PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 11294973-1 2001 In the current study, the identification of the rat and human UDP-glucuronosyltransferase (UGT) isoforms responsible for the glucuronidation of diclofenac was determined. Diclofenac 144-154 UDP glucuronosyltransferase family 1 member A complex locus Homo sapiens 62-89 11294973-1 2001 In the current study, the identification of the rat and human UDP-glucuronosyltransferase (UGT) isoforms responsible for the glucuronidation of diclofenac was determined. Diclofenac 144-154 UDP glucuronosyltransferase family 1 member A complex locus Homo sapiens 91-94 11294973-2 2001 Recombinant human UGT1A9 catalyzed the glucuronidation of diclofenac at a moderate rate of 166-pmol/min/mg protein, while UGT1A6 and 2B15 catalyzed the glucuronidation of diclofenac at low rates (<20-pmol/min/mg protein). Diclofenac 58-68 UDP glucuronosyltransferase family 1 member A9 Homo sapiens 18-24 11294973-2 2001 Recombinant human UGT1A9 catalyzed the glucuronidation of diclofenac at a moderate rate of 166-pmol/min/mg protein, while UGT1A6 and 2B15 catalyzed the glucuronidation of diclofenac at low rates (<20-pmol/min/mg protein). Diclofenac 171-181 UDP glucuronosyltransferase family 1 member A9 Homo sapiens 18-24 11294973-2 2001 Recombinant human UGT1A9 catalyzed the glucuronidation of diclofenac at a moderate rate of 166-pmol/min/mg protein, while UGT1A6 and 2B15 catalyzed the glucuronidation of diclofenac at low rates (<20-pmol/min/mg protein). Diclofenac 171-181 UDP glucuronosyltransferase family 1 member A6 Homo sapiens 122-128 11294973-3 2001 Conversely, human UGT2B7 displayed a high rate of diclofenac glucuronide formation (>500 pmol/min/mg protein). 1-O-(2-((2',6'-dichlorophenyl)amino)phenylacetyl)glucopyranuronic acid 50-72 UDP glucuronosyltransferase family 2 member B7 Homo sapiens 18-24 11294973-4 2001 Recombinant rat UGT2B1 catalyzed the glucuronidation of diclofenac at a rate of 250-pmol/min/mg protein. Diclofenac 56-66 UDP glucuronosyltransferase family 2 member B17 Rattus norvegicus 16-22 11294973-7 2001 Morphine is a known substrate for rat UGT2B1 and human UGT2B7 and both total morphine glucuronidation (3-O- and 6-O-glucuronides) and diclofenac glucuronidation reactions showed a strong correlation with one another in human liver microsome samples. Morphine 0-8 UDP glucuronosyltransferase family 2 member B17 Rattus norvegicus 38-44 11294973-7 2001 Morphine is a known substrate for rat UGT2B1 and human UGT2B7 and both total morphine glucuronidation (3-O- and 6-O-glucuronides) and diclofenac glucuronidation reactions showed a strong correlation with one another in human liver microsome samples. Morphine 0-8 UDP glucuronosyltransferase family 2 member B7 Homo sapiens 55-61 11294973-9 2001 These data suggested that rat UGT2B1 and human UGT2B7 were the major UGT isoforms involved in the glucuronidation of diclofenac. Diclofenac 117-127 UDP glucuronosyltransferase family 2 member B17 Rattus norvegicus 30-36 11294973-9 2001 These data suggested that rat UGT2B1 and human UGT2B7 were the major UGT isoforms involved in the glucuronidation of diclofenac. Diclofenac 117-127 UDP glucuronosyltransferase family 2 member B7 Homo sapiens 47-53 11294973-9 2001 These data suggested that rat UGT2B1 and human UGT2B7 were the major UGT isoforms involved in the glucuronidation of diclofenac. Diclofenac 117-127 UDP glucuronosyltransferase family 1 member A complex locus Homo sapiens 30-33