World Library  
Flag as Inappropriate
Email this Article

Fluorolintane

Article Id: WHEBN0047025874
Reproduction Date:

Title: Fluorolintane  
Author: World Heritage Encyclopedia
Language: English
Subject: Lefetamine, Diphenidine, Midafotel, 2,5-Dimethoxy-4-isopropylamphetamine, Macromerine
Collection:
Publisher: World Heritage Encyclopedia
Publication
Date:
 

Fluorolintane

Fluorolintane
Systematic (IUPAC) name
1-(1-(2-fluorophenyl)-2-phenylethyl)pyrrolidine
Chemical data
Formula C18H20FN
Molecular mass 269.36 g·mol−1

Fluorolintane (also known as 2-FPPP) is a dissociative anesthetic drug that has been sold online as a designer drug.[1]

Fluorolintane and related diarylethylamines are antagonists of the NMDA receptor[2] and have been studied in vitro as potential treatments for neurotoxic injury,[3] depression[4] and as sympathomimetic.[5]

See also

References

  1. ^ Jason Wallach, Pierce V. Kavanagh, Gavin McLaughlin, Noreen Morris, John D. Power, Simon P. Elliott, Marion S. Mercier, David Lodge, Hamilton Morris, Nicola M. Dempster, Simon D. Brandt (May 2014). "Preparation and characterization of the ‘research chemical’ diphenidine, its pyrrolidine analogue, and their 2,2-diphenylethyl isomers". Drug Testing and Analysis 7 (5): 358–367.  
  2. ^ Michael L. Berger, Anna Schweifer, Patrick Rebernik, Friedrich Hammerschmidt (May 2009). "NMDA receptor affinities of 1,2-diphenylethylamine and 1-(1,2-diphenylethyl)piperidine enantiomers and of related compounds". Bioorganic & Medicinal Chemistry 17 (1): 3456–3462.  
  3. ^ Nancy M. Gray, Brian K. Cheng. "Patent EP 0346791 B1 - 1,2-diarylethylamines for treatment of neurotoxic injury". Retrieved 17 June 2015. 
  4. ^ Brooke D Aspergren, Richard V Heinzelman (1963). "Patent US 3083139 A - Therapeutic 1-(1, 2-diphenylethyl) pyrrolidine for the management of depression". Retrieved 22 June 2015. 
  5. ^ R. V. Heinzelman , B. D. Aspergren (July 1953). "Compounds Containing the Pyrrolidine Ring. Analogs of Sympathomimetic Amines". Journal of the American Chemistry Society 75 (14): 3409–3413.  
This article was sourced from Creative Commons Attribution-ShareAlike License; additional terms may apply. World Heritage Encyclopedia content is assembled from numerous content providers, Open Access Publishing, and in compliance with The Fair Access to Science and Technology Research Act (FASTR), Wikimedia Foundation, Inc., Public Library of Science, The Encyclopedia of Life, Open Book Publishers (OBP), PubMed, U.S. National Library of Medicine, National Center for Biotechnology Information, U.S. National Library of Medicine, National Institutes of Health (NIH), U.S. Department of Health & Human Services, and USA.gov, which sources content from all federal, state, local, tribal, and territorial government publication portals (.gov, .mil, .edu). Funding for USA.gov and content contributors is made possible from the U.S. Congress, E-Government Act of 2002.
 
Crowd sourced content that is contributed to World Heritage Encyclopedia is peer reviewed and edited by our editorial staff to ensure quality scholarly research articles.
 
By using this site, you agree to the Terms of Use and Privacy Policy. World Heritage Encyclopedia™ is a registered trademark of the World Public Library Association, a non-profit organization.
 



Copyright © World Library Foundation. All rights reserved. eBooks from World eBook Library are sponsored by the World Library Foundation,
a 501c(4) Member's Support Non-Profit Organization, and is NOT affiliated with any governmental agency or department.