{"ATC Code":"C - Cardiovascular system","Abbreviation":"","Actives":["Epinine"],"Aliases":["Ibopaminum","Ibopamina","SB 7505","SB-7505","Propanoic acid, 2-methyl-, 4-(2-(methylamino)ethyl)-1,2-phenylene ester","N-methyldopamine diisobutyrate","(4-(2-(methylamino)ethyl)-2-(2-methylpropanoyloxy)phenyl) 2-methylpropanoate","5-(2-(methylamino)ethyl)-2-((2-methylpropanoyl)oxy)phenyl 2-methylpropanoate","5-[2-(methylamino)ethyl]-2-[(2-methylpropanoyl)oxy]phenyl 2-methylpropanoate","C01CA16","S01FB03","266-229-5","4-(2-(Methylamino)ethyl)-o-phenylene diisobutyrate","4-(2-(methylamino)ethyl)-1,2-phenylene bis(2-methylpropanoate)","4-[2-(methylamino)ethyl]-o-phenylene diisobutyrate","SB 7505; SB 7505 (pharmaceutical); SKF 100168","Ibopamino","SKF 100168","Escandine","Trazyl","4-(2-(Methylamino)ethyl)-2-phenylendiisobutyrat","DB13316","D04488","L013392","Q5984366"],"CAS":"66195-31-1","ChEBI":"CHEBI:135306","ChEMBL":"CHEMBL307739","ChemicalClasses":["carboxylic acid","catecholamine"],"Chirality":"achiral","Classes":["Prodrug","Sympathomimetic"],"EINECS":"266-229-5","Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"266-229-5","Formating":[],"HMDB ID":"HMDB0041906","HeavyAtomCount":22,"IUPACName":"[4-[2-(methylamino)ethyl]-2-(2-methylpropanoyloxy)phenyl] 2-methylpropanoate","InChI":"InChI=1S/C17H25NO4/c1-11(2)16(19)21-14-7-6-13(8-9-18-5)10-15(14)22-17(20)12(3)4/h6-7,10-12,18H,8-9H2,1-5H3","InChIKey":"WDKXLLJDNUBYCY-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)","MolecularFormula":"C\u003csub\u003e17\u003c/sub\u003eH\u003csub\u003e25\u003c/sub\u003eNO\u003csub\u003e4\u003c/sub\u003e","MolecularWeight":"307.4 g/mol","PubChemId":68555,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Ibopamine","Name":"Ibopamine","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB13316","Name":"Ibopamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/68555","Name":"Ibopamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL307739","Name":"Ibopamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:135306","Name":"Ibopamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=66195-31-1","Name":"Ibopamine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0041906","Name":"Ibopamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/D04488","Name":"Ibopamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/8ZCA2I2L11","Name":"Ibopamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID3023138","Name":"Ibopamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 68555, Ibopamine. Accessed July 19, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/68555\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/68555\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Ibopamine. UNII: 8ZCA2I2L11. Global Substance Registration System. Accessed July 19, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/8ZCA2I2L11\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/8ZCA2I2L11\u003c/a\u003e"],"SMILES":"CC(C)C(=O)OC1=C(C=C(C=C1)CCNC)OC(=O)C(C)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 0 156.967 85.644\"\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 0h157v86H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M119.822 84.734v-15.24M119.822 69.494l13.198-7.62M119.822 69.494l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M105.405 62.578V50.556M107.843 62.578V50.556\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M105.405 50.556v6.011M107.843 50.556v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m106.624 61.874-9.92 5.728M90.142 67.598l-9.914-5.724\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m80.228 61.874.004-15.248M77.79 60.467l.004-12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m80.232 46.626-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m67.034 39.006-13.203 7.628M67.035 41.822l-10.766 6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.831 46.634-.005 15.249\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.826 61.883 13.198 7.62M56.265 60.475l10.759 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m80.228 61.874-13.204 7.629M53.831 46.634l-13.198-7.62M40.633 39.014l-13.198 7.62M27.435 46.634 17.39 40.835M11.083 40.835 1.038 46.634M80.232 46.626l9.919-5.724M93.432 35.087l.002-11.319\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m93.434 25.176-10.531-6.083M94.654 23.064l-10.532-6.082\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m82.903 19.093 5.265 3.041M84.122 16.982l5.266 3.041\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m93.434 23.768 13.2-7.618M106.634 16.15l.002-15.24M106.634 16.15l13.197 7.622\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M108.883 46.631q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.387 1.459.392.53 1.22.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.226.524-.393.524-.393 1.452M95.685 69.491q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 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\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M16.177 41.464h-.72l-2.62-4.066h-.029l.029.595q.024.358.024.733v2.738h-.565v-4.899h.714l2.608 4.054h.029l-.018-.328-.023-.476q-.006-.262-.006-.482v-2.768h.577zM16.04 36.003h-.619v-2.286h-2.512v2.286h-.613v-4.899h.613v2.071h2.512v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M95.691 39.005q0 .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-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.459.393.529 1.221.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.208-.523-.834 0-1.227.523-.393.524-.393 1.453M82.497 16.143q0 .756-.256 1.327-.256.566-.757.882-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.888-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.501.31.757.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m96.704 67.602 4.96-2.864M90.142 67.598l-4.957-2.862\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m17.39 40.835 5.023 2.899M17.39 40.835l5.023 2.899M11.083 40.835l-5.022 2.899M11.083 40.835l-5.022 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m90.151 40.902-4.96 2.862M93.432 35.087l.001-5.659\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"mol\"\u003e\u003cg fill=\"#1ff01f\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M153.65 40.971q-.785 0-1.238.53-.452.523-.452 1.446 0 .911.416 1.447.423.53 1.268.53.322 0 .608-.054.291-.059.565-.143v.536q-.274.101-.565.149-.292.053-.697.053-.744 0-1.25-.309-.5-.31-.75-.875-.25-.572-.25-1.34 0-.744.268-1.309.274-.566.803-.881.53-.322 1.28-.322.78 0 1.352.286l-.244.524q-.227-.102-.506-.185-.274-.083-.608-.083m2.757 4.423h-.601v-5.215h.601zM150.743 45.394h-.619v-2.286h-2.512v2.286h-.613v-4.899h.613v2.071h2.512v-2.071h.619z\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Ibopamine hydrochloride","UNII":"3VXW2HU8GS"}],"Salts":["hydrochloride"],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 134.059 85.644\"\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 0h135v86H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M119.822 84.734v-15.24M119.822 69.494l13.198-7.62M119.822 69.494l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M105.405 62.578V50.556M107.843 62.578V50.556\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M105.405 50.556v6.011M107.843 50.556v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m106.624 61.874-9.92 5.728M90.142 67.598l-9.914-5.724\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m80.228 61.874.004-15.248M77.79 60.467l.004-12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m80.232 46.626-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m67.034 39.006-13.203 7.628M67.035 41.822l-10.766 6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.831 46.634-.005 15.249\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.826 61.883 13.198 7.62M56.265 60.475l10.759 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m80.228 61.874-13.204 7.629M53.831 46.634l-13.198-7.62M40.633 39.014l-13.198 7.62M27.435 46.634 17.39 40.835M11.083 40.835 1.038 46.634M80.232 46.626l9.919-5.724M93.432 35.087l.002-11.319\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m93.434 25.176-10.531-6.083M94.654 23.064l-10.532-6.082\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m82.903 19.093 5.265 3.041M84.122 16.982l5.266 3.041\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m93.434 23.768 13.2-7.618M106.634 16.15l.002-15.24M106.634 16.15l13.197 7.622\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M108.883 46.631q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.387 1.459.392.53 1.22.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.226.524-.393.524-.393 1.452M95.685 69.491q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 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\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M16.177 41.464h-.72l-2.62-4.066h-.029l.029.595q.024.358.024.733v2.738h-.565v-4.899h.714l2.608 4.054h.029l-.018-.328-.023-.476q-.006-.262-.006-.482v-2.768h.577zM16.04 36.003h-.619v-2.286h-2.512v2.286h-.613v-4.899h.613v2.071h2.512v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M95.691 39.005q0 .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-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.459.393.529 1.221.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.208-.523-.834 0-1.227.523-.393.524-.393 1.453M82.497 16.143q0 .756-.256 1.327-.256.566-.757.882-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.888-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.501.31.757.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m96.704 67.602 4.96-2.864M90.142 67.598l-4.957-2.862\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m17.39 40.835 5.023 2.899M17.39 40.835l5.023 2.899M11.083 40.835l-5.022 2.899M11.083 40.835l-5.022 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m90.151 40.902-4.96 2.862M93.432 35.087l.001-5.659\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":{"Cognitive Effects":["Thought acceleration","Wakefulness"],"Physical Effects":["Stamina enhancement","Dehydration","Dry mouth","Restless legs","Shakiness","Abnormal heartbeat","Increased blood pressure","Increased heart rate","Vasoconstriction"],"Visual Effects":[]},"Title":"Ibopamine","UNII":"8ZCA2I2L11","Wikipedia":"Ibopamine","XLogP":2.9}