has been cited by the following article(s):
[1]
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Chiral Serum Pharmacokinetics of 4-Fluoroamphetamine after Controlled Oral Administration: Can (R)/(S)-Concentration Ratios Help in Interpreting Forensic Cases?
Journal of Analytical Toxicology,
2021
DOI:10.1093/jat/bkaa156
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[2]
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4-Fluoromethamphetamine (4-FMA) induces in vitro hepatotoxicity mediated by CYP2E1, CYP2D6, and CYP3A4 metabolism
Toxicology,
2021
DOI:10.1016/j.tox.2021.152988
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[3]
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4-Fluoromethamphetamine (4-FMA) induces in vitro hepatotoxicity mediated by CYP2E1, CYP2D6, and CYP3A4 metabolism
Toxicology,
2021
DOI:10.1016/j.tox.2021.152988
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[4]
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Indirect chiral separation of 8 novel amphetamine derivatives as potential new psychoactive compounds by GC–MS and HPLC
Science & Justice,
2017
DOI:10.1016/j.scijus.2016.08.007
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[5]
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Differentiation of ring-substituted bromoamphetamine analogs by gas chromatography–tandem mass spectrometry
Forensic Toxicology,
2016
DOI:10.1007/s11419-015-0296-3
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[6]
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The Toxicology of New Psychoactive Substances
Therapeutic Drug Monitoring,
2016
DOI:10.1097/FTD.0000000000000263
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