{"ATC Code":"N - Nervous system","Abbreviation":"","Aliases":["5,5-Diallylbarbituric acid","Allobarbitone","Diallylbarbital","Diallymal","Alobarbital","Diallylbarbituric acid","Allobarbitalum","2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-di-2-propenyl-","diallylmal","diallyl barbituric acid","N05CA21","5,5-bis(prop-2-en-1-yl)-1,3-diazinane-2,4,6-trione","200-140-4","Allylbarbitural","Barbidal","Barballyl","Dormallyl","Novallyl","Curral","Diadol","Malilum","Alnox","Malil","Allbarbital","Dorm"],"CAS":"52-43-7","ChEBI":"CHEBI:134875","ChEMBL":"CHEMBL267719","ChemicalClasses":["barbiturate"],"Chirality":"achiral","EINECS":"200-140-4","EliminationHalfLife":"","Erowid Experience Reports":[],"Esters":[],"European Community (EC) Number":"200-140-4","Formating":[],"HMDB ID":"HMDB0248157","HeavyAtomCount":15,"IUPACName":"5,5-bis(prop-2-enyl)-1,3-diazinane-2,4,6-trione","InChI":"InChI=1S/C10H12N2O3/c1-3-5-10(6-4-2)7(13)11-9(15)12-8(10)14/h3-4H,1-2,5-6H2,(H2,11,12,13,14,15)","InChIKey":"FDQGNLOWMMVRQL-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e12\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003eO\u003csub\u003e3\u003c/sub\u003e","MolecularWeight":"208.21 g/mol","PubChemId":5842,"RefCount":4,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Allobarbital","Name":"Allobarbital","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q418905","Name":"Allobarbital","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB13577","Name":"Allobarbital","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/5842","Name":"Allobarbital","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL267719","Name":"Allobarbital","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:134875","Name":"Allobarbital","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=52-43-7","Name":"Allobarbital","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0248157","Name":"Allobarbital","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/D02817","Name":"Allobarbital","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/8NT43GG2HA","Name":"Allobarbital","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID9022572","Name":"Allobarbital","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 5842, Allobarbital. Accessed July 13, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/5842\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/5842\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Allobarbital. UNII: 8NT43GG2HA. Global Substance Registration System. Accessed July 13, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/8NT43GG2HA\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/8NT43GG2HA\u003c/a\u003e","Anvisa. RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial. Diário Oficial da União. March 31, 2023. Accessed July 13, 2025. \u003ca href=https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-784-de-31-de-marco-de-2023-474904992\u003ehttps://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-784-de-31-de-marco-de-2023-474904992\u003c/a\u003e"],"SMILES":"C=CCC1(C(=O)NC(=O)NC1=O)CC=C","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Brazil","ref":["3"],"schedule":"B1 substance"},{"gov":"Canada","ref":[],"schedule":"Schedule IV substance"},{"act":"Controlled Substances Act (CSA)","gov":"United States","ref":[],"schedule":"Schedule I"},{"gov":"Germany","ref":[],"schedule":"Anlage III substance"}],"StereoisomerData":[],"Stereoisomers":["(+)-Allobarbital","(-)-Allobarbital"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 58.437 87.543\"\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 0h59v88H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m33.801 12.729 9.795-11.676M36.574 13.217l8.89-10.597\"/\u003e\u003c/g\u003e\u003cpath d=\"m33.801 12.729 5.214 14.32M39.015 27.049l-9.794 11.676M29.221 38.725l-13.204 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M16.017 47.761 5.485 41.68M17.236 45.649 6.704 39.568\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m5.485 41.68 5.266 3.041M6.704 39.568l5.266 3.04\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m16.017 46.353-.003 11.399M19.166 63.422l10.045 5.8\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m30.43 68.517.002 12.023M27.991 68.518l.002 12.022\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m30.432 80.54-.001-6.011M27.993 80.54l-.001-6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m29.211 69.222 10.05-5.807M42.415 57.743l.004-11.398M29.221 38.725l13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m41.199 45.641 10.529-6.077M42.418 47.753l10.529-6.077\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m51.728 39.564-5.265 3.038M52.947 41.676l-5.264 3.039\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m29.221 38.725-9.799-11.673M19.422 27.052l5.209-14.322\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M24.631 12.73 14.833 1.058M21.859 13.22 12.965 2.626\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M5.078 38.73q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887Q.56 39.48.56 38.718q0-.75.244-1.309.25-.566.756-.882.506-.315 1.274-.315.732 0 1.232.315.5.31.756.876.256.565.256 1.327m-3.863 0q0 .923.387 1.459.393.529 1.22.529.84 0 1.221-.529.387-.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\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M17.953 64.051h-.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-.262-.006-.482v-2.768h.577zM13.51 64.051h-.619v-2.286h-2.512v2.286h-.613v-4.899h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M31.472 84.459q0 .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 1.232.316.5.309.756.875t.256 1.328m-3.863 0q0 .922.387 1.458.393.53 1.22.53.84 0 1.221-.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=\"M44.355 64.043h-.721l-2.619-4.066h-.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.578zM48.661 64.043h-.619v-2.286h-2.513v2.286h-.613v-4.9h.613v2.072h2.513v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M57.877 38.724q0 .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-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.863 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.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=\"#3050f8\" d=\"m16.014 57.752.001-5.699M16.014 57.752l.001-5.699M19.166 63.422l5.022 2.9M19.166 63.422l5.022 2.9M39.261 63.415l-5.025 2.904M42.415 57.743l.002-5.699\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Allobarbital","UNII":"8NT43GG2HA","Wikidata":"Q418905","Wikipedia":"Allobarbital","XLogP":1}