Determination of the metabolites of the new designer drugs bk-MBDB and bk-MDEA in human urine

Author:

Zaitsu Kei,Katagi Munehiro,Kamata Hiroe T.,Kamata Tooru,Shima Noriaki,Miki Akihiro,Tsuchihashi Hitoshi,Mori Yasushige

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine,Law

Reference19 articles.

1. Methcathinone and 2-methylamino-1-(3,4-methylenedioxyphenyl)propan-1-one (methylone) selectively inhibit plasma membrane monoamine transporters;Cozzi;Soc. Neurosci. Abstr.,1998

2. Inhibition of plasma membrane monoamine transporters by β-ketoamphetamines;Cozzi;Eur. J. Phamacol.,1999

3. Amphetamine-like effects in human of the khat alkaloid;Brenneisen;Br. J. Clin. Phamacol.,1990

4. In vitro characterization of ephedrine-related stereoisomers at biogenic amine transporters and the receptorome reveals selective actions as norepinephrine transporter substrates;Rothman;J. Pharmacol. Exp. Ther.,2003

5. Metabolism of the recently encountered designer drug, methylone in humans and rats;Kamata;Xenobiotica,2006

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