{"Abbreviation":["TBG"],"Aliases":["RefChem:187084","8-methoxy-3-methyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole","orb1689772","GTPL13551","EX-A6452","BT182116","DA-58231","En300-37278326","8-methoxy-3-methyl-1H,2H,3H,4H,5H,6H-azepino[4,5-b]indole"],"CAS":"2483829-58-7","ChemicalClasses":["hexahydroazepinoindole"],"Chirality":"achiral","DurationOfAction":"","EliminationHalfLife":"","Esters":[],"European Community (EC) Number":"893-229-8","Formating":[],"HeavyAtomCount":17,"IUPACName":"8-methoxy-3-methyl-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indole","InChI":"InChI=1S/C14H18N2O/c1-16-7-5-12-11-4-3-10(17-2)9-14(11)15-13(12)6-8-16/h3-4,9,15H,5-8H2,1-2H3","InChIKey":"FNGNYGCPNKZYOG-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e14\u003c/sub\u003eH\u003csub\u003e18\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003eO","MolecularWeight":"230.31 g/mol","PubChemId":146026994,"RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Tabernanthalog","Name":"Tabernanthalog","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q105715202","Name":"Tabernanthalog","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/146026994","Name":"Tabernanthalog","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=2483829-58-7","Name":"Tabernanthalog","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID301336754","Name":"Tabernanthalog","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 146026994, Tabernanthalog. Accessed October 10, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/146026994\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/146026994\u003c/a\u003e"],"SMILES":"CN1CCC2=C(CC1)NC3=C2C=CC(=C3)OC","SaltData":[],"Salts":[],"Scheduling":[],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 120.814 47.063\"\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 0h121v48H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m119.813 7.361-11.222 3.646M102.411 9.028l-7.624-7.973M94.787 1.055 79.608 2.421M79.608 2.421 71.213 15.14\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M75.922 29.634 71.213 15.14M73.056 28.703l-3.615-11.125\"/\u003e\u003c/g\u003e\u003cpath d=\"m75.922 29.634 14.268 5.355M90.19 34.989l13.083-7.817M104.799 15.908l-1.526 11.264M75.922 29.634l-9.256 6.725M60.519 36.359l-9.256-6.725\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m51.263 29.634 4.71-14.494M49.379 27.542l3.84-11.817\"/\u003e\u003c/g\u003e\u003cpath d=\"M71.213 15.14h-15.24M55.973 15.14 45.775 3.814\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M45.775 3.814 30.868 6.983M44.905 6.492 32.752 9.075\"/\u003e\u003c/g\u003e\u003cpath d=\"m30.868 6.983-4.709 14.494\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m26.159 21.477 10.197 11.326M28.913 20.892l8.314 9.233\"/\u003e\u003c/g\u003e\u003cpath d=\"m51.263 29.634-14.907 3.169M26.159 21.477l-11.278 2.397M8.59 21.69l-7.536-8.37\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M107.26 14.52h-.721l-2.619-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566V9.621h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482V9.621h.578z\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M65.534 41.042h-.721l-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.578zM65.397 46.503h-.62v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M13.511 24.643q0 .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-.565.756-.881t1.274-.316q.732 0 1.232.316.5.31.756.875.256.566.256 1.328m-3.863 0q0 .922.386 1.458.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524-.392.524-.392 1.453\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m108.591 11.007 5.611-1.823M102.411 9.028l-3.812-3.986M104.799 15.908l-.763 5.632M66.666 36.359l4.628-3.363M60.519 36.359l-4.628-3.363\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m14.881 23.874 5.639-1.199M8.59 21.69l-3.768-4.185\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Tabernanthalog","Wikidata":"Q105715202","Wikipedia":"Tabernanthalog","XLogP":2.4}