{"id":11216,"date":"2022-11-21T05:05:22","date_gmt":"2022-11-20T21:05:22","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11216"},"modified":"2022-11-21T05:05:22","modified_gmt":"2022-11-20T21:05:22","slug":"spink-edwards-team-published-research-in-journal-of-medicinal-chemistry-in-58-cas-890590-91-7","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11216","title":{"rendered":"Spink, Edward&#8217;s team published research in Journal of Medicinal Chemistry  in 58 | CAS: 890590-91-7"},"content":{"rendered":"<p>Spink, Edward published the artcile<b><i>Structure-Activity Relationship for the Oxadiazole Class of Antibiotics<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/890590-91-7.html\">Related Products of pyrazoles-derivatives<\/a>,  the publication is  Journal of Medicinal Chemistry (2015), 58(3), 1380-1389, database is CAplus and MEDLINE.<\/p>\n<p>The structure-activity relationship (SAR) for the newly discovered oxadiazole class of antibiotics is described with evaluation of 120 derivatives of the lead structure. This class of antibiotics was discovered by in silico docking and scoring against the crystal structure of a penicillin-binding protein. They impair cell-wall biosynthesis and exhibit activities against the Gram-pos. bacterium Staphylococcus aureus, including methicillin-resistant S. aureus (MRSA) and vancomycin-resistant and linezolid-resistant S. aureus. Compound <strong>I<\/strong> was efficacious in a mouse model of MRSA infection, exhibiting a long half-life, a high volume of distribution, and low clearance. This antibiotic is bactericidal and is orally bioavailable in mice. This class of antibiotics holds great promise in recourse against infections by MRSA.<\/p>\n<p>Journal of Medicinal Chemistry published new progress about 890590-91-7. 890590-91-7 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Carboxylic acid, name is 3-Isopropyl-1H-pyrazole-5-carboxylic acid, and the molecular formula is C4H10O2, <a href=\"https:\/\/www.ambeed.com\/products\/890590-91-7.html\">Related Products of pyrazoles-derivatives<\/a>.<\/p>\n<p>Referemce:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">https:\/\/en.wikipedia.org\/wiki\/Pyrazole<\/a>,<br \/><a href=\"Pyrazole - Wikipedia\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Journal of Medicinal Chemistry published new progress about 890590-91-7. 890590-91-7 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Carboxylic acid, name is 3-Isopropyl-1H-pyrazole-5-carboxylic acid, and the molecular formula is C4H10O2, <a href=\"https:\/\/www.ambeed.com\/products\/890590-91-7.html\">Related Products of pyrazoles-derivatives<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[131],"tags":[717],"class_list":["post-11216","post","type-post","status-publish","format-standard","hentry","category-pyrazoles-derivatives","tag-m-w150-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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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":"Spink, Edward's team published research in Journal of Medicinal Chemistry in 58 | CAS: 890590-91-7 | pyrazoles-derivatives","description":"Spink, Edward published the artcileStructure-Activity Relationship for the Oxadiazole Class of Antibiotics, Related Products of pyrazoles-derivatives, the publication is Journal of Medicinal Chemistry (2015), 58(3), 1380-1389, database is CAplus and MEDLINE.","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=11216","og_locale":"en_US","og_type":"article","og_title":"Spink, Edward's team published research in Journal of Medicinal Chemistry in 58 | CAS: 890590-91-7 | pyrazoles-derivatives","og_description":"Spink, Edward published the artcileStructure-Activity Relationship for the Oxadiazole Class of Antibiotics, Related Products of pyrazoles-derivatives, the publication is Journal of Medicinal Chemistry (2015), 58(3), 1380-1389, database is CAplus and MEDLINE.","og_url":"https:\/\/www.pyrazoles-derivatives.com\/?p=11216","og_site_name":"pyrazoles-derivatives","article_published_time":"2022-11-20T21:05:22+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=11216","url":"https:\/\/www.pyrazoles-derivatives.com\/?p=11216","name":"Spink, Edward's team published research in Journal of Medicinal Chemistry in 58 | CAS: 890590-91-7 | pyrazoles-derivatives","isPartOf":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/#website"},"datePublished":"2022-11-20T21:05:22+00:00","author":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1"},"description":"Spink, Edward published the artcileStructure-Activity Relationship for the Oxadiazole Class of Antibiotics, Related Products of pyrazoles-derivatives, the publication is Journal of Medicinal Chemistry (2015), 58(3), 1380-1389, database is CAplus and MEDLINE.","breadcrumb":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=11216#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.pyrazoles-derivatives.com\/?p=11216"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=11216#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"\u9996\u9875","item":"https:\/\/www.pyrazoles-derivatives.com\/"},{"@type":"ListItem","position":2,"name":"Spink, Edward&#8217;s team published research in Journal of Medicinal Chemistry in 58 | CAS: 890590-91-7"}]},{"@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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