{"Abbreviation":"","Aliases":["NEDPA","Benzeneethanamine, N-ethyl-α-phenyl-","N-Ethyl-α-phenylbenzeneethanamine","(1,2-Diphenylethyl)(ethyl)amine","n-ethyl-1,2-diphenylethylamine","Phenethylamine, N-ethyl-α-phenyl-","N-ethyl-1,2-diphenylethan-1-amine","Benzeneethanamine, n-ethyl-α-phenyl-"],"CAS":"60951-19-1","ChemicalClasses":["diarylethylamine"],"Chirality":"racemic","EliminationHalfLife":"","Esters":[],"Formating":[],"HeavyAtomCount":17,"IUPACName":"N-ethyl-1,2-diphenylethanamine","InChI":"InChI=1S/C16H19N/c1-2-17-16(15-11-7-4-8-12-15)13-14-9-5-3-6-10-14/h3-12,16-17H,2,13H2,1H3","InChIKey":"IGFZMQXEKIZPDR-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e16\u003c/sub\u003eH\u003csub\u003e19\u003c/sub\u003eN","MolecularWeight":"225.33 g/mol","Opticalactivity":"( + / - )","PubChemId":110821,"Record Description":["Ephenidine (also known as NEDPA and EPE) is a dissociative anesthetic that has been sold online as a designer drug.[1][2] It is illegal in some countries as a structural isomer of the banned opioid drug lefetamine, but has been sold in countries where it is not yet banned. Ephenidine and related diarylethylamines have been studied in vitro as treatments for neurotoxic injuries, and are antagonists of the NMDA receptor.","Wikipedia|List of designer drugs|Dissociatives|Diarylethylamines"],"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Ephenidine","Name":"Ephenidine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q20708135","Name":"Ephenidine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/110821","Name":"Ephenidine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=60951-19-1","Name":"Ephenidine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/NG69VG2948","Name":"Ephenidine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID601032416","Name":"Ephenidine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 110821, Ephenidine. Accessed July 13, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/110821\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/110821\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Ephenidine. UNII: NG69VG2948. Global Substance Registration System. Accessed July 13, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/NG69VG2948\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/NG69VG2948\u003c/a\u003e"],"SMILES":"CCNC(CC1=CC=CC=C1)C2=CC=CC=C2","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Australia","ref":[],"schedule":"Unscheduled substance"},{"gov":"Canada","ref":[],"schedule":"Schedule I substance"},{"act":"Neue-psychoaktive-Stoffe-Gesetz (NpSG)","gov":"Germany","ref":[],"schedule":"Neuer-Psychoaktiver-Stoff"},{"gov":"United Kingdom","ref":[],"schedule":"PSA substance"}],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"CCN[C@H](Cc1ccccc1)c1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.469 62.849\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" 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