{"Abbreviation":"","Aliases":["B. S. 7573-a","B.S. 7573-a","9-Acridineethanamine, N-(1-methyl-2-phenylethyl)-","BS-7573-A","9-(2-((α-Methylphenethyl)amino)ethyl)acridine","9-{2-((α-Methylphenethyl)amino)ethyl}acridine","Acridorexum","BS 7573-a","HY-164022","CS-1097708","Q19595771"],"CAS":"47487-22-9","ChEMBL":"CHEMBL2105932","ChemicalClasses":["amphetamine"],"Chirality":"racemic","Classes":["Stimulant"],"Erowid Experience Reports":null,"Esters":[],"Formating":[],"HeavyAtomCount":26,"IUPACName":"N-(2-acridin-9-ylethyl)-1-phenylpropan-2-amine","InChI":"InChI=1S/C24H24N2/c1-18(17-19-9-3-2-4-10-19)25-16-15-20-21-11-5-7-13-23(21)26-24-14-8-6-12-22(20)24/h2-14,18,25H,15-17H2,1H3","InChIKey":"SZSWKYIWACGNDZ-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e24\u003c/sub\u003eH\u003csub\u003e24\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"340.5 g/mol","Opticalactivity":"( + / - )","PubChemId":297931,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Acridorex","Name":"Acridorex","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/297931","Name":"Acridorex","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2105932","Name":"Acridorex","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=47487-22-9","Name":"Acridorex","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/7SGV5HQH8B","Name":"Acridorex","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID30866131","Name":"Acridorex","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 297931, Acridorex. Accessed July 20, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/297931\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/297931\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Acridorex. UNII: 7SGV5HQH8B. Global Substance Registration System. Accessed July 20, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/7SGV5HQH8B\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/7SGV5HQH8B\u003c/a\u003e"],"SMILES":"CC(CC1=CC=CC=C1)NCCC2=C3C=CC=CC3=NC4=CC=CC=C42","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"C[C@H](Cc1ccccc1)NCCc1c2ccccc2nc2ccccc12","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 147.196 78.285\"\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 0h148v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M54.157 31.527h-.7M54.448 34.065h-1.283M54.74 36.604h-1.867M55.032 39.142h-2.45M55.324 41.681H52.29M55.615 44.22h-3.617M55.907 46.758h-4.201\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.807 31.527-13.191-7.616M40.616 23.911l-13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.425 31.527-13.196-7.625M24.987 32.934l-10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.229 23.902 1.038 31.518\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 31.518.005 15.24M3.477 32.926l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 46.758 13.196 7.624\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 54.382 13.191-7.615M14.239 51.567l10.752-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.425 31.527.005 15.24M53.807 31.527l10.037-5.796M70.151 25.731l10.037 5.796M80.188 31.527l13.191-7.616M93.379 23.911l13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m106.57 31.527-.005 15.24M109.008 32.934l-.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"M106.565 46.767 93.37 54.391\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m93.37 54.391-.005 15.24M95.808 55.798l-.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m93.365 69.631 13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m106.556 77.247 13.195-7.625M106.555 74.431l10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m119.751 69.622.005-15.24M106.565 46.767l13.191 7.615\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m119.756 54.382 10.043-5.802M119.756 51.567l8.823-5.098\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m129.799 48.58-5.021 2.901M128.579 46.469l-4.411 2.549\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m132.953 42.908.004-11.39\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m132.957 31.518 13.196-7.624M132.956 28.702l10.759-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m146.153 23.894.005-15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m146.158 8.654-13.191-7.616M143.719 10.062l-10.752-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m132.967 1.038-13.196 7.624\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m119.771 8.662-.005 15.24M122.209 10.07l-.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m106.57 31.527 13.196-7.625M132.957 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.938 26.361h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.017-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM68.801 20.9h-.619v-2.286H65.67V20.9h-.613V16h.613v2.072h2.512V16h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M134.893 49.208h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.844 25.731-5.018 2.898M63.844 25.731l-5.018 2.898M70.151 25.731l5.018 2.898M70.151 25.731l5.018 2.898M132.953 42.908l.002-5.695\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-Acridorex","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"C[C@@H](Cc1ccccc1)NCCc1c2ccccc2nc2ccccc12","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 147.196 78.285\"\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 0h148v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M54.157 31.527h-.7l-1.751 15.231h4.201z\" class=\"bond\"/\u003e\u003cpath d=\"m53.807 31.527-13.191-7.616M40.616 23.911l-13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.425 31.527-13.196-7.625M24.987 32.934l-10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.229 23.902 1.038 31.518\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 31.518.005 15.24M3.477 32.926l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 46.758 13.196 7.624\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 54.382 13.191-7.615M14.239 51.567l10.752-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.425 31.527.005 15.24M53.807 31.527l10.037-5.796M70.151 25.731l10.037 5.796M80.188 31.527l13.191-7.616M93.379 23.911l13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m106.57 31.527-.005 15.24M109.008 32.934l-.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"M106.565 46.767 93.37 54.391\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m93.37 54.391-.005 15.24M95.808 55.798l-.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m93.365 69.631 13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m106.556 77.247 13.195-7.625M106.555 74.431l10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m119.751 69.622.005-15.24M106.565 46.767l13.191 7.615\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m119.756 54.382 10.043-5.802M119.756 51.567l8.823-5.098\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m129.799 48.58-5.021 2.901M128.579 46.469l-4.411 2.549\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m132.953 42.908.004-11.39\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m132.957 31.518 13.196-7.624M132.956 28.702l10.759-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m146.153 23.894.005-15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m146.158 8.654-13.191-7.616M143.719 10.062l-10.752-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m132.967 1.038-13.196 7.624\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m119.771 8.662-.005 15.24M122.209 10.07l-.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m106.57 31.527 13.196-7.625M132.957 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.938 26.361h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.017-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM68.801 20.9h-.619v-2.286H65.67V20.9h-.613V16h.613v2.072h2.512V16h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M134.893 49.208h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.844 25.731-5.018 2.898M63.844 25.731l-5.018 2.898M70.151 25.731l5.018 2.898M70.151 25.731l5.018 2.898M132.953 42.908l.002-5.695\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Acridorex","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Acridorex","(S)-Acridorex"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 147.196 78.285\"\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 0h148v79H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M53.807 46.758V31.527M53.807 31.527l-13.191-7.616M40.616 23.911l-13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.425 31.527-13.196-7.625M24.987 32.934l-10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.229 23.902 1.038 31.518\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 31.518.005 15.24M3.477 32.926l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 46.758 13.196 7.624\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 54.382 13.191-7.615M14.239 51.567l10.752-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.425 31.527.005 15.24M53.807 31.527l10.037-5.796M70.151 25.731l10.037 5.796M80.188 31.527l13.191-7.616M93.379 23.911l13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m106.57 31.527-.005 15.24M109.008 32.934l-.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"M106.565 46.767 93.37 54.391\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m93.37 54.391-.005 15.24M95.808 55.798l-.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m93.365 69.631 13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m106.556 77.247 13.195-7.625M106.555 74.431l10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m119.751 69.622.005-15.24M106.565 46.767l13.191 7.615\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m119.756 54.382 10.043-5.802M119.756 51.567l8.823-5.098\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m129.799 48.58-5.021 2.901M128.579 46.469l-4.411 2.549\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m132.953 42.908.004-11.39\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m132.957 31.518 13.196-7.624M132.956 28.702l10.759-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m146.153 23.894.005-15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m146.158 8.654-13.191-7.616M143.719 10.062l-10.752-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m132.967 1.038-13.196 7.624\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m119.771 8.662-.005 15.24M122.209 10.07l-.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m132.957 31.518-13.191-7.616M106.57 31.527l13.196-7.625\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.938 26.361h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.017-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM68.801 20.9h-.619v-2.286H65.67V20.9h-.613V16h.613v2.072h2.512V16h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M134.893 49.208h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.844 25.731-5.018 2.898M63.844 25.731l-5.018 2.898M70.151 25.731l5.018 2.898M70.151 25.731l5.018 2.898M132.953 42.908l.002-5.695\" 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":"Acridorex","UNII":"7SGV5HQH8B","Wikipedia":"Acridorex","XLogP":5.7}