PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
25953703-4	2015	Their rank order potency for TPO inhibition was MBT=CMBT>ABT>BTZ, whereas HBT and MTBT exhibited no inhibitory activity.	benzothiazole	67-70	thyroid peroxidase S homeolog	Xenopus laevis	29-32
25953703-4	2015	Their rank order potency for TPO inhibition was MBT=CMBT>ABT>BTZ, whereas HBT and MTBT exhibited no inhibitory activity.	5-chloro-2-mercaptobenzothiazole	52-56	thyroid peroxidase S homeolog	Xenopus laevis	29-32
26971167-6	2016	At 7 days, exposure to butachlor up-regulated the mRNA expression of genes involved in THs synthesis and metabolism (tshalpha, tg, tpo and dio1) and THs receptors (tralpha and trbeta).	butachlor	23-32	thyroid peroxidase S homeolog	Xenopus laevis	131-134
25953703-8	2015	The 2 most potent chemicals for TPO inhibition, MBT and CMBT, produced responses in vivo indicative of T4 synthesis inhibition including induction of sodium iodide symporter mRNA and decreases in glandular and circulating thyroid hormones.	Sodium Iodide	150-163	thyroid peroxidase S homeolog	Xenopus laevis	32-35
25953703-4	2015	Their rank order potency for TPO inhibition was MBT=CMBT>ABT>BTZ, whereas HBT and MTBT exhibited no inhibitory activity.	abt	60-63	thyroid peroxidase S homeolog	Xenopus laevis	29-32
23178179-3	2013	2-Mercaptobenzothiazole (MBT), a high production volume chemical, was tested and shown to inhibit thyroid peroxidase (TPO) enzyme activity in vitro, a key enzyme necessary for the synthesis of thyroid hormone.	captax	0-23	thyroid peroxidase S homeolog	Xenopus laevis	118-121
23178179-3	2013	2-Mercaptobenzothiazole (MBT), a high production volume chemical, was tested and shown to inhibit thyroid peroxidase (TPO) enzyme activity in vitro, a key enzyme necessary for the synthesis of thyroid hormone.	captax	25-28	thyroid peroxidase S homeolog	Xenopus laevis	118-121