{"id":11653,"date":"2022-12-01T06:40:04","date_gmt":"2022-11-30T22:40:04","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11653"},"modified":"2022-12-01T06:40:04","modified_gmt":"2022-11-30T22:40:04","slug":"lemurell-malins-team-published-research-in-journal-of-medicinal-chemistry-in-62-cas-724710-02-5","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11653","title":{"rendered":"Lemurell, Malin&#8217;s team published research in Journal of Medicinal Chemistry  in 62 | CAS: 724710-02-5"},"content":{"rendered":"<p>Lemurell, Malin published the artcile<b><i>Novel Chemical Series of 5-Lipoxygenase-Activating Protein Inhibitors for Treatment of Coronary Artery Disease<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/724710-02-5.html\">HPLC of Formula: 724710-02-5<\/a>,  the publication is  Journal of Medicinal Chemistry (2019), 62(9), 4325-4349, database is CAplus and MEDLINE.<\/p>\n<p>5-Lipoxygenase (5-LO)-activating protein (FLAP) inhibitors have proven to attenuate 5-LO pathway activity and leukotriene production in human clin. trials. However, previous clin. candidates have been discontinued and the link between FLAP inhibition and outcome in inflammatory diseases remains to be established. We here describe a novel series of FLAP inhibitors identified from a screen of 10k compounds and the medicinal chem. strategies undertaken to progress this series. Compound <strong>I<\/strong> showed good overall properties and a pIC<sub>50<\/sub> hWB<sub>free<\/sub> of 8.1 and an lipophilic ligand efficiency of 5.2. Target engagement for <strong>I<\/strong> was established in dogs using ex vivo measurement of leukotriene B<sub>4<\/sub> (LTB<sub>4<\/sub>) levels in blood with good correlation to in vitro potency. A predicted human dose of 280 mg b.i.d. suggests a wide margin to any identified in vitro off-target effects and sufficient exposure to achieve an 80% reduction of LTB<sub>4<\/sub> levels in humans. Compound <strong>I<\/strong> is progressed to preclin. in vivo safety studies.<\/p>\n<p>Journal of Medicinal Chemistry published new progress about 724710-02-5. 724710-02-5 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Pyrazole,Boronic Acids,Boronic acid and ester, name is (1H-Pyrazol-5-yl)boronic acid, and the molecular formula is C3H5BN2O2, <a href=\"https:\/\/www.ambeed.com\/products\/724710-02-5.html\">HPLC of Formula: 724710-02-5<\/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 724710-02-5. 724710-02-5 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Pyrazole,Boronic Acids,Boronic acid and ester, name is (1H-Pyrazol-5-yl)boronic acid, and the molecular formula is C3H5BN2O2, <a href=\"https:\/\/www.ambeed.com\/products\/724710-02-5.html\">HPLC of Formula: 724710-02-5<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[801,131],"tags":[732],"class_list":["post-11653","post","type-post","status-publish","format-standard","hentry","category-724710-02-5","category-pyrazoles-derivatives","tag-m-w100-150"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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