{"ATC Code":"N - Nervous system","Abbreviation":"","Actives":["Amphetamine","Theophylline"],"Aliases":["Fenetylline","Phenethylline","Amfetyline","Captagon","Fenetyllin","Amphetaminoethyltheophylline","Theophyllineethylamphetamine","Fenetylinum","Fenetilina","Fitton","Humburg 814","Fenetillina","Fenetyllinum","Homburg-814","Theophylline, 7-(2-((α-methylphenethyl)amino)ethyl)-","D323","7-(2-((α-Methylphenethyl)amino)ethyl)theophylline","1H-purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-7-(2-((1-methyl-2-phenylethyl)amino)ethyl)-","7-ethyltheophyllineamphetamine","1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-7-[2-[(1-methyl-2-phenylethyl)amino]ethyl]-","N06BA10","1,3-dimethyl-7-(2-((1-phenylpropan-2-yl)amino)ethyl)-2,3,6,7-tetrahydro-1H-purine-2,6-dione","609-418-3","Fenetylline, (+)-","Fenethylline, (+)-"],"CAS":"3736-08-1","ChEBI":"CHEBI:135451","ChEMBL":"CHEMBL2111152","ChemicalClasses":["amphetamine"],"Chirality":"racemic","Classes":["Codrug","Prodrug","Stimulant"],"DEA no":1503,"Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"609-418-3","Formating":[],"HMDB ID":"HMDB0252198","HeavyAtomCount":25,"Human Drugs":"Pharmaceuticals","IUPACName":"1,3-dimethyl-7-[2-(1-phenylpropan-2-ylamino)ethyl]purine-2,6-dione","InChI":"InChI=1S/C18H23N5O2/c1-13(11-14-7-5-4-6-8-14)19-9-10-23-12-20-16-15(23)17(24)22(3)18(25)21(16)2/h4-8,12-13,19H,9-11H2,1-3H3","InChIKey":"NMCHYWGKBADVMK-UHFFFAOYSA-N","MeSH Pharmacological Classification":"A loosely defined group of drugs that tend to increase behavioral alertness, agitation, or excitation. They work by a variety of mechanisms, but usually not by direct excitation of neurons. The many drugs that have such actions as side effects to their main therapeutic use are not included here. (See all compounds classified as Central Nervous System Stimulants.)","Melting Point":"227-229","MolecularFormula":"C\u003csub\u003e18\u003c/sub\u003eH\u003csub\u003e23\u003c/sub\u003eN\u003csub\u003e5\u003c/sub\u003eO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"341.4 g/mol","Opticalactivity":"( + / - )","PubChemId":19527,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Fenethylline","Name":"Fenethylline","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB01482","Name":"Fenethylline","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/19527","Name":"Fenethylline","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2111152","Name":"Fenethylline","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:135451","Name":"Fenethylline","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=3736-08-1","Name":"Fenethylline","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0252198","Name":"Fenethylline","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/D07944","Name":"Fenethylline","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/YZ0N7VL5R3","Name":"Fenethylline","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID50859686","Name":"Fenethylline","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 19527, Fenethylline. Accessed July 19, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/19527\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/19527\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Fenethylline. UNII: YZ0N7VL5R3. Global Substance Registration System. Accessed July 19, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/YZ0N7VL5R3\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/YZ0N7VL5R3\u003c/a\u003e"],"SMILES":"CC(CC1=CC=CC=C1)NCCN2C=NC3=C2C(=O)N(C(=O)N3C)C","SaltData":[{"AcidCount":1,"AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 190.944 63.251\"\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 0h191v64H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M53.836 54.584v-15.24M53.836 39.344l-13.198-7.62M40.638 31.724l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath 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43.772h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.733v2.738h-.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=\"m63.881 33.545-5.023 2.9M63.881 33.545l-5.023 2.9M70.187 33.545l5.022 2.9M70.187 33.545l5.022 2.9M103.476 37.524l-5.023-2.9M107.03 43.187l.589 5.638M125.197 53.958l2.739-4.732M109.848 37.908l5.315-2.37M136.803 16.199 131 17.433M141.342 11.714l1.741-5.357M142.991 18.692l3.659 4.066M146.82 37.541l1.745-5.359M142.279 42.026l-5.803 1.234M148.466 44.519l3.659 4.065\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Fenethylline","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Fenethylline","(S)-Fenethylline"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 168.036 63.251\"\u003e\u003crect width=\"100%\" height=\"100%\" 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0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"none\" d=\"M147.53 43.772h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.733v2.738h-.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=\"m63.881 33.545-5.023 2.9M63.881 33.545l-5.023 2.9M70.187 33.545l5.022 2.9M70.187 33.545l5.022 2.9M103.476 37.524l-5.023-2.9M107.03 43.187l.589 5.638M125.197 53.958l2.739-4.732M109.848 37.908l5.315-2.37M136.803 16.199 131 17.433M142.991 18.692l3.659 4.066M146.82 37.541l1.745-5.359M142.279 42.026l-5.803 1.234M148.466 44.519l3.659 4.065M141.342 11.714l1.741-5.357\" 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":[]},"Therapeutic Uses":"Central Nervous System Stimulants","Title":"Fenethylline","UNII":"YZ0N7VL5R3","Wikipedia":"Fenethylline","XLogP":1.4}