{"Abbreviation":"","Aliases":["Perviton","Fenatin","N-(α-Methylphenethyl)nicotinamide","Nicotinoyl-β-phenylisopropylamine","3-Pyridinecarboxamide, N-(1-methyl-2-phenylethyl)-","Phenatin","N-(1-Methyl-2-phenylethyl)nicotinamide","Nicotinic acid β-phenylisopropylamide","Nicotinamide, N-(α-methylphenethyl)-","Oprea1_859298","N(α-Methylphenethyl)nicotinamide","Ag-205/40091803","N-(1-Phenylpropan-2-yl)pyridine-3-carboximidic acid","Q27271334","3-Pyridinecarboxamide, N-(1-methyl-2-phenylethyl)- (VA"],"CAS":"139-68-4","ChemicalClasses":["amphetamine"],"Chirality":"racemic","Classes":["Stimulant"],"Erowid Experience Reports":null,"Esters":[],"Formating":[],"HeavyAtomCount":18,"IUPACName":"N-(1-phenylpropan-2-yl)pyridine-3-carboxamide","InChI":"InChI=1S/C15H16N2O/c1-12(10-13-6-3-2-4-7-13)17-15(18)14-8-5-9-16-11-14/h2-9,11-12H,10H2,1H3,(H,17,18)","InChIKey":"KJRJJAZBUWXZFN-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Drugs that bind to but do not activate histamine receptors, thereby blocking the actions of histamine or histamine agonists. Classical antihistaminics block the histamine H1 receptors only. (See all compounds classified as Histamine Antagonists.)","MolecularFormula":"C\u003csub\u003e15\u003c/sub\u003eH\u003csub\u003e16\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003eO","MolecularWeight":"240.30 g/mol","Opticalactivity":"( + / - )","PubChemId":120640,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Phenatine","Name":"Phenatine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/120640","Name":"Phenatine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=139-68-4","Name":"Phenatine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/90O34W851E","Name":"Phenatine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID40930271","Name":"Phenatine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 120640, Phenatine. Accessed July 19, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/120640\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/120640\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Phenatine. UNII: 90O34W851E. Global Substance Registration System. Accessed July 19, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/90O34W851E\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/90O34W851E\u003c/a\u003e"],"SMILES":"CC(CC1=CC=CC=C1)NC(=O)C2=CN=CC=C2","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"C[C@H](Cc1ccccc1)NC(=O)c1cccnc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 122.333 55.444\"\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 0h123v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M54.186 31.537h-.7M54.436 33.714h-1.2M54.686 35.892h-1.7M54.936 38.069h-2.2M55.186 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class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-Phenatine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"C[C@@H](Cc1ccccc1)NC(=O)c1cccnc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 122.333 55.444\"\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 0h123v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M54.186 31.537h-.7l-1.75 15.24h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m53.836 31.537-13.198-7.62M40.638 23.917l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 31.537-13.204-7.628M25.002 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stroke=\"#3050f8\" d=\"m63.881 25.738-5.023 2.899M63.881 25.738l-5.023 2.899M70.187 25.738l5.022 2.899M70.187 25.738l5.022 2.899M116.679 25.727l-5.025 2.904\" 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":"Phenatine","UNII":"90O34W851E","Wikipedia":"Phenatine","XLogP":2.2}