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Contents

   



(Top)
  


1 See also  




2 References  













Eclanamine






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From Wikipedia, the free encyclopedia
  

Eclanamine
Clinical data
ATC code
  • None
Identifiers

  • N-(3,4-dichlorophenyl)-N-[(1R,2R)-2-(dimethylamino)cyclopentyl]propanamide

CAS Number
  • maleate: 67450-45-7 checkY
    • PubChem CID
    ChemSpider
    UNII
  • maleate: J2C169J769 checkY
    • Chemical and physical data
    FormulaC16H22Cl2N2O
    Molar mass329.27 g·mol−1
    3D model (JSmol)

    • Clc2ccc(N(C(=O)CC)[C@@H]1CCC[C@H]1N(C)C)cc2Cl

    • InChI=1S/C16H22Cl2N2O/c1-4-16(21)20(11-8-9-12(17)13(18)10-11)15-7-5-6-14(15)19(2)3/h8-10,14-15H,4-7H2,1-3H3/t14-,15-/m1/s1

    • Key:YCRFSKUCDBJWLX-HUUCEWRRSA-N

    Eclanamine (U-48,753) is a drug which was patented as an antidepressant, but was never marketed.[1] It acts by inhibiting the reuptakeofserotonin and norepinephrine.[2]

    See also[edit]

    References[edit]

    1. ^ Triggle DJ (1997). Dictionary of pharmacological agents. London: Chapman & Hall. ISBN 978-0-412-46630-4.
  • ^ Rees DC (1992). "Chemical structures and biological activities of non-peptide selective kappa opioid ligands". Progress in Medicinal Chemistry. 29: 109–39 (128). doi:10.1016/s0079-6468(08)70006-7. ISBN 978-0-444-89472-4. PMID 1335584.

    • Retrieved from "https://en.wikipedia.org/w/index.php?title=Eclanamine&oldid=1082621559"
    Categories: 
    ●Drugs not assigned an ATC code
     ●Carboxamides
     ●Dimethylamino compounds
     ●Antidepressants
     ●Serotonin–norepinephrine reuptake inhibitors
     ●Cyclopentanes
     Hidden categories: 
    ●Articles with short description
     ●Short description matches Wikidata
     ●Articles without EBI source
     ●Chemical pages without DrugBank identifier
     ●Articles without KEGG source
     ●Multiple chemicals in Infobox drug
     ●Chemicals using indexlabels
     ●Chemical articles with multiple CAS registry numbers
     ●Drugs with no legal status
     ●Articles containing unverified chemical infoboxes
      


    ●This page was last edited on 14 April 2022, at 05:18 (UTC).
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