{"Abbreviation":"","Aliases":["Thioseconal","5-Allyl-5-(1-methylbutyl)-2-thiobarbituric acid","4,6(1H,5H)-Pyrimidinedione, dihydro-5-(1-methylbutyl)-5-(2-propenyl)-2-thioxo-","dihydro-5-(1-methylbutyl)-5-(2-propenyl)-2-thioxo-4,6(1H,5H)-pyrimidinedione","Thioquinalbarbitone","5-Allyl-5-(1-methylbutyl)-2-thioxodihydro-4,6(1H,5H)-pyrimidinedione","5-allyl-5-(1-methylbutyl)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione","4,6-dihydroxy-5-(pentan-2-yl)-5-(prop-2-en-1-yl)-2,5-dihydropyrimidine-2-thione","5-(pentan-2-yl)-5-(prop-2-en-1-yl)-2-sulfanylidene-1,3-diazinane-4,6-dione","201-018-3","5-Allyl-5-(1-methylbutyl)-2-thiobarbitursaeure","Surital","Barbituric acid, 5-allyl-5-(1-methylbutyl)-2-thio-","5-(pentan-2-yl)-5-(prop-2-en-1-yl)-2-sulfanylidenedihydropyrimidine-4,6(1H,5H)-dione","Spectrum_001812","Spectrum2_000384","Spectrum3_001782","Spectrum4_000577","Spectrum5_001901","Dihydro-5-(1-methylbutyl)-5-(2-propenyl)-2-thioxo-4,6-(1H,5H)-pyrimidinedione","BSPBio_003303","KBioGR_001014","KBioSS_002307","DivK1c_000990","Thiamylal, analytical standard"],"Biological Half-Life":"Although no studies have been performed on humans, the half-life in cats is 14.3 hours.","CAS":"77-27-0","ChEBI":"CHEBI:9536","ChEMBL":"CHEMBL440","ChemicalClasses":["thiobarbiturate"],"Chirality":"racemic","Drug Indication":"Used for the production of complete anaesthesia of short duration, for the induction of general anaesthesia, and for inducing a hypnotic state.","EINECS":"201-018-3","EliminationHalfLife":"14.3 h (cats)","Erowid Experience Reports":[],"Esters":[],"European Community (EC) Number":"201-018-3","Formating":[],"HMDB ID":"HMDB0015285","HeavyAtomCount":17,"Human Drugs":"Human drug -\u003e Discontinued","IUPACName":"5-pentan-2-yl-5-prop-2-enyl-2-sulfanylidene-1,3-diazinane-4,6-dione","InChI":"InChI=1S/C12H18N2O2S/c1-4-6-8(3)12(7-5-2)9(15)13-11(17)14-10(12)16/h5,8H,2,4,6-7H2,1,3H3,(H2,13,14,15,16,17)","InChIKey":"XLOMZPUITCYLMJ-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Ultrashort-acting anesthetics that are used for induction. Loss of consciousness is rapid and induction is pleasant, but there is no muscle relaxation and reflexes frequently are not reduced adequately. Repeated administration results in accumulation and prolongs the recovery time. Since these agents have little if any analgesic activity, they are seldom used alone except in brief minor procedures. (From AMA Drug Evaluations Annual, 1994, p174) (See all compounds classified as Anesthetics, Intravenous.)","Melting Point":"132-133 °C","MolecularFormula":"C\u003csub\u003e12\u003c/sub\u003eH\u003csub\u003e18\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003eO\u003csub\u003e2\u003c/sub\u003eS","MolecularWeight":"254.35 g/mol","Opticalactivity":"( + / - )","Pharmacodynamics":"Thiamylal, a barbiturate, is used in combination with acetaminophen or aspirin and caffeine for its sedative and relaxant effects in the treatment of tension headaches, migraines, and pain. Barbiturates act as nonselective depressants of the central nervous system (CNS), capable of producing all levels of CNS mood alteration from excitation to mild sedation, hypnosis, and deep coma. In sufficiently high therapeutic doses, barbiturates induce anesthesia.","Physical Description":"Solid","PubChemId":3032285,"RefCount":4,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Thiamylal","Name":"Thiamylal","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q906102","Name":"Thiamylal","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB01154","Name":"Thiamylal","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/3032285","Name":"Thiamylal","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL440","Name":"Thiamylal","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:9536","Name":"Thiamylal","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=77-27-0","Name":"Thiamylal","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0015285","Name":"Thiamylal","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/D06106","Name":"Thiamylal","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/01T23W89FR","Name":"Thiamylal","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID3048441","Name":"Thiamylal","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 3032285, Thiamylal. Accessed July 13, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/3032285\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/3032285\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Thiamylal. UNII: 01T23W89FR. Global Substance Registration System. Accessed July 13, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/01T23W89FR\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/01T23W89FR\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":"CCCC(C)C1(C(=O)NC(=S)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"}],"Solubility":"5.06e-02 g/L","StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"C=CCC1([C@@H](C)CCC)C(=O)NC(=S)NC1=O","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 58.437 101.816\"\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\" 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