{"ATC Code":"A - Alimentary tract and metabolism","Abbreviation":"","Actives":["Amphetamine"],"Aliases":["K98M4N387W","N-(3-Chloropropyl)-α-methylphenethylamine","Phenethylamine, N-(3-chloropropyl)-α-methyl-","(3-chloropropyl)(1-phenylpropan-2-yl)amine","chloropropylamphetamine","241-279-0","Mefenorex, (+)-","N-(3-Chloropropyl)-α-methylbenzeneethanamine","85052999IT","n-(3-chloropropyl)-α-methylphenethylamine","Mefenorexum","111051-41-3","111051-42-4","Benzeneethanamine, N-(3-chloropropyl)-α-methyl-","Tox21_113684","DB13852","Ncgc00249908-01","Cas-17243-57-1","D07891","3-Chloro-N-(1-methyl-2-phenylethyl)-1-propanamine #","Q10579342","Benzeneethanamine, N-(3-chloropropyl)-α-methyl-, (+)-","Benzeneethanamine, n-(3-chloropropyl)-α-methyl","Benzeneethanamine, n-(3-chloropropyl)-α-methyl-, (+)-","Benzeneethanamine, n-(3-chloropropyl)-α-methyl-"],"CAS":"17243-57-1","ChEBI":"CHEBI:134883","ChEMBL":"CHEMBL2110962","ChemicalClasses":["amphetamine"],"Chirality":"racemic","Classes":["Prodrug","Stimulant"],"DEA no":1580,"EINECS":"241-279-0","Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"241-279-0","Formating":[],"HeavyAtomCount":14,"Human Drugs":"Pharmaceuticals","IUPACName":"N-(3-chloropropyl)-1-phenylpropan-2-amine","InChI":"InChI=1S/C12H18ClN/c1-11(14-9-5-8-13)10-12-6-3-2-4-7-12/h2-4,6-7,11,14H,5,8-10H2,1H3","InChIKey":"XXVROGAVTTXONC-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Drugs that mimic the effects of stimulating postganglionic adrenergic sympathetic nerves. Included here are drugs that directly stimulate adrenergic receptors and drugs that act indirectly by provoking the release of adrenergic transmitters. (See all compounds classified as Sympathomimetics.)","MolecularFormula":"C\u003csub\u003e12\u003c/sub\u003eH\u003csub\u003e18\u003c/sub\u003eClN","MolecularWeight":"211.73 g/mol","Opticalactivity":"( - )","PubChemId":21777,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Mefenorex","Name":"Mefenorex","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB13852","Name":"Mefenorex","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/21777","Name":"Mefenorex","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2110962","Name":"Mefenorex","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:134883","Name":"Mefenorex","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=17243-57-1","Name":"Mefenorex","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/D07891","Name":"Mefenorex","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/7FT4O2NC8G","Name":"Mefenorex","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID6057665","Name":"Mefenorex","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 21777, Mefenorex. Accessed July 19, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/21777\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/21777\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Mefenorex. UNII: 7FT4O2NC8G. Global Substance Registration System. Accessed July 19, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/7FT4O2NC8G\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/7FT4O2NC8G\u003c/a\u003e"],"SMILES":"CC(CC1=CC=CC=C1)NCCCCl","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"C[C@H](Cc1ccccc1)NCCCCl","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 123.638 39.997\"\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 0h124v40H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M54.186 16.091h-.7M54.436 18.268h-1.2M54.686 20.445h-1.7M54.936 22.622h-2.2M55.186 24.799h-2.7M55.436 26.977h-3.2M55.686 29.154h-3.7M55.936 31.331h-4.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 16.091-13.198-7.62M40.638 8.471l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.44 16.091 14.236 8.462M25.002 17.498l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 8.462-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.082.005 15.249M3.477 17.49l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.331 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 38.959 13.198-7.62M14.247 36.143l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 16.091.004 15.248M53.836 16.091l10.045-5.8M70.187 10.291l10.045 5.8M80.232 16.091l13.199-7.62M93.431 8.471l13.198 7.62M106.629 16.091l10.241-5.913\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 10.921h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 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12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.331 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 38.959 13.198-7.62M14.247 36.143l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 16.091.004 15.248M53.836 16.091l10.045-5.8M70.187 10.291l10.045 5.8M80.232 16.091l13.199-7.62M93.431 8.471l13.198 7.62M106.629 16.091l10.241-5.913\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 10.921h-.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-.483V6.021h.578zM68.838 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M120.321 6.494q-.786 0-1.238.53-.452.524-.452 1.447 0 .911.416 1.446.423.53 1.268.53.322 0 .607-.053.292-.06.566-.143v.536q-.274.101-.566.148-.291.054-.696.054-.744 0-1.25-.31-.5-.309-.75-.875-.25-.571-.25-1.339 0-.744.268-1.31.273-.565.803-.881.53-.321 1.28-.321.78 0 1.352.285l-.245.524q-.226-.101-.506-.184-.273-.084-.607-.084m2.757 4.424h-.601V5.703h.601z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 10.291-5.023 2.9M63.881 10.291l-5.023 2.9M70.187 10.291l5.022 2.9M70.187 10.291l5.022 2.9\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m116.87 10.178-5.12 2.957\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Mefenorex","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Mefenorex","(S)-Mefenorex"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 123.638 39.997\"\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 0h124v40H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M53.836 31.331v-15.24M53.836 16.091l-13.198-7.62M40.638 8.471l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.44 16.091 14.236 8.462M25.002 17.498l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 8.462-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.082.005 15.249M3.477 17.49l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.331 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 38.959 13.198-7.62M14.247 36.143l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 16.091.004 15.248M53.836 16.091l10.045-5.8M70.187 10.291l10.045 5.8M80.232 16.091l13.199-7.62M93.431 8.471l13.198 7.62M106.629 16.091l10.241-5.913\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 10.921h-.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-.483V6.021h.578zM68.838 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M120.321 6.494q-.786 0-1.238.53-.452.524-.452 1.447 0 .911.416 1.446.423.53 1.268.53.322 0 .607-.053.292-.06.566-.143v.536q-.274.101-.566.148-.291.054-.696.054-.744 0-1.25-.31-.5-.309-.75-.875-.25-.571-.25-1.339 0-.744.268-1.31.273-.565.803-.881.53-.321 1.28-.321.78 0 1.352.285l-.245.524q-.226-.101-.506-.184-.273-.084-.607-.084m2.757 4.424h-.601V5.703h.601z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 10.291-5.023 2.9M63.881 10.291l-5.023 2.9M70.187 10.291l5.022 2.9M70.187 10.291l5.022 2.9\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m116.87 10.178-5.12 2.957\" 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":"Mefenorex","UNII":"7FT4O2NC8G","Wikipedia":"Mefenorex","XLogP":3.1}