About: In vivo and in vitro metabolism of 3,4-(methylenedioxy)methamphetamine in the rat: identification of metabolites using an ion trap detector

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About: In vivo and in vitro metabolism of 3,4-(methylenedioxy)methamphetamine in the rat: identification of metabolites using an ion trap detector Goto Sponge NotDistinct Permalink

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scientific article published on 01 November 1988

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 1988 (uk) im November 1988 veröffentlichter wissenschaftlicher Artikel (de) գիտական հոդված հրատարակված 1988 թվականի նոյեմբերի 1-ին (hy) scientific article published on 01 November 1988 (en) artículu científicu espublizáu en payares de 1988 (ast)
publication date	wds:Q69933538-C89A2B00-5C72-44C3-8484-A1F52859A6B9
publication date	1988-11-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q69933538-15E3C3E6-CBBD-4445-9455-4A9631BB0762 wds:Q69933538-9D70FF2B-DD53-4B2E-ACA1-FA3F07312C63
author name string	H K Lim R L Foltz
rdfs:label	In vivo and in vitro metabolism of 3,4-(methylenedioxy)methamphetamine in the rat: identification of metabolites using an ion trap detector (en) In vivo and in vitro metabolism of 3,4-(methylenedioxy)methamphetamine in the rat: identification of metabolites using an ion trap detector (nl)
skos:prefLabel	In vivo and in vitro metabolism of 3,4-(methylenedioxy)methamphetamine in the rat: identification of metabolites using an ion trap detector (en) In vivo and in vitro metabolism of 3,4-(methylenedioxy)methamphetamine in the rat: identification of metabolites using an ion trap detector (nl)
name	In vivo and in vitro metabolism of 3,4-(methylenedioxy)methamphetamine in the rat: identification of metabolites using an ion trap detector (en) In vivo and in vitro metabolism of 3,4-(methylenedioxy)methamphetamine in the rat: identification of metabolites using an ion trap detector (nl)
title	wds:Q69933538-3068F4B9-F951-4237-8932-9208B4DD3C19
title	In vivo and in vitro metabolism of 3,4-(methylenedioxy)methamphetamine in the rat: identification of metabolites using an ion trap detector (en)
page(s)	wds:Q69933538-F17FED79-6DE1-4432-9089-29C909039F11
page(s)	370-378
instance of	wds:Q69933538-0A02A258-A857-446E-BC36-ACDDEE5761FF
instance of	scholarly article
PubMed ID	wds:Q69933538-1AA16CF7-5760-432D-B96D-EA1C85B31D24
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2908769
PubMed ID	2908769
published in	wds:Q69933538-D363F5B9-4574-4895-A263-BB1F8550C0EE
published in	Chemical Research in Toxicology
issue	wds:Q69933538-C3979259-E25C-415A-8306-E7D092D89621
volume	wds:Q69933538-CC6C9DB2-4671-4DBC-BDFB-B76C6C60A222
issue	6
volume	1
DOI	wds:Q69933538-193E5FF1-3C92-4D44-9E56-DC702E0DF2A6
DOI	http://dx.doi.org/10.1021/TX00006A008
DOI	10.1021/TX00006A008
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q69933538
is cites work of	The Neuropsychopharmacology and Toxicology of 3,4-methylenedioxy-N-ethyl-amphetamine (MDEA). The pre-clinical behavioural pharmacology of 3,4-methylenedioxymethamphetamine (MDMA). Toxicity of amphetamines: an update Quantification of 3,4-methylenedioxymetamphetamine and its metabolites in plasma and urine by gas chromatography with nitrogen-phosphorus detection. Identification of the human cytochromes P450 involved in the oxidative metabolism of "Ecstasy"-related designer drugs Acute and long-term effects of MDMA on cerebral dopamine biochemistry and function A comparative study on the acute and long-term effects of MDMA and 3,4-dihydroxymethamphetamine (HHMA) on brain monoamine levels after i.p. or striatal administration in mice 2,5-Bis-(glutathion-S-yl)-alpha-methyldopamine, a putative metabolite of (+/-)-3,4-methylenedioxyamphetamine, decreases brain serotonin concentrations Pro-oxidant effects of Ecstasy and its metabolites in mouse brain synaptosomes Agony and ecstasy: a review of MDMA effects and toxicity The relationship between core body temperature and 3,4-methylenedioxymethamphetamine metabolism in rats: implications for neurotoxicity. Lost in translation: preclinical studies on 3,4-methylenedioxymethamphetamine provide information on mechanisms of action, but do not allow accurate prediction of adverse events in humans Inhibitory metabolite complex formation of methylenedioxymethamphetamine with rat and human cytochrome P450. Particular involvement of CYP 2D Identification, synthesis, and biological evaluation of metabolites of the experimental cancer treatment drugs indotecan (LMP400) and indimitecan (LMP776) and investigation of isomerically hydroxylated indenoisoquinoline analogues as topoisomerase I Synthesis and capillary electrophoretic analysis of enantiomerically enriched reference standards of MDMA and its main metabolites. High-performance thin-layer chromatographic determination of N-ethyl-3,4-methylenedioxyamphetamine and its major metabolites in urine and comparison with high-performance liquid chromatography Identification of someN-hydroxylated metabolites of (±)-3,4-methylenedioxymethamphetamine in horse urine by gas chromatography-mass spectrometry Serotonergic neurotoxic thioether metabolites of 3,4-methylenedioxymethamphetamine (MDMA, "ecstasy"): synthesis, isolation, and characterization of diastereoisomers. Lethal monointoxication by overdosage of MDEA. The use of toxicokinetics for the safety assessment of drugs acting in the brain Hair analysis for drug abuse. XV. Disposition of 3, 4-methylenedioxymethamphetamine (MDMA) and its related compounds into rat hair and application to hair analysis for MDMA abuse Synthesis, in vitro formation, and behavioural effects of glutathione regioisomers of alpha-methyldopamine with relevance to MDA and MDMA (ecstasy). Attenuation of ecstasy-induced neurotoxicity by N-acetylcysteine. National Scientific Medical Meeting. 26-27 March 1999. Abstracts
is cites work of	wds:Q35745285-4D06934B-E57E-4FBD-A2F8-816367CA28FE wds:Q43261577-9D2362C3-1ECC-4298-BDEA-B1D7A0919CFF wds:Q73094230-E986C586-ED50-492D-BD87-85CCDC8CE19D wds:Q40945435-52AFBCE7-2F08-4DAB-93F1-D2B68437003D wds:Q78184469-866C496A-77CA-45FB-8808-07BAEC2F5A55 wds:Q84586372-4BD4F956-6C88-4C98-8E3F-783241D98199 wds:Q73064891-AD2AB688-3FD3-4753-8C7C-DC3A7A3FF0A8 wds:Q40432284-910AC68C-E727-4FD4-808C-368D3F9EFD22 wds:Q44590396-A03F3095-F672-444A-A6F8-7C24AB137FD4 wds:Q42165763-A2BD5347-ECDC-4127-B07F-6E9707B1D288 wds:Q35146115-59E68069-BB57-48D5-ACC0-958FC4C09126 wds:Q34011998-516F2C99-87FD-48D3-B41F-91936D23C3E1 wds:Q41741838-2A0AC157-87AA-4B0E-BFDE-78B856B18DBF wds:Q41474235-B6BF1DD7-8581-4F0F-8DB6-251E36169949 wds:Q30341737-55B37B53-65CD-4E60-9997-6AF0D8B9305C wds:Q73755207-42FAD404-2AE4-42B5-9629-C168478F635D wds:Q22252794-D3F5B80F-4640-47D1-8071-537F5EF88DE8 wds:Q26859367-247EC50F-AD23-4CAD-A267-7EA022991E55 wds:Q34424134-33F44166-DEB9-4E15-AA21-6C9393BBFA7E wds:Q36525254-82B9D0CD-2939-4765-8799-E3F78F48491F wds:Q33877774-832A16FE-CB89-43F1-8794-806445E583BE wds:Q46115283-5B98E9A2-F636-49F3-AD81-0440AC124FF2 wds:Q44614898-E50EC1C8-3DFA-4BBB-A3DE-EAA0A212247F wds:Q64960952-08F1F291-CDFE-4274-8415-EF403EB1A4C0

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