词条 | Butallylonal |
释义 |
| Watchedfields = changed | verifiedrevid = 414038144 | IUPAC_name = 5-sec-Butyl-5-(beta-bromoallyl)barbituric acid | image = Butallylonal structure.svg | width = 155 | tradename = | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_AU = | legal_CA = Schedule IV | legal_UK = | legal_US = | legal_status = | routes_of_administration = | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 1142-70-7 | ATC_prefix = none | ATC_suffix = | PubChem = 14362 | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 13723 | ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL = 469253 | C=11 | H=15 | Br=1 | N=2 | O=3 | molecular_weight = 303.15 g/mol | smiles = O=C1NC(=O)NC(=O)C1(C(C)CC)CC(\\Br)=C | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C11H15BrN2O3/c1-4-6(2)11(5-7(3)12)8(15)13-10(17)14-9(11)16/h6H,3-5H2,1-2H3,(H2,13,14,15,16,17) | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = FWZMBTIUIQUJFF-UHFFFAOYSA-N }} Butallylonal is a barbiturate derivative invented in the 1920s.[1] It has sedative properties, and was used primarily as an anaesthetic in veterinary medicine.[2] Butallylonal is considered similar in effects to pentobarbital but is longer in action, being considered an intermediate-acting barbiturate rather than short-acting. References1. ^{{cite patent|country=US|number=1739662}} {{GABAAR PAMs}}{{sedative-stub}}2. ^{{cite journal | doi = 10.1007/BF01907782 | vauthors = Mittmann U, Schmidt HD, Schmier J, Wirth RH | title = Hemorrhagic shock with fixed hypotension and with spontaneous recovery of blood pressure. A comparison of two shock models | journal = Basic Research in Cardiology | year = 1976 | volume = 71 | issue = 1 | pages = 47–59 | pmid = 1259685}} 4 : Barbiturates|Organobromides|Alkene derivatives|GABAA receptor positive allosteric modulators |
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