{"id":10997,"date":"2022-11-16T03:23:12","date_gmt":"2022-11-15T19:23:12","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=10997"},"modified":"2022-11-16T03:23:12","modified_gmt":"2022-11-15T19:23:12","slug":"gummadi-venkateshwar-raos-team-published-research-in-bioorganic-medicinal-chemistry-letters-in-2013-09-01-cas-1415825-05-6","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=10997","title":{"rendered":"Gummadi, Venkateshwar Rao&#8217;s team published research in Bioorganic &#038; Medicinal Chemistry Letters  in 2013-09-01 | CAS: 1415825-05-6"},"content":{"rendered":"<p>Gummadi, Venkateshwar Rao published the artcile<b><i>Discovery of 7-azaindole based anaplastic lymphoma kinase (ALK) inhibitors: Wild type and mutant (L1196M) active compounds with unique binding mode<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/1415825-05-6.html\">Product Details of C16H20BFN2O2<\/a>,  the main research area is  azaindole derivative ALK inhibitor preparation antiproliferative cancer; 7-Azaindole; AODVBYYJEPEEKR-UHFFFAOYSA-N; ATZJNUYRMAFPBF-UHFFFAOYSA-N; Anaplastic large cell lymphoma (ALCL); Anaplastic lymphoma kinase (ALK); Cancer; FADONZKXBUVWLH-UHFFFAOYSA-N; FPQUAATUWBOAGG-UHFFFAOYSA-N; HCWGKZMWRCORGX-UHFFFAOYSA-N; ISOJIFQFHFOCFC-UHFFFAOYSA-N; JJYRLIVLBDHFEU-UHFFFAOYSA-N; KNRKBZCJMLVHPB-UHFFFAOYSA-N; Karpas299; LKQKEJPUPWXICV-UHFFFAOYSA-N; LRWNZUVVRSBHQU-UHFFFAOYSA-N; MGARIFYNPCFMQT-UHFFFAOYSA-N; NAKSXXPCEJGLLQ-UHFFFAOYSA-N; PGSYBTKGCJXUAV-UHFFFAOYSA-N; SDWMCZUOCJDBOJ-UHFFFAOYSA-N; WIWKHKMJZYIJLG-UHFFFAOYSA-N; WXMICXPDNXUCTC-UHFFFAOYSA-N; XUQBNEPFDRSOCA-UHFFFAOYSA-N; ZHUGMFFQPPOJNL-UHFFFAOYSA-N.<\/p>\n<p>We have identified a novel 7-azaindole series of anaplastic lymphoma kinase (ALK) inhibitors. Compounds 7b, 7m and 7n demonstrate excellent potencies in biochem. and cellular assays. X-ray crystal structure of one of the compounds (7k) revealed a unique binding mode with the benzyl group occupying the back pocket, explaining its potency towards ALK and selectivity over tested kinases particularly Aurora-A. This binding mode is in contrast to that of known ALK inhibitors such as Crizotinib and NVP-TAE684 which occupy the ribose binding pocket, close to DFG motif.<\/p>\n<p>Bioorganic &#038; Medicinal Chemistry Letters published new progress about Antitumor agents. 1415825-05-6 belongs to class pyrazoles-derivatives, name is 1-(2-Fluorobenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, and the molecular formula is C16H20BFN2O2, <a href=\"https:\/\/www.ambeed.com\/products\/1415825-05-6.html\">Product Details of C16H20BFN2O2<\/a>.<\/p>\n<p>Referemce:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">Pyrazole &#8211; Wikipedia<\/a>,<br \/><a href=\"https:\/\/www.sciencedirect.com\/topics\/chemistry\/pyrazoles\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Bioorganic &#038; Medicinal Chemistry Letters published new progress about Antitumor agents. 1415825-05-6 belongs to class pyrazoles-derivatives, name is 1-(2-Fluorobenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, and the molecular formula is C16H20BFN2O2, <a href=\"https:\/\/www.ambeed.com\/products\/1415825-05-6.html\">Product Details of C16H20BFN2O2<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[782,131],"tags":[778],"class_list":["post-10997","post","type-post","status-publish","format-standard","hentry","category-1415825-05-6","category-pyrazoles-derivatives","tag-m-w200-350"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Gummadi, Venkateshwar Rao&#039;s team published research in Bioorganic &amp; Medicinal Chemistry Letters in 2013-09-01 | CAS: 1415825-05-6 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Gummadi, Venkateshwar Rao published the artcileDiscovery of 7-azaindole based anaplastic lymphoma kinase (ALK) inhibitors: Wild type and mutant (L1196M) active compounds with unique binding mode, Product Details of C16H20BFN2O2, the main research area is azaindole derivative ALK inhibitor preparation antiproliferative cancer; 7-Azaindole; AODVBYYJEPEEKR-UHFFFAOYSA-N; ATZJNUYRMAFPBF-UHFFFAOYSA-N; Anaplastic large cell lymphoma (ALCL); Anaplastic lymphoma kinase (ALK); Cancer; FADONZKXBUVWLH-UHFFFAOYSA-N; FPQUAATUWBOAGG-UHFFFAOYSA-N; HCWGKZMWRCORGX-UHFFFAOYSA-N; ISOJIFQFHFOCFC-UHFFFAOYSA-N; JJYRLIVLBDHFEU-UHFFFAOYSA-N; KNRKBZCJMLVHPB-UHFFFAOYSA-N; Karpas299; LKQKEJPUPWXICV-UHFFFAOYSA-N; LRWNZUVVRSBHQU-UHFFFAOYSA-N; MGARIFYNPCFMQT-UHFFFAOYSA-N; NAKSXXPCEJGLLQ-UHFFFAOYSA-N; PGSYBTKGCJXUAV-UHFFFAOYSA-N; SDWMCZUOCJDBOJ-UHFFFAOYSA-N; WIWKHKMJZYIJLG-UHFFFAOYSA-N; 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