892491-46-2Relevant academic research and scientific papers
Identification, optimisation and in vivo evaluation of oxadiazole DGAT-1 inhibitors for the treatment of obesity and diabetes
McCoull, William,Addie, Matthew S.,Birch, Alan M.,Birtles, Susan,Buckett, Linda K.,Butlin, Roger J.,Bowker, Suzanne S.,Boyd, Scott,Chapman, Stephen,Davies, Robert D.M.,Donald, Craig S.,Green, Clive P.,Jenner, Chloe,Kemmitt, Paul D.,Leach, Andrew G.,Moody, Graeme C.,Morentin Gutierrez, Pablo,Newcombe, Nicholas J.,Nowak, Thorsten,Packer, Martin J.,Plowright, Alleyn T.,Revill, John,Schofield, Paul,Sheldon, Chris,Stokes, Steve,Turnbull, Andrew V.,Wang, Steven J.Y.,Whalley, David P.,Matthew Wood
, p. 3873 - 3878 (2012/07/03)
A novel series of DGAT-1 inhibitors was discovered from an oxadiazole amide high throughput screening (HTS) hit. Optimisation of potency and ligand lipophilicity efficiency (LLE) resulted in a carboxylic acid containing clinical candidate 53 (AZD3988), wh
OXADIAZOLE DERIVATIVES AS DGAT INHIBITORS
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Page/Page column 315, (2008/06/13)
Compounds of formula (I), and salts and pro-drugs thereof: Formula (I) wherein for example R1 is optionally substituted aryl or heteroaryl; Y is a linking group selected from, for example, a direct bond, and a (substituted) alkyl chain; R2
OXADIAZOLE DERIVATIVES AS DGAT INHIBITORS
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Page/Page column 61, (2008/06/13)
Compounds of Formula (I): wherein R1- R2, W and Y are as described m the specification, and their salts and pro-drugs, are inhibitors of DGAT and are thereby useful in the treatment of, for example, obesity. Processes for preparing c
