755753-54-9Relevant academic research and scientific papers
Synthesis and evaluation of heteroarylalanine diacids as potent and selective neutral endopeptidase inhibitors
Glossop, Melanie S.,Bazin, Richard J.,Dack, Kevin N.,Fox, David N.A.,MacDonald, Graeme A.,Mills, Mark,Owen, Dafydd R.,Phillips, Chris,Reeves, Keith A.,Ringer, Tracy J.,Strang, Ross S.,Watson, Christine A.L.
, p. 3404 - 3406 (2011/07/07)
Heteroarylalanine derivatives 4 were designed as potential inhibitors of neutral endopeptidase (NEP EC 3.4.24.11). Selectivity over other zinc metalloproteinases was explored through occupation of the S2′ subsite within NEP. Structural optimisation led to
NEUTRAL ENDOPEPTIDASE INHIBITOR POLYMORPH
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, (2008/06/13)
Disclosed are (2S)-2-{1-[(1S)-1-Isobutoxycarbonyl-2-(5-phenyl-oxazol-2-yl)-ethylcarbamoyl]-cyclopentylmethyl}-4-methoxy-butyric, Potassium-(2S)-2-{1-[(1S)-1-Isobutoxycarbonyl-2-(5-phenyl-oxazol-2-yl)-ethylcarbamoyl]-cyclopentylmethyl}-4-methoxy-butyrate,
