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 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 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