PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8164250-7	1994	The separation of the four stereoisomers using chiral amines and the stereoselective synthesis of the 2-(mercaptomethyl)-3-phenylbutanoyl moiety showed that inhibitors with the 2S,3R configuration are the most potent on both NEP and ACE.	2-(mercaptomethyl)-3-phenylbutanoyl	102-137	angiotensin I converting enzyme (peptidyl-dipeptidase A) 1	Mus musculus	233-236