{"Abbreviation":["3-BMC"],"Aliases":["3-Bromomethcathinone","Dtxsid40438606","Dtxcid90839765","3-Bmc","1-Propanone, 1-(3-bromophenyl)-2-(methylamino)-","Unii-789qe5va57","1-(3-Bromophenyl)-2-(methylamino)-1-propanone","3-bmap","Schembl30457585","NS00017589"],"CAS":"486459-02-3","ChemicalClasses":["cathinone"],"Chirality":"racemic","Classes":["Stimulant"],"Esters":[],"Formating":[],"HeavyAtomCount":13,"IUPACName":"1-(3-bromophenyl)-2-(methylamino)propan-1-one","InChI":"InChI=1S/C10H12BrNO/c1-7(12-2)10(13)8-4-3-5-9(11)6-8/h3-7,12H,1-2H3","InChIKey":"PXLYROINIXKFAW-UHFFFAOYSA-N","MeSH Headers":[{"Id":"M0573074","Link":"https://id.nlm.nih.gov/mesh/M0573074.html","Name":"3-bromomethcathinone","Ref":12},{"Id":"DescTree","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":"MeSH Tree","Ref":14},{"Id":"PubMed from MeSH","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":null,"Ref":22}],"MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e12\u003c/sub\u003eBrNO","MolecularWeight":"242.11 g/mol","Opticalactivity":"( + / - )","PD":"PD048346","PubChemId":10354356,"Records":{"UNII":{"Impurities":[]}},"RefChem":"93248","RefCount":3,"RefCur":"","References":[{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q82254398","Name":"Brophedrone","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/10354356","Name":"Brophedrone","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD048346","Name":"Brophedrone","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=486459-02-3","Name":"Brophedrone","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/789QE5VA57","Name":"Brophedrone","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID40438606","Name":"Brophedrone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 10354356, 3-Bromomethcathinone. Accessed April 29, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/10354356\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/10354356\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Brophedrone. UNII: 789QE5VA57. Global Substance Registration System. Accessed April 29, 2026. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/789QE5VA57\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/789QE5VA57\u003c/a\u003e"],"SMILES":"CC(C(=O)C1=CC(=CC=C1)Br)NC","SaltData":[{"AcidCount":1,"Amine":"Brophedrone","AmineCount":1,"Formula":"Cl","Name":"hydrochloride","RName":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 122.346 49.848\"\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=\"#1ff01f\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h123v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M72.003 41.181v-15.24M72.003 25.941l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M57.586 19.025V7.002M60.024 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M57.586 7.002v6.011M60.024 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.805 18.321-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.607 25.941-13.203-7.628M43.169 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.404 18.313-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.205 25.933.005 15.248M21.644 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m19.21 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.413 48.81 13.199-7.62M32.414 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.607 25.941.005 15.249M19.205 25.933 7.537 19.198M72.003 25.941l10.045-5.799M88.355 20.142 98.4 25.941\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M61.064 3.078q0 .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-.881T58.82.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.523-.392 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 15.288q.917 0 1.387.273.47.268.47.941 0 .435-.244.72-.238.286-.69.364v.035q.309.048.559.179t.393.375q.149.238.149.619 0 .667-.458 1.03-.459.363-1.245.363H.56v-4.899zm.119 2.089q.631 0 .863-.202.238-.203.238-.601 0-.405-.285-.578-.286-.179-.911-.179h-.81v1.56zm-.905.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.94-.238zm5.476-1.446q.101 0 .22.011.125.006.208.03l-.071.554q-.089-.018-.196-.03-.108-.018-.203-.018-.28 0-.53.155-.244.155-.393.435-.148.273-.148.648v1.959h-.602v-3.673h.494l.066.667h.03q.178-.298.458-.518t.667-.22\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M87.142 20.771h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.055h.03l-.018-.328q-.012-.22-.023-.476-.006-.262-.006-.482v-2.769h.577zM87.005 15.31h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#a62929\" d=\"m7.537 19.198 5.834 3.368\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m82.048 20.142-5.023 2.899M82.048 20.142l-5.023 2.899M88.355 20.142l5.022 2.899M88.355 20.142l5.022 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"mol\"\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M119.029 23.072q-.785 0-1.238.53-.452.524-.452 1.447 0 .911.417 1.447.422.529 1.268.529.321 0 .607-.053.291-.06.565-.143v.536q-.274.101-.565.149-.292.053-.697.053-.744 0-1.25-.309-.5-.31-.75-.876-.25-.571-.25-1.339 0-.744.268-1.31.274-.565.804-.881.529-.321 1.279-.321.78 0 1.352.286l-.244.523q-.227-.101-.506-.184-.274-.084-.608-.084m2.757 4.424h-.601v-5.215h.601zM116.122 27.496h-.619V25.21h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Brophedrone hydrochloride","UNII":"LK47N4W2NS"}],"Salts":["hydrochloride"],"StereoisomerData":[{"ChemicalClasses":["cathinone"],"SMILES":"CN[C@H](C)C(=O)C1=CC(Br)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 99.438 49.848\"\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 0h100v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m98.4 25.941-10.045-5.799M82.048 20.142l-10.045 5.799\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M72.353 25.941h-.7M72.603 28.118h-1.2M72.853 30.295h-1.7M73.103 32.473h-2.2M73.353 34.65h-2.7M73.603 36.827h-3.2M73.853 39.004h-3.7M74.103 41.181h-4.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m72.003 25.941-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M57.586 19.025V7.002M60.024 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M57.586 7.002v6.011M60.024 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.805 18.321-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.607 25.941-13.203-7.628M43.169 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.404 18.313-13.199 7.62M19.205 25.933 7.537 19.198\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.205 25.933.005 15.248M21.644 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m19.21 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.413 48.81 13.199-7.62M32.414 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.607 25.941.005 15.249\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M87.142 20.771h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.055h.03l-.018-.328q-.012-.22-.023-.476-.006-.262-.006-.482v-2.769h.577zM87.005 15.31h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M61.064 3.078q0 .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-.881T58.82.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.523-.392 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 15.288q.917 0 1.387.273.47.268.47.941 0 .435-.244.72-.238.286-.69.364v.035q.309.048.559.179t.393.375q.149.238.149.619 0 .667-.458 1.03-.459.363-1.245.363H.56v-4.899zm.119 2.089q.631 0 .863-.202.238-.203.238-.601 0-.405-.285-.578-.286-.179-.911-.179h-.81v1.56zm-.905.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.94-.238zm5.476-1.446q.101 0 .22.011.125.006.208.03l-.071.554q-.089-.018-.196-.03-.108-.018-.203-.018-.28 0-.53.155-.244.155-.393.435-.148.273-.148.648v1.959h-.602v-3.673h.494l.066.667h.03q.178-.298.458-.518t.667-.22\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m88.355 20.142 5.022 2.899M88.355 20.142l5.022 2.899M82.048 20.142l-5.023 2.899M82.048 20.142l-5.023 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#a62929\" d=\"m7.537 19.198 5.834 3.368\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-Brophedrone"},{"ChemicalClasses":["cathinone"],"SMILES":"CN[C@@H](C)C(=O)C1=CC(Br)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 99.438 49.848\"\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 0h100v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m98.4 25.941-10.045-5.799M82.048 20.142l-10.045 5.799\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M72.353 25.941h-.7l-1.75 15.24h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m72.003 25.941-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M57.586 19.025V7.002M60.024 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M57.586 7.002v6.011M60.024 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.805 18.321-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.607 25.941-13.203-7.628M43.169 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.404 18.313-13.199 7.62M19.205 25.933 7.537 19.198\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.205 25.933.005 15.248M21.644 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m19.21 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.413 48.81 13.199-7.62M32.414 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.607 25.941.005 15.249\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M87.142 20.771h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.055h.03l-.018-.328q-.012-.22-.023-.476-.006-.262-.006-.482v-2.769h.577zM87.005 15.31h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M61.064 3.078q0 .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-.881T58.82.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.523-.392 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 15.288q.917 0 1.387.273.47.268.47.941 0 .435-.244.72-.238.286-.69.364v.035q.309.048.559.179t.393.375q.149.238.149.619 0 .667-.458 1.03-.459.363-1.245.363H.56v-4.899zm.119 2.089q.631 0 .863-.202.238-.203.238-.601 0-.405-.285-.578-.286-.179-.911-.179h-.81v1.56zm-.905.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.94-.238zm5.476-1.446q.101 0 .22.011.125.006.208.03l-.071.554q-.089-.018-.196-.03-.108-.018-.203-.018-.28 0-.53.155-.244.155-.393.435-.148.273-.148.648v1.959h-.602v-3.673h.494l.066.667h.03q.178-.298.458-.518t.667-.22\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m88.355 20.142 5.022 2.899M88.355 20.142l5.022 2.899M82.048 20.142l-5.023 2.899M82.048 20.142l-5.023 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#a62929\" d=\"m7.537 19.198 5.834 3.368\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Brophedrone"}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Brophedrone","(S)-Brophedrone"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 99.438 49.848\"\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 0h100v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M72.003 41.181v-15.24M72.003 25.941l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M57.586 19.025V7.002M60.024 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M57.586 7.002v6.011M60.024 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.805 18.321-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.607 25.941-13.203-7.628M43.169 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.404 18.313-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.205 25.933.005 15.248M21.644 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m19.21 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.413 48.81 13.199-7.62M32.414 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.607 25.941.005 15.249M19.205 25.933 7.537 19.198M72.003 25.941l10.045-5.799M88.355 20.142 98.4 25.941\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M61.064 3.078q0 .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-.881T58.82.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.386 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.392.523-.392 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 15.288q.917 0 1.387.273.47.268.47.941 0 .435-.244.72-.238.286-.69.364v.035q.309.048.559.179t.393.375q.149.238.149.619 0 .667-.458 1.03-.459.363-1.245.363H.56v-4.899zm.119 2.089q.631 0 .863-.202.238-.203.238-.601 0-.405-.285-.578-.286-.179-.911-.179h-.81v1.56zm-.905.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.94-.238zm5.476-1.446q.101 0 .22.011.125.006.208.03l-.071.554q-.089-.018-.196-.03-.108-.018-.203-.018-.28 0-.53.155-.244.155-.393.435-.148.273-.148.648v1.959h-.602v-3.673h.494l.066.667h.03q.178-.298.458-.518t.667-.22\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M87.142 20.771h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.055h.03l-.018-.328q-.012-.22-.023-.476-.006-.262-.006-.482v-2.769h.577zM87.005 15.31h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#a62929\" d=\"m7.537 19.198 5.834 3.368\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m82.048 20.142-5.023 2.899M82.048 20.142l-5.023 2.899M88.355 20.142l5.022 2.899M88.355 20.142l5.022 2.899\" 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":"Brophedrone","UNII":"789QE5VA57","Wikidata":"Q82254398","XLogP":2.3}