1463484-39-0Relevant articles and documents
Discovery and Early Clinical Development of LY3202626, a Low-Dose, CNS-Penetrant BACE Inhibitor
McKinzie, David L.,Winneroski, Leonard L.,Green, Steven J.,Hembre, Erik J.,Erickson, Jon A.,Willis, Brian A.,Monk, Scott A.,Aluise, Christopher D.,Baker, Thomas K.,Lopez, Jose E.,Hendle, J?rg,Beck, James P.,Brier, Richard A.,Boggs, Leonard N.,Borders, Anthony R.,Cocke, Patrick J.,Garcia-Losada, Pablo,Lowe, Stephen L.,Mathes, Brian M.,May, Patrick C.,Porter, Warren J.,Stout, Stephanie L.,Timm, David E.,Watson, Brian M.,Yang, Zhixiang,Mergott, Dustin J.
, p. 8076 - 8100 (2021/06/28)
The beta-site APP cleaving enzyme 1, known as BACE1, has been a widely pursued Alzheimer's disease drug target owing to its critical role in the production of amyloid-beta. We have previously reported the clinical development of LY2811376 and LY2886721. L
TOSYLATE SALT OF N-[3-[(4AR,7AS)-2-AMINO-6-(5-FLUOROPYRIMIDIN-2-YL)-4,4A,5,7-TETRAHYDROPYRROLO[3,4-D][1,3]THIAZIN-7A-YL]-4-FLUORO-PHENYL]-5-METHOXY-PYRAZINE-2-CARBOXAMIDE
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, (2016/08/23)
The present invention provides a tosylate salt of N-[3-[(4aR,7aS)-2-amino-6-(5- fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro- phenyl]-5-methoxy-pyrazine-2-carboxamide.
TETRAHYDROPYRROLOTHIAZINE COMPOUNDS
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Paragraph 0108; 0109, (2013/10/08)
The present invention provides compounds of Formula I: wherein A is selected from the group consisting of; R1 is H or F; R2 is H, —CH2OH, C1-C3 alkyl, R3 is H, F, or CN; R4 is H, F; or CN; and R5 is H, —CH3, or —OCH3; or a pharmaceutically acceptable salt thereof.