Therapeutic Targets Database
BIDD Pharmainformatics Databases


TTD Drug ID: DAP000686

Drug Information
SynonymsVIROVYVQCGLCII-UHFFFAOYSA-; component of Dexamyl; Talamo; Eunoctal; Amytal; Dormytal; ZINC04811698; Amobarbitalum [INN-Latin]; Amital; Sumital; 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-5-(3-methylbutyl)-; Isomyl; NSC120800; Binoctal; Amobarbital [INN:JAN]; Amobarbitone; Amospan; Oprea1_587446; 5-Ethyl-5-isopentylbarbituric acid; Amylobarbitone; 5-Ethyl-5-isopentylbarbitursaeure; Amylobarbital; CCRIS 5454; IDI1_000994; MolPort-004-285-843; amobarbital; DB01351; Isoamylethylbarbituric acid; DivK1c_000994; component of Amo-Dextrosule; Amobarbitalum; Somnal; CBDivE_006514; Amobarbitale [DCIT]; 5-Ethyl-5-isoamylmalonyl urea; KBio1_000994; 64-43-7 (hydrochloride); D00555; AMAL; UNII-GWH6IJ239E; 5-ethyl-5-(3-methylbutyl)-1,3-diazinane-2,4,6-trione; 5-Ethyl-5-(3-methylbutyl)-2,4,6(1H,3H,5H)-pyrimidinetrione; Barbamyl; Mylodorm; CID2164; LS-7196; Amybal; Dorlotyn; 5-Isoamyl-5-ethylbarbituric acid; Amobarbitale; Schiwanox; NSC 10815; NINDS_000994; HSDB 3286; Pentymal; NSC32406; DEA No. 2126; InChI=1/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16); NSC10815; Barbamil; 57-43-2; Isomytal (TN); Amobarbital suppository dosage form; Stadadorm; ZINC04811699; CHEMBL267894; component of Q-Caps; Isomytal; EINECS 200-330-7; Robarb; Amasust; Amylbarbitone; component of 15-90; Amobarbital (JP15/INN); 5-Ethyl-5-(3-methylbutyl)barbituric acid; Barbamyl acid; WLN: T6VMVMV FHJ F2 F2Y1&1; Sednotic; Barbituric acid, 5-ethyl-5-isopentyl-; Pentymalum; AC1L1D2C; C07536; Ethylisopentylbarbituric acid; BIDD:PXR0091; 5-Ethyl-5-isoamylbarbituric acid; CHEBI:2673; 5-ethyl-5-(3-methylbutyl)pyrimidine-2,4,6(1H,3H,5H)-trione
[ICD9: 307.41, 307.42, 327.0, 780.51, 780.52   ICD10: F51.0, G47.0]
Approved    [1]

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Canonical SMILESCCC1(C(=O)NC(=O)NC1=O)CCC(C)C    
Therapeutic ClassHypnotics and Sedatives
CAS NumberCAS 57-43-2
PubChem Compound IDCID 2164.
PubChem Substance IDSID 9739.
SuperDrug ATC IDN05CA02
SuperDrug CAS ID000057432;
TargetGamma-aminobutyric acid receptor subunit alpha-1Antagonist[2][3]
Ref 1Drug information of Amobarbital, 2008 To Reference
Ref 2DrugBank: a knowledgebase for drugs, drug actions and drug targets. Nucleic Acids Res. 2008 Jan;36(Database issue):D901-6. Epub 2007 Nov 29. To Reference
Ref 3Effect of barbiturates on polyphosphoinositide biosynthesis and protein kinase C activity in synaptosomes. Neuropharmacology. 1989 Dec;28(12):1317-23. To Reference


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