MEAI (English Wikipedia)

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

Last modified:

Ref.Un. Ref.Website
Global rank English rank
5th place
5th place
2nd place
2nd place
15th place
8th place
low place
low place
14th place
9th place
4th place
4th place
low place
low place
low place
low place
low place
low place
9,451st place
4,978th place
3rd place
3rd place
185th place
154th place
1,041st place
901st place
110th place
65th place
1,154th place
606th place
776th place
2,100th place
182nd place
172nd place
1st place
1st place
950th place
813th place
16th place
11th place
13th place
14th place
46th place
29th place
low place
low place
3,066th place
1,749th place
low place
low place

adsabs.harvard.edu (Global: 14th place; English: 9th place)

ui.adsabs.harvard.edu

  • Shimshoni JA, Winkler I, Edery N, Golan E, van Wettum R, Nutt D (March 2017). "Toxicological evaluation of 5-methoxy-2-aminoindane (MEAI): Binge mitigating agent in development". Toxicology and Applied Pharmacology. 319: 59–68. Bibcode:2017ToxAP.319...59S. doi:10.1016/j.taap.2017.01.018. PMID 28167221. S2CID 205304106. 5-Methoxy-2-aminoindane (MEAI or Chaperon) is a psychoactive compound of the aminoindane class with a mechanism of action described by one patent as being possibly mediated by binding to the dopamine D3 receptor (Haadsma-Svensson et al., 1994). In recent years MEAI has been recreationally used by many people, mainly in the UK, who report a mild euphoric, alcohol-like tipsy experience (Nutt, 2013; Slezak, 2014). Typically recreational users ingest orally MEAI at doses of up to 1–2 mg/kg body weight in a session and report an onset of effect of up to 4 h with reduced desire to consume alcoholic beverages.
  • Shimshoni JA, Sobol E, Golan E, Ben Ari Y, Gal O (March 2018). "Pharmacokinetic and pharmacodynamic evaluation of 5-methoxy-2-aminoindane (MEAI): A new binge-mitigating agent". Toxicology and Applied Pharmacology. 343: 29–39. Bibcode:2018ToxAP.343...29S. doi:10.1016/j.taap.2018.02.009. PMID 29458138. S2CID 3879333.
  • Nutt DJ, King LA, Phillips LD (November 2010). "Drug harms in the UK: a multicriteria decision analysis". Lancet. 376 (9752): 1558–1565. Bibcode:2010Lanc..376.1558N. doi:10.1016/S0140-6736(10)61462-6. PMID 21036393. S2CID 5667719.

aipsin.com (Global: low place; English: low place)

  • "5-MeO-AI". АИПСИН (in Russian). Retrieved 1 January 2026.

benedictwermter.com (Global: low place; English: low place)

books.google.com (Global: 3rd place; English: 3rd place)

cbc.ca (Global: 110th place; English: 65th place)

clearmindmedicine.com (Global: low place; English: low place)

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

espacenet.com (Global: 950th place; English: 813th place)

worldwide.espacenet.com

  • US 5708018, Haadsma-Svensson SR, Andersson BR, Sonesson CA, Lin CH, Waters RN, Svensson KA, Carlsson PA, Hansson LO, Stjernlof NP, "2-aminoindans as selective dopamine D3 ligands", published 1998-01-13, assigned to Pharmacia & Upjohn Co.

globes.co.il (Global: 776th place; English: 2,100th place)

independent.co.uk (Global: 46th place; English: 29th place)

netfirms.com (Global: 9,451st place; English: 4,978th place)

bitnest.netfirms.com

newscientist.com (Global: 1,041st place; English: 901st place)

newswire.ca (Global: 3,066th place; English: 1,749th place)

nih.gov (Global: 5th place; English: 5th place)

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

archives.nida.nih.gov

openlibrary.org (Global: 185th place; English: 154th place)

ozmosi.com (Global: low place; English: low place)

pryzm.ozmosi.com

patents.google.com (Global: 1,154th place; English: 606th place)

  • US 10406123B2, Golan E, "Binge behavior regulators", issued 2019-09-10
  • US 20170360067, Golan E, "Alcoholic beverage substitutes", issued 2017-12-21

patsnap.com (Global: low place; English: low place)

synapse.patsnap.com

semanticscholar.org (Global: 15th place; English: 8th place)

api.semanticscholar.org

  • Shimshoni JA, Winkler I, Edery N, Golan E, van Wettum R, Nutt D (March 2017). "Toxicological evaluation of 5-methoxy-2-aminoindane (MEAI): Binge mitigating agent in development". Toxicology and Applied Pharmacology. 319: 59–68. Bibcode:2017ToxAP.319...59S. doi:10.1016/j.taap.2017.01.018. PMID 28167221. S2CID 205304106. 5-Methoxy-2-aminoindane (MEAI or Chaperon) is a psychoactive compound of the aminoindane class with a mechanism of action described by one patent as being possibly mediated by binding to the dopamine D3 receptor (Haadsma-Svensson et al., 1994). In recent years MEAI has been recreationally used by many people, mainly in the UK, who report a mild euphoric, alcohol-like tipsy experience (Nutt, 2013; Slezak, 2014). Typically recreational users ingest orally MEAI at doses of up to 1–2 mg/kg body weight in a session and report an onset of effect of up to 4 h with reduced desire to consume alcoholic beverages.
  • 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.
  • 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.
  • Shimshoni JA, Sobol E, Golan E, Ben Ari Y, Gal O (March 2018). "Pharmacokinetic and pharmacodynamic evaluation of 5-methoxy-2-aminoindane (MEAI): A new binge-mitigating agent". Toxicology and Applied Pharmacology. 343: 29–39. Bibcode:2018ToxAP.343...29S. doi:10.1016/j.taap.2018.02.009. PMID 29458138. S2CID 3879333.
  • Nutt DJ, King LA, Phillips LD (November 2010). "Drug harms in the UK: a multicriteria decision analysis". Lancet. 376 (9752): 1558–1565. Bibcode:2010Lanc..376.1558N. doi:10.1016/S0140-6736(10)61462-6. PMID 21036393. S2CID 5667719.

springer.com (Global: 182nd place; English: 172nd place)

link.springer.com

theguardian.com (Global: 16th place; English: 11th place)

thewalrus-factchecking.com (Global: low place; English: low place)

web.archive.org (Global: 1st place; English: 1st place)

worldcat.org (Global: 4th place; English: 4th place)

search.worldcat.org

youtube.com (Global: 13th place; English: 14th place)