PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10751038-0	2000	Structure activity relationship of human microsomal epoxide hydrolase inhibition by amide and acid analogues of valproic acid.	Valproic Acid	112-125	epoxide hydrolase 1	Homo sapiens	41-69	
10751038-1	2000	PURPOSE: The purpose of this study was to evaluate the in vitro inhibitory potency of various amide analogues and derivatives of valproic acid toward human microsomal epoxide hydrolase (mEH).	Valproic Acid	129-142	epoxide hydrolase 1	Homo sapiens	156-184	
1540232-0	1992	Interaction of valproic acid and some analogues with microsomal epoxide hydrolase.	Valproic Acid	15-28	epoxide hydrolase 1	Homo sapiens	53-81	
2501059-0	1989	Inhibition of human liver microsomal epoxide hydrolase by valproate and valpromide: in vitro/in vivo correlation.	Valproic Acid	58-67	epoxide hydrolase 1	Homo sapiens	26-54	
2501059-2	1989	In this study, therapeutic concentrations of valproic acid (less than 1 mmol/L) and valpromide (less than 10 mumol/L) inhibited hydrolysis of carbamazepine epoxide and styrene oxide in human liver microsomes and in preparations of purified human liver microsomal epoxide hydrolase.	Valproic Acid	45-58	epoxide hydrolase 1	Homo sapiens	252-280	
2501059-6	1989	Valproic acid and valpromide are the first drugs known to inhibit microsomal epoxide hydrolase, an important detoxification enzyme, at therapeutic concentrations.	Valproic Acid	0-13	epoxide hydrolase 1	Homo sapiens	66-94