167304-98-5Relevant academic research and scientific papers
Dual metalloprotease inhibitors: Mercaptoacetyl-based fused heterocyclic dipeptide mimetics as inhibitors of angiotensin-converting enzyme and neutral endopeptidase
Robl, Jeffrey A.,Sun, Chong-Qing,Stevenson, Jay,Ryono, Denis E.,Simpkins, Ligaya M.,Cimarusti, Maria P.,Dejneka, Tamara,Slusarchyk, William A.,Chao, Sam,Stratton, Leslie,Misra, Raj N.,Bednarz, Mark S.,Asaad, Magdi M.,Cheung, Hong Son,Abboa-Offei, Benoni E.,Smith, Patricia L.,Mathers, Parker D.,Fox, Maxine,Schaeffer, Thomas R.,Seymour, Andrea A.,Trippodo, Nick C.
, p. 1570 - 1577 (2007/10/03)
A series of 7,6- and 7,5-fused bicyclic thiazepinones and oxazepinones were generated and incorporated as conformationally restricted dipeptide surrogates in mercaptoacyl dipeptides. These compounds are potent inhibitors of angiotensin-converting enzyme (
COMPOUNDS CONTAINING A FUSED BICYCLE RING AND PROCESSES THEREFOR
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, (2008/06/13)
Compounds of the formula STR1 wherein X is O or S--(O) t ; n is one or two; m is zero or one; Y is CH 2, O, or S--(O) t provided that Y is O or S--(O) t only when m is one; and A is STR2 are dual inhibitors of NEP and ACE. Compounds wherein A is STR3 are selective ACE inhibitors. Also disclosed are methods of preparation and intermediates.
