{"Abbreviation":["3-MeO-PCP"],"Aliases":["1-(1-(3-Methoxyphenyl)cyclohexyl)piperidine","3-MeO-PCP","3-MeO-phencyclidine","RefChem:907135","C18H27NO","5FUR-144","Piperidine, 1-[1-(3-methoxyphenyl)cyclohexyl]-","Piperidine, 1-(1-(3-methoxyphenyl)cyclohexyl)-","AS-19179","1-1-3-methoxyphenyl cyclohexyl -piperidine","C22809"],"CAS":"72242-03-6","ChemicalClasses":["arylcyclohexylamine"],"Chirality":"achiral","Esters":[],"Formating":[],"HMDB ID":"HMDB0243769","HeavyAtomCount":20,"IUPACName":"1-[1-(3-methoxyphenyl)cyclohexyl]piperidine","InChI":"InChI=1S/C18H27NO/c1-20-17-10-8-9-16(15-17)18(11-4-2-5-12-18)19-13-6-3-7-14-19/h8-10,15H,2-7,11-14H2,1H3","InChIKey":"BQQSZHHKGPOXLN-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e18\u003c/sub\u003eH\u003csub\u003e27\u003c/sub\u003eNO","MolecularWeight":"273.4 g/mol","PD":"PD048286","PubChemId":11778080,"Record Description":["3-Hydroxyphencyclidine (3-HO-PCP) is a dissociative anesthetic that has been sold online as a designer drug.[1] 3-HO-PCP binds to the NMDA and opioid receptors.","Wikipedia|List of designer drugs|Dissociatives|Arylcyclohexylamines","Wikipedia|NMDA receptor antagonist|Uncompetitive channel blockers"],"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/3-MeO-PCP","Name":"3-Methoxyphencyclidine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q223096","Name":"3-Methoxyphencyclidine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/11778080","Name":"3-Methoxyphencyclidine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD048286","Name":"3-Methoxyphencyclidine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=72242-03-6","Name":"3-Methoxyphencyclidine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0243769","Name":"3-Methoxyphencyclidine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C22809","Name":"3-Methoxyphencyclidine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/28A91R606X","Name":"3-Methoxyphencyclidine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID50222578","Name":"3-Methoxyphencyclidine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 11778080, 3-Methoxyphencyclidine. Accessed September 6, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/11778080\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/11778080\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 3-Methoxyphencyclidine. UNII: 28A91R606X. Global Substance Registration System. Accessed September 6, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/28A91R606X\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/28A91R606X\u003c/a\u003e"],"SMILES":"COC1=CC=CC(=C1)C2(CCCCC2)N3CCCCC3","SaltData":[{"AcidCount":1,"Amine":"3-Methoxyphencyclidine","AmineCount":1,"Formula":"Cl","Name":"hydrocloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.15 96.244\"\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=\"#1ff01f\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h95v97H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m16.544 1.053 7.266 8.623M25.006 16.465l-3.825 10.574\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath 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