PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
1330177-7	1992	The estimated KB values obtained for these two compounds, assuming competitive antagonism, were 40 +/- 14 nM and 8.6 +/- 2.8 nM for D-Arg,[Hyp3,D-Phe7]-bradykinin and D-Arg[Hyp3,Thi5,8,D-Phe7]-bradykinin respectively.	d-phe7	144-150	kininogen 1	Bos taurus	152-162	
2902216-7	1988	Thus, high-affinity binding is blocked by B2 antagonists, D-Arg[Hyp3, thienylalanine5,8,D-Phe7]-BK and [thienylalanine5,8, D-Phe7]-BK and low-affinity binding is blocked by B1 antagonist des-Arg9[Leu8]-BK.	d-phe7	88-94	kininogen 1	Bos taurus	96-98	
2175399-4	1990	The response was markedly inhibited by the bradykinin B2 antagonist [Thi5,8,D-Phe7] bradykinin but not the B1 antagonist [Des-Arg9,Leu8] bradykinin.	d-phe7	76-82	kininogen 1	Bos taurus	43-53	
2175399-4	1990	The response was markedly inhibited by the bradykinin B2 antagonist [Thi5,8,D-Phe7] bradykinin but not the B1 antagonist [Des-Arg9,Leu8] bradykinin.	d-phe7	76-82	kininogen 1	Bos taurus	84-94	
2175399-4	1990	The response was markedly inhibited by the bradykinin B2 antagonist [Thi5,8,D-Phe7] bradykinin but not the B1 antagonist [Des-Arg9,Leu8] bradykinin.	d-phe7	76-82	kininogen 1	Bos taurus	84-94	
2902216-7	1988	Thus, high-affinity binding is blocked by B2 antagonists, D-Arg[Hyp3, thienylalanine5,8,D-Phe7]-BK and [thienylalanine5,8, D-Phe7]-BK and low-affinity binding is blocked by B1 antagonist des-Arg9[Leu8]-BK.	d-phe7	123-129	kininogen 1	Bos taurus	131-133	
2902216-7	1988	Thus, high-affinity binding is blocked by B2 antagonists, D-Arg[Hyp3, thienylalanine5,8,D-Phe7]-BK and [thienylalanine5,8, D-Phe7]-BK and low-affinity binding is blocked by B1 antagonist des-Arg9[Leu8]-BK.	d-phe7	123-129	kininogen 1	Bos taurus	131-133