{"Abbreviation":["PCPy"],"Aliases":["PCPy","1-(1-Phenylcyclohexyl)pyrrolidine","Roliciclidina","Rolicyclidinum","RefChem:179781","PHP (1-(1-phenylcyclohexyl)pyrrolidine)","Pyrrolidine, 1-(1-phenylcyclohexyl)-","Ncgc00160464-01","1-(1-phenylcyclohexyl)-pyrrolidine","Tox21_111832","Pyrrolidine, 1-(1-phenylcyclohexyl)","DB01549","Cas-2201-39-0","D12706"],"CAS":"2201-39-0","ChEBI":"CHEBI:60805","ChEMBL":"CHEMBL1719398","ChemicalClasses":["arylcyclohexylamine"],"Chirality":"achiral","DEA no":7458,"Drug Indication":"Rolicyclidine has anesthetic properties and can induce a sedative effect.","Esters":[],"Formating":[],"HeavyAtomCount":17,"IUPACName":"1-(1-phenylcyclohexyl)pyrrolidine","InChI":"InChI=1S/C16H23N/c1-3-9-15(10-4-1)16(11-5-2-6-12-16)17-13-7-8-14-17/h1,3-4,9-10H,2,5-8,11-14H2","InChIKey":"FYOWWXMGDATDQY-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e16\u003c/sub\u003eH\u003csub\u003e23\u003c/sub\u003eN","MolecularWeight":"229.36 g/mol","Pharmacodynamics":"Rolicyclidine is similar in effects to phencyclidine but is slightly less potent and has less stimulant effects. Instead it acts by inducing a sedative effect described as being somewhat similar to a barbiturate, but with additional PCP-like dissociative, anaesthetic and hallucinogenic effects.","PubChemId":62436,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Rolicyclidine","Name":"Rolicyclidine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q570183","Name":"Rolicyclidine","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB01549","Name":"Rolicyclidine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/62436","Name":"Rolicyclidine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1719398","Name":"Rolicyclidine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:60805","Name":"Rolicyclidine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=2201-39-0","Name":"Rolicyclidine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/D12706","Name":"Rolicyclidine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/183O9O9JE3","Name":"Rolicyclidine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID8046167","Name":"Rolicyclidine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 62436, Rolicyclidine. Accessed September 6, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/62436\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/62436\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Rolicyclidine. UNII: 183O9O9JE3. Global Substance Registration System. Accessed September 6, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/183O9O9JE3\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/183O9O9JE3\u003c/a\u003e"],"SMILES":"C1CCC(CC1)(C2=CC=CC=C2)N3CCCC3","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Australia","ref":[],"schedule":"S9 substance"},{"gov":"Brazil","ref":[],"schedule":"F2 substance"},{"gov":"Canada","ref":[],"schedule":"Schedule III substance"},{"gov":"United Kingdom","ref":[],"schedule":"Class A substance"},{"act":"Controlled Substances Act (CSA)","gov":"United States","ref":[],"schedule":"Schedule I"},{"gov":"Germany","ref":[],"schedule":"Anlage I substance"},{"act":"Convention on Psychotropic Substances 1971","gov":"United Nations","ref":[],"schedule":"Schedule I drug"}],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 67.399 70.224\"\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\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h68v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m35.637 69.185 13.196-7.624M48.833 61.561l.004-15.24M48.837 46.321l-13.191-7.616M35.646 38.705 22.451 46.33M22.451 46.33l-.005 15.24M35.637 69.185 22.446 61.57M35.646 38.705l-9.793-11.666\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m10.846 29.694 15.007-2.655M11.808 27.047l12.235-2.164\"/\u003e\u003c/g\u003e\u003cpath d=\"M10.846 29.694 1.053 18.028\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m6.267 3.708-5.214 14.32M8.077 5.864 3.826 17.539\"/\u003e\u003c/g\u003e\u003cpath d=\"m6.267 3.708 15.007-2.655\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M31.067 12.719 21.274 1.053M28.294 13.208 20.312 3.7\"/\u003e\u003c/g\u003e\u003cpath d=\"m25.853 27.039 5.214-14.32M35.646 38.705l6.949-8.283M44.488 23.228l-2.722-10.934M41.766 12.294l12.911-8.123M54.677 4.171l11.669 9.79M66.346 13.961l-5.754 14.126M48.773 27.268l11.819.819\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M47.377 29.486h-.721l-2.619-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m42.595 30.422-3.475 4.141M44.488 23.228l-1.361-5.467M48.773 27.268l5.91.41\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Rolicyclidine","UNII":"183O9O9JE3","Wikidata":"Q570183","Wikipedia":"Rolicyclidine","XLogP":3.3}