{"Abbreviation":"","Aliases":["deoxyepinephrine","Desoxyepinephrine","Deoxyadrenaline","Epyamine","Epinin","Deoxyephinephrine","1,2-Benzenediol, 4-(2-(methylamino)ethyl)-","4-(2-Methylamino-ethyl)-benzene-1,2-diol","3,4-dihydroxy-N-methylphenethylamine","N-methyl-3,4-dihydroxyphenethylamine","1-(3,4-dihydroxyphenyl)-2-methylaminoethane","1,2-Benzenediol, 4-[2-(methylamino)ethyl]-","Desoxyadrenaline","207-919-8","Methyldopamine","N-Methyldopamine","4-(2-Methylaminoethyl)pyrocatechol","N-2-(3,4-dihydroxyphenyl)ethylmethylamine","4-(β-Methylaminoethyl)catechol","4-[2-(Methylamino)ethyl]-1,2-benzenediol","4-(2-(Methylamino)ethyl)-1,2-Benzenediol","Deoxiepinephrine","Lopac-D-5886","Biomol-NT_000002","Lopac0_000390"],"CAS":"501-15-5","ChEBI":"CHEBI:10554","ChEMBL":"CHEMBL31088","ChemicalClasses":["phenethylamine"],"Chirality":"achiral","Classes":["Sympathomimetic","Neurotransmitter"],"EINECS":"207-919-8","Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"207-919-8","Formating":[],"HMDB ID":"HMDB0032020","HeavyAtomCount":12,"IUPACName":"4-[2-(methylamino)ethyl]benzene-1,2-diol","InChI":"InChI=1S/C9H13NO2/c1-10-5-4-7-2-3-8(11)9(12)6-7/h2-3,6,10-12H,4-5H2,1H3","InChIKey":"NGKZFDYBISXGGS-UHFFFAOYSA-N","Melting Point":"188 - 189 °C","MolecularFormula":"C\u003csub\u003e9\u003c/sub\u003eH\u003csub\u003e13\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"167.20 g/mol","Physical Description":"Solid","PubChemId":4382,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Nifekalant","Name":"Epinine","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB13917","Name":"Epinine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/4382","Name":"Epinine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL31088","Name":"Epinine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:10554","Name":"Epinine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=501-15-5","Name":"Epinine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0032020","Name":"Epinine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C07453","Name":"Epinine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/R7339QLN1C","Name":"Epinine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID10198205","Name":"Epinine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 4382, Epinine. Accessed July 19, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/4382\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/4382\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Epinine. UNII: R7339QLN1C. Global Substance Registration System. Accessed July 19, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/R7339QLN1C\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/R7339QLN1C\u003c/a\u003e"],"SMILES":"CNCCC1=CC(=C(C=C1)O)O","SaltData":[{"AcidCount":1,"AmineCount":1,"Formula":"Br","Name":"hydrobromide","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 124.881 42.032\"\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=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h125v43H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m99.519 16.091-10.045-5.8M83.168 10.291l-10.045 5.8M73.123 16.091l-13.199-7.62M59.924 8.471l-13.198 7.62\" class=\"bond\"/\u003e\u003cg 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