100959-50-0Relevant academic research and scientific papers
The method for manufacturing the same and hydroxybenzenesulfonic deriv. phenethyloxy substd. (by machine translation)
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Paragraph 0188, (2016/11/21)
PROBLEM TO BE SOLVED: having a harmful effect substd. rnethylphenylsilicone compd. hydroxybenzenesulfonic deriv. synthesizable substd. phenethyloxy easily and efficiently and to provide a manufacturing method thereof. SOLUTION: phenethyloxy substd. represented by hydroxybenzenesulfonic deriv. eq. (1). (= O or = S; Y 1-Y 3 is H, Br, mercapto group, amino group, nitro group, or thiocyanate group; X is H or a halogen atom; R 1 and R 2 the A is a halogen atom or the alkyl group or a halogen atom halopyridine C 1-C 4 of) selected drawing: no (by machine translation)
Novel Series of Dihydropyridinone P2X7 Receptor Antagonists
Lopez-Tapia, Francisco,Walker, Keith A. M.,Brotherton-Pleiss, Christine,Caroon, Joanie,Nitzan, Dov,Lowrie, Lee,Gleason, Shelley,Zhao, Shu-Hai,Berger, Jacob,Cockayne, Debra,Phippard, Deborah,Suttmann, Rebecca,Fitch, William L.,Bourdet, David,Rege, Pankaj,Huang, Xiaojun,Broadbent, Scott,Dvorak, Charles,Zhu, Jiang,Wagner, Paul,Padilla, Fernando,Loe, Brad,Jahangir, Alam,Alker, André
supporting information, p. 8413 - 8426 (2015/11/24)
Identification of singleton P2X7 inhibitor 1 from HTS gave a pharmacophore that eventually turned into potential clinical candidates 17 and 19. During development, a number of issues were successfully addressed, such as metabolic stability, plasma stability, GSH adduct formation, and aniline mutagenicity. Thus, careful modification of the molecule, such as conversion of the 1,4-dihydropyridinone to the 1,2-dihydropyridinone system, proper substitution at C-5″, and in some cases addition of fluorine atoms to the aniline ring allowed for the identification of a novel class of potent P2X7 inhibitors suitable for evaluating the role of P2X7 in inflammatory, immune, neurologic, or musculoskeletal disorders.
