1211517-76-8Relevant articles and documents
ALDOSTERONE SYNTHASE INHIBITORS
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Page/Page column 34; 35, (2016/12/26)
The present invention relates to compounds of formula I: and pharmaceutically acceptable salts thereof, wherein R1, R2 and R3, are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.
Discovery of benzimidazole CYP11B2 inhibitors with in vivo activity in rhesus monkeys
Hoyt, Scott B.,Park, Min K.,London, Clare,Xiong, Yusheng,Tata, Jim,Bennett, D. Jonathan,Cooke, Andrew,Cai, Jiaqiang,Carswell, Emma,Robinson, John,MacLean, John,Brown, Lindsay,Belshaw, Simone,Clarkson, Thomas R.,Liu, Kun,Liang, Gui-Bai,Struthers, Mary,Cully, Doris,Wisniewski, Tom,Ren, Ning,Bopp, Charlene,Sok, Andrea,Cai, Tian-Quan,Stribling, Sloan,Pai, Lee-Yuh,Ma, Xiuying,Metzger, Joe,Verras, Andreas,McMasters, Daniel,Chen, Qing,Tung, Elaine,Tang, Wei,Salituro, Gino,Buist, Nicole,Kuethe, Jeff,Rivera, Nelo,Clemas, Joe,Zhou, Gaochao,Gibson, Jack,Maxwell, Carrie Ann,Lassman, Mike,McLaughlin, Theresa,Castro-Perez, Jose,Szeto, Daphne,Forrest, Gail,Hajdu, Richard,Rosenbach, Mark,Ali, Amjad
supporting information, p. 573 - 578 (2015/05/27)
We report the discovery of a benzimidazole series of CYP11B2 inhibitors. Hit-to-lead and lead optimization studies identified compounds such as 32, which displays potent CYP11B2 inhibition, high selectivity versus related CYP targets, and good pharmacokin
TRIAZOLOPYRIDYL COMPOUNDS AS ALDOSTERONE SYNTHASE INHIBITORS
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Page/Page column 36, (2013/04/10)
This invention relates to triazolopyridyl compounds of the structural formula: [Formula should be inserted here] or their pharmaceutically acceptable salts, wherein the variable are defined herein. The inventive compounds selectively inhibit aldosterone synthase. This invention also provides for pharmaceutical compositions comprising the compounds of Formula I or their salts as well as potentially to methods for the treatment, amelioration or prevention of conditions that could be treated by inhibiting aldosterone synthase.