Alphenal (Alphenal, Efrodal, Prophenal, Sanudorm), also known as 5-allyl-5-phenylbarbituric acid, is a barbiturate derivative developed in the 1920s.[1] It has primarily anticonvulsant properties, and was used occasionally for the treatment of epilepsy or convulsions, although not as commonly, as better known barbiturates such as phenobarbital.[2][3][4][5]
^Martin JR, Godel T, Hunkeler W, Jenck F, Moreau JL, Sleight AJ, Widmer U (December 2000). "Psychopharmacological Agents". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.1619250313011820.a01. ISBN0471238961.
^Brandenberger H, Maes RA (1997). Analytical Toxicology: For Clinical, Forensic, and Pharmaceutical Chemists. Walter de Gruyter. p. 348. ISBN978-3-11-010731-9. Retrieved 19 May 2012.
^García PC, Cruz SV, Mirón CE (28 January 2005). Fundamentos de síntesis de fármacos. Edicions Universitat Barcelona. p. 161. ISBN978-84-475-2876-9. Retrieved 19 May 2012.
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alphenal, efrodal, prophenal, sanudorm, also, known, allyl, phenylbarbituric, acid, barbiturate, derivative, developed, 1920s, primarily, anticonvulsant, properties, used, occasionally, treatment, epilepsy, convulsions, although, commonly, better, known, barbi. Alphenal Alphenal Efrodal Prophenal Sanudorm also known as 5 allyl 5 phenylbarbituric acid is a barbiturate derivative developed in the 1920s 1 It has primarily anticonvulsant properties and was used occasionally for the treatment of epilepsy or convulsions although not as commonly as better known barbiturates such as phenobarbital 2 3 4 5 AlphenalClinical dataOther names5 Phenyl 5 allylbarbituric acidRoutes ofadministrationOralATC codenoneLegal statusLegal statusCA Schedule IV US Schedule III Rx onlyIdentifiersIUPAC name 5 phenyl 5 prop 2 enyl 1 3 diazinane 2 4 6 trioneCAS Number115 43 5 YPubChem CID8274ChemSpider7975 YUNII7T7L08Q9JICompTox Dashboard EPA DTXSID60150919ECHA InfoCard100 003 718Chemical and physical dataFormulaC 13H 12N 2O 3Molar mass244 250 g mol 13D model JSmol Interactive imageSMILES O C1NC O NC O C1 c2ccccc2 C C CInChI InChI 1S C13H12N2O3 c1 2 8 13 9 6 4 3 5 7 9 10 16 14 12 18 15 11 13 17 h2 7H 1 8H2 H2 14 15 16 17 18 YKey WOIGZSBYKGQJGL UHFFFAOYSA N Y verify LD50 Mouse Oral 280 mg kgReferences edit DE 526854 Verfahren zur Darstellung von C C disubstituierten Barbitursaeuren issued 11 June 1931 assigned to Hoffmann La Roche Carissimi M 1962 Nuovi Barbiturici Alogenati Farmaco Ediozione Scientifica 17 6 390 413 Martin JR Godel T Hunkeler W Jenck F Moreau JL Sleight AJ Widmer U December 2000 Psychopharmacological Agents Kirk Othmer Encyclopedia of Chemical Technology doi 10 1002 0471238961 1619250313011820 a01 ISBN 0471238961 Brandenberger H Maes RA 1997 Analytical Toxicology For Clinical Forensic and Pharmaceutical Chemists Walter de Gruyter p 348 ISBN 978 3 11 010731 9 Retrieved 19 May 2012 Garcia PC Cruz SV Miron CE 28 January 2005 Fundamentos de sintesis de farmacos Edicions Universitat Barcelona p 161 ISBN 978 84 475 2876 9 Retrieved 19 May 2012 nbsp This anticonvulsant related article is a stub You can help Wikipedia by expanding it vte nbsp This sedative related article is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Alphenal amp oldid 1202781235, wikipedia, wiki, book, books, library,
