{"Abbreviation":[],"Aliases":["3-(1-(1-(4-bromophenyl)ethyl)piperidin-4-yl)-1H-benzimidazol-2-one","2H-Benzimidazol-2-one, 1-[1-[1-(4-bromophenyl)ethyl]-4-piperidinyl]-1,3-dihydro-","1-(1-(1-(4-Bromophenyl)ethyl)-4-piperidinyl)-1,3-dihydro-2H-benzimidazol-2-one","1-(1-(1-(4-Bromophenyl)ethyl)piperidin-4-yl)-1,3-dihydro-2H-benzo(d)imidazol-2-one","1-[1-[1-(4-Bromophenyl)ethyl]-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-one","1-{1-[1-(4-Bromophenyl)ethyl]piperidin-4-yl}-1,3-dihydro-2H-benzo[d]imidazol-2-one","GTPL12956","compound 21","C22777","1-(1-(1-(4-Bromophenyl)ethyl)piperidin-4-yl)-1,3-dihydro-2H-benzimidazol-2-one","1-[1-[1-(4-Bromophenyl)ethyl]-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-one; 2H-Benzimidazol-2-one, 1-[1-[1-(4-bromophenyl)ethyl]-4-piperidinyl]-1,3-dihydro- (ACI); 1-[1-[1-(4-Bromophenyl)ethyl]-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-one (ACI); Brorphine"],"CAS":"2244737-98-0","ChEMBL":"CHEMBL4203403","ChemicalClasses":["benzimidazole"],"Chirality":"racemic","Classes":["Opioid"],"DEA no":9098,"Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":25,"IUPACName":"3-[1-[1-(4-bromophenyl)ethyl]piperidin-4-yl]-1H-benzimidazol-2-one","InChI":"InChI=1S/C20H22BrN3O/c1-14(15-6-8-16(21)9-7-15)23-12-10-17(11-13-23)24-19-5-3-2-4-18(19)22-20(24)25/h2-9,14,17H,10-13H2,1H3,(H,22,25)","InChIKey":"CNOFBGYRMCBVLO-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Compounds with activity like OPIATE ALKALOIDS, acting at OPIOID RECEPTORS. Properties include induction of ANALGESIA or NARCOSIS. (See all compounds classified as Analgesics, Opioid.)","MolecularFormula":"C\u003csub\u003e20\u003c/sub\u003eH\u003csub\u003e22\u003c/sub\u003eBrN\u003csub\u003e3\u003c/sub\u003eO","MolecularWeight":"400.3 g/mol","PubChemId":145975294,"RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Brorphine","Name":"Brorphine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/145975294","Name":"Brorphine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL4203403","Name":"Brorphine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=2244737-98-0","Name":"Brorphine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C22777","Name":"Brorphine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/38H2BE6LU4","Name":"Brorphine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID201027168","Name":"Brorphine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 145975294, Brorphine. Accessed July 28, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/145975294\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/145975294\u003c/a\u003e"],"SMILES":"CC(C1=CC=C(C=C1)Br)N2CCC(CC2)N3C4=CC=CC=C4NC3=O","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"C[C@H](C1=CC=C(Br)C=C1)N1CCC(N2C(=O)NC3=CC=CC=C32)CC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 77.17 138.747\"\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 0h78v139H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m60.931 90.623-.145.685M63.475 90.862l-.265 1.256M66.019 91.102l-.386 1.826M68.563 91.341l-.506 2.397M71.107 91.58l-.627 2.969M73.651 91.82l-.747 3.539M76.195 92.059l-.868 4.11\"/\u003e\u003c/g\u003e\u003cpath d=\"m60.859 90.965-10.178 11.332\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m55.406 116.786-4.725-14.489M52.651 116.205l-3.852-11.813\"/\u003e\u003c/g\u003e\u003cpath d=\"m55.406 116.786-10.179 11.343\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m30.324 124.983 14.903 3.146M32.206 122.888l12.147 2.564\"/\u003e\u003c/g\u003e\u003cpath d=\"m30.324 124.983-8.401 9.354M30.324 124.983l-4.725-14.489\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m35.778 99.151-10.179 11.343M36.652 101.828l-8.298 9.247\"/\u003e\u003c/g\u003e\u003cpath d=\"m50.681 102.297-14.903-3.146M60.859 90.965l-3.491-10.699M52.823 75.787 41.222 73.34M41.222 73.34l-4.724-14.481M36.498 58.859l10.187-11.334M46.685 47.525l-3.491-10.7M44.565 29.462l6.331-8.704\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M50.009 19.538h12.459M50.009 21.977h12.459\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M62.468 19.538h-6.229M62.468 21.977h-6.229\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m50.896 20.758-6.331-8.705M38.687 9.524l-11.248 3.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 13.142-13.2-7.616M25.001 14.55 14.239 8.341\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.239 5.526 1.038 13.142\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M1.038 13.142v15.231M3.477 14.55v12.415\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 28.373 13.201 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 35.989 13.2-7.616M14.239 33.174l10.762-6.209\"/\u003e\u003c/g\u003e\u003cpath d=\"M27.439 13.142v15.231M38.687 31.991l-11.248-3.618M46.685 47.525l14.912 3.145M61.597 50.67l4.724 14.48M59.011 73.284l7.31-8.134\" class=\"bond\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M16.099 133.288q.917 0 1.387.273.471.268.471.941 0 .435-.244.72-.238.286-.691.364v.035q.31.048.56.179t.393.375q.148.238.148.619 0 .667-.458 1.03t-1.244.363H14.7v-4.899zm.119 2.089q.631 0 .864-.202.238-.203.238-.601 0-.405-.286-.578-.286-.179-.911-.179h-.809v1.56zm-.904.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.941-.238zm5.475-1.446q.101 0 .22.011.125.006.209.03l-.072.554q-.089-.018-.196-.03-.107-.018-.202-.018-.28 0-.53.155-.244.155-.393.435-.149.273-.149.648v1.959h-.601v-3.673h.494l.065.667h.03q.179-.298.458-.518.28-.22.667-.22\" class=\"atom\"/\u003e\u003cpath stroke=\"none\" d=\"M58.075 78.935h-.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.578zM43.901 35.494h-.72l-2.62-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578z\" class=\"atom\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M68.387 20.755q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.263-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881.507-.316 1.274-.316.733 0 1.233.316.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M43.901 10.921h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM43.764 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#a62929\" d=\"m21.923 134.337 4.2-4.677\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m57.368 80.266 1.746 5.349M52.823 75.787l-5.8-1.223M43.194 36.825l1.746 5.35M44.565 29.462l3.165-4.352M44.565 12.053l3.165 4.352M44.565 12.053l3.165 4.352M38.687 9.524l-5.624 1.809M38.687 9.524l-5.624 1.809M38.687 31.991l-5.624-1.809M59.011 73.284l3.655-4.067\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-Brorphine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"C[C@@H](C1=CC=C(Br)C=C1)N1CCC(N2C(=O)NC3=CC=CC=C32)CC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.755 138.747\"\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 0h77v139H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m60.931 90.623-.145.685 14.541 4.861.434-2.055.434-2.055z\" class=\"bond\"/\u003e\u003cpath d=\"m60.859 90.965-10.178 11.332\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m55.406 116.786-4.725-14.489M52.651 116.205l-3.852-11.813\"/\u003e\u003c/g\u003e\u003cpath d=\"m55.406 116.786-10.179 11.343\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m30.324 124.983 14.903 3.146M32.206 122.888l12.147 2.564\"/\u003e\u003c/g\u003e\u003cpath d=\"m30.324 124.983-8.401 9.354M30.324 124.983l-4.725-14.489\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m35.778 99.151-10.179 11.343M36.652 101.828l-8.298 9.247\"/\u003e\u003c/g\u003e\u003cpath d=\"m50.681 102.297-14.903-3.146M60.859 90.965l-3.491-10.699M52.823 75.787 41.222 73.34M41.222 73.34l-4.724-14.481M36.498 58.859l10.187-11.334M46.685 47.525l-3.491-10.7M44.565 29.462l6.331-8.704\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M50.009 19.538h12.459M50.009 21.977h12.459\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M62.468 19.538h-6.229M62.468 21.977h-6.229\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m50.896 20.758-6.331-8.705M38.687 9.524l-11.248 3.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 13.142-13.2-7.616M25.001 14.55 14.239 8.341\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.239 5.526 1.038 13.142\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M1.038 13.142v15.231M3.477 14.55v12.415\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 28.373 13.201 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 35.989 13.2-7.616M14.239 33.174l10.762-6.209\"/\u003e\u003c/g\u003e\u003cpath d=\"M27.439 13.142v15.231M38.687 31.991l-11.248-3.618M46.685 47.525l14.912 3.145M61.597 50.67l4.724 14.48M59.011 73.284l7.31-8.134\" class=\"bond\"/\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M16.099 133.288q.917 0 1.387.273.471.268.471.941 0 .435-.244.72-.238.286-.691.364v.035q.31.048.56.179t.393.375q.148.238.148.619 0 .667-.458 1.03t-1.244.363H14.7v-4.899zm.119 2.089q.631 0 .864-.202.238-.203.238-.601 0-.405-.286-.578-.286-.179-.911-.179h-.809v1.56zm-.904.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.941-.238zm5.475-1.446q.101 0 .22.011.125.006.209.03l-.072.554q-.089-.018-.196-.03-.107-.018-.202-.018-.28 0-.53.155-.244.155-.393.435-.149.273-.149.648v1.959h-.601v-3.673h.494l.065.667h.03q.179-.298.458-.518.28-.22.667-.22\" class=\"atom\"/\u003e\u003cpath stroke=\"none\" d=\"M58.075 78.935h-.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.578zM43.901 35.494h-.72l-2.62-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578z\" class=\"atom\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M68.387 20.755q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.263-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881.507-.316 1.274-.316.733 0 1.233.316.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M43.901 10.921h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM43.764 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#a62929\" d=\"m21.923 134.337 4.2-4.677\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m57.368 80.266 1.746 5.349M52.823 75.787l-5.8-1.223M43.194 36.825l1.746 5.35M44.565 29.462l3.165-4.352M44.565 12.053l3.165 4.352M44.565 12.053l3.165 4.352M38.687 9.524l-5.624 1.809M38.687 9.524l-5.624 1.809M38.687 31.991l-5.624-1.809M59.011 73.284l3.655-4.067\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Brorphine","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Brorphine","(S)-Brorphine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.736 139.882\"\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 0h77v140H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m75.761 45.768-14.902 3.149M60.859 48.917 50.681 37.585\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m35.769 40.733 14.912-3.148M36.642 38.057l12.157-2.567\"/\u003e\u003c/g\u003e\u003cpath d=\"M35.769 40.733 25.58 29.4\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M30.302 14.919 25.58 29.4M32.184 17.014l-3.849 11.803\"/\u003e\u003c/g\u003e\u003cpath d=\"m30.302 14.919 14.912-3.148\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M55.403 23.104 45.214 11.771M52.648 23.687l-8.307-9.24\"/\u003e\u003c/g\u003e\u003cpath d=\"m50.681 37.585 4.722-14.481M30.302 14.919l-8.976-9.994M60.859 48.917l-3.491 10.699M59.011 66.598l7.31 8.134M66.321 74.732l-4.724 14.48M61.597 89.212l-14.912 3.146M46.685 92.358 36.498 81.023M36.498 81.023l4.724-14.48M52.823 64.096l-11.601 2.447M46.685 92.358l-3.491 10.699M38.687 107.891l-11.248 3.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 111.509-13.2-7.616M25.001 112.917l-10.762-6.209\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.239 103.893-13.201 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M1.038 111.509v15.232M3.477 112.917v12.415\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 126.741 13.201 7.615\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 134.356 13.2-7.615M14.239 131.541l10.762-6.209\"/\u003e\u003c/g\u003e\u003cpath d=\"M27.439 111.509v15.232M27.439 126.741l11.248 3.618M44.565 127.829l6.331-8.704M44.565 110.42l6.331 8.705\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M50.009 117.906h12.459M50.009 120.344h12.459\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M62.468 117.906h-6.229M62.468 120.344h-6.229\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath fill=\"#a62929\" stroke=\"none\" d=\"M16.078.56q.916 0 1.387.274.47.268.47.94 0 .435-.244.721-.238.286-.691.363v.036q.31.047.56.178t.393.375q.149.238.149.619 0 .667-.459 1.03-.458.363-1.244.363h-1.72V.56zm.119 2.09q.631 0 .863-.203.238-.202.238-.601 0-.405-.286-.578-.286-.178-.911-.178h-.809v1.56zm-.905.512v1.774h.988q.655 0 .905-.25.256-.256.256-.667 0-.381-.268-.619-.262-.238-.941-.238zm5.475-1.447q.102 0 .221.012.125.006.208.03l-.071.553q-.09-.018-.197-.03-.107-.017-.202-.017-.28 0-.53.154-.244.155-.393.435-.149.274-.149.649v1.958h-.601V1.786h.494l.066.667h.029q.179-.298.459-.518.279-.22.666-.22\" class=\"atom\"/\u003e\u003cpath stroke=\"none\" d=\"M58.075 65.847h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM43.901 109.288h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.482v-2.769h.578z\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M43.901 133.861h-.72l-2.62-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.327-.024-.477q-.006-.262-.006-.482v-2.768h.578zM43.764 139.322h-.619v-2.286h-2.512v2.286h-.614v-4.899h.614v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M68.387 119.122q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.263-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.507-.315 1.274-.315.733 0 1.233.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.221.53.839 0 1.22-.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=\"#a62929\" d=\"m21.326 4.925 4.488 4.997\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m57.368 59.616 1.746-5.349M59.011 66.598l3.655 4.067M52.823 64.096l-5.8 1.224M43.194 103.057l1.746-5.349M38.687 107.891l-5.624 1.809M38.687 130.359l-5.624-1.809M44.565 127.829l3.165-4.352M44.565 110.42l3.165 4.353\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":{"Cognitive Effects":["Cognitive euphoria","Thought deceleration","Anxiety suppression","Compulsive redosing","Increased music appreciation"],"Physical Effects":["Respiratory depression","Pain relief","Itchiness","Constipation","Cough suppression","Sedation","Nausea","Pupil constriction","Stomach cramp","Difficulty urinating"],"Visual Effects":["Double vision"]},"Title":"Brorphine","UNII":"38H2BE6LU4","Wikipedia":"Brorphine","XLogP":4.6}