PMID-sentid Pub_year Sent_text compound_name comp_offset prot_official_name organism prot_offset 18674515-0 2008 The human UDP-glucuronosyltransferase UGT1A3 is highly selective towards N2 in the tetrazole ring of losartan, candesartan, and zolarsartan. zolasartan(2-) 128-139 UDP glucuronosyltransferase family 1 member A3 Homo sapiens 38-44 18674515-1 2008 Losartan, candesartan, and zolarsartan are AT(1) receptor antagonists that inhibit the effect of angiotensin II. zolasartan(2-) 27-38 angiotensinogen Homo sapiens 97-111 18674515-8 2008 Moreover, the tetrazole-N2 of zolarsartan was only conjugated by UGT1A3, whereas the tetrazole-N1 of this aglycone was accessible to other enzymes, including UGT1A5. zolasartan(2-) 30-41 UDP glucuronosyltransferase family 1 member A3 Homo sapiens 65-71 18674515-8 2008 Moreover, the tetrazole-N2 of zolarsartan was only conjugated by UGT1A3, whereas the tetrazole-N1 of this aglycone was accessible to other enzymes, including UGT1A5. zolasartan(2-) 30-41 UDP glucuronosyltransferase family 1 member A5 Homo sapiens 158-164