{"id":11236,"date":"2022-11-21T05:06:50","date_gmt":"2022-11-20T21:06:50","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11236"},"modified":"2022-11-21T05:06:50","modified_gmt":"2022-11-20T21:06:50","slug":"bryan-marian-c-s-team-published-research-in-bioorganic-medicinal-chemistry-letters-in-23-cas-724710-02-5","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11236","title":{"rendered":"Bryan, Marian C.&#8217;s team published research in Bioorganic &amp; Medicinal Chemistry Letters  in 23 | CAS: 724710-02-5"},"content":{"rendered":"<p>Bryan, Marian C. published the artcile<b><i>N-substituted azaindoles as potent inhibitors of Cdc7 kinase<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/724710-02-5.html\">Category: pyrazoles-derivatives<\/a>,  the publication is  Bioorganic &amp; Medicinal Chemistry Letters (2013), 23(7), 2056-2060, database is CAplus and MEDLINE.<\/p>\n<p>Cdc7 kinase is responsible for the initiation and regulation of DNA replication and was proposed as a target for cancer therapy. We have identified a class of Cdc7 inhibitors based on a substituted indole core. Synthesis of focused indole and azaindole analogs yielded potent and selective 5-azaindole Cdc7 inhibitors with improved intrinsic metabolic stability (ie 36). In parallel, quantum mech. conformational anal. helped to rationalize SAR observations, led to a proposal of the preferred binding conformation in the absence of co-crystallog. data, and allowed the design of 7-azaindole 37 as a second lead in this series.<\/p>\n<p>Bioorganic &amp; Medicinal Chemistry Letters 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\">Category: pyrazoles-derivatives<\/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>Bioorganic &amp; Medicinal Chemistry Letters 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\">Category: pyrazoles-derivatives<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[131],"tags":[732],"class_list":["post-11236","post","type-post","status-publish","format-standard","hentry","category-pyrazoles-derivatives","tag-m-w100-150"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Bryan, Marian C.&#039;s team published research in Bioorganic &amp; 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