelli, Donatella; Sparatore, Anna published the article \u300aSynthesis and antiplasmodial activity of new heteroaryl derivatives of 7-chloro-4-aminoquinoline\u300b about this compound( cas:22600-77-7 )  in Bioorganic &#038; Medicinal Chemistry. Keywords: quinoline heteroarylmethylamino heteroarylamino preparation antiplasmodial activity; antimalarial aminoquinoline chloro preparation. Let&#8217;s learn more about this compound (cas:22600-77-7).<\/p>\n<p>With the aim to investigate the effect of different heterocyclic rings linked to the 4-aminoquinoline nucleus on the antimalarial activity, a set of 7-chloro-4-(heteroarylmethylamino)quinoline and 7-chloro-4-(heteroarylamino)quinoline derivatives was synthesized and tested in vitro against D-10 (CQ-S) and W-2 (CQ-R) strains of Plasmodium falciparum. All compounds exhibited from moderate to high antiplasmodial activities. The activity was strongly influenced both by the presence of a methylenic group, as a spacer between the 4-aminoquinoline and the heterocyclic ring, and by the presence of a basic head. The most potent mols. inhibited the growth of both CQ-S and CQ-R strains of P. falciparum with IC50 < 30 nM and were not toxic against human endothelial cells. These results confirm that the presence of an heteroaryl moiety in the side chain of 7-chloro-4-aminoquinoline is useful for the design and development of new powerful antimalarial agents.\n\nThis compound((1H-Imidazol-2-yl)methanamine dihydrochloride)<a href=\"https:\/\/www.ambeed.com\/products\/22600-77-7.html\">Computed Properties of  C4H9Cl2N3<\/a> was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.<\/p>\n<p>Reference:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">Pyrazole &#8211; Wikipedia<\/a>,<br \/><a href=\"https:\/\/www.sciencedirect.com\/topics\/chemistry\/pyrazoles\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/A><\/p>\n","protected":false},"excerpt":{"rendered":"<p>This compound((1H-Imidazol-2-yl)methanamine dihydrochloride)<a href=\"https:\/\/www.ambeed.com\/products\/22600-77-7.html\">Computed Properties of  C4H9Cl2N3<\/a> was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[730,131],"tags":[126],"class_list":["post-9744","post","type-post","status-publish","format-standard","hentry","category-22600-77-7","category-pyrazoles-derivatives","tag-m-w100-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>The Absolute Best Science Experiment for 22600-77-7 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (1H-Imidazol-2-yl)methanamine dihydrochloride( cas:22600-77-7 ) is researched.Computed Properties of C4H9Cl2N3.Casagrande, Manolo; Barteselli, Anna; Basilico, Nicoletta; Parapini, Silvia; Taramelli, Donatella; Sparatore, Anna published the article \u300aSynthesis and antiplasmodial activity of new heteroaryl derivatives of 7-chloro-4-aminoquinoline\u300b about this compound( cas:22600-77-7 ) in Bioorganic &amp; Medicinal Chemistry. Keywords: quinoline heteroarylmethylamino heteroarylamino preparation antiplasmodial activity; antimalarial aminoquinoline chloro preparation. Let&#039;s learn more about this compound (cas:22600-77-7).\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.pyrazoles-derivatives.com\/?p=9744\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"The Absolute Best Science Experiment for 22600-77-7 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (1H-Imidazol-2-yl)methanamine dihydrochloride( cas:22600-77-7 ) is researched.Computed Properties of C4H9Cl2N3.Casagrande, Manolo; Barteselli, Anna; Basilico, Nicoletta; Parapini, Silvia; Taramelli, Donatella; Sparatore, Anna published the article \u300aSynthesis and antiplasmodial activity of new heteroaryl derivatives of 7-chloro-4-aminoquinoline\u300b about this compound( cas:22600-77-7 ) in Bioorganic &amp; Medicinal Chemistry. Keywords: quinoline heteroarylmethylamino heteroarylamino preparation antiplasmodial activity; antimalarial aminoquinoline chloro preparation. 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Compound: (1H-Imidazol-2-yl)methanamine dihydrochloride( cas:22600-77-7 ) is researched.Computed Properties of C4H9Cl2N3.Casagrande, Manolo; Barteselli, Anna; Basilico, Nicoletta; Parapini, Silvia; Taramelli, Donatella; Sparatore, Anna published the article \u300aSynthesis and antiplasmodial activity of new heteroaryl derivatives of 7-chloro-4-aminoquinoline\u300b about this compound( cas:22600-77-7 ) in Bioorganic & Medicinal Chemistry. Keywords: quinoline heteroarylmethylamino heteroarylamino preparation antiplasmodial activity; antimalarial aminoquinoline chloro preparation. 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Pyrazole derivatives play an important role in antitumor agents.\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.pyrazoles-derivatives.com\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\",\"name\":\"Jessica.F\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/en.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/en.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"caption\":\"Jessica.F\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"The Absolute Best Science Experiment for 22600-77-7 | pyrazoles-derivatives","description":"The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (1H-Imidazol-2-yl)methanamine dihydrochloride( cas:22600-77-7 ) is researched.Computed Properties of C4H9Cl2N3.Casagrande, Manolo; Barteselli, Anna; Basilico, Nicoletta; Parapini, Silvia; Taramelli, Donatella; Sparatore, Anna published the article \u300aSynthesis and antiplasmodial activity of new heteroaryl derivatives of 7-chloro-4-aminoquinoline\u300b about this compound( cas:22600-77-7 ) in Bioorganic & Medicinal Chemistry. Keywords: quinoline heteroarylmethylamino heteroarylamino preparation antiplasmodial activity; antimalarial aminoquinoline chloro preparation. Let's learn more about this compound (cas:22600-77-7).","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.pyrazoles-derivatives.com\/?p=9744","og_locale":"en_US","og_type":"article","og_title":"The Absolute Best Science Experiment for 22600-77-7 | pyrazoles-derivatives","og_description":"The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (1H-Imidazol-2-yl)methanamine dihydrochloride( cas:22600-77-7 ) is researched.Computed Properties of C4H9Cl2N3.Casagrande, Manolo; Barteselli, Anna; Basilico, Nicoletta; Parapini, Silvia; Taramelli, Donatella; Sparatore, Anna published the article \u300aSynthesis and antiplasmodial activity of new heteroaryl derivatives of 7-chloro-4-aminoquinoline\u300b about this compound( cas:22600-77-7 ) in Bioorganic & Medicinal Chemistry. Keywords: quinoline heteroarylmethylamino heteroarylamino preparation antiplasmodial activity; antimalarial aminoquinoline chloro preparation. Let's learn more about this compound (cas:22600-77-7).","og_url":"https:\/\/www.pyrazoles-derivatives.com\/?p=9744","og_site_name":"pyrazoles-derivatives","article_published_time":"2022-04-19T20:14:58+00:00","author":"Jessica.F","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Jessica.F","Est. reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=9744","url":"https:\/\/www.pyrazoles-derivatives.com\/?p=9744","name":"The Absolute Best Science Experiment for 22600-77-7 | pyrazoles-derivatives","isPartOf":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/#website"},"datePublished":"2022-04-19T20:14:58+00:00","author":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1"},"description":"The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. 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Let's learn more about this compound (cas:22600-77-7).","breadcrumb":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=9744#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.pyrazoles-derivatives.com\/?p=9744"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=9744#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"\u9996\u9875","item":"https:\/\/www.pyrazoles-derivatives.com\/"},{"@type":"ListItem","position":2,"name":"The Absolute Best Science Experiment for 22600-77-7"}]},{"@type":"WebSite","@id":"https:\/\/www.pyrazoles-derivatives.com\/#website","url":"https:\/\/www.pyrazoles-derivatives.com\/","name":"pyrazoles-derivatives","description":"Several pyrazole derivatives possess important pharmacological activities and they have been proved useful materials in drug research. 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