{"id":10687,"date":"2022-10-27T02:54:57","date_gmt":"2022-10-26T18:54:57","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=10687"},"modified":"2022-10-27T02:54:57","modified_gmt":"2022-10-26T18:54:57","slug":"terakado-masahiko-team-published-research-in-acs-medicinal-chemistry-letters-in-2017-37622-90-5","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=10687","title":{"rendered":"Terakado, Masahiko team published research in ACS Medicinal Chemistry Letters  in 2017 | 37622-90-5"},"content":{"rendered":"<p>Pyrazole and its derivatives are considered a pharmacologically important active scaffold that possesses almost all types of pharmacological activities. 37622-90-5, formula is C6H8N2O2, Name is  Ethyl 4-pyrazolecarboxylate.  Pyrazole is a weak base, with pKb 11.5 (pKa of the conjugated acid 2.49 at 25 \u00b0C).Pyrazole used as a ligand to prepare organometallic compounds. <a href=\"https:\/\/www.ambeed.com\/products\/37622-90-5.html\">Category: pyrazoles-derivatives<\/a>.<\/p>\n<p>Terakado, Masahiko;Suzuki, Hidehiro;Hashimura, Kazuya;Tanaka, Motoyuki;Ueda, Hideyuki;Hirai, Keisuke;Asada, Masaki;Ikura, Masahiro;Matsunaga, Naoki;Saga, Hiroshi;Shinozaki, Koji;Karakawa, Naoko;Takada, Yuka;Minami, Masashi;Egashira, Hiromu;Sugiura, Yoshihiro;Yamada, Masanori;Nakade, Shinji;Takaoka, Yoshikazu research published \u300a Discovery of a Slow Tight Binding LPA1 Antagonist (ONO-0300302) for the Treatment of Benign Prostatic Hyperplasia\u300b, the research content is summarized as follows. Scaffold hopping from the amide group of lead compound ONO-7300243 (1) to a secondary alc. successfully gave a novel chemotype lysophosphatidic acid receptor 1 (LPA<sub>1<\/sub>) antagonist 4. Wash-out experiments using rat isolated urethra showed that compound 4 possesses a tight binding feature to the LPA<sub>1<\/sub> receptor. Further modification of two Ph groups of 1 to pyrrole and an indane moiety afforded an optimized compound ONO-0300302 (19). Despite its high i.v. clearance, 19 inhibited significantly an LPA-induced increase of intraurethral pressure (IUP) in rat (3 mg\/kg, p.o.) and dog (1 mg\/kg, p.o.) over 12 h. Binding experiments with [<sup>3<\/sup>H]-ONO-0300302 suggest that the observed long duration action is because of the slow tight binding character of 19.<\/p>\n<p>37622-90-5, Ethyl 4-pyrazolecarboxylate, also known as Ethyl pyrazole-4-carboxylate, is a useful research compound. Its molecular formula is C6H8N2O2 and its molecular weight is 140.14 g\/mol. The purity is usually 95%.<\/p>\n<p>Ethyl pyrazole-4-carboxylate is a low yield, transition metal salt that is used in the synthesis of pyrazoles. It can be synthesized by the reaction of sodium ethoxide with ethyl chloroformate and a Grignard reagent. Sodium ethoxide is added to a suspension of sodium chloride and dried ethyl chloroformate, followed by addition of magnesium turnings. The mixture is refluxed for one hour, cooled, and filtered to give crystals. Ethyl pyrazole-4-carboxylate is used in the preparation of ethyl esters from aliphatic alcohols by reacting with boron trichloride or phosphorus pentachloride. It participates in certain chemical reactions as a byproduct and can damage equipment during chemical reactions. The yield of this compound can be increased by using an excess amount of Grignard reagent or adding hexamethylenetetramine to the reaction mixture, <a href=\"https:\/\/www.ambeed.com\/products\/37622-90-5.html\">Category: pyrazoles-derivatives<\/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>37622-90-5, Ethyl 4-pyrazolecarboxylate, also known as Ethyl pyrazole-4-carboxylate, is a useful research compound. Its molecular formula is C6H8N2O2 and its molecular weight is 140.14 g\/mol. The purity is usually 95%.<\/p>\n<p>Ethyl pyrazole-4-carboxylate is a low yield, transition metal salt that is used in the synthesis of pyrazoles. It can be synthesized by the reaction of sodium ethoxide with ethyl chloroformate and a Grignard reagent. Sodium ethoxide is added to a suspension of sodium chloride and dried ethyl chloroformate, followed by addition of magnesium turnings. The mixture is refluxed for one hour, cooled, and filtered to give crystals. Ethyl pyrazole-4-carboxylate is used in the preparation of ethyl esters from aliphatic alcohols by reacting with boron trichloride or phosphorus pentachloride. It participates in certain chemical reactions as a byproduct and can damage equipment during chemical reactions. The yield of this compound can be increased by using an excess amount of Grignard reagent or adding hexamethylenetetramine to the reaction mixture, <a href=\"https:\/\/www.ambeed.com\/products\/37622-90-5.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":[218,131],"tags":[732],"class_list":["post-10687","post","type-post","status-publish","format-standard","hentry","category-37622-90-5","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>Terakado, Masahiko team published research in ACS Medicinal Chemistry Letters in 2017 | 37622-90-5 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Pyrazole and its derivatives are considered a pharmacologically important active scaffold that possesses almost all types of pharmacological activities. 37622-90-5, formula is C6H8N2O2, Name is Ethyl 4-pyrazolecarboxylate. 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