{"Abbreviation":["TMT","MCPA"],"Aliases":["3,4,5-Trimethoxytranylcypromine","Cyclopropanamine, 2-(3,4,5-trimethoxyphenyl)-","RefChem:1082743","2-(3,4,5-Trimethoxyphenyl)-cyclopropylamine","Cyclopropylamine, 2-(3,4,5-trimethoxyphenyl)-","2-(3,4,5-Trimethoxyphenyl)cyclopropanamine","2-(3,4,5-trimethoxyphenyl) cyclopropylamine","En300-1848414"],"CAS":"17061-21-1","ChemicalClasses":["phenylcyclopropylamine"],"Chirality":"racemic","Classes":["Psychedelic"],"DurationOfAction":"","EliminationHalfLife":"","Esters":[],"Formating":[],"HeavyAtomCount":16,"IUPACName":"2-(3,4,5-trimethoxyphenyl)cyclopropan-1-amine","InChI":"InChI=1S/C12H17NO3/c1-14-10-4-7(8-6-9(8)13)5-11(15-2)12(10)16-3/h4-5,8-9H,6,13H2,1-3H3","InChIKey":"HNYWYOQSLRJIMG-UHFFFAOYSA-N","LD50":[{"dosages":[{"amount":"76500 μg/kg","route":"intraperitoneal"}],"organism":"Mouse"}],"MolecularFormula":"C\u003csub\u003e12\u003c/sub\u003eH\u003csub\u003e17\u003c/sub\u003eNO\u003csub\u003e3\u003c/sub\u003e","MolecularWeight":"223.27 g/mol","PubChemId":28236,"RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/3,4,5-Trimethoxytranylcypromine","Name":"3,4,5-Trimethoxytranylcypromine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q82914011","Name":"3,4,5-Trimethoxytranylcypromine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/28236","Name":"3,4,5-Trimethoxytranylcypromine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=17061-21-1","Name":"3,4,5-Trimethoxytranylcypromine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID90937795","Name":"3,4,5-Trimethoxytranylcypromine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 28236, 3,4,5-Trimethoxytranylcypromine. Accessed October 9, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/28236\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/28236\u003c/a\u003e"],"SMILES":"COC1=CC(=CC(=C1OC)OC)C2CC2N","SaltData":[],"Salts":[],"Scheduling":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"COC1=CC([C@@H]2C[C@@H]2N)=CC(OC)=C1OC","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 72.442 87.275\"\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 0h73v88H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m2.864 69.647-.019-11.319M6.114 52.508l9.91-5.744\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m16.024 46.764 13.152 7.541M18.461 45.351l10.711 6.141\"/\u003e\u003c/g\u003e\u003cpath d=\"m29.176 54.305 13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m55.385 54.628.351-.606M53.041 53.607l.644-1.111M50.697 52.586l.936-1.615M48.353 51.565l1.229-2.12M46.009 50.544l1.521-2.625M43.665 49.523l1.814-3.13M41.321 48.502l2.106-3.634\"/\u003e\u003c/g\u003e\u003cpath d=\"m55.561 54.325 15.248.021M70.809 54.346l-7.65 13.19M55.561 54.325l7.598 13.211M63.159 67.536l-.021 11.39\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m42.374 46.685.046-15.161M39.94 45.275l.037-12.346\"/\u003e\u003c/g\u003e\u003cpath d=\"m42.42 31.524-13.203-7.628M29.217 23.896l.002-11.319M32.498 6.764l9.921-5.726\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m29.217 23.896-13.198 7.62M29.216 26.712l-10.758 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m16.024 46.764-.005-15.248M16.019 31.516l-9.924-5.727M2.819 19.977 2.817 8.658\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M5.097 54.404q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.31.756.875.256.566.256 1.328m-3.863 0q0 .922.387 1.458.393.53 1.22.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M65.071 85.226h-.72l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM69.378 85.226h-.62V82.94h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62zM71.882 86.715h-1.943v-.3l.772-.779q.221-.221.371-.393.154-.175.232-.339.079-.168.079-.364 0-.243-.146-.368-.143-.129-.372-.129-.214 0-.379.075-.16.075-.328.207l-.193-.242q.171-.147.393-.247.225-.1.507-.1.411 0 .65.207t.24.575q0 .229-.097.433-.093.2-.264.396-.168.196-.393.418l-.615.604v.017h1.486z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M31.479 8.653q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.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 1.233.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.22.529.84 0 1.221-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.209-.523-.833 0-1.226.523-.393.524-.393 1.453M5.078 23.895q0 .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 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m2.845 58.328.009 5.66M6.114 52.508l4.955-2.872\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.138 78.926.01-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m29.219 12.577-.001 5.659M32.498 6.764l4.961-2.863M6.095 25.789l4.962 2.863M2.819 19.977l-.001-5.66\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(12S,14S)-3,4,5-Trimethoxytranylcypromine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"COC1=CC([C@H]2C[C@@H]2N)=CC(OC)=C1OC","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 72.442 87.275\"\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 0h73v88H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m2.864 69.647-.019-11.319M6.114 52.508l9.91-5.744\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m16.024 46.764 13.152 7.541M18.461 45.351l10.711 6.141\"/\u003e\u003c/g\u003e\u003cpath d=\"m29.176 54.305 13.198-7.62\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m55.385 54.628.351-.606-13.354-9.932v2.595l-2.247 1.297z\" class=\"bond\"/\u003e\u003cpath d=\"m55.561 54.325 15.248.021M70.809 54.346l-7.65 13.19M55.561 54.325l7.598 13.211M63.159 67.536l-.021 11.39\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m42.374 46.685.046-15.161M39.94 45.275l.037-12.346\"/\u003e\u003c/g\u003e\u003cpath d=\"m42.42 31.524-13.203-7.628M29.217 23.896l.002-11.319M32.498 6.764l9.921-5.726\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m29.217 23.896-13.198 7.62M29.216 26.712l-10.758 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m16.024 46.764-.005-15.248M16.019 31.516l-9.924-5.727M2.819 19.977 2.817 8.658\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M5.097 54.404q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.31.756.875.256.566.256 1.328m-3.863 0q0 .922.387 1.458.393.53 1.22.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M65.071 85.226h-.72l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM69.378 85.226h-.62V82.94h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62zM71.882 86.715h-1.943v-.3l.772-.779q.221-.221.371-.393.154-.175.232-.339.079-.168.079-.364 0-.243-.146-.368-.143-.129-.372-.129-.214 0-.379.075-.16.075-.328.207l-.193-.242q.171-.147.393-.247.225-.1.507-.1.411 0 .65.207t.24.575q0 .229-.097.433-.093.2-.264.396-.168.196-.393.418l-.615.604v.017h1.486z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M31.479 8.653q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.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 1.233.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.22.529.84 0 1.221-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.209-.523-.833 0-1.226.523-.393.524-.393 1.453M5.078 23.895q0 .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 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m2.845 58.328.009 5.66M6.114 52.508l4.955-2.872\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.138 78.926.01-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m29.219 12.577-.001 5.659M32.498 6.764l4.961-2.863M6.095 25.789l4.962 2.863M2.819 19.977l-.001-5.66\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(12R,14S)-3,4,5-Trimethoxytranylcypromine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"COC1=CC([C@@H]2C[C@H]2N)=CC(OC)=C1OC","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 72.442 87.275\"\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 0h73v88H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m2.864 69.647-.019-11.319M6.114 52.508l9.91-5.744\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m16.024 46.764 13.152 7.541M18.461 45.351l10.711 6.141\"/\u003e\u003c/g\u003e\u003cpath d=\"m29.176 54.305 13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m55.385 54.628.351-.606M53.041 53.607l.644-1.111M50.697 52.586l.936-1.615M48.353 51.565l1.229-2.12M46.009 50.544l1.521-2.625M43.665 49.523l1.814-3.13M41.321 48.502l2.106-3.634\"/\u003e\u003c/g\u003e\u003cpath d=\"m55.561 54.325 15.248.021M70.809 54.346l-7.65 13.19M55.561 54.325l7.598 13.211M63.159 67.536l-.021 11.39\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m42.374 46.685.046-15.161M39.94 45.275l.037-12.346\"/\u003e\u003c/g\u003e\u003cpath d=\"m42.42 31.524-13.203-7.628M29.217 23.896l.002-11.319M32.498 6.764l9.921-5.726\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m29.217 23.896-13.198 7.62M29.216 26.712l-10.758 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m16.024 46.764-.005-15.248M16.019 31.516l-9.924-5.727M2.819 19.977 2.817 8.658\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M5.097 54.404q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.31.756.875.256.566.256 1.328m-3.863 0q0 .922.387 1.458.393.53 1.22.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M65.071 85.226h-.72l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM69.378 85.226h-.62V82.94h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62zM71.882 86.715h-1.943v-.3l.772-.779q.221-.221.371-.393.154-.175.232-.339.079-.168.079-.364 0-.243-.146-.368-.143-.129-.372-.129-.214 0-.379.075-.16.075-.328.207l-.193-.242q.171-.147.393-.247.225-.1.507-.1.411 0 .65.207t.24.575q0 .229-.097.433-.093.2-.264.396-.168.196-.393.418l-.615.604v.017h1.486z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M31.479 8.653q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.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 1.233.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.22.529.84 0 1.221-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.209-.523-.833 0-1.226.523-.393.524-.393 1.453M5.078 23.895q0 .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 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m2.845 58.328.009 5.66M6.114 52.508l4.955-2.872\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.138 78.926.01-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m29.219 12.577-.001 5.659M32.498 6.764l4.961-2.863M6.095 25.789l4.962 2.863M2.819 19.977l-.001-5.66\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(12S,14R)-3,4,5-Trimethoxytranylcypromine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"COC1=CC([C@H]2C[C@H]2N)=CC(OC)=C1OC","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 72.442 87.275\"\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 0h73v88H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m2.864 69.647-.019-11.319M6.114 52.508l9.91-5.744\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m16.024 46.764 13.152 7.541M18.461 45.351l10.711 6.141\"/\u003e\u003c/g\u003e\u003cpath d=\"m29.176 54.305 13.198-7.62\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m55.385 54.628.351-.606-13.354-9.932v2.595l-2.247 1.297z\" class=\"bond\"/\u003e\u003cpath d=\"m55.561 54.325 15.248.021M70.809 54.346l-7.65 13.19M55.561 54.325l7.598 13.211M63.159 67.536l-.021 11.39\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m42.374 46.685.046-15.161M39.94 45.275l.037-12.346\"/\u003e\u003c/g\u003e\u003cpath d=\"m42.42 31.524-13.203-7.628M29.217 23.896l.002-11.319M32.498 6.764l9.921-5.726\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m29.217 23.896-13.198 7.62M29.216 26.712l-10.758 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m16.024 46.764-.005-15.248M16.019 31.516l-9.924-5.727M2.819 19.977 2.817 8.658\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M5.097 54.404q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.31.756.875.256.566.256 1.328m-3.863 0q0 .922.387 1.458.393.53 1.22.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M65.071 85.226h-.72l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM69.378 85.226h-.62V82.94h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62zM71.882 86.715h-1.943v-.3l.772-.779q.221-.221.371-.393.154-.175.232-.339.079-.168.079-.364 0-.243-.146-.368-.143-.129-.372-.129-.214 0-.379.075-.16.075-.328.207l-.193-.242q.171-.147.393-.247.225-.1.507-.1.411 0 .65.207t.24.575q0 .229-.097.433-.093.2-.264.396-.168.196-.393.418l-.615.604v.017h1.486z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M31.479 8.653q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.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 1.233.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.22.529.84 0 1.221-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.209-.523-.833 0-1.226.523-.393.524-.393 1.453M5.078 23.895q0 .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 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m2.845 58.328.009 5.66M6.114 52.508l4.955-2.872\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.138 78.926.01-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m29.219 12.577-.001 5.659M32.498 6.764l4.961-2.863M6.095 25.789l4.962 2.863M2.819 19.977l-.001-5.66\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(12R,14R)-3,4,5-Trimethoxytranylcypromine","UNII":null}],"StereoisomerType":"diastereomer","Stereoisomers":["(12S,14S)-3,4,5-Trimethoxytranylcypromine","(12R,14S)-3,4,5-Trimethoxytranylcypromine","(12S,14R)-3,4,5-Trimethoxytranylcypromine","(12R,14R)-3,4,5-Trimethoxytranylcypromine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 72.442 87.275\"\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 0h73v88H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m2.864 69.647-.019-11.319M6.114 52.508l9.91-5.744\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m16.024 46.764 13.152 7.541M18.461 45.351l10.711 6.141\"/\u003e\u003c/g\u003e\u003cpath d=\"m29.176 54.305 13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m42.374 46.685.046-15.161M39.94 45.275l.037-12.346\"/\u003e\u003c/g\u003e\u003cpath d=\"m42.42 31.524-13.203-7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m29.217 23.896-13.198 7.62M29.216 26.712l-10.758 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m16.024 46.764-.005-15.248M16.019 31.516l-9.924-5.727M2.819 19.977 2.817 8.658M29.217 23.896l.002-11.319M32.498 6.764l9.921-5.726M42.374 46.685l13.187 7.64M55.561 54.325l15.248.021M70.809 54.346l-7.65 13.19M55.561 54.325l7.598 13.211M63.159 67.536l-.021 11.39\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M5.097 54.404q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.31.756.875.256.566.256 1.328m-3.863 0q0 .922.387 1.458.393.53 1.22.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.833 0-1.226.524t-.393 1.453M5.078 23.895q0 .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 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452M31.479 8.653q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.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 1.233.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.22.529.84 0 1.221-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.209-.523-.833 0-1.226.523-.393.524-.393 1.453\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M65.071 85.226h-.72l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM69.378 85.226h-.62V82.94h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62zM71.882 86.715h-1.943v-.3l.772-.779q.221-.221.371-.393.154-.175.232-.339.079-.168.079-.364 0-.243-.146-.368-.143-.129-.372-.129-.214 0-.379.075-.16.075-.328.207l-.193-.242q.171-.147.393-.247.225-.1.507-.1.411 0 .65.207t.24.575q0 .229-.097.433-.093.2-.264.396-.168.196-.393.418l-.615.604v.017h1.486z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m2.845 58.328.009 5.66M6.114 52.508l4.955-2.872M6.095 25.789l4.962 2.863M2.819 19.977l-.001-5.66M29.219 12.577l-.001 5.659M32.498 6.764l4.961-2.863\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.138 78.926.01-5.695\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":null,"Title":"3,4,5-Trimethoxytranylcypromine","Wikidata":"Q82914011","Wikipedia":"3,4,5-Trimethoxytranylcypromine","XLogP":1.1}
