{"id":11740,"date":"2022-12-02T03:52:42","date_gmt":"2022-12-01T19:52:42","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11740"},"modified":"2022-12-02T03:52:42","modified_gmt":"2022-12-01T19:52:42","slug":"wang-zhens-team-published-research-in-journal-of-medicinal-chemistry-in-64-cas-763120-58-7","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11740","title":{"rendered":"Wang, Zhen&#8217;s team published research in Journal of Medicinal Chemistry  in 64 | CAS: 763120-58-7"},"content":{"rendered":"<p>Wang, Zhen published the artcile<b><i>Discovery of an Orally Bioavailable Small-Molecule Inhibitor for the \u03b2-Catenin\/B-Cell Lymphoma 9 Protein-Protein Interaction<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/763120-58-7.html\">Product Details of C3H5BN2O2<\/a>,  the publication is  Journal of Medicinal Chemistry (2021), 64(16), 12109-12131, database is CAplus and MEDLINE.<\/p>\n<p>Aberrant activation of Wnt\/\u03b2-catenin signaling is strongly associated with many diseases including cancer invasion and metastasis. Small-mol. targeting of the central signaling node of this pathway, \u03b2-catenin, is a biol. rational approach to abolish hyperactivation of \u03b2-catenin signaling but has been demonstrated to be a difficult task. Herein, we report a drug-like small mol., ZW4864, that binds with \u03b2-catenin and selectively disrupts the protein-protein interaction (PPI) between B-cell lymphoma 9 (BCL9) and \u03b2-catenin while sparing the \u03b2-catenin\/E-cadherin PPI. ZW4864 dose-dependently suppresses \u03b2-catenin signaling activation, downregulates oncogenic \u03b2-catenin target genes, and abrogates invasiveness of \u03b2-catenin-dependent cancer cells. More importantly, ZW4864 shows good pharmacokinetic properties and effectively suppresses \u03b2-catenin target gene expression in the patient-derived xenograft mouse model. This study offers a selective chem. probe to explore \u03b2-catenin-related biol. and a drug-like small-mol. \u03b2-catenin\/BCL9 disruptor for future drug development.<\/p>\n<p>Journal of Medicinal Chemistry published new progress about 763120-58-7. 763120-58-7 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Boronic Acids,Boronic acid and ester, name is 1H-Pyrazole-4-boronic acid, and the molecular formula is C22H12F6O6S2, <a href=\"https:\/\/www.ambeed.com\/products\/763120-58-7.html\">Product Details of 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>Journal of Medicinal Chemistry published new progress about 763120-58-7. 763120-58-7 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Boronic Acids,Boronic acid and ester, name is 1H-Pyrazole-4-boronic acid, and the molecular formula is C22H12F6O6S2, <a href=\"https:\/\/www.ambeed.com\/products\/763120-58-7.html\">Product Details of 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":[802,131],"tags":[732],"class_list":["post-11740","post","type-post","status-publish","format-standard","hentry","category-763120-58-7","category-pyrazoles-derivatives","tag-m-w100-150"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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