PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
19218247-4	2009	Herein we demonstrate for the first time that human AKR1C enzymes (AKR1C1-4) are able to reduce conjugated steroids such as Dht-17beta-glucuronide (DhtG), Dht-17beta-sulfate (DhtS), and Tib-17beta-sulfate (TibS).	dihydrotestosterone glucuronide	124-146	aldo-keto reductase family 1 member C1	Homo sapiens	67-75
19218247-4	2009	Herein we demonstrate for the first time that human AKR1C enzymes (AKR1C1-4) are able to reduce conjugated steroids such as Dht-17beta-glucuronide (DhtG), Dht-17beta-sulfate (DhtS), and Tib-17beta-sulfate (TibS).	dihydrotestosterone glucuronide	148-152	aldo-keto reductase family 1 member C1	Homo sapiens	67-75
19218247-6	2009	The product profile of the reduction of each steroid conjugate by the individual AKR1C isoform was similar to that of the corresponding free steroid except for the reduction of DhtG catalyzed by AKR1C2, where a complete inversion in stereochemical preference to 3beta-reduction (with DhtG) from 3alpha-reduction (with Dht and DhtS) was observed.	dihydrotestosterone glucuronide	177-181	aldo-keto reductase family 1 member C2	Homo sapiens	195-201
19218247-6	2009	The product profile of the reduction of each steroid conjugate by the individual AKR1C isoform was similar to that of the corresponding free steroid except for the reduction of DhtG catalyzed by AKR1C2, where a complete inversion in stereochemical preference to 3beta-reduction (with DhtG) from 3alpha-reduction (with Dht and DhtS) was observed.	dihydrotestosterone glucuronide	284-288	aldo-keto reductase family 1 member C2	Homo sapiens	195-201
11129427-1	2000	BACKGROUND: UDP-glucuronosyltransferase 2B15 (UGT2B15) catalyzes the inactivation of dihydrotestosterone (DHT) by forming the DHT-glucuronide and is expressed in normal and hyperplastic prostate tissue.	dihydrotestosterone glucuronide	126-141	UDP glucuronosyltransferase family 2 member B15	Homo sapiens	12-44
16595710-4	2006	Among the 12 UGT isoforms tested, only UGT1A8 was capable of producing DHT diglucuronide from DHT.	dihydrotestosterone glucuronide	71-88	UDP glucuronosyltransferase family 1 member A complex locus	Homo sapiens	13-16
16595710-4	2006	Among the 12 UGT isoforms tested, only UGT1A8 was capable of producing DHT diglucuronide from DHT.	dihydrotestosterone glucuronide	71-88	UDP glucuronosyltransferase family 1 member A8	Homo sapiens	39-45
11129427-1	2000	BACKGROUND: UDP-glucuronosyltransferase 2B15 (UGT2B15) catalyzes the inactivation of dihydrotestosterone (DHT) by forming the DHT-glucuronide and is expressed in normal and hyperplastic prostate tissue.	dihydrotestosterone glucuronide	126-141	UDP glucuronosyltransferase family 2 member B15	Homo sapiens	46-53
9202245-4	1997	The formation of DHT glucuronide (DHT-G) was inhibited by 47% when LNCaP cells were treated for 6 days with 10 ng/ml of EGF.	dihydrotestosterone glucuronide	17-32	epidermal growth factor	Homo sapiens	120-123
30959153-4	2019	Using vesicular transport assay with recombinant human MRP2, MRP3, MRP4, MDR1 and BCRP, we first identified that TG, AG, EtioG, and DHTG were primarily substrates of MRP2 and MRP3, although lower levels of transport were also observed with MDR1 and BCRP vesicles.	dihydrotestosterone glucuronide	132-136	ATP binding cassette subfamily C member 2	Homo sapiens	55-59
30959153-4	2019	Using vesicular transport assay with recombinant human MRP2, MRP3, MRP4, MDR1 and BCRP, we first identified that TG, AG, EtioG, and DHTG were primarily substrates of MRP2 and MRP3, although lower levels of transport were also observed with MDR1 and BCRP vesicles.	dihydrotestosterone glucuronide	132-136	ATP binding cassette subfamily C member 3	Homo sapiens	61-65
30959153-4	2019	Using vesicular transport assay with recombinant human MRP2, MRP3, MRP4, MDR1 and BCRP, we first identified that TG, AG, EtioG, and DHTG were primarily substrates of MRP2 and MRP3, although lower levels of transport were also observed with MDR1 and BCRP vesicles.	dihydrotestosterone glucuronide	132-136	ATP binding cassette subfamily C member 4	Homo sapiens	67-71
30959153-4	2019	Using vesicular transport assay with recombinant human MRP2, MRP3, MRP4, MDR1 and BCRP, we first identified that TG, AG, EtioG, and DHTG were primarily substrates of MRP2 and MRP3, although lower levels of transport were also observed with MDR1 and BCRP vesicles.	dihydrotestosterone glucuronide	132-136	ATP binding cassette subfamily B member 1	Homo sapiens	73-77
30959153-4	2019	Using vesicular transport assay with recombinant human MRP2, MRP3, MRP4, MDR1 and BCRP, we first identified that TG, AG, EtioG, and DHTG were primarily substrates of MRP2 and MRP3, although lower levels of transport were also observed with MDR1 and BCRP vesicles.	dihydrotestosterone glucuronide	132-136	BCR pseudogene 1	Homo sapiens	82-86
30959153-4	2019	Using vesicular transport assay with recombinant human MRP2, MRP3, MRP4, MDR1 and BCRP, we first identified that TG, AG, EtioG, and DHTG were primarily substrates of MRP2 and MRP3, although lower levels of transport were also observed with MDR1 and BCRP vesicles.	dihydrotestosterone glucuronide	132-136	ATP binding cassette subfamily C member 2	Homo sapiens	166-170
30959153-4	2019	Using vesicular transport assay with recombinant human MRP2, MRP3, MRP4, MDR1 and BCRP, we first identified that TG, AG, EtioG, and DHTG were primarily substrates of MRP2 and MRP3, although lower levels of transport were also observed with MDR1 and BCRP vesicles.	dihydrotestosterone glucuronide	132-136	ATP binding cassette subfamily C member 3	Homo sapiens	175-179
30959153-4	2019	Using vesicular transport assay with recombinant human MRP2, MRP3, MRP4, MDR1 and BCRP, we first identified that TG, AG, EtioG, and DHTG were primarily substrates of MRP2 and MRP3, although lower levels of transport were also observed with MDR1 and BCRP vesicles.	dihydrotestosterone glucuronide	132-136	ATP binding cassette subfamily B member 1	Homo sapiens	240-244
30959153-4	2019	Using vesicular transport assay with recombinant human MRP2, MRP3, MRP4, MDR1 and BCRP, we first identified that TG, AG, EtioG, and DHTG were primarily substrates of MRP2 and MRP3, although lower levels of transport were also observed with MDR1 and BCRP vesicles.	dihydrotestosterone glucuronide	132-136	BCR pseudogene 1	Homo sapiens	249-253
30959153-9	2019	The glucuronides of inactive androgens, AG and EtioG were preferentially transported by MRP3, whereas the glucuronides of active androgens, TG and DHTG were mainly transported by MRP2 in liver.	dihydrotestosterone glucuronide	147-151	ATP binding cassette subfamily C member 2	Homo sapiens	179-183
9569009-8	1998	Results show a dose dependent inhibition of DHT glucuronide (DHT-G) formation following treatment (6 days) with acidic FGF (aFGF) and basic FGF (bFGF).	dihydrotestosterone glucuronide	44-59	fibroblast growth factor 1	Homo sapiens	112-122
9569009-8	1998	Results show a dose dependent inhibition of DHT glucuronide (DHT-G) formation following treatment (6 days) with acidic FGF (aFGF) and basic FGF (bFGF).	dihydrotestosterone glucuronide	44-59	fibroblast growth factor 1	Homo sapiens	124-128
9569009-8	1998	Results show a dose dependent inhibition of DHT glucuronide (DHT-G) formation following treatment (6 days) with acidic FGF (aFGF) and basic FGF (bFGF).	dihydrotestosterone glucuronide	44-59	fibroblast growth factor 2	Homo sapiens	134-143
9569009-8	1998	Results show a dose dependent inhibition of DHT glucuronide (DHT-G) formation following treatment (6 days) with acidic FGF (aFGF) and basic FGF (bFGF).	dihydrotestosterone glucuronide	44-59	fibroblast growth factor 2	Homo sapiens	145-149