PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
1718269-4	1991	These binding sites resembled mammalian angiotensin II receptors by their high affinity and by their sensitivity to dithiothreitol.	Dithiothreitol	116-130	angiotensinogen	Homo sapiens	40-54	
11068047-1	2000	Dithiothreitol (DTT) treatment of angiotensin II (Ang II) type 2 (AT(2)) receptor potentiates ligand binding, but the underlying mechanism is not known.	Dithiothreitol	0-14	angiotensinogen	Homo sapiens	34-48	
11068047-1	2000	Dithiothreitol (DTT) treatment of angiotensin II (Ang II) type 2 (AT(2)) receptor potentiates ligand binding, but the underlying mechanism is not known.	Dithiothreitol	0-14	angiotensinogen	Homo sapiens	50-56	
11068047-1	2000	Dithiothreitol (DTT) treatment of angiotensin II (Ang II) type 2 (AT(2)) receptor potentiates ligand binding, but the underlying mechanism is not known.	Dithiothreitol	16-19	angiotensinogen	Homo sapiens	34-48	
11068047-1	2000	Dithiothreitol (DTT) treatment of angiotensin II (Ang II) type 2 (AT(2)) receptor potentiates ligand binding, but the underlying mechanism is not known.	Dithiothreitol	16-19	angiotensinogen	Homo sapiens	50-56	
7965763-5	1994	Binding sites exhibited the characteristics of the AT1 class of ANG II receptor, ligand binding being sensitive to dithiothreitol, completely inhibited by nonpeptide AT1 antagonists (Losartan, EXP3174 and SKF108566) and not inhibited by the AT2 antagonist (PD123319).	Dithiothreitol	115-129	angiotensinogen	Homo sapiens	64-70	
8075862-13	1994	Specific binding of [125I]-(Sar1, Ile8)AII to each structure was completely inhibited by 10 microM dithiothreitol and was inhibited by unlabelled ligands with the rank order of potency (Sar1, Ile8)AII > AII > losartan = SKF108566 > PD123319 indicating an AT1 subclass of angiotensin receptor.	Dithiothreitol	99-113	angiotensinogen	Homo sapiens	39-42	
3925269-3	1985	DTT-treated high molecular weight (HMW) angiotensinogen was very similar to low molecular weight (LMW) angiotensinogen with respect to molecular weight, pH profile for angiotensin formation by human kidney renin, thermostability, Km value and isoelectric point.	Dithiothreitol	0-3	angiotensinogen	Homo sapiens	40-55	
28204818-6	2017	Confocal imaging analysis revealed that both LDL uptake by cells and LDL retention in human umbilical venous walls were highly elevated after Ang II exposure, while MbetaCD and DTT significantly inhibited the effects of Ang II.	Dithiothreitol	177-180	angiotensinogen	Homo sapiens	220-226	
24755153-8	2014	Functional significance of glutathionylation in intact vessels was supported by Ang II-induced impairment of endothelium-dependent vasorelaxation that was abolished by the disulfide reducing agent, dithiothreitol.	Dithiothreitol	198-212	angiotensinogen	Homo sapiens	80-86