PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 15618670-1 2002 The participation of cytochrome P-450 (CYP) isoforms in the metabolism of selegiline was investigated. Selegiline 74-84 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 21-37 15618670-1 2002 The participation of cytochrome P-450 (CYP) isoforms in the metabolism of selegiline was investigated. Selegiline 74-84 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 39-42 15618670-2 2002 Experiments using recombinant CYP isoforms expressed in human lymphoblastoid cells showed CYP2B6 to be the major CYP isoform involved with the metabolism of selegiline. Selegiline 157-167 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 30-33 15618670-2 2002 Experiments using recombinant CYP isoforms expressed in human lymphoblastoid cells showed CYP2B6 to be the major CYP isoform involved with the metabolism of selegiline. Selegiline 157-167 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 90-93 10862503-2 2000 In the current work we have studied the cytochrome P450 (CYP)-catalyzed oxidative metabolism of selegiline to desmethylselegiline and 1-methamphetamine and the effects of selegiline, desmethylselegiline and 1-methamphetamine on hepatic CYP enzymes in human liver microsomes in vitro. Selegiline 96-106 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 40-55 10862503-2 2000 In the current work we have studied the cytochrome P450 (CYP)-catalyzed oxidative metabolism of selegiline to desmethylselegiline and 1-methamphetamine and the effects of selegiline, desmethylselegiline and 1-methamphetamine on hepatic CYP enzymes in human liver microsomes in vitro. Selegiline 96-106 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 57-60 10862503-2 2000 In the current work we have studied the cytochrome P450 (CYP)-catalyzed oxidative metabolism of selegiline to desmethylselegiline and 1-methamphetamine and the effects of selegiline, desmethylselegiline and 1-methamphetamine on hepatic CYP enzymes in human liver microsomes in vitro. Selegiline 96-106 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 236-239 10862503-2 2000 In the current work we have studied the cytochrome P450 (CYP)-catalyzed oxidative metabolism of selegiline to desmethylselegiline and 1-methamphetamine and the effects of selegiline, desmethylselegiline and 1-methamphetamine on hepatic CYP enzymes in human liver microsomes in vitro. Selegiline 119-129 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 40-55 10862503-2 2000 In the current work we have studied the cytochrome P450 (CYP)-catalyzed oxidative metabolism of selegiline to desmethylselegiline and 1-methamphetamine and the effects of selegiline, desmethylselegiline and 1-methamphetamine on hepatic CYP enzymes in human liver microsomes in vitro. Selegiline 119-129 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 57-60 10862503-8 2000 In studies with CYP-specific model activities, both selegiline and desmethylselegiline inhibited the CYP2C19-mediated S-mephenytoin 4"-hydroxylation with average IC50 values of 21 microM and 26 microM, respectively. Selegiline 52-62 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 16-19 10862503-11 2000 Inhibitory potencies of selegiline, desmethylselegiline and 1-methamphetamine towards other CYP-model activities were much lower. Selegiline 24-34 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 92-95