PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27208893-0	2016	Drug interaction study of natural steroids from herbs specifically toward human UDP-glucuronosyltransferase (UGT) 1A4 and their quantitative structure activity relationship (QSAR) analysis for prediction.	Steroids	34-42	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	80-117	
9622078-11	1998	The steroid form of the UDPGT transcript was expressed in LNCaP cells and was enhanced in biochanin A-treated LNCaP cells.	Steroids	4-11	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	24-29	
27208893-4	2016	Some natural steroids such as gitogenin, tigogenin, and solasodine were found to be the novel selective inhibitors of UGT1A4, and did not inhibit the activities of major human CYP isoforms.	Steroids	13-21	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	118-124	
27208893-7	2016	And this inhibition of steroids towards UGT1A4 was also verified in human primary hepatocytes.	Steroids	23-31	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	40-46	
27208893-8	2016	Furthermore, a quantitative structure-activity relationship (QSAR) of steroids with inhibitory effects toward human UGT1A4 isoform was established using the computational methods.	Steroids	70-78	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	116-122	
27208893-9	2016	Our findings elucidate the potential for in vivo HDI effects of steroids in herbal medicine and foods, with the clinical dr ugs eliminated by UGT1A4, and reveal the vital pharamcophoric requirement of natural steroids for UGT1A4 inhibition activity.	Steroids	64-72	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	142-148	
27208893-9	2016	Our findings elucidate the potential for in vivo HDI effects of steroids in herbal medicine and foods, with the clinical dr ugs eliminated by UGT1A4, and reveal the vital pharamcophoric requirement of natural steroids for UGT1A4 inhibition activity.	Steroids	64-72	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	222-228	
15057901-13	2004	Two polymorphisms of the hepatic UGT1A4 protein show a differential metabolic activity toward mutagenic amines and endogenous steroids, altering hepatic metabolism and detoxification.	Steroids	126-134	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	33-39	
18497089-7	2008	MCF-7 cells cultured steroid-free additionally expressed CYP1A2 as well as UGT1A4, 1A8, and 1A9.	Steroids	21-28	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	75-81