{"id":9913,"date":"2022-09-21T02:23:07","date_gmt":"2022-09-20T18:23:07","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=9913"},"modified":"2022-09-21T02:23:07","modified_gmt":"2022-09-20T18:23:07","slug":"klug-dana-m-team-published-research-on-rsc-medicinal-chemistry-in-2020-269410-08-4","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=9913","title":{"rendered":"Klug, Dana M. team published research on RSC Medicinal Chemistry  in 2020 | 269410-08-4"},"content":{"rendered":"<p>Pyrazole is an organic compound with the formula C3H3N2H. It is a heterocycle characterized by a 5-membered ring of three carbon atoms and two adjacent nitrogen atoms, which are in ortho-substitution. 269410-08-4, formula is C9H15BN2O2, Name is  4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole.  Pyrazoles are a class of compounds that have the ring C3N2 with adjacent nitrogen atoms.Notable drugs containing a pyrazole ring are celecoxib (celebrex) and the anabolic steroid stanozolol. <a href=\"https:\/\/www.ambeed.com\/products\/269410-08-4.html\">Application In Synthesis of  269410-08-4<\/a>.<\/p>\n<p>Klug, Dana M.;Diaz-Gonzalez, Rosario;DeLano, Travis J.;Mavrogiannaki, Eftychia M.;Buskes, Melissa J.;Dalton, Raeann M.;Fisher, John K.;Schneider, Katherine M.;Hilborne, Vivian;Fritsche, Melanie G.;Simpson, Quillon J.;Tear, Westley F.;Devine, William G.;Perez-Moreno, Guiomar;Ceballos-Perez, Gloria;Garcia-Hernandez, Raquel;Bosch-Navarrete, Cristina;Ruiz-Perez, Luis Miguel;Gamarro, Francisco;Gonzalez-Pacanowska, Dolores;Martinez-Martinez, Maria Santos;Manzano-Chinchon, Pilar;Navarro, Miguel;Pollastri, Michael P.;Ferrins, Lori research published \u300a Structure-property studies of an imidazoquinoline chemotype with antitrypanosomal activity\u300b, the research content is summarized as follows. Human African trypanosomiasis is a neglected tropical disease (NTD) that is fatal if left untreated. Although approx. 13 million people live in moderate- to high-risk areas for infection, current treatments are plagued by problems with safety, efficacy, and emerging resistance. In an effort to fill the drug development pipeline for HAT, we have expanded previous work exploring the chemotype represented by the compound NEU-1090, with a particular focus on improvement of absorption, distribution, metabolism and elimination (ADME) properties. These efforts resulted in several compounds with substantially improved aqueous solubility, although these modifications typically resulted in a loss of trypanosomal activity. We herein report the results of our investigation into the antiparasitic activity, toxicity, and ADME properties of this class of compounds in the interest of informing the NTD drug discovery community and avoiding duplication of effort.<\/p>\n<p>269410-08-4, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, also known as 4-Pyrazoleboronic acid pinacol ester , is a useful research compound. Its molecular formula is C9H15BN2O2 and its molecular weight is 194.04 g\/mol. The purity is usually 95%.<\/p>\n<p>4-Pyrazoleboronic acid pinacol ester is a useful reagent for Suzuki-Miyaura cross-couplings as well as Ruthenium-catalyzed asymmetric hydrogenation. 4-Pyrazoleboronic acid pinacol ester is also a useful reagent for preparing VEGF, Aurora, RHO (ROCK), Janus Kinase 2, c-MET, ALK, S-nitrsoflutathione reductase, CDC7, Acetyl-CoA carboxylase inhibitors.<\/p>\n<p>4-Pyrazoleboronic acid pinacol ester is used in the preparation of Rho kinase (ROCK) inhibitors as wella s other biologically active compounds.<\/p>\n<p>4-Pyrazoleboronic acid pinacol ester is an organic compound that is the product of a bifunctional coupling reaction between 4-pyrazolecarboxylic acid and pinacol. It has been shown to inhibit protein S6 kinase, which is involved in the regulation of cell growth and proliferation. This compound has also been shown to be effective against cancer cells, including those that are resistant to conventional chemotherapeutic drugs. 4-Pyrazoleboronic acid pinacol ester may also be used as a precursor for other compounds with pharmaceutical activity., <a href=\"https:\/\/www.ambeed.com\/products\/269410-08-4.html\">Application In Synthesis of  269410-08-4<\/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>269410-08-4, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, also known as 4-Pyrazoleboronic acid pinacol ester , is a useful research compound. Its molecular formula is C9H15BN2O2 and its molecular weight is 194.04 g\/mol. The purity is usually 95%.<\/p>\n<p>4-Pyrazoleboronic acid pinacol ester is a useful reagent for Suzuki-Miyaura cross-couplings as well as Ruthenium-catalyzed asymmetric hydrogenation. 4-Pyrazoleboronic acid pinacol ester is also a useful reagent for preparing VEGF, Aurora, RHO (ROCK), Janus Kinase 2, c-MET, ALK, S-nitrsoflutathione reductase, CDC7, Acetyl-CoA carboxylase inhibitors.<\/p>\n<p>4-Pyrazoleboronic acid pinacol ester is used in the preparation of Rho kinase (ROCK) inhibitors as wella s other biologically active compounds.<\/p>\n<p>4-Pyrazoleboronic acid pinacol ester is an organic compound that is the product of a bifunctional coupling reaction between 4-pyrazolecarboxylic acid and pinacol. It has been shown to inhibit protein S6 kinase, which is involved in the regulation of cell growth and proliferation. This compound has also been shown to be effective against cancer cells, including those that are resistant to conventional chemotherapeutic drugs. 4-Pyrazoleboronic acid pinacol ester may also be used as a precursor for other compounds with pharmaceutical activity., <a href=\"https:\/\/www.ambeed.com\/products\/269410-08-4.html\">Application In Synthesis of  269410-08-4<\/a><\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[734,131],"tags":[717],"class_list":["post-9913","post","type-post","status-publish","format-standard","hentry","category-269410-08-4","category-pyrazoles-derivatives","tag-m-w150-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Klug, Dana M. team published research on RSC Medicinal Chemistry in 2020 | 269410-08-4 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Pyrazole is an organic compound with the formula C3H3N2H. It is a heterocycle characterized by a 5-membered ring of three carbon atoms and two adjacent nitrogen atoms, which are in ortho-substitution. 269410-08-4, formula is C9H15BN2O2, Name is 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole. Pyrazoles are a class of compounds that have the ring C3N2 with adjacent nitrogen atoms.Notable drugs containing a pyrazole ring are celecoxib (celebrex) and the anabolic steroid stanozolol. 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Pyrazoles are a class of compounds that have the ring C3N2 with adjacent nitrogen atoms.Notable drugs containing a pyrazole ring are celecoxib (celebrex) and the anabolic steroid stanozolol. 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