{"id":11570,"date":"2022-11-30T04:43:00","date_gmt":"2022-11-29T20:43:00","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11570"},"modified":"2022-11-30T04:43:00","modified_gmt":"2022-11-29T20:43:00","slug":"lee-dahyes-team-published-research-in-journal-of-medicinal-chemistry-in-62-cas-1190875-39-8","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11570","title":{"rendered":"Lee, Dahye&#8217;s team published research in Journal of Medicinal Chemistry  in 62 | CAS: 1190875-39-8"},"content":{"rendered":"<p>Lee, Dahye published the artcile<b><i>Discovery of Novel Pyruvate Dehydrogenase Kinase 4 Inhibitors for Potential Oral Treatment of Metabolic Diseases<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/1190875-39-8.html\">Name:  (1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-pyrazol-4-yl)boronic acid<\/a>,  the publication is  Journal of Medicinal Chemistry (2019), 62(2), 575-588, database is CAplus and MEDLINE.<\/p>\n<p>Pyruvate dehydrogenase kinase 4 (PDK4) activation is associated with metabolic diseases including hyperglycemia, insulin resistance, allergies, and cancer. Structural modifications of hit anthraquinone led to the identification of a new series of allosteric PDK4 inhibitors. Among this series, compound 8c showed promising in vitro activity with an IC<sub>50<\/sub> value of 84 nM. Good metabolic stability, pharmacokinetic profiles, and possible metabolites were suggested. Compound 8c improved glucose tolerance in diet-induced obese mice and ameliorated allergic reactions in a passive cutaneous anaphylaxis mouse model. Addnl., compound 8c exhibited anticancer activity by controlling cell proliferation, transformation, and apoptosis. From the mol. docking studies, compound 8c displayed optimal fitting in the lipoamide binding site (allosteric) with a full fitness, providing a new scaffold for drug development toward PDK4 inhibitors.<\/p>\n<p>Journal of Medicinal Chemistry published new progress about 1190875-39-8. 1190875-39-8 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Piperidine,Boronic acid and ester,Amide,Boronic Acids,Boronic Acids,Boronic acid and ester,, name is (1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-pyrazol-4-yl)boronic acid, and the molecular formula is C13H22BN3O4, <a href=\"https:\/\/www.ambeed.com\/products\/1190875-39-8.html\">Name:  (1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-pyrazol-4-yl)boronic acid<\/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 1190875-39-8. 1190875-39-8 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Piperidine,Boronic acid and ester,Amide,Boronic Acids,Boronic Acids,Boronic acid and ester,, name is (1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-pyrazol-4-yl)boronic acid, and the molecular formula is C13H22BN3O4, <a href=\"https:\/\/www.ambeed.com\/products\/1190875-39-8.html\">Name:  (1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-pyrazol-4-yl)boronic acid<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[807,131],"tags":[740],"class_list":["post-11570","post","type-post","status-publish","format-standard","hentry","category-1190875-39-8","category-pyrazoles-derivatives","tag-m-w250-300"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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