{"Abbreviation":["α-PHP"],"Aliases":["α-PHP","1-Phenyl-2-(1-pyrrolidinyl)-1-hexanone","Hexanophenone, 2-(1-pyrrolidinyl)-","α-pyrrolidinohexanophenone","1-Hexanone, 1-phenyl-2-(1-pyrrolidinyl)-","J3.226.366f","1-phenyl-2-(pyrrolidin-1-yl)hexan-1-one","RefChem:555927","824-478-2","α-Pyrrolidinohexanophenone (Other names: α-PHP; α-pyrrolidinohexanophenone; 1-phenyl-2-(pyrrolidin-1-yl)hexan-1-one)","PV-7","C22753"],"CAS":"13415-86-6","ChemicalClasses":["pyrrolidinophenone"],"Chirality":"racemic","Classes":["Stimulant"],"Esters":[],"European Community (EC) Number":"824-478-2","Formating":["alpha-pyrrolidinohexiophenone"],"HeavyAtomCount":18,"IUPACName":"1-phenyl-2-pyrrolidin-1-ylhexan-1-one","InChI":"InChI=1S/C16H23NO/c1-2-3-11-15(17-12-7-8-13-17)16(18)14-9-5-4-6-10-14/h4-6,9-10,15H,2-3,7-8,11-13H2,1H3","InChIKey":"KYIJLDDXQWBNGX-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e16\u003c/sub\u003eH\u003csub\u003e23\u003c/sub\u003eNO","MolecularWeight":"245.36 g/mol","Opticalactivity":"( + / - )","PD":"PD046435","PubChemId":102107923,"Record Description":["Wikipedia|List of designer drugs|Stimulants|Pyrrolidines and Pyrrolidinophenones","\u0026#945;-Pyrrolidinohexiophenone (\u0026#945;-PHP, alpha-PHP, \u0026#945;-Pyrrolidinohexanophenone, PV-7) is a synthetic stimulant drug of the cathinone class developed in the 1960s[1] which has been reported as a novel designer drug. It is a longer chain homologue of \u0026#945;-PVP, having an extra carbon on the alkyl side chain, and is a structural isomer of pyrovalerone. Sweden's public health agency suggested to classify \u0026#945;-PHP as narcotic on June 1, 2015. As of October 2015 \u0026#945;-PHP is a controlled substance in China."],"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/α-Pyrrolidinohexiophenone","Name":"α-Pyrrolidinohexiophenone","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q21098929","Name":"α-Pyrrolidinohexiophenone","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/102107923","Name":"α-Pyrrolidinohexiophenone","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD046435","Name":"α-Pyrrolidinohexiophenone","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=13415-86-6","Name":"α-Pyrrolidinohexiophenone","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C22753","Name":"α-Pyrrolidinohexiophenone","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/297J9K8A4G","Name":"α-Pyrrolidinohexiophenone","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID301016924","Name":"α-Pyrrolidinohexiophenone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 102107923, α-Pyrrolidinohexiophenone. Accessed August 28, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/102107923\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/102107923\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. α-Pyrrolidinohexiophenone. UNII: 297J9K8A4G. Global Substance Registration System. Accessed August 28, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/297J9K8A4G\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/297J9K8A4G\u003c/a\u003e"],"SMILES":"CCCCC(C(=O)C1=CC=CC=C1)N2CCCC2","SaltData":[{"AcidCount":1,"Amine":"α-Pyrrolidinohexiophenone","AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 115.132 73.75\"\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 0h116v74H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m80.232 72.712-13.198-7.62M67.034 65.092v-15.24M67.034 49.852l-13.198-7.62M53.836 42.232v-15.24M53.836 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class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M42.897 4.129q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.882.506-.315 1.274-.315.732 0 1.232.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.221.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M68.975 21.822h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.482v-2.769h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 21.193-5.023 2.9M70.254 20.804l5.335 2.372M67.44 15.53l.595-5.637\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"mol\"\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M111.816 35.024q-.786 0-1.239.53-.452.523-.452 1.446 0 .911.417 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class=\"bond\"\u003e\u003cpath d=\"M39.419 20.076V8.053M41.857 20.076V8.053\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.419 8.053v6.012M41.857 8.053v6.012\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.638 19.372-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 26.992-13.204-7.628M25.002 28.4l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 19.364-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 26.984.005 15.248M3.477 28.391l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 42.232 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 49.861 13.198-7.62M14.247 47.045l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 26.992.004 15.249M53.836 26.992l10.045-5.799M70.254 20.804l10.67 4.744M80.924 25.548l10.245-11.312M91.169 14.236l-7.62-13.198M83.549 1.038 68.63 4.255M67.44 15.53l1.19-11.275\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M42.897 4.129q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.882.506-.315 1.274-.315.732 0 1.232.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.221.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M68.975 21.822h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.482v-2.769h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 21.193-5.023 2.9M70.254 20.804l5.335 2.372M67.44 15.53l.595-5.637\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":{"Cognitive Effects":["Analysis enhancement","Ego inflation","Focus enhancement","Increased music appreciation","Motivation enhancement","Thought acceleration","Wakefulness","Disinhibition","Suggestibility suppression","Cognitive euphoria","Compulsive redosing","Mania"],"Physical Effects":["Increased libido","Stamina enhancement","Stimulation","Appetite suppression","Dehydration","Dry mouth","Restless legs","Shakiness","Teeth grinding","Abnormal heartbeat","Increased blood pressure","Increased heart rate","Vasoconstriction"],"Visual Effects":[]},"Title":"α-Pyrrolidinohexiophenone","UNII":"297J9K8A4G","Wikidata":"Q21098929","Wikipedia":"α-Pyrrolidinohexiophenone","XLogP":4}