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Volumn 3, Issue 7-8, 2011, Pages 483-495

In vitro approaches to studying the metabolism of new psychoactive compounds

Author keywords

Cytosol; Drug; Hepatocyte; Microsome; S9 mix

Indexed keywords

COMMERCE; DRUG PRODUCTS; ENZYMES; MASS SPECTROMETRY; PHYSIOLOGY; RISK ASSESSMENT;

EID: 79960641733     PISSN: 19427603     EISSN: 19427611     Source Type: Journal    
DOI: 10.1002/dta.295     Document Type: Review
Times cited : (60)

References (76)
  • 1
    • 85153026883 scopus 로고    scopus 로고
    • US Department of Health and Human Services. Guidance for Industry: Safety Testing of Drug Metabolites, Available at: .
    • US Department of Health and Human Services. Guidance for Industry: Safety Testing of Drug Metabolites, 2008, Available at: .
    • (2008)
  • 2
    • 19944368433 scopus 로고    scopus 로고
    • Metabolism of designer drugs of abuse
    • R. F. Staack, H. H. Maurer. Metabolism of designer drugs of abuse. Curr. Drug Metab. 2005, 6, 259.
    • (2005) Curr. Drug Metab. , vol.6 , pp. 259
    • Staack, R.F.1    Maurer, H.H.2
  • 3
    • 77953493759 scopus 로고    scopus 로고
    • Metabolism of designer drugs of abuse: an updated review
    • M. R. Meyer, H. H. Maurer. Metabolism of designer drugs of abuse: an updated review. Curr. Drug Metab. 2010, 11, 468.
    • (2010) Curr. Drug Metab. , vol.11 , pp. 468
    • Meyer, M.R.1    Maurer, H.H.2
  • 6
    • 6344250770 scopus 로고    scopus 로고
    • 57 varieties: the human cytochromes P450
    • D. F. Lewis. 57 varieties: the human cytochromes P450. Pharmacogenomics 2004, 5, 305.
    • (2004) Pharmacogenomics , vol.5 , pp. 305
    • Lewis, D.F.1
  • 8
    • 0035139012 scopus 로고    scopus 로고
    • Screening for detection of new antidepressants, neuroleptics, hypnotics, and their metabolites in urine by GC-MS developed using rat liver microsomes
    • J. Bickeboeller-Friedrich, H. H. Maurer. Screening for detection of new antidepressants, neuroleptics, hypnotics, and their metabolites in urine by GC-MS developed using rat liver microsomes. Ther. Drug Monit. 2001, 23, 61.
    • (2001) Ther. Drug Monit. , vol.23 , pp. 61
    • Bickeboeller-Friedrich, J.1    Maurer, H.H.2
  • 9
    • 1842432478 scopus 로고    scopus 로고
    • Identification of human cytochrome P450 2D6 as major enzyme involved in the O-demethylation of the designer drug p-methoxymethamphetamine
    • R. F. Staack, D. S. Theobald, L. D. Paul, D. Springer, T. Kraemer, H. H. Maurer. Identification of human cytochrome P450 2D6 as major enzyme involved in the O-demethylation of the designer drug p-methoxymethamphetamine. Drug Metab. Dispos. 2004, 32, 379.
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 379
    • Staack, R.F.1    Theobald, D.S.2    Paul, L.D.3    Springer, D.4    Kraemer, T.5    Maurer, H.H.6
  • 10
    • 1642457236 scopus 로고    scopus 로고
    • Cytochrome P450 dependent metabolism of the new designer drug 1-(3-trifluoromethylphenyl)piperazine (TFMPP). In vivo studies in wistar and dark agouti rats as well as in vitro studies in human liver microsomes
    • R. F. Staack, L. D. Paul, D. Springer, T. Kraemer, H. H. Maurer. Cytochrome P450 dependent metabolism of the new designer drug 1-(3-trifluoromethylphenyl)piperazine (TFMPP). In vivo studies in wistar and dark agouti rats as well as in vitro studies in human liver microsomes. Biochem. Pharmacol. 2004, 67, 235.
    • (2004) Biochem. Pharmacol. , vol.67 , pp. 235
    • Staack, R.F.1    Paul, L.D.2    Springer, D.3    Kraemer, T.4    Maurer, H.H.5
  • 11
    • 1542314455 scopus 로고    scopus 로고
    • In vivo metabolism of the new designer drug 1-(4-methoxyphenyl)piperazine (MeOPP) in rat and identification of the human cytochrome P450 enzymes responsible for the major metabolic step
    • R. F. Staack, D. S. Theobald, L. D. Paul, D. Springer, T. Kraemer, H. H. Maurer. In vivo metabolism of the new designer drug 1-(4-methoxyphenyl)piperazine (MeOPP) in rat and identification of the human cytochrome P450 enzymes responsible for the major metabolic step. Xenobiotica 2004, 34, 179.
    • (2004) Xenobiotica , vol.34 , pp. 179
    • Staack, R.F.1    Theobald, D.S.2    Paul, L.D.3    Springer, D.4    Kraemer, T.5    Maurer, H.H.6
  • 12
    • 0042025298 scopus 로고    scopus 로고
    • Identification of cytochrome p450 enzymes involved in the metabolism of 4'-methyl-alpha-pyrrolidinopropiophenone, a novel scheduled designer drug, in human liver microsomes
    • D. Springer, L. D. Paul, R. F. Staack, T. Kraemer, H. H. Maurer. Identification of cytochrome p450 enzymes involved in the metabolism of 4'-methyl-alpha-pyrrolidinopropiophenone, a novel scheduled designer drug, in human liver microsomes. Drug Metab. Dispos. 2003, 31, 979.
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 979
    • Springer, D.1    Paul, L.D.2    Staack, R.F.3    Kraemer, T.4    Maurer, H.H.5
  • 13
    • 37549045269 scopus 로고    scopus 로고
    • Identification of cytochrome P450 enzymes involved in the metabolism of the new designer drug 4'-methyl-alpha-pyrrolidinobutyrophenone
    • F. T. Peters, M. R. Meyer, D. S. Theobald, H. H. Maurer. Identification of cytochrome P450 enzymes involved in the metabolism of the new designer drug 4'-methyl-alpha-pyrrolidinobutyrophenone. Drug Metab. Dispos. 2008, 36, 163.
    • (2008) Drug Metab. Dispos. , vol.36 , pp. 163
    • Peters, F.T.1    Meyer, M.R.2    Theobald, D.S.3    Maurer, H.H.4
  • 14
    • 0242351749 scopus 로고    scopus 로고
    • Identification of cytochrome P450 enzymes involved in the metabolism of 4'-methoxy-alpha-pyrrolidinopropiophenone (MOPPP), a designer drug, in human liver microsomes
    • D. Springer, R. F. Staack, L. D. Paul, T. Kraemer, H. H. Maurer. Identification of cytochrome P450 enzymes involved in the metabolism of 4'-methoxy-alpha-pyrrolidinopropiophenone (MOPPP), a designer drug, in human liver microsomes. Xenobiotica 2003, 33, 989.
    • (2003) Xenobiotica , vol.33 , pp. 989
    • Springer, D.1    Staack, R.F.2    Paul, L.D.3    Kraemer, T.4    Maurer, H.H.5
  • 15
    • 20144386490 scopus 로고    scopus 로고
    • Identification of cytochrome P450 enzymes involved in the metabolism of 3', 4'-methylenedioxy-alpha-pyrrolidinopropiophenone (MDPPP), a designer drug, in human liver microsomes
    • D. Springer, R. F. Staack, L. D. Paul, T. Kraemer, H. H. Maurer. Identification of cytochrome P450 enzymes involved in the metabolism of 3', 4'-methylenedioxy-alpha-pyrrolidinopropiophenone (MDPPP), a designer drug, in human liver microsomes. Xenobiotica 2005, 35, 227.
    • (2005) Xenobiotica , vol.35 , pp. 227
    • Springer, D.1    Staack, R.F.2    Paul, L.D.3    Kraemer, T.4    Maurer, H.H.5
  • 16
    • 55949120153 scopus 로고    scopus 로고
    • Identification of cytochrome P450 enzymes involved in the metabolism of the designer drugs N-(1-phenylcyclohexyl)-3-ethoxypropanamine and N-(1-phenylcyclohexyl)-3-methoxy-propanamine
    • C. Sauer, F. T. Peters, A. E. Schwaninger, M. R. Meyer, H. H. Maurer. Identification of cytochrome P450 enzymes involved in the metabolism of the designer drugs N-(1-phenylcyclohexyl)-3-ethoxypropanamine and N-(1-phenylcyclohexyl)-3-methoxy-propanamine. Chem. Res. Toxicol. 2008, 21, 1949.
    • (2008) Chem. Res. Toxicol. , vol.21 , pp. 1949
    • Sauer, C.1    Peters, F.T.2    Schwaninger, A.E.3    Meyer, M.R.4    Maurer, H.H.5
  • 17
    • 58249130589 scopus 로고    scopus 로고
    • Investigations on the cytochrome P450 (CYP) isoenzymes involved in the metabolism of the designer drugs N-(1-phenyl cyclohexyl)-2-ethoxyethanamine and N-(1-phenylcyclohexyl)-2-methoxyethanamine
    • C. Sauer, F. T. Peters, A. E. Schwaninger, M. R. Meyer, H. H. Maurer. Investigations on the cytochrome P450 (CYP) isoenzymes involved in the metabolism of the designer drugs N-(1-phenyl cyclohexyl)-2-ethoxyethanamine and N-(1-phenylcyclohexyl)-2-methoxyethanamine. Biochem. Pharmacol. 2009, 77, 444.
    • (2009) Biochem. Pharmacol. , vol.77 , pp. 444
    • Sauer, C.1    Peters, F.T.2    Schwaninger, A.E.3    Meyer, M.R.4    Maurer, H.H.5
  • 18
    • 67649201776 scopus 로고    scopus 로고
    • New designer drug alpha-pyrrolidinovalerophenone (PVP): studies on its metabolism and toxicological detection in rat urine using gas chromatographic/mass spectrometric techniques
    • C. Sauer, F. T. Peters, C. Haas, M. R. Meyer, G. Fritschi, H. H. Maurer. New designer drug alpha-pyrrolidinovalerophenone (PVP): studies on its metabolism and toxicological detection in rat urine using gas chromatographic/mass spectrometric techniques. J. Mass Spectrom. 2009, 44, 952.
    • (2009) J. Mass Spectrom. , vol.44 , pp. 952
    • Sauer, C.1    Peters, F.T.2    Haas, C.3    Meyer, M.R.4    Fritschi, G.5    Maurer, H.H.6
  • 19
    • 78650716854 scopus 로고    scopus 로고
    • Studies on the metabolism of the alpha-pyrrolidinophenone designer drug methylenedioxy-pyrovalerone (MDPV) in rat and human urine and human liver microsomes using GC-MS and LC-high-resolution-MS and its detectability in urine by GC-MS
    • M. R. Meyer, P. Du, F. Schuster, H. H. Maurer. Studies on the metabolism of the alpha-pyrrolidinophenone designer drug methylenedioxy-pyrovalerone (MDPV) in rat and human urine and human liver microsomes using GC-MS and LC-high-resolution-MS and its detectability in urine by GC-MS. J. Mass Spectrom. 2010, 45, 1426.
    • (2010) J. Mass Spectrom. , vol.45 , pp. 1426
    • Meyer, M.R.1    Du, P.2    Schuster, F.3    Maurer, H.H.4
  • 20
    • 38649136220 scopus 로고    scopus 로고
    • Designer drug 2,5-dimethoxy-4-methyl-amphetamine (DOM, STP): involvement of the cytochrome P450 isoenzymes in formation of its main metabolite and detection of the latter in rat urine as proof of a drug intake using gas chromatography-mass spectrometry
    • A. H. Ewald, M. Puetz, H. H. Maurer. Designer drug 2, 5-dimethoxy-4-methyl-amphetamine (DOM, STP): involvement of the cytochrome P450 isoenzymes in formation of its main metabolite and detection of the latter in rat urine as proof of a drug intake using gas chromatography-mass spectrometry. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 2008, 862, 252.
    • (2008) J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. , vol.862 , pp. 252
    • Ewald, A.H.1    Puetz, M.2    Maurer, H.H.3
  • 21
    • 56549131437 scopus 로고    scopus 로고
    • 2,5-Dimethoxyamphetamine-derived designer drugs: studies on the identification of cytochrome P450 (CYP) isoenzymes involved in formation of their main metabolites and on their capability to inhibit CYP2D6
    • A. H. Ewald, H. H. Maurer. 2, 5-Dimethoxyamphetamine-derived designer drugs: studies on the identification of cytochrome P450 (CYP) isoenzymes involved in formation of their main metabolites and on their capability to inhibit CYP2D6. Toxicol. Lett. 2008, 183, 52.
    • (2008) Toxicol. Lett. , vol.183 , pp. 52
    • Ewald, A.H.1    Maurer, H.H.2
  • 22
    • 33845191282 scopus 로고    scopus 로고
    • Identification of monoamine oxidase and cytochrome P450 isoenzymes involved in the deamination of phenethylamine-derived designer drugs (2C-series)
    • D. S. Theobald, H. H. Maurer. Identification of monoamine oxidase and cytochrome P450 isoenzymes involved in the deamination of phenethylamine-derived designer drugs (2C-series). Biochem. Pharmacol. 2007, 73, 287.
    • (2007) Biochem. Pharmacol. , vol.73 , pp. 287
    • Theobald, D.S.1    Maurer, H.H.2
  • 25
    • 79951911231 scopus 로고    scopus 로고
    • Current knowledge of the isoenzymes involved in the metabolism and transport of frequently abused opioids, anesthetics, cognitive enhancers, plant-derived hallucinogens, and of nicotine with aspects on pharmacogenomics
    • M. R. Meyer, H. H. Maurer. Current knowledge of the isoenzymes involved in the metabolism and transport of frequently abused opioids, anesthetics, cognitive enhancers, plant-derived hallucinogens, and of nicotine with aspects on pharmacogenomics. Pharmacogenomics 2011, 12, 215.
    • (2011) Pharmacogenomics , vol.12 , pp. 215
    • Meyer, M.R.1    Maurer, H.H.2
  • 26
    • 54349126394 scopus 로고    scopus 로고
    • The role of human hepatic cytochrome P450 isozymes in the metabolism of racemic 3,4-methylenedioxy-methamphetamine and its enantiomers
    • M. R. Meyer, F. T. Peters, H. H. Maurer. The role of human hepatic cytochrome P450 isozymes in the metabolism of racemic 3, 4-methylenedioxy-methamphetamine and its enantiomers. Drug Metab. Dispos. 2008, 36, 2345.
    • (2008) Drug Metab. Dispos. , vol.36 , pp. 2345
    • Meyer, M.R.1    Peters, F.T.2    Maurer, H.H.3
  • 27
    • 66649134714 scopus 로고    scopus 로고
    • The role of human hepatic cytochrome P450 isozymes in the metabolism of racemic 3,4-methylenedioxyethylamphetamine and its single enantiomers
    • M. R. Meyer, F. T. Peters, H. H. Maurer. The role of human hepatic cytochrome P450 isozymes in the metabolism of racemic 3, 4-methylenedioxyethylamphetamine and its single enantiomers. Drug Metab. Dispos. 2009, 37, 1152.
    • (2009) Drug Metab. Dispos. , vol.37 , pp. 1152
    • Meyer, M.R.1    Peters, F.T.2    Maurer, H.H.3
  • 28
    • 64249104432 scopus 로고    scopus 로고
    • Stereoselective differences in the cytochrome P450-dependent dealkylation and demethylenation of N-methyl-benzodioxolyl-butanamine (MBDB, Eden) enantiomers
    • M. R. Meyer, F. T. Peters, H. H. Maurer. Stereoselective differences in the cytochrome P450-dependent dealkylation and demethylenation of N-methyl-benzodioxolyl-butanamine (MBDB, Eden) enantiomers. Biochem. Pharmacol. 2009, 77, 17.
    • (2009) Biochem. Pharmacol. , vol.77 , pp. 17
    • Meyer, M.R.1    Peters, F.T.2    Maurer, H.H.3
  • 29
    • 68349154511 scopus 로고    scopus 로고
    • Investigations on the human hepatic cytochrome P450 isozymes involved in the metabolism of 3,4-methylenedioxy-amphetamine (MDA) and benzodi-oxolyl-butanamine (BDB) enantiomers
    • M. R. Meyer, F. T. Peters, H. H. Maurer. Investigations on the human hepatic cytochrome P450 isozymes involved in the metabolism of 3, 4-methylenedioxy-amphetamine (MDA) and benzodi-oxolyl-butanamine (BDB) enantiomers. Toxicol. Lett. 2009, 190, 54.
    • (2009) Toxicol. Lett. , vol.190 , pp. 54
    • Meyer, M.R.1    Peters, F.T.2    Maurer, H.H.3
  • 30
    • 19444375492 scopus 로고    scopus 로고
    • Mammalian flavin-containing monooxygenases: structure/function, genetic polymorphisms and role in drug metabolism
    • S. K. Krueger, D. E. Williams. Mammalian flavin-containing monooxygenases: structure/function, genetic polymorphisms and role in drug metabolism. Pharmacol. Ther. 2005, 106, 357.
    • (2005) Pharmacol. Ther. , vol.106 , pp. 357
    • Krueger, S.K.1    Williams, D.E.2
  • 31
    • 0034280122 scopus 로고    scopus 로고
    • Human flavin-containing monooxygenase: substrate specificity and role in drug metabolism
    • J. R. Cashman. Human flavin-containing monooxygenase: substrate specificity and role in drug metabolism. Curr. Drug Metab. 2000, 1, 181.
    • (2000) Curr. Drug Metab. , vol.1 , pp. 181
    • Cashman, J.R.1
  • 32
    • 0030854077 scopus 로고    scopus 로고
    • Baculovirus-mediated expression and purification of human FMO3: catalytic, immunochemical, and structural characterization
    • R. L. Haining, A. P. Hunter, A. J. Sadeque, R. M. Philpot, A. E. Rettie. Baculovirus-mediated expression and purification of human FMO3: catalytic, immunochemical, and structural characterization. Drug Metab. Dispos. 1997, 25, 790.
    • (1997) Drug Metab. Dispos. , vol.25 , pp. 790
    • Haining, R.L.1    Hunter, A.P.2    Sadeque, A.J.3    Philpot, R.M.4    Rettie, A.E.5
  • 33
    • 34250676097 scopus 로고    scopus 로고
    • Genetic polymorphisms of human flavin-containing monooxygenase 3: implications for drug metabolism and clinical perspectives
    • I. M. Hisamuddin, V. W. Yang. Genetic polymorphisms of human flavin-containing monooxygenase 3: implications for drug metabolism and clinical perspectives. Pharmacogenomics 2007, 8, 635.
    • (2007) Pharmacogenomics , vol.8 , pp. 635
    • Hisamuddin, I.M.1    Yang, V.W.2
  • 35
    • 70350510900 scopus 로고    scopus 로고
    • Flavin-containing monooxygenase 1-catalysed N,N-dimethyl-amphetamine N-oxidation
    • S. K. Lee, M. J. Kang, C. Jin, M. K. In, D. H. Kim, H. H. Yoo. Flavin-containing monooxygenase 1-catalysed N, N-dimethyl-amphetamine N-oxidation. Xenobiotica 2009, 39, 680.
    • (2009) Xenobiotica , vol.39 , pp. 680
    • Lee, S.K.1    Kang, M.J.2    Jin, C.3    In, M.K.4    Kim, D.H.5    Yoo, H.H.6
  • 37
    • 0034128936 scopus 로고    scopus 로고
    • Human UDP-glucuronosyltransferases: metabolism, expression, and disease
    • R. H. Tukey, C. P. Strassburg. Human UDP-glucuronosyltransferases: metabolism, expression, and disease. Annu. Rev. Pharmacol. Toxicol. 2000, 40, 581.
    • (2000) Annu. Rev. Pharmacol. Toxicol. , vol.40 , pp. 581
    • Tukey, R.H.1    Strassburg, C.P.2
  • 38
    • 0037423299 scopus 로고    scopus 로고
    • Expression and characterization of recombinant human UDP-glucuronosyltransferases (UGTs). UGT1A9 is more resistant to detergent inhibition than other UGTs and was purified as an active dimeric enzyme
    • M. Kurkela, J. A. Garcia-Horsman, L. Luukkanen, S. Morsky, J. Taskinen, M. Baumann, R. Kostiainen, J. Hirvonen, M. Finel. Expression and characterization of recombinant human UDP-glucuronosyltransferases (UGTs). UGT1A9 is more resistant to detergent inhibition than other UGTs and was purified as an active dimeric enzyme. J. Biol. Chem. 2003, 278, 3536.
    • (2003) J. Biol. Chem. , vol.278 , pp. 3536
    • Kurkela, M.1    Garcia-Horsman, J.A.2    Luukkanen, L.3    Morsky, S.4    Taskinen, J.5    Baumann, M.6    Kostiainen, R.7    Hirvonen, J.8    Finel, M.9
  • 39
    • 0041856580 scopus 로고    scopus 로고
    • Glucuronidation of anabolic androgenic steroids by recombinant human UDP-glucuronosyltransferases
    • T. Kuuranne, M. Kurkela, M. Thevis, W. Schanzer, M. Finel, R. Kostiainen. Glucuronidation of anabolic androgenic steroids by recombinant human UDP-glucuronosyltransferases. Drug Metab. Dispos. 2003, 31, 1117.
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 1117
    • Kuuranne, T.1    Kurkela, M.2    Thevis, M.3    Schanzer, W.4    Finel, M.5    Kostiainen, R.6
  • 41
    • 70350333887 scopus 로고    scopus 로고
    • The role of human UDP-glucuronyltransferases on the formation of the methylenedioxymethamphetamine (ecstasy) phase II metabolites R- and S-3-methoxymethamphetamine 4-O-glucuronides
    • A. E. Schwaninger, M. R. Meyer, J. Zapp, H. H. Maurer. The role of human UDP-glucuronyltransferases on the formation of the methylenedioxymethamphetamine (ecstasy) phase II metabolites R- and S-3-methoxymethamphetamine 4-O-glucuronides. Drug Metab. Dispos. 2009, 37, 2212.
    • (2009) Drug Metab. Dispos. , vol.37 , pp. 2212
    • Schwaninger, A.E.1    Meyer, M.R.2    Zapp, J.3    Maurer, H.H.4
  • 42
    • 3242766775 scopus 로고
    • Amine oxidases. XVII. Mode of action of 1-isonicotinyl-2-isopropylhydrazine on monoamine oxidase
    • J. Barsky, W. L. Pacha, S. Sarkar, E. A. Zeller. Amine oxidases. XVII. Mode of action of 1-isonicotinyl-2-isopropylhydrazine on monoamine oxidase. J. Biol. Chem. 1959, 234, 389.
    • (1959) J. Biol. Chem. , vol.234 , pp. 389
    • Barsky, J.1    Pacha, W.L.2    Sarkar, S.3    Zeller, E.A.4
  • 44
    • 0028278638 scopus 로고
    • The functional role of monoamine oxidases A and B in the mammalian central nervous system
    • M. D. Berry, A. V. Juorio, I. A. Paterson. The functional role of monoamine oxidases A and B in the mammalian central nervous system. Prog. Neurobiol. 1994, 42, 375.
    • (1994) Prog. Neurobiol. , vol.42 , pp. 375
    • Berry, M.D.1    Juorio, A.V.2    Paterson, I.A.3
  • 47
    • 79952616759 scopus 로고    scopus 로고
    • Sulfation the 3,4-methylenedioxymethamphetamine (MDMA) metabolites 3,4-dihydroxymethamphetamine (DHMA) and 4-hydroxy-3-methoxymethamphetamine (HMMA) and their capability to inhibit human sulfotransferases
    • A. E. Schwaninger, M. R. Meyer, J. Zapp, H. H. Maurer. Sulfation the 3, 4-methylenedioxymethamphetamine (MDMA) metabolites 3, 4-dihydroxymethamphetamine (DHMA) and 4-hydroxy-3-methoxymethamphetamine (HMMA) and their capability to inhibit human sulfotransferases. Toxicol. Lett. 2011, 202, 120.
    • (2011) Toxicol. Lett. , vol.202 , pp. 120
    • Schwaninger, A.E.1    Meyer, M.R.2    Zapp, J.3    Maurer, H.H.4
  • 48
    • 0037097059 scopus 로고    scopus 로고
    • Studies on the metabolism and toxicological detection of the new designer drug N-benzylpiperazine in urine using gas chromatography-mass spectrometry
    • R. F. Staack, G. Fritschi, H. H. Maurer. Studies on the metabolism and toxicological detection of the new designer drug N-benzylpiperazine in urine using gas chromatography-mass spectrometry. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 2002, 773, 35.
    • (2002) J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. , vol.773 , pp. 35
    • Staack, R.F.1    Fritschi, G.2    Maurer, H.H.3
  • 49
    • 1642367231 scopus 로고    scopus 로고
    • New designer drug 1-(3,4-methylenedioxybenzyl) piperazine (MDBP): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry
    • R. F. Staack, H. H. Maurer. New designer drug 1-(3, 4-methylenedioxybenzyl) piperazine (MDBP): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry. J. Mass Spectrom. 2004, 39, 255.
    • (2004) J. Mass Spectrom. , vol.39 , pp. 255
    • Staack, R.F.1    Maurer, H.H.2
  • 50
    • 67449103235 scopus 로고    scopus 로고
    • Enantioselectivity in the methylation of the catecholic phase I metabolites of methylenedioxy designer drugs and their capability to inhibit catechol-O-methyltransferase-catalyzed dopamine 3-methylation
    • M. R. Meyer, H. H. Maurer. Enantioselectivity in the methylation of the catecholic phase I metabolites of methylenedioxy designer drugs and their capability to inhibit catechol-O-methyltransferase-catalyzed dopamine 3-methylation. Chem. Res. Toxicol. 2009, 22, 1205.
    • (2009) Chem. Res. Toxicol. , vol.22 , pp. 1205
    • Meyer, M.R.1    Maurer, H.H.2
  • 51
    • 4744359958 scopus 로고    scopus 로고
    • Standardization of conditions for the metabolic activation of N-nitrosodiethylamine in mutagenicity tests
    • C. A. Aiub, L. F. Pinto, I. Felzenszwalb. Standardization of conditions for the metabolic activation of N-nitrosodiethylamine in mutagenicity tests. Genet. Mol. Res. 2004, 3, 264.
    • (2004) Genet. Mol. Res. , vol.3 , pp. 264
    • Aiub, C.A.1    Pinto, L.F.2    Felzenszwalb, I.3
  • 52
    • 0020371778 scopus 로고
    • Comparative genotoxicity studies of ethyl carbamate and related chemicals: further support for vinyl carbamate as a proximate carcinogenic metabolite
    • J. W. Allen, R. Langenbach, S. Nesnow, K. Sasseville, S. Leavitt, J. Campbell, K. Brock, Y. Sharief. Comparative genotoxicity studies of ethyl carbamate and related chemicals: further support for vinyl carbamate as a proximate carcinogenic metabolite. Carcinogenesis 1982, 3, 1437.
    • (1982) Carcinogenesis , vol.3 , pp. 1437
    • Allen, J.W.1    Langenbach, R.2    Nesnow, S.3    Sasseville, K.4    Leavitt, S.5    Campbell, J.6    Brock, K.7    Sharief, Y.8
  • 53
    • 37749045357 scopus 로고    scopus 로고
    • Development of an in vitro assay for the investigation of metabolism-induced drug hepatotoxicity
    • M. Otto, S. H. Hansen, L. Dalgaard, J. Dubois, L. Badolo. Development of an in vitro assay for the investigation of metabolism-induced drug hepatotoxicity. Cell Biol. Toxicol. 2008, 24, 87.
    • (2008) Cell Biol. Toxicol. , vol.24 , pp. 87
    • Otto, M.1    Hansen, S.H.2    Dalgaard, L.3    Dubois, J.4    Badolo, L.5
  • 54
    • 77955858928 scopus 로고    scopus 로고
    • Toxicological determination and in vitro metabolism of the designer drug methylenedioxypyrovalerone (MPDV) by gas chromatography/mass spectrometry and liquid chromatography/quadrupole time-of-flight mass spectrometry
    • S. Strano-Rossi, A. B. Cadwallader, X. de la Torre, F. Botre. Toxicological determination and in vitro metabolism of the designer drug methylenedioxypyrovalerone (MPDV) by gas chromatography/mass spectrometry and liquid chromatography/quadrupole time-of-flight mass spectrometry. Rapid Commun. Mass Spectrom. 2010, 24, 2706.
    • (2010) Rapid Commun. Mass Spectrom. , vol.24 , pp. 2706
    • Strano-Rossi, S.1    Cadwallader, A.B.2    de la Torre, X.3    Botre, F.4
  • 55
    • 60749083654 scopus 로고    scopus 로고
    • Metabolic stability: main enzymes involved and best tools to assess it
    • R. Laine. Metabolic stability: main enzymes involved and best tools to assess it. Curr. Drug Metab. 2008, 9, 921.
    • (2008) Curr. Drug Metab. , vol.9 , pp. 921
    • Laine, R.1
  • 56
    • 0032968777 scopus 로고    scopus 로고
    • Cryopreserved human hepatocytes: characterization of drug-metabolizing enzyme activities and applications in higher throughput screening assays for hepatotoxicity, metabolic stability, and drug-drug interaction potential
    • A. P. Li, C. Lu, J. A. Brent, C. Pham, A. Fackett, C. E. Ruegg, P. M. Silber. Cryopreserved human hepatocytes: characterization of drug-metabolizing enzyme activities and applications in higher throughput screening assays for hepatotoxicity, metabolic stability, and drug-drug interaction potential. Chem. Biol. Interact. 1999, 121, 17.
    • (1999) Chem. Biol. Interact. , vol.121 , pp. 17
    • Li, A.P.1    Lu, C.2    Brent, J.A.3    Pham, C.4    Fackett, A.5    Ruegg, C.E.6    Silber, P.M.7
  • 60
    • 0032866401 scopus 로고    scopus 로고
    • The use of heterologously expressed drug metabolizing enzymes-state of the art and prospects for the future
    • C. L. Crespi, V. P. Miller. The use of heterologously expressed drug metabolizing enzymes-state of the art and prospects for the future. Pharmacol Ther. 1999, 84, 121.
    • (1999) Pharmacol Ther. , vol.84 , pp. 121
    • Crespi, C.L.1    Miller, V.P.2
  • 61
    • 33645961595 scopus 로고    scopus 로고
    • The impact of in vitro binding on in vitro-in vivo extrapolations, projections of metabolic clearance and clinical drug-drug interactions
    • K. Grime, R. J. Riley. The impact of in vitro binding on in vitro-in vivo extrapolations, projections of metabolic clearance and clinical drug-drug interactions. Curr. Drug Metab. 2006, 7, 251.
    • (2006) Curr. Drug Metab. , vol.7 , pp. 251
    • Grime, K.1    Riley, R.J.2
  • 62
    • 0033674502 scopus 로고    scopus 로고
    • Comparison between cytochrome P450 (CYP) content and relative activity approaches to scaling from cDNA-expressed CYPs to human liver microsomes: ratios of accessory proteins as sources of discrepancies between the approaches
    • K. Venkatakrishnan, L. L. von Moltke, M. H. Court, J. S. Harmatz, C. L. Crespi, D. J. Greenblatt. Comparison between cytochrome P450 (CYP) content and relative activity approaches to scaling from cDNA-expressed CYPs to human liver microsomes: ratios of accessory proteins as sources of discrepancies between the approaches. Drug Metab. Dispos. 2000, 28, 1493.
    • (2000) Drug Metab. Dispos. , vol.28 , pp. 1493
    • Venkatakrishnan, K.1    von Moltke, L.L.2    Court, M.H.3    Harmatz, J.S.4    Crespi, C.L.5    Greenblatt, D.J.6
  • 63
    • 0035079928 scopus 로고    scopus 로고
    • Application of the relative activity factor approach in scaling from heterologously expressed cytochromes p450 to human liver microsomes: studies on amitriptyline as a model substrate
    • K. Venkatakrishnan, L. L. von Moltke, D. J. Greenblatt. Application of the relative activity factor approach in scaling from heterologously expressed cytochromes p450 to human liver microsomes: studies on amitriptyline as a model substrate. J. Pharmacol. Exp. Ther. 2001, 297, 326.
    • (2001) J. Pharmacol. Exp. Ther. , vol.297 , pp. 326
    • Venkatakrishnan, K.1    von Moltke, L.L.2    Greenblatt, D.J.3
  • 64
    • 0034770465 scopus 로고    scopus 로고
    • Human drug metabolism and the cytochromes P450: application and relevance of in vitro models
    • K. Venkatakrishnan, L. L. Von Moltke, D. J. Greenblatt. Human drug metabolism and the cytochromes P450: application and relevance of in vitro models. J. Clin. Pharmacol. 2001, 41, 1149.
    • (2001) J. Clin. Pharmacol. , vol.41 , pp. 1149
    • Venkatakrishnan, K.1    Von Moltke, L.L.2    Greenblatt, D.J.3
  • 65
    • 0028674392 scopus 로고
    • Eds: B. Testa, U. A. Meyer). Academic Press: London
    • C. L. Crespi. Advances in Drug Research, Vol. 26 (Eds: B. Testa, U. A. Meyer ). Academic Press: London, 1995, pp. 179-235.
    • (1995) Advances in Drug Research, Vol. 26 , pp. 179-235
    • Crespi, C.L.1
  • 66
    • 73149100796 scopus 로고    scopus 로고
    • Contribution of the different UDP-glucuronosyltransferase (UGT) isoforms to buprenorphine and norbuprenorphine metabolism and relationship with the main UGT polymorphisms in a bank of human liver microsomes
    • K. Rouguieg, N. Picard, F. L. Sauvage, J. M. Gaulier, P. Marquet. Contribution of the different UDP-glucuronosyltransferase (UGT) isoforms to buprenorphine and norbuprenorphine metabolism and relationship with the main UGT polymorphisms in a bank of human liver microsomes. Drug Metab. Dispos. 2010, 38, 40.
    • (2010) Drug Metab. Dispos. , vol.38 , pp. 40
    • Rouguieg, K.1    Picard, N.2    Sauvage, F.L.3    Gaulier, J.M.4    Marquet, P.5
  • 67
    • 40649125544 scopus 로고    scopus 로고
    • New designer drugs N-(1-phenylcyclohexyl)-2-ethoxyethanamine (PCEEA) and N-(1-phenylcyclohexyl)-2-methoxyethanamine (PCMEA): Studies on their metabolism and toxicological detection in rat urine using gas chromatographic/mass spectrometric techniques
    • C. Sauer, F. T. Peters, R. F. Staack, G. Fritschi, H. H. Maurer. New designer drugs N-(1-phenylcyclohexyl)-2-ethoxyethanamine (PCEEA) and N-(1-phenylcyclohexyl)-2-methoxyethanamine (PCMEA): Studies on their metabolism and toxicological detection in rat urine using gas chromatographic/mass spectrometric techniques. J. Mass Spectrom. 2008, 43, 305.
    • (2008) J. Mass Spectrom. , vol.43 , pp. 305
    • Sauer, C.1    Peters, F.T.2    Staack, R.F.3    Fritschi, G.4    Maurer, H.H.5
  • 68
    • 70349158718 scopus 로고    scopus 로고
    • Studies on the metabolism of mitragynine, the main alkaloid of the herbal drug Kratom, in rat and human urine using liquid chromatography-linear ion trap mass spectrometry
    • A. A. Philipp, D. K. Wissenbach, S. W. Zoerntlein, O. N. Klein, J. Kanogsunthornrat, H. H. Maurer. Studies on the metabolism of mitragynine, the main alkaloid of the herbal drug Kratom, in rat and human urine using liquid chromatography-linear ion trap mass spectrometry. J. Mass Spectrom. 2009, 44, 1249.
    • (2009) J. Mass Spectrom. , vol.44 , pp. 1249
    • Philipp, A.A.1    Wissenbach, D.K.2    Zoerntlein, S.W.3    Klein, O.N.4    Kanogsunthornrat, J.5    Maurer, H.H.6
  • 70
    • 34250716024 scopus 로고    scopus 로고
    • Biotechnological synthesis of drug metabolites using human cytochrome P450 2D6 heterologously expressed in fission yeast exemplified for the designer drug metabolite 4'-hydroxymethyl-alpha-pyrrolidinobutyrophenone
    • F. T. Peters, C. A. Dragan, D. R. Wilde, M. R. Meyer, J. Zapp, M. Bureik, H. H. Maurer. Biotechnological synthesis of drug metabolites using human cytochrome P450 2D6 heterologously expressed in fission yeast exemplified for the designer drug metabolite 4'-hydroxymethyl-alpha-pyrrolidinobutyrophenone. Biochem. Pharmacol. 2007, 74, 511.
    • (2007) Biochem. Pharmacol. , vol.74 , pp. 511
    • Peters, F.T.1    Dragan, C.A.2    Wilde, D.R.3    Meyer, M.R.4    Zapp, J.5    Bureik, M.6    Maurer, H.H.7
  • 71
    • 58249142504 scopus 로고    scopus 로고
    • Isolation and purification of the designer drug metabolite O-Deethyl-(1-phenylcyclohexyl)-3-ethoxypropanamine (O-Deethyl-PCEPA)-Biotechnologically synthesized using fission yeast expressing CYP2D6
    • in, Proceedings of the XVth GTFCh Symposium, Mosbach, Germany, 18-21 April 2007. (Eds.: F. Pragst, R. Aderjan), GTFCH, Bad Vilbel: Germany
    • F. T. Peters, A. E. Schwaninger, C. A. Dragan, C. Sauer, G. Fritschi, M. Bureik, H. H. Maurer. Isolation and purification of the designer drug metabolite O-Deethyl-(1-phenylcyclohexyl)-3-ethoxypropanamine (O-Deethyl-PCEPA)-Biotechnologically synthesized using fission yeast expressing CYP2D6, in Current Contributions to Forensic and Clinical Toxicology, Proceedings of the XVth GTFCh Symposium, Mosbach, Germany, 18-21 April 2007. (Eds.: F. Pragst, R. Aderjan ), GTFCH, Bad Vilbel: Germany, 2008, pp. 204-210.
    • (2008) Current Contributions to Forensic and Clinical Toxicology , pp. 204-210
    • Peters, F.T.1    Schwaninger, A.E.2    Dragan, C.A.3    Sauer, C.4    Fritschi, G.5    Bureik, M.6    Maurer, H.H.7
  • 72
    • 58249126709 scopus 로고    scopus 로고
    • Use of fission yeast heterologously expressing human cytochrome P450 2B6 in biotechnological synthesis of the designer drug metabolite N-(1-phenylcyclohexyl)-2-hydroxyethanamine
    • F. T. Peters, C. A. Dragan, A. E. Schwaninger, C. Sauer, J. Zapp, M. Bureik, H. H. Maurer. Use of fission yeast heterologously expressing human cytochrome P450 2B6 in biotechnological synthesis of the designer drug metabolite N-(1-phenylcyclohexyl)-2-hydroxyethanamine. Forensic Sci. Int. 2009, 184, 69.
    • (2009) Forensic Sci. Int. , vol.184 , pp. 69
    • Peters, F.T.1    Dragan, C.A.2    Schwaninger, A.E.3    Sauer, C.4    Zapp, J.5    Bureik, M.6    Maurer, H.H.7
  • 73
    • 76749093063 scopus 로고    scopus 로고
    • Biotechnological synthesis of drug metabolites using human cytochrome P450 isozymes heterologously expressed in fission yeast
    • F. T. Peters, M. Bureik, H. H. Maurer. Biotechnological synthesis of drug metabolites using human cytochrome P450 isozymes heterologously expressed in fission yeast. Bioanalysis 2009, 1, 821.
    • (2009) Bioanalysis , vol.1 , pp. 821
    • Peters, F.T.1    Bureik, M.2    Maurer, H.H.3
  • 74
    • 79952470677 scopus 로고    scopus 로고
    • Production of human phase 1 and 2 metabolites by whole-chell biotransformation with recombinant microbes
    • A. Zollner, D. Buchheit, M. R. Meyer, H. H. Maurer, F. T. Peters, M. Bureik. Production of human phase 1 and 2 metabolites by whole-chell biotransformation with recombinant microbes. Bioanalysis 2010, 2, 1277.
    • (2010) Bioanalysis , vol.2 , pp. 1277
    • Zollner, A.1    Buchheit, D.2    Meyer, M.R.3    Maurer, H.H.4    Peters, F.T.5    Bureik, M.6
  • 75
    • 65949101646 scopus 로고    scopus 로고
    • 4-Hydroxy-3-methoxymethamphetamine glucuronide as a phase II metabolite of 3,4-methylenedioxymethamphetamine: enzyme-assisted synthesis and involvement of human hepatic uridine 5'-diphosphate-glucuronosyltransferase 2B15 in the glucuronidation
    • T. Shoda, K. Fukuhara, Y. Goda, H. Okuda. 4-Hydroxy-3-methoxymethamphetamine glucuronide as a phase II metabolite of 3, 4-methylenedioxymethamphetamine: enzyme-assisted synthesis and involvement of human hepatic uridine 5'-diphosphate-glucuronosyltransferase 2B15 in the glucuronidation. Chem. Pharm. Bull. (Tokyo) 2009, 57, 472.
    • (2009) Chem. Pharm. Bull. (Tokyo) , vol.57 , pp. 472
    • Shoda, T.1    Fukuhara, K.2    Goda, Y.3    Okuda, H.4


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