Methylendioxypyrovaleron (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Methylendioxypyrovaleron" in German language version.

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  • Joshua C. Yohannan, Joseph S. Bozenko, Jr.: The Characterization of 3,4-Methylenedioxypyrovalerone (MDPV). In: Microgram Journal. Band 7, Nr. 1, 2010, S. 12–15 (dea.gov [PDF; 689 kB] Volltext).

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  • M. Coppola, R. Mondola: 3,4-Methylenedioxypyrovalerone (MDPV): Chemistry, pharmacology and toxicology of a new designer drug of abuse marketed online. In: Toxicology Letters. Band 208, Nr. 1, 5. Januar 2006, S. 12–15, doi:10.1016/j.toxlet.2011.10.002.
  • Simmler LD u. a.: Pharmacological characterization of designer cathinones in vitro. In: British Journal of Pharmacology. Band 168, Heft 2, 2013, S. 458–470, doi:10.1111/j.1476-5381.2012.02145.x, PMID 22897747, PMC 3572571 (freier Volltext).
  • Baumann MH, Partilla JS, Lehner KR, Thorndike EB, Hoffman AF, Holy M, Rothman RB, Goldberg SR, Lupica CR, Sitte HH, Brandt SD, Tella SR, Cozzi NV, Schindler CW: Powerful cocaine-like actions of 3,4-methylenedioxypyrovalerone (MDPV), a principal constituent of psychoactive ‘bath salts’ products. In: Neuropsychopharmacology. 38. Jahrgang, Nr. 4, 2013, S. 552–62, doi:10.1038/npp.2012.204, PMID 23072836, PMC 3572453 (freier Volltext).
  • F. Westphal, T. Junge, P. Rösner, F. Sönnichsen, F. Schuster: Mass and NMR spectroscopic characterization of 3,4-methylenedioxypyrovalerone: A designer drug with alpha-pyrrolidinophenone structure. In: Forensic Science International. 190. Jahrgang, Nr. 1–3, 2009, S. 1, doi:10.1016/j.forsciint.2009.05.001, PMID 19500924.
  • Araújo AM, Valente MJ, Carvalho M, Dias da Silva D, Gaspar H, Carvalho F, de Lourdes Bastos M, Guedes de Pinho P: Raising awareness of new psychoactive substances: chemical analysis and in vitro toxicity screening of 'legal high' packages containing synthetic cathinones. In: Arch. Toxicol. 89. Jahrgang, Nr. 5, 2015, S. 757–71, doi:10.1007/s00204-014-1278-7, PMID 24903018.
  • Brittany L. Murray, Christine M. Murphy, Michael C. Beuhler: Death Following Recreational Use of Designer Drug “Bath Salts” Containing 3,4-Methylenedioxypyrovalerone (MDPV). In: Journal of Medical Toxicology. 8. Jahrgang, Nr. 1, 2012, S. 69–75, doi:10.1007/s13181-011-0196-9.
  • John Wyman, Eric Lavins, David Engelhart et al.: Postmortem Tissue Distribution of MDPV Following Lethal Intoxication by “Bath Salts”. In: Journal of Analytical Toxicology. 37. Jahrgang, 2013, S. 182–185, doi:10.1093/jat/bkt001.
  • B. Desharnais, Y. Dazé, L.M. Huppertz et al.: A case of fatal idiosyncratic reaction to the designer drug 3,4-methylenedioxypyrovalerone (MDPV) and review of the literature. In: Forensic Sci Med Pathol. 13. Jahrgang, 2017, S. 350–354, doi:10.1007/s12024-017-9894-1.
  • Edward A. Ross, Gary M. Reisfield, Mary C. Watson, Chris W. Chronister, Bruce A. Goldberger: Psychoactive “Bath Salts” Intoxication with Methylenedioxypyrovalerone. In: The American Journal of Medicine. 125. Jahrgang, Nr. 9, 2012, S. 854–858, doi:10.1016/j.amjmed.2012.02.019.
  • S. Fröhlich, E. Lambe, J. O’Dea: Acute liver failure following recreational use of psychotropic “head shop” compounds. In: Irish Journal of Medical Science. 180. Jahrgang, Nr. 1, 2010, S. 263–264, doi:10.1007/s11845-010-0636-6.
  • Heather A. Borek, Christopher P. Holstege: Hyperthermia and Multiorgan Failure After Abuse of “Bath Salts” Containing 3,4-Methylenedioxypyrovalerone. In: Annals of Emergency Medicine. 60. Jahrgang, Nr. 1, 2012, S. 103–105, doi:10.1016/j.annemergmed.2012.01.005.
  • R. Kolanos, J. S. Partilla, M. H. Baumann, B. A. Hutsell, M. L. Banks, S. S. Negus, R. A. Glennon: Stereoselective Actions of Methylenedioxypyrovalerone (MDPV) To Inhibit Dopamine and Norepinephrine Transporters and Facilitate Intracranial Self-Stimulation in Rats. In: ACS Chemical Neuroscience. 6. Jahrgang, Nr. 5, 2015, S. 771–777, doi:10.1021/acschemneuro.5b00006.
  • Shekar A, Aguilar JI, Galli G, Cozzi NV, Brandt SD, Ruoho AE, Baumann MH, Matthies HJ, Galli A: Atypical dopamine efflux caused by 3,4-methylenedioxypyrovalerone (MDPV) via the human dopamine transporter. In: J. Chem. Neuroanat. 2017, doi:10.1016/j.jchemneu.2017.01.004, PMID 28163218.
  • Meyer MR, Du P, Schuster F, Maurer HH: Studies on the metabolism of the α-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. In: J Mass Spectrom. 45. Jahrgang, Nr. 12, 2010, S. 1426–42, doi:10.1002/jms.1859, PMID 21053377.
  • Baumann MH, Bukhari MO, Lehner KR, Anizan S, Rice KC, Concheiro M, Huestis MA: Neuropharmacology of 3,4-Methylenedioxypyrovalerone (MDPV), Its Metabolites, and Related Analogs. In: Curr Top Behav Neurosci. 2016, doi:10.1007/7854_2016_53, PMID 27830575.
  • Negreira N, Erratico C, Kosjek T, van Nuijs AL, Heath E, Neels H, Covaci A: In vitro Phase I and Phase II metabolism of α-pyrrolidinovalerophenone (α-PVP), methylenedioxypyrovalerone (MDPV) and methedrone by human liver microsomes and human liver cytosol. In: Anal Bioanal Chem. 407. Jahrgang, Nr. 19, 2015, S. 5803–16, doi:10.1007/s00216-015-8763-6, PMID 26014283.
  • Valente MJ, Araújo AM, Silva R, Bastos Mde L, Carvalho F, Guedes de Pinho P, Carvalho M: 3,4-Methylenedioxypyrovalerone (MDPV): in vitro mechanisms of hepatotoxicity under normothermic and hyperthermic conditions. In: Arch. Toxicol. 90. Jahrgang, Nr. 8, 2016, S. 1959–73, doi:10.1007/s00204-015-1653-z, PMID 26676947.
  • Valente MJ, Bastos ML, Fernandes E, Carvalho F, Guedes de Pinho P, Carvalho M: Neurotoxicity of β-Keto Amphetamines: Deathly Mechanisms Elicited by Methylone and MDPV in Human Dopaminergic SH-SY5Y Cells. In: ACS Chem Neurosci. 2017, doi:10.1021/acschemneuro.6b00421, PMID 28067045.
  • Wood MR, Lalancette RA, Bernal I: Crystallographic investigations of select cathinones: emerging illicit street drugs known as `bath salts'. In: Acta Crystallogr C Struct Chem. 71. Jahrgang, Pt 1, 2015, S. 32–8, doi:10.1107/S2053229614025637, PMID 25567572.
  • Schindler CW, Thorndike EB, Suzuki M, Rice KC, Baumann MH: Pharmacological mechanisms underlying the cardiovascular effects of the "bath salt" constituent 3,4-methylenedioxypyrovalerone (MDPV). In: Br. J. Pharmacol. 173. Jahrgang, Nr. 24, 2016, S. 3492–3501, doi:10.1111/bph.13640, PMID 27714779.

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  • Patent US3314970A: Pyrrolidino Ketones. Angemeldet am 14. Oktober 1964, veröffentlicht am 18. April 1967, Anmelder: Boehringer Ingelheim G.m.b.H., Erfinder: Ernst Seger.
  • Patentanmeldung DE1545591A1: Verfahren zur Herstellung von alpha-Aminoketonen mit heterocyclischer Aminogruppe. Angemeldet am 28. Mai 1965, veröffentlicht am 7. August 1969, Anmelder: C.H. Boehringer Sohn, Erfinder: Herbert Köppe et al.

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  • Simmler LD u. a.: Pharmacological characterization of designer cathinones in vitro. In: British Journal of Pharmacology. Band 168, Heft 2, 2013, S. 458–470, doi:10.1111/j.1476-5381.2012.02145.x, PMID 22897747, PMC 3572571 (freier Volltext).
  • Baumann MH, Partilla JS, Lehner KR, Thorndike EB, Hoffman AF, Holy M, Rothman RB, Goldberg SR, Lupica CR, Sitte HH, Brandt SD, Tella SR, Cozzi NV, Schindler CW: Powerful cocaine-like actions of 3,4-methylenedioxypyrovalerone (MDPV), a principal constituent of psychoactive ‘bath salts’ products. In: Neuropsychopharmacology. 38. Jahrgang, Nr. 4, 2013, S. 552–62, doi:10.1038/npp.2012.204, PMID 23072836, PMC 3572453 (freier Volltext).
  • F. Westphal, T. Junge, P. Rösner, F. Sönnichsen, F. Schuster: Mass and NMR spectroscopic characterization of 3,4-methylenedioxypyrovalerone: A designer drug with alpha-pyrrolidinophenone structure. In: Forensic Science International. 190. Jahrgang, Nr. 1–3, 2009, S. 1, doi:10.1016/j.forsciint.2009.05.001, PMID 19500924.
  • Araújo AM, Valente MJ, Carvalho M, Dias da Silva D, Gaspar H, Carvalho F, de Lourdes Bastos M, Guedes de Pinho P: Raising awareness of new psychoactive substances: chemical analysis and in vitro toxicity screening of 'legal high' packages containing synthetic cathinones. In: Arch. Toxicol. 89. Jahrgang, Nr. 5, 2015, S. 757–71, doi:10.1007/s00204-014-1278-7, PMID 24903018.
  • Shekar A, Aguilar JI, Galli G, Cozzi NV, Brandt SD, Ruoho AE, Baumann MH, Matthies HJ, Galli A: Atypical dopamine efflux caused by 3,4-methylenedioxypyrovalerone (MDPV) via the human dopamine transporter. In: J. Chem. Neuroanat. 2017, doi:10.1016/j.jchemneu.2017.01.004, PMID 28163218.
  • Meyer MR, Du P, Schuster F, Maurer HH: Studies on the metabolism of the α-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. In: J Mass Spectrom. 45. Jahrgang, Nr. 12, 2010, S. 1426–42, doi:10.1002/jms.1859, PMID 21053377.
  • Baumann MH, Bukhari MO, Lehner KR, Anizan S, Rice KC, Concheiro M, Huestis MA: Neuropharmacology of 3,4-Methylenedioxypyrovalerone (MDPV), Its Metabolites, and Related Analogs. In: Curr Top Behav Neurosci. 2016, doi:10.1007/7854_2016_53, PMID 27830575.
  • Negreira N, Erratico C, Kosjek T, van Nuijs AL, Heath E, Neels H, Covaci A: In vitro Phase I and Phase II metabolism of α-pyrrolidinovalerophenone (α-PVP), methylenedioxypyrovalerone (MDPV) and methedrone by human liver microsomes and human liver cytosol. In: Anal Bioanal Chem. 407. Jahrgang, Nr. 19, 2015, S. 5803–16, doi:10.1007/s00216-015-8763-6, PMID 26014283.
  • Valente MJ, Araújo AM, Silva R, Bastos Mde L, Carvalho F, Guedes de Pinho P, Carvalho M: 3,4-Methylenedioxypyrovalerone (MDPV): in vitro mechanisms of hepatotoxicity under normothermic and hyperthermic conditions. In: Arch. Toxicol. 90. Jahrgang, Nr. 8, 2016, S. 1959–73, doi:10.1007/s00204-015-1653-z, PMID 26676947.
  • Valente MJ, Bastos ML, Fernandes E, Carvalho F, Guedes de Pinho P, Carvalho M: Neurotoxicity of β-Keto Amphetamines: Deathly Mechanisms Elicited by Methylone and MDPV in Human Dopaminergic SH-SY5Y Cells. In: ACS Chem Neurosci. 2017, doi:10.1021/acschemneuro.6b00421, PMID 28067045.
  • Wood MR, Lalancette RA, Bernal I: Crystallographic investigations of select cathinones: emerging illicit street drugs known as `bath salts'. In: Acta Crystallogr C Struct Chem. 71. Jahrgang, Pt 1, 2015, S. 32–8, doi:10.1107/S2053229614025637, PMID 25567572.
  • Schindler CW, Thorndike EB, Suzuki M, Rice KC, Baumann MH: Pharmacological mechanisms underlying the cardiovascular effects of the "bath salt" constituent 3,4-methylenedioxypyrovalerone (MDPV). In: Br. J. Pharmacol. 173. Jahrgang, Nr. 24, 2016, S. 3492–3501, doi:10.1111/bph.13640, PMID 27714779.