| 词条 | Tetrabarbital |
| 释义 |
| IUPAC_name = 5-ethyl-5-(hexan-3-yl)pyrimidine-2,4,6(1H,3H,5H)-trione | image = Tetrabarbital-2d.svg | width = 143 | CAS_number = 76-23-3 | ATC_prefix = None | ATC_suffix = | UNII = 3K441526FO | PubChem = 101534 | ChemSpiderID = 91745 | C = 12 | H = 20 | N = 2 | O = 3 | molecular_weight = 240.299 g/mol | smiles = O=C1NC(=O)NC(=O)C1(C(CC)CCC)CC | StdInChI = 1S/C12H20N2O3/c1-4-7-8(5-2)12(6-3)9(15)13-11(17)14-10(12)16/h8H,4-7H2,1-3H3,(H2,13,14,15,16,17) | StdInChIKey = ZLUNGGZJSQDFPH-UHFFFAOYSA-N | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | pregnancy_category = | legal_status = | routes_of_administration = }}Tetrabarbital (INN; Butysal, Butysedal, Tetramal) is a barbiturate derivative used as a hypnotic.[1][2] See also
References1. ^{{cite book | author1 = C. R Ganellin | author2 = D. J Triggle | author3 = F.. Macdonald | title = Dictionary of pharmacological agents | url = https://books.google.com/books?id=DeX7jgInYFMC&pg=PA842 | accessdate = 28 November 2011 | year = 1997 | publisher = CRC Press | isbn = 978-0-412-46630-4 | page = 842}} {{Hypnotics}}{{GABAAR PAMs}}2. ^{{cite web | url = http://whqlibdoc.who.int/hq/2004/WHO_EDM_QSM_2004.5.pdf | author = World Health Organization | title = The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substance | year = 2004 | format = PDF}} 5 : Barbiturates|Hypnotics|Pyrimidines|Sedatives|GABAA receptor positive allosteric modulators |
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