{"id":10992,"date":"2022-11-15T03:40:13","date_gmt":"2022-11-14T19:40:13","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=10992"},"modified":"2022-11-15T03:40:13","modified_gmt":"2022-11-14T19:40:13","slug":"encinas-lourdess-team-published-research-in-journal-of-medicinal-chemistry-in-2014-02-27-cas-769132-77-6","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=10992","title":{"rendered":"Encinas, Lourdes’s team published research in Journal of Medicinal Chemistry in 2014-02-27 | CAS: 769132-77-6"},"content":{"rendered":"

Encinas, Lourdes published the artcileEncoded Library Technology as a Source of Hits for the Discovery and Lead Optimization of a Potent and Selective Class of Bactericidal Direct Inhibitors of Mycobacterium tuberculosis InhA<\/i><\/b>, Formula: C9H14N2O2<\/a>, the main research area is pyrrolidinylpyrazolecarboxamide benzofuranylcarbonyl derivative preparation tuberculostatic structure activity.<\/p>\n

Tuberculosis (TB) is one of the world’s oldest and deadliest diseases, killing a person every 20 s. InhA, the enoyl-ACP reductase from Mycobacterium tuberculosis, is the target of the frontline antitubercular drug isoniazid (INH). Compounds that directly target InhA and do not require activation by mycobacterial catalase peroxidase KatG are promising candidates for treating infections caused by INH resistant strains. The application of the encoded library technol. (ELT) to the discovery of direct InhA inhibitors yielded compound I endowed with good enzymic potency but with low antitubercular potency. This work reports the hit identification, the selected strategy for potency optimization, the structure-activity relationships of a hundred analogs synthesized, and the results of the in vivo efficacy studies performed with the lead compound II.<\/p>\n

Journal of Medicinal Chemistry published new progress about Crystal structure. 769132-77-6 belongs to class pyrazoles-derivatives, name is 3-Isobutyl-1-methyl-1H-pyrazole-5-carboxylic acid, and the molecular formula is C9H14N2O2, Formula: C9H14N2O2<\/a>.<\/p>\n

Referemce:
Pyrazole – Wikipedia<\/a>,
Pyrazoles – an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

Journal of Medicinal Chemistry published new progress about Crystal structure. 769132-77-6 belongs to class pyrazoles-derivatives, name is 3-Isobutyl-1-methyl-1H-pyrazole-5-carboxylic acid, and the molecular formula is C9H14N2O2, Formula: C9H14N2O2<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[774,131],"tags":[717],"class_list":["post-10992","post","type-post","status-publish","format-standard","hentry","category-769132-77-6","category-pyrazoles-derivatives","tag-m-w150-200"],"yoast_head":"\nEncinas, Lourdes's team published research in Journal of Medicinal Chemistry in 2014-02-27 | CAS: 769132-77-6 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Encinas, Lourdes published the artcileEncoded Library Technology as a Source of Hits for the Discovery and Lead Optimization of a Potent and Selective Class of Bactericidal Direct Inhibitors of Mycobacterium tuberculosis InhA, Formula: C9H14N2O2, the main research area is pyrrolidinylpyrazolecarboxamide benzofuranylcarbonyl derivative preparation tuberculostatic structure activity.\" \/>\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=10992\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Encinas, Lourdes's team published research in Journal of Medicinal Chemistry in 2014-02-27 | CAS: 769132-77-6 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"Encinas, Lourdes published the artcileEncoded Library Technology as a Source of Hits for the Discovery and Lead Optimization of a Potent and Selective Class of Bactericidal Direct Inhibitors of Mycobacterium tuberculosis InhA, Formula: C9H14N2O2, the main research area is pyrrolidinylpyrazolecarboxamide benzofuranylcarbonyl derivative preparation tuberculostatic structure activity.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.pyrazoles-derivatives.com\/?p=10992\" \/>\n<meta property=\"og:site_name\" content=\"pyrazoles-derivatives\" \/>\n<meta property=\"article:published_time\" content=\"2022-11-14T19:40:13+00:00\" \/>\n<meta name=\"author\" content=\"Jessica.F\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Jessica.F\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=10992\",\"url\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=10992\",\"name\":\"Encinas, Lourdes's team published research in Journal of Medicinal Chemistry in 2014-02-27 | CAS: 769132-77-6 | pyrazoles-derivatives\",\"isPartOf\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#website\"},\"datePublished\":\"2022-11-14T19:40:13+00:00\",\"author\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\"},\"description\":\"Encinas, Lourdes published the artcileEncoded Library Technology as a Source of Hits for the Discovery and Lead Optimization of a Potent and Selective Class of Bactericidal Direct Inhibitors of Mycobacterium tuberculosis InhA, Formula: C9H14N2O2, the main research area is pyrrolidinylpyrazolecarboxamide benzofuranylcarbonyl derivative preparation tuberculostatic structure activity.\",\"breadcrumb\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=10992#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.pyrazoles-derivatives.com\/?p=10992\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=10992#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"\u9996\u9875\",\"item\":\"https:\/\/www.pyrazoles-derivatives.com\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Encinas, Lourdes’s team published research in Journal of Medicinal Chemistry in 2014-02-27 | CAS: 769132-77-6\"}]},{\"@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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