MDAI (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "MDAI" in English language version.

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admin.ch (Global: 279th place; English: 551st place)

  • "812.121.11" (PDF). Verordnung des EDI über die Verzeichnisse der Betäubungsmittel, psychotropen Stoffe, Vorläuferstoffe und Hilfschemikalien (Regulation of the EDI about the directories of drugs, psychotropic substances, precursors and auxiliary chemicals) (in German). Das Eidgenössische Departement des Innern (EDI). December 2011.

doi.org (Global: 2nd place; English: 2nd place)

finlex.fi (Global: 3,070th place; English: 5,496th place)

in.gov.br (Global: 3,151st place; English: 5,932nd place)

laegemiddelstyrelsen.dk (Global: low place; English: low place)

mdma.ch (Global: low place; English: low place)

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nih.gov (Global: 4th place; English: 4th place)

pubmed.ncbi.nlm.nih.gov

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psu.edu (Global: 207th place; English: 136th place)

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semanticscholar.org (Global: 11th place; English: 8th place)

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  • Corkery JM, Elliott S, Schifano F, Corazza O, Ghodse AH (July 2013). "MDAI (5,6-methylenedioxy-2-aminoindane; 6,7-dihydro-5H-cyclopenta[f][1,3]benzodioxol-6-amine; 'sparkle'; 'mindy') toxicity: a brief overview and update". Human Psychopharmacology. 28 (4): 345–355. doi:10.1002/hup.2298. PMID 23881883. S2CID 12322724.
  • Gallagher CT, Assi S, Stair JL, Fergus S, Corazza O, Corkery JM, et al. (March 2012). "5,6-Methylenedioxy-2-aminoindane: from laboratory curiosity to 'legal high'". Human Psychopharmacology. 27 (2): 106–112. doi:10.1002/hup.1255. PMID 22389075. S2CID 205924978.
  • Páleníček T, Lhotková E, Žídková M, Balíková M, Kuchař M, Himl M, et al. (August 2016). "Emerging toxicity of 5,6-methylenedioxy-2-aminoindane (MDAI): Pharmacokinetics, behaviour, thermoregulation and LD50 in rats". Progress in Neuro-Psychopharmacology & Biological Psychiatry. 69: 49–59. doi:10.1016/j.pnpbp.2016.04.004. PMID 27083855. S2CID 33032545.
  • Brandt SD, Sumnall HR, Measham F, Cole J (July 2010). "Second generation mephedrone. The confusing case of NRG-1". BMJ. 341 c3564. doi:10.1136/bmj.c3564. PMID 20605894. S2CID 20354123.
  • Setola V, Hufeisen SJ, Grande-Allen KJ, Vesely I, Glennon RA, Blough B, et al. (June 2003). "3,4-methylenedioxymethamphetamine (MDMA, "Ecstasy") induces fenfluramine-like proliferative actions on human cardiac valvular interstitial cells in vitro". Molecular Pharmacology. 63 (6): 1223–1229. doi:10.1124/mol.63.6.1223. PMID 12761331. S2CID 839426.
  • Rothman RB, Baumann MH, Dersch CM, Romero DV, Rice KC, Carroll FI, et al. (January 2001). "Amphetamine-type central nervous system stimulants release norepinephrine more potently than they release dopamine and serotonin". Synapse. 39 (1): 32–41. doi:10.1002/1098-2396(20010101)39:1<32::AID-SYN5>3.0.CO;2-3. PMID 11071707. S2CID 15573624.
  • Oberlender R, Nichols DE (1988). "Drug discrimination studies with MDMA and amphetamine". Psychopharmacology. 95 (1): 71–6. doi:10.1007/bf00212770. PMID 2898791. S2CID 19664637.
  • Oberlender R, Nichols DE (March 1991). "Structural variation and (+)-amphetamine-like discriminative stimulus properties". Pharmacology, Biochemistry, and Behavior. 38 (3): 581–6. doi:10.1016/0091-3057(91)90017-V. PMID 2068194. S2CID 19069907. PMID
  • Kovar KA (July 1998). "Chemistry and pharmacology of hallucinogens, entactogens and stimulants". Pharmacopsychiatry. 31 (Suppl 2): 69–72. doi:10.1055/s-2007-979349. PMID 9754836. S2CID 28388528.
  • Nichols DE, Johnson MP, Oberlender R (January 1991). "5-Iodo-2-aminoindan, a nonneurotoxic analogue of p-iodoamphetamine". Pharmacology, Biochemistry, and Behavior. 38 (1): 135–9. CiteSeerX 10.1.1.670.504. doi:10.1016/0091-3057(91)90601-w. PMID 1826785. S2CID 20485505.
  • Johnson MP, Huang XM, Nichols DE (December 1991). "Serotonin neurotoxicity in rats after combined treatment with a dopaminergic agent followed by a nonneurotoxic 3,4-methylenedioxymethamphetamine (MDMA) analogue". Pharmacology, Biochemistry, and Behavior. 40 (4): 915–22. doi:10.1016/0091-3057(91)90106-c. PMID 1726189. S2CID 7199902.
  • Cozzi NV, Frescas S, Marona-Lewicka D, Huang X, Nichols DE (March 1998). "Indan analogs of fenfluramine and norfenfluramine have reduced neurotoxic potential". Pharmacology, Biochemistry, and Behavior. 59 (3): 709–15. doi:10.1016/s0091-3057(97)00557-1. PMID 9512076. S2CID 41048219.

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