{"Abbreviation":"","Aliases":["Bromantan","bromontan","2-bromophenyl-1-amino adamantane","N-(4-Bromophenyl)tricyclo(3.3.1.13,7)decan-2-amine","Tricyclo(3.3.1.13,7)decan-2-amine, N-(4-bromophenyl)-","Tricyclo[3.3.1.13,7]decan-2-amine, N-(4-bromophenyl)-","Ladasten","N-(2-adamantyl)-n-(4-bromophenyl)amine","Tricyclo[3.3.1.13,7]decan-2-amine,N-(4-bromophenyl)-","2-(4-Bromophenyl)aminoadamantane","Tricyclo[3.3.1.13,7]decan-2-amine, N-(4-bromophenyl)-; N-(4-Bromophenyl)tricyclo[3.3.1.13,7]decan-2-amine; Bromantan; Bromantane","Albb-035069","UWC73727","N-(4-bromophenyl)-2-adamantanamine","AS-54469","N-(2-adamantyl)-N-(p-bromophenyl)-amine","N-(2-Adamantyl)-N-(4-bromophenyl)-amine","En300-154642","S10385","A842407","Q385533","Z440843598"],"CAS":"87913-26-6","ChEMBL":"CHEMBL4303520","ChemicalClasses":["aniline"],"Chirality":"racemic","Classes":["Stimulant"],"Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"687-739-8","Formating":[],"HeavyAtomCount":18,"IUPACName":"N-(4-bromophenyl)adamantan-2-amine","InChI":"InChI=1S/C16H20BrN/c17-14-1-3-15(4-2-14)18-16-12-6-10-5-11(8-12)9-13(16)7-10/h1-4,10-13,16,18H,5-9H2","InChIKey":"LWJALJDRFBXHKX-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Substances that augment, stimulate, activate, potentiate, or modulate the immune response at either the cellular or humoral level. The classical agents (Freund\u0026apos;s adjuvant, BCG, Corynebacterium parvum, et al.) contain bacterial antigens. Some are endogenous (e.g., histamine, interferon, transfer factor, tuftsin, interleukin-1). Their mode of action is either non-specific, resulting in increased immune responsiveness to a wide variety of antigens, or antigen-specific, i.e., affecting a restricted type of immune response to a narrow group of antigens. The therapeutic efficacy of many biological response modifiers is related to their antigen-specific immunoadjuvanticity. (See all compounds classified as Adjuvants, Immunologic.)","MolecularFormula":"C\u003csub\u003e16\u003c/sub\u003eH\u003csub\u003e20\u003c/sub\u003eBrN","MolecularWeight":"306.24 g/mol","PubChemId":4660557,"RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Bromantane","Name":"Bromantane","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/4660557","Name":"Bromantane","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL4303520","Name":"Bromantane","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=87913-26-6","Name":"Bromantane","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/N1ILS53XWK","Name":"Bromantane","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID40405333","Name":"Bromantane","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 4660557, Bromantane. Accessed July 25, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/4660557\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/4660557\u003c/a\u003e"],"SMILES":"C1C2CC3CC1CC(C2)C3NC4=CC=C(C=C4)Br","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"Brc1ccc(N[C@H]2[C@@H]3C[C@H]4C[C@H](C[C@@H]2C4)C3)cc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 109.733 50.887\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h110v51H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m7.771 37.915 11.426-6.597\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.197 31.318 13.196 7.624M21.635 29.911l10.758 6.215\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.393 38.942 13.19-7.615\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.583 31.327-.004-15.24M43.145 29.919l-.004-12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.579 16.087 10.037-5.796M71.96 16.087l-10.037-5.796M71.96 16.087l.003 15.231\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m72.138 31.015-.35.606 13.377 9.908v-4.871z\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m98.539 31.617-.35-.606M96.778 32.922l-.599-1.04M95.018 34.227l-.85-1.473M93.257 35.532l-1.1-1.906M91.497 36.836l-1.35-2.338M89.736 38.141l-1.6-2.772M87.975 39.446l-1.85-3.205M86.215 40.751l-2.1-3.638\"/\u003e\u003c/g\u003e\u003cpath d=\"m98.364 31.314 8.228 15.027\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m93.539 39.832-.298.634 15.932 9.861-2.044-3.734-1.468-2.681z\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M93.39 40.499a.376.376 0 0 1-.35-.35v-3.638l.313.059.112-.013.275-.131v3.723c0 .175-.175.35-.35.35m.349-6.179-.7-1.123v-8.28s.175-.35.35-.35c.176 0 .351.175.351.35v7.022l-.276.089-.252.515-.097.209h.069l.556.434v.238l-.465-.115.465.731v.284z\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m85.473 8.312-.626.313M86.697 10.27l-1.017.509M87.921 12.229l-1.409.704M89.145 14.187l-1.8.9M90.369 16.145l-2.191 1.096M91.594 18.103l-2.583 1.292M92.818 20.061l-2.974 1.488M94.042 22.02l-3.366 1.683M95.266 23.978l-3.757 1.879\"/\u003e\u003c/g\u003e\u003cpath d=\"m71.96 16.087 13.2-7.618M85.16 8.469l13.202 7.613M98.364 31.314l-.002-15.232M93.39 40.149l-13.911 6.196M71.963 31.318l7.516 15.027M45.579 16.087 32.383 8.462\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.383 8.462-13.191 7.616M32.382 11.278l-10.751 6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m19.197 31.318-.005-15.24\" class=\"bond\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 35.907q.917 0 1.387.274.47.267.47.94 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-.178-.911-.178h-.81v1.559zm-.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 .22.012.125.005.208.029l-.071.554q-.089-.018-.196-.03-.108-.018-.203-.018-.28 0-.53.155-.244.155-.393.435-.148.274-.148.649v1.958h-.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=\"M60.71 10.921h-.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-.483V6.021h.577zM60.573 5.459h-.619V3.173h-2.512v2.286h-.613V.56h.613v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#a62929\" d=\"m7.771 37.915 5.713-3.298\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m55.616 10.291-5.019 2.898M55.616 10.291l-5.019 2.898M61.923 10.291l5.018 2.898M61.923 10.291l5.018 2.898\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1r,3R)-5r)-7S)-9Tet_CCW)-Bromantane","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"Brc1ccc(N[C@H]2[C@H]3C[C@@H]4C[C@@H](C[C@H]2C4)C3)cc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 108.509 49.268\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h109v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m7.771 37.915 11.426-6.597\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.197 31.318 13.196 7.624M21.635 29.911l10.758 6.215\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.393 38.942 13.19-7.615\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.583 31.327-.004-15.24M43.145 29.919l-.004-12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.579 16.087 10.037-5.796M71.96 16.087l-10.037-5.796M71.96 16.087l.003 15.231\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m72.138 31.015-.35.606M74.149 31.886l-.6 1.04M76.16 32.757l-.85 1.473M78.17 33.628l-1.099 1.906M80.181 34.499l-1.349 2.339M82.192 35.37l-1.599 2.773M84.203 36.241l-1.849 3.206M86.214 37.112l-2.099 3.639\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M85.165 41.529v-4.871l7.271-3.153.03 2.614-7.3 5.41zm9.213-6.828-.023-2.028 3.834-1.662.35.606z\" class=\"bond\"/\u003e\u003cpath d=\"m98.364 31.314 8.228 15.027\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m93.539 39.832-.298.634M95.863 40.6l-.545 1.162M98.187 41.368l-.793 1.69M100.511 42.136l-1.04 2.218M102.835 42.904l-1.288 2.746M105.159 43.672l-1.536 3.274M107.483 44.44l-1.783 3.803\"/\u003e\u003c/g\u003e\u003cpath d=\"m93.39 40.149-.002-15.232\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m85.473 8.312-.626.313 8.892 22.793v-9.746z\" class=\"bond\"/\u003e\u003cpath d=\"m71.96 16.087 13.2-7.618M85.16 8.469l13.202 7.613M98.364 31.314l-.002-15.232M93.39 40.149l-13.911 6.196M71.963 31.318l7.516 15.027M45.579 16.087 32.383 8.462\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.383 8.462-13.191 7.616M32.382 11.278l-10.751 6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m19.197 31.318-.005-15.24\" class=\"bond\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 35.907q.917 0 1.387.274.47.267.47.94 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-.178-.911-.178h-.81v1.559zm-.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 .22.012.125.005.208.029l-.071.554q-.089-.018-.196-.03-.108-.018-.203-.018-.28 0-.53.155-.244.155-.393.435-.148.274-.148.649v1.958h-.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=\"M60.71 10.921h-.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-.483V6.021h.577zM60.573 5.459h-.619V3.173h-2.512v2.286h-.613V.56h.613v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#a62929\" d=\"m7.771 37.915 5.713-3.298\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m55.616 10.291-5.019 2.898M55.616 10.291l-5.019 2.898M61.923 10.291l5.018 2.898M61.923 10.291l5.018 2.898\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1r,3S)-5r)-7R)-9Tet_CW)-Bromantane","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(1r,3R)-5r)-7S)-9Tet_CCW)-Bromantane","(1r,3S)-5r)-7R)-9Tet_CW)-Bromantane"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 108.659 48.57\"\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 0h109v49H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m107.61 24.523-9.26 14.02M98.35 38.543l-.003-15.24M98.347 23.303l-13.194-7.626M85.153 15.677l8.904-14.636M94.057 1.041l1.234 14.529M107.61 24.523 95.291 15.57\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M82.111 23.555a.4.4 0 0 1-.315-.196c-.088-.152-.024-.391.128-.478l6.807-3.929.701.404-7.158 4.131a.23.23 0 0 1-.163.068m9.406-5.402-.701-.404 4.3-2.482a.3.3 0 0 1 .158-.039c.127 0 .26.063.32.167a.376.376 0 0 1-.128.479z\" class=\"bond\"/\u003e\u003cpath d=\"M82.099 23.184 71.963 38.531M71.963 38.531l13.194 7.626M98.35 38.543l-13.193 7.614M71.963 38.531l-.003-15.24M85.153 15.677 71.96 23.291M71.96 23.291l-10.037-5.796M55.616 17.495l-10.037 5.796\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.583 38.531-.004-15.24M43.145 37.123l-.004-12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.583 38.531-13.19 7.615\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.197 38.522 13.196 7.624M21.635 37.115l10.758 6.215\"/\u003e\u003c/g\u003e\u003cpath d=\"m19.197 38.522-.005-15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.383 15.666-13.191 7.616M32.382 18.482 21.631 24.69\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.579 23.291-13.196-7.625M19.197 38.522 7.771 45.119\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M60.71 18.124h-.72l-2.619-4.066h-.03l.03.596q.023.357.023.732v2.738h-.565v-4.899h.714l2.608 4.054h.029l-.017-.327-.024-.477q-.006-.261-.006-.482v-2.768h.577zM60.573 12.663h-.619v-2.286h-2.512v2.286h-.613V7.764h.613v2.072h2.512V7.764h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M1.959 43.111q.917 0 1.387.274.47.267.47.94 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-.178-.911-.178h-.81V45.2zm-.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-.148.649v1.958h-.602v-3.673h.494l.066.667h.03q.178-.298.458-.518t.667-.22\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m61.923 17.495 5.018 2.898M61.923 17.495l5.018 2.898M55.616 17.495l-5.019 2.898M55.616 17.495l-5.019 2.898\" class=\"hi\"/\u003e\u003cpath stroke=\"#a62929\" d=\"m7.771 45.119 5.713-3.299\" 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":"Bromantane","UNII":"N1ILS53XWK","Wikipedia":"Bromantane","XLogP":5}