PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 29458047-0 2018 Effects of cytochrome P450 single nucleotide polymorphisms on methadone metabolism and pharmacodynamics. Methadone 62-71 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 11-26 29458047-4 2018 Methadone is primarily metabolized in the liver by cytochrome P450 (CYP) enzymes, predominately by CYP2B6, followed by CYP3A4, 2C19, 2D6, and to a lesser extent, CYP2C18, 3A7, 2C8, 2C9, 3A5, and 1A2. Methadone 0-9 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 51-66 29458047-4 2018 Methadone is primarily metabolized in the liver by cytochrome P450 (CYP) enzymes, predominately by CYP2B6, followed by CYP3A4, 2C19, 2D6, and to a lesser extent, CYP2C18, 3A7, 2C8, 2C9, 3A5, and 1A2. Methadone 0-9 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 68-71 29458047-4 2018 Methadone is primarily metabolized in the liver by cytochrome P450 (CYP) enzymes, predominately by CYP2B6, followed by CYP3A4, 2C19, 2D6, and to a lesser extent, CYP2C18, 3A7, 2C8, 2C9, 3A5, and 1A2. Methadone 0-9 cytochrome P450 family 2 subfamily B member 6 Homo sapiens 99-105 29458047-4 2018 Methadone is primarily metabolized in the liver by cytochrome P450 (CYP) enzymes, predominately by CYP2B6, followed by CYP3A4, 2C19, 2D6, and to a lesser extent, CYP2C18, 3A7, 2C8, 2C9, 3A5, and 1A2. Methadone 0-9 cytochrome P450 family 2 subfamily C member 18 Homo sapiens 162-169 29458047-6 2018 Several SNPs in the CYP2B6, 3A4, 2C19, 2D6, and 3A5 genes result in increases in methadone plasma concentrations, decreased N-demethylation, and decreased methadone clearance. Methadone 81-90 cytochrome P450 family 2 subfamily B member 6 Homo sapiens 20-26 29458047-6 2018 Several SNPs in the CYP2B6, 3A4, 2C19, 2D6, and 3A5 genes result in increases in methadone plasma concentrations, decreased N-demethylation, and decreased methadone clearance. Methadone 155-164 cytochrome P450 family 2 subfamily B member 6 Homo sapiens 20-26 29458047-7 2018 In particular, carriers of CYP2B6*6/*6 may have a greater risk for detrimental adverse effects, as methadone metabolism and clearance are diminished in these individuals. Methadone 99-108 cytochrome P450 family 2 subfamily B member 6 Homo sapiens 27-33 29458047-8 2018 CYP2B6*4, on the other hand, has been observed to decrease plasma concentrations of methadone due to increased methadone clearance. Methadone 84-93 cytochrome P450 family 2 subfamily B member 6 Homo sapiens 0-6 29458047-8 2018 CYP2B6*4, on the other hand, has been observed to decrease plasma concentrations of methadone due to increased methadone clearance. Methadone 111-120 cytochrome P450 family 2 subfamily B member 6 Homo sapiens 0-6 29458047-9 2018 The involvement, contribution, and understanding the role of SNPs in CYP2B6, and other CYP genes, in methadone metabolism can improve the therapeutic uses of methadone in patient outcome and the development of personalized medicine. Methadone 101-110 cytochrome P450 family 2 subfamily B member 6 Homo sapiens 69-75 29458047-9 2018 The involvement, contribution, and understanding the role of SNPs in CYP2B6, and other CYP genes, in methadone metabolism can improve the therapeutic uses of methadone in patient outcome and the development of personalized medicine. Methadone 101-110 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 69-72 29458047-9 2018 The involvement, contribution, and understanding the role of SNPs in CYP2B6, and other CYP genes, in methadone metabolism can improve the therapeutic uses of methadone in patient outcome and the development of personalized medicine. Methadone 158-167 cytochrome P450 family 2 subfamily B member 6 Homo sapiens 69-75 29458047-9 2018 The involvement, contribution, and understanding the role of SNPs in CYP2B6, and other CYP genes, in methadone metabolism can improve the therapeutic uses of methadone in patient outcome and the development of personalized medicine. Methadone 158-167 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 69-72