PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
14584950-0	2003	Design, synthesis, and SAR of potent and selective dipeptide-derived inhibitors for dipeptidyl peptidases.	Dipeptides	51-60	sarcosine dehydrogenase	Homo sapiens	23-26	
21256035-0	2011	Synthesis and SAR studies on azetidine-containing dipeptides as HCMV inhibitors.	Dipeptides	50-60	sarcosine dehydrogenase	Homo sapiens	14-17	
21256035-1	2011	SAR studies on an azetidine-containing dipeptide prototype inhibitor of HCMV are described.	Dipeptides	39-48	sarcosine dehydrogenase	Homo sapiens	0-3	
27390066-3	2016	The SAR studies revealed several potent compounds, particularly among the phosphinic dipeptide analogues, that were strong inhibitors of ERAP2 (Ki=100-350nM).	Dipeptides	85-94	sarcosine dehydrogenase	Homo sapiens	4-7	
11948437-1	2002	Structurally constraint dipeptidomimetics represent an important class of conformationally rigid dipeptide surrogates and molecular scaffolds, which are frequently employed in peptide-based structure-activity relationships (SAR) and construction of combinatorial libraries.	Dipeptides	97-106	sarcosine dehydrogenase	Homo sapiens	224-227	
31709757-7	2020	From the SAR model created, a multiple regression equation was derived to predict the biological activity of the dipeptide DPP-IV inhibitors.	Dipeptides	113-122	sarcosine dehydrogenase	Homo sapiens	9-12