PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 8248926-4 1993 A polyclonal antibody raised against CYP4B1 prevented the covalent binding of [14C]-ipomeanol to lung microsomal protein in vitro. 4-ipomeanol 84-93 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 37-43 8248926-0 1993 CYP4B1 activates 4-ipomeanol in rat lung. 4-ipomeanol 17-28 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 0-6 8248926-1 1993 Inhibition of pulmonary CYP4B1 activity by pretreatment of rats with p-xylene decreased the ability of lung microsomes to N-hydroxylate 2-aminofluorene and prevented the lung damage normally seen after dosing with ipomeanol. 4-ipomeanol 214-223 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 24-30 8248926-7 1993 The CYP4B1 substrate 2-aminofluorene, when dosed to rats, caused a sixfold decrease in ipomeanol toxicity. 4-ipomeanol 87-96 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 4-10 24899949-1 2010 OBJECTIVE: We determined the cytotoxic properties of cytochrome P450 4B1 (CYP4B1) activated 4-ipomeanol (4-ipo) and 2-aminoanthracene (2-AA) in rat glioma to verify the CYP4B1/4-ipo or 2-AA system for prodrug-activating gene therapy. 4-ipomeanol 92-103 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 53-72 23682585-0 2013 Synthesis and evaluation of a 18F-labeled 4-ipomeanol as an imaging agent for CYP4B1 gene prodrug activation therapy. 4-ipomeanol 42-53 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 78-84 23682585-1 2013 We report the development of a (18)F-labeled 4-ipomeanol (4-IM), which is metabolized by the CYP4B1 enzyme, to image tumors and monitor enzyme-activating anticancer prodrugs. 4-ipomeanol 45-56 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 93-99 23682585-1 2013 We report the development of a (18)F-labeled 4-ipomeanol (4-IM), which is metabolized by the CYP4B1 enzyme, to image tumors and monitor enzyme-activating anticancer prodrugs. 4-ipomeanol 58-62 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 93-99 24899949-1 2010 OBJECTIVE: We determined the cytotoxic properties of cytochrome P450 4B1 (CYP4B1) activated 4-ipomeanol (4-ipo) and 2-aminoanthracene (2-AA) in rat glioma to verify the CYP4B1/4-ipo or 2-AA system for prodrug-activating gene therapy. 4-ipomeanol 105-110 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 53-72 24899949-1 2010 OBJECTIVE: We determined the cytotoxic properties of cytochrome P450 4B1 (CYP4B1) activated 4-ipomeanol (4-ipo) and 2-aminoanthracene (2-AA) in rat glioma to verify the CYP4B1/4-ipo or 2-AA system for prodrug-activating gene therapy. 4-ipomeanol 105-110 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 74-80 24899949-1 2010 OBJECTIVE: We determined the cytotoxic properties of cytochrome P450 4B1 (CYP4B1) activated 4-ipomeanol (4-ipo) and 2-aminoanthracene (2-AA) in rat glioma to verify the CYP4B1/4-ipo or 2-AA system for prodrug-activating gene therapy. 4-ipomeanol 92-103 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 74-80 24899949-1 2010 OBJECTIVE: We determined the cytotoxic properties of cytochrome P450 4B1 (CYP4B1) activated 4-ipomeanol (4-ipo) and 2-aminoanthracene (2-AA) in rat glioma to verify the CYP4B1/4-ipo or 2-AA system for prodrug-activating gene therapy. 4-ipomeanol 92-97 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 53-72 24899949-1 2010 OBJECTIVE: We determined the cytotoxic properties of cytochrome P450 4B1 (CYP4B1) activated 4-ipomeanol (4-ipo) and 2-aminoanthracene (2-AA) in rat glioma to verify the CYP4B1/4-ipo or 2-AA system for prodrug-activating gene therapy. 4-ipomeanol 92-97 cytochrome P450, family 4, subfamily b, polypeptide 1 Rattus norvegicus 74-80