Designer drug 2,4,5-trimethoxyamphetamine (TMA-2): Studies on its metabolism and toxicological detection in rat urine using gas chromatographic/mass spectrometric techniques
ANIMAL EXPERIMENT;
ARTICLE;
CONTROLLED STUDY;
DEAMINATION;
DEMETHYLATION;
DOSE RESPONSE;
DRUG ACETYLATION;
DRUG EXCRETION;
DRUG HYDROLYSIS;
DRUG METABOLISM;
DRUG URINE LEVEL;
GAS CHROMATOGRAPHY;
LIQUID LIQUID EXTRACTION;
MALE;
MASS SPECTROMETRY;
NONHUMAN;
PRIORITY JOURNAL;
RAT;
URINALYSIS;
URINARY EXCRETION;
European Monitoring Centre for Drugs and Drug Addiction (EMCDDA). 2004
European Monitoring Centre for Drugs and Drug Addiction (EMCDDA). Report on the risk assessment of TMA-2 in the framework of the joint action on new synthetic drugs. http://www.emcdda.eu.int/multimedia/publications/ risk_assessments/TMA2.2003-1639. pdf, 2004.
Intelligence alert large fentanyl/MDA/TMA laboratory in Azuza, California-possibly the "OC-80" tablet source
Drug Enforcement Administration-Office of Forensic Sciences
Drug Enforcement Administration-Office of Forensic Sciences. Intelligence alert large fentanyl/MDA/TMA laboratory in Azuza, California-possibly the "OC-80" tablet source. Microgram 2006; 39: 45.
Dihydrobenzofuran analogues of hallucinogens. 3. Models of 4-substituted (2,5-dimethoxyphenyl)alkylamine derivatives with rigidified methoxy groups
Monte AP, Marona-Lewicka D, Parker MA, Wainscott DB, Nelson DL, Nichols DE. Dihydrobenzofuran analogues of hallucinogens. 3. Models of 4-substituted (2,5-dimethoxyphenyl)alkylamine derivatives with rigidified methoxy groups. J. Med. Chem. 1996; 39: 2953.
Toxicokinetics of amphetamines: Metabolism and toxicokinetic data of designer drugs, of amphetamine, methamphetamine and their N-alkyl derivatives
[review]
Kraemer T, Maurer HH. Toxicokinetics of amphetamines: Metabolism and toxicokinetic data of designer drugs, of amphetamine, methamphetamine and their N-alkyl derivatives [review]. Ther. Drug Monit. 2002; 24: 277.
Studies on the metabolism and toxicological detection of the designer drug 4-methylthioamphetamine (4-MTA). In human urine using gas chromatography-mass spectrometry
Ewald AH, Peters FT, Weise M, Maurer HH. Studies on the metabolism and toxicological detection of the designer drug 4-methylthioamphetamine (4-MTA). in human urine using gas chromatography-mass spectrometry. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 2005; 824: 123.
Designer drugs 2,5-dimethoxy-4-bromoamphetamine (DOB) and 2,5-dimethoxy-4-bromomethamphetamine (MDOB): Studies on their metabolism and toxicological detection in rat urine using gas chromatographic/mass spectrometric techniques
Ewald AH, Fritschi G, Bork WR, Maurer HH. Designer drugs 2,5-dimethoxy-4-bromoamphetamine (DOB) and 2,5-dimethoxy-4-bromomethamphetamine (MDOB): Studies on their metabolism and toxicological detection in rat urine using gas chromatographic/mass spectrometric techniques. J. Mass Spectrom. 2006; 41: 487.
Quantitative measurement of demethylation of 14C-methoxyl labeled DMPEA and TMA-2 in rats
Sargent T, Shulgin AT, Kusubov N III. Quantitative measurement of demethylation of 14C-methoxyl labeled DMPEA and TMA-2 in rats. Psychopharmacol. Commun. 1976; 2: 199.
Position of chromatographic techniques in screening for detection of drugs or poisons in clinical and forensic toxicology and/or doping control
[review]
Maurer HH. Position of chromatographic techniques in screening for detection of drugs or poisons in clinical and forensic toxicology and/or doping control [review]. Clin. Chem. Lab. Med. 2004; 42: 1310.
New designer drug 2,5-dimethoxy-4-propylthiophenethylamine (2C-T-7): Studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry
Theobald DS, Fehn S, Maurer HH. New designer drug 2,5-dimethoxy-4- propylthiophenethylamine (2C-T-7): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry. J. Mass Spectrom. 2005; 40: 105.
New designer drug 2,5-dimethoxy-4-ethylthio-beta-phenethylamine (2C-T-2): Studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry
Theobald DS, Staack RF, Puetz M, Maurer HH. New designer drug 2,5-dimethoxy-4-ethylthio-beta-phenethylamine (2C-T-2): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry. J. Mass Spectrom. 2005; 40: 1157.
Pfleger K, Maurer HH, Weber A. Mass Spectral Library of Drugs, Poisons, Pesticides, Pollutants and their Metabolites. 4th ed. Agilent Technologies: Palo Alto, 2006; in preparation.
de-Zeeuw RA, Franke JP, Maurer HH, Pfleger K. Gas Chromatographic Retention Indices of Toxicologically Relevant Substances and their Metabolites (Report of the DFG Commission for Clinical Toxicological Analysis, Special Issue of the TIAFT Bulletin). 3rd ed. VCH publishers: Weinheim, New York, Basle, 1992.
Abuse of Nutmeg (Myristica fragrans Houtt.): Studies on the metabolism and the toxicological detection of its ingredients elemicin, Myristicin and safrole in rat and human urine using gas chromatography/mass spectrometry
(in press)
Beyer J, Ehlers D, Maurer HH. Abuse of Nutmeg (Myristica fragrans Houtt.): Studies on the metabolism and the toxicological detection of its ingredients elemicin, Myristicin and safrole in rat and human urine using gas chromatography/mass spectrometry. Ther. Drug Monit. 2006; 28: (in press).
Studies on the metabolism and the toxicological analysis of the new piperazine-like designer drug N-benzylpiperazine in urine using gas chromatography-mass spectrometry
Staack RF, Fritschi G, Maurer HH. Studies on the metabolism and the toxicological analysis of the new piperazine-like designer drug N-benzylpiperazine in urine using gas chromatography-mass spectrometry. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 2002; 773: 35.
Screening for detection of new antidepressants, neuroleptics, hypnotics, and their metabolites in urine by GC-MS developed using rat liver microsomes
Bickeboeller-Friedrich J, Maurer HH. 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.