{"id":11640,"date":"2022-12-01T06:38:33","date_gmt":"2022-11-30T22:38:33","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11640"},"modified":"2022-12-01T06:38:33","modified_gmt":"2022-11-30T22:38:33","slug":"kharbanda-anupreets-team-published-research-in-european-journal-of-medicinal-chemistry-in-225-cas-724710-02-5","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11640","title":{"rendered":"Kharbanda, Anupreet&#8217;s team published research in European Journal of Medicinal Chemistry  in 225 | CAS: 724710-02-5"},"content":{"rendered":"<p>Kharbanda, Anupreet published the artcile<b><i>Discovery of 4-aminoquinolines as highly selective TGF\u03b2R1 inhibitors with an attenuated MAP4K4 profile for potential applications in immuno-oncology<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/724710-02-5.html\">Formula: C3H5BN2O2<\/a>,  the publication is  European Journal of Medicinal Chemistry (2021), 113763, database is CAplus and MEDLINE.<\/p>\n<p>The tumor microenvironment contains high concentrations of TGF\u03b2, a crucial immunosuppressive cytokine. TGF\u03b2 stimulates immune escape by promoting peripheral immune tolerance to avoid tumoricidal attack. Small-mol. inhibitors of TGF\u03b2R1 are a prospective method for next-generation immunotherapies. In the present study, we identified selective 4-aminoquinoline-based inhibitors of TGF\u03b2R1 through structural and rational-based design strategies. This led to the identification of [N-(2-(2,5-difluorophenyl)pyridin-4-yl)-7-(4-(methylsulfonyl)phenyl)quinolin-4-amine], which was found to be selective for TGF\u03b2R1 with the exception of MAP4K4 in the kinase profiling assay. The compound was then further optimized to remove MAP4K4 activity, since MAP4K4 is vital for proper T-cell function and its inhibition could exacerbate tumor immunosuppression. Optimization efforts led to [7-(4-(methylsulfonyl)phenyl)-N-(2-(m-tolyl)pyridin-4-yl)quinolin-4-amine] that inhibited TGF\u03b2R1 at an IC<sub>50<\/sub> of 0.79 \u00b1 0.19 nM with 2000-fold selectivity against MAP4K4. 7-(4-(Methylsulfonyl)phenyl)-N-(2-(m-tolyl)pyridin-4-yl)quinolin-4-amine, represents a highly selective TGF\u03b2R1 inhibitor that has potential applications in immuno-oncol.<\/p>\n<p>European 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\">Formula: C3H5BN2O2<\/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>European 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\">Formula: C3H5BN2O2<\/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-11640","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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