Heptobarbital

Chemical compound
  • None
Legal statusLegal status Identifiers
  • 5-methyl-5-phenylpyrimidine-2,4,6(1H,3H,5H)-trione
CAS Number
  • 76-94-8
PubChem CID
  • 66160
ChemSpider
  • 59547
UNII
  • GFR227X6YY
CompTox Dashboard (EPA)
  • DTXSID00226900 Edit this at Wikidata
ECHA InfoCard100.000.905 Edit this at WikidataChemical and physical dataFormulaC11H10N2O3Molar mass218.212 g·mol−13D model (JSmol)
  • Interactive image
  • O=C1NC(=O)NC(=O)C1(c2ccccc2)C
InChI
  • InChI=1S/C11H10N2O3/c1-11(7-5-3-2-4-6-7)8(14)12-10(16)13-9(11)15/h2-6H,1H3,(H2,12,13,14,15,16)
  • Key:LSAOZCAKUIANSQ-UHFFFAOYSA-N

Heptobarbital (Rutonal), also known as phenylmethylbarbituric acid is a barbiturate derivative.[1][2][3] It has often been confused with methylphenobarbital because both drugs contain a methylphenyl moiety and are overall very similar in structure.

See also

  • Barbiturate

References

  1. ^ Martin JR, Godel T, Hunkeler W, Jenck F, Moreau JL, Sleight AJ, Widmer U (11 January 2001). Kirk-Othmer Encyclopedia of Chemical Technology, 4th Edition. Vol. 5. Wiley Interscience. doi:10.1002/0471238961.1619250313011820.a01. ISBN 978-0-471-41961-7. {{cite book}}: |journal= ignored (help)
  2. ^ Hvorost A (2010). "Phenylmethylbarbituric Acid". Analysis of Drugs and Poisons. Archived from the original on 7 April 2012. Retrieved 28 November 2011.
  3. ^ Sinnema YA (January 1967). "The identification and determination of barbiturates in serum". Zeitschrift für klinische Chemie und klinische Biochemie. 5 (1): 21–5. doi:10.1515/cclm.1967.5.1.21. PMID 5594996. S2CID 15422152.
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GABAA receptor positive modulators
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See also: Receptor/signaling modulators • GABA receptor modulators • GABA metabolism/transport modulators