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| synonyms = 5,5-Diallylbarbituric acid, Allobarbital
| synonyms = 5,5-Diallylbarbituric acid, Allobarbital
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'''Allobarbital''', also known as '''allobarbitone''' and branded as '''Cibalgine''' or '''Dial-Ciba''' (in combination with [[ethyl carbamate]]), is a [[barbiturate]] derivative invented in 1912 by Ernst Preiswerk and Ernst Grether working for [[Ciba Specialty Chemicals|CIBA]]. It was used primarily as an [[anticonvulsant]]<ref>{{cite journal|last1=Chocholova L. |last2=Radil-Weiss |first2=T. |title=Effect of allobarbital on focal epilepsy in rats |journal=Physiologia Bohemoslovaca |year=1971 |volume=20 |issue=4 |pages=325-34}}</ref> although it has now largely been replaced by newer drugs with improved safety profiles. Other uses for allobarbital included as an adjutant to boost the activity of [[analgesic]] drugs, and use in the treatment of [[insomnia]] and [[anxiety]].
'''Allobarbital''', also known as '''allobarbitone''' and branded as '''Cibalgine''' or '''Dial-Ciba''' (in combination with [[ethyl carbamate]]), is a [[barbiturate]] derivative invented in 1912 by Ernst Preiswerk and Ernst Grether working for [[Ciba Specialty Chemicals|CIBA]]. It was used primarily as an [[anticonvulsant]]<ref>{{cite journal|last1=Chocholova L. |last2=Radil-Weiss |first2=T. |title=Effect of allobarbital on focal epilepsy in rats |journal=Physiologia Bohemoslovaca |year=1971 |volume=20 |issue=4 |pages=325–34|pmid=4335127 }}</ref> although it has now largely been replaced by newer drugs with improved safety profiles. Other uses for allobarbital included as an adjutant to boost the activity of [[analgesic]] drugs, and use in the treatment of [[insomnia]] and [[anxiety]].


Allobarbital was never particularly widely used compared to better known barbiturates such as [[phenobarbital]] and [[secobarbital]], although it saw more use in some European countries such as [[Bulgaria]] and [[Slovakia]],<ref>{{cite journal|last1=Getova |first1=D. |last2=Georgiev |first2=V. |title=GABA-ergic mechanisms in the anticonvulsive activity of newly synthesized barbiturates. I. Effects of barbiturates on the convulsive action of GABA-antagonists. |journal=Acta Physiologica et Pharmacologica Bulgarica |year=1987 |volume=13 |issue=3 |pages=43-50}}</ref> and is still used in for example Poland, but only as compound.<ref>{{Citation
Allobarbital was never particularly widely used compared to better known barbiturates such as [[phenobarbital]] and [[secobarbital]], although it saw more use in some European countries such as [[Bulgaria]] and [[Slovakia]],<ref>{{cite journal|last1=Getova |first1=D. |last2=Georgiev |first2=V. |title=GABA-ergic mechanisms in the anticonvulsive activity of newly synthesized barbiturates. I. Effects of barbiturates on the convulsive action of GABA-antagonists |journal=Acta Physiologica et Pharmacologica Bulgarica |year=1987 |volume=13 |issue=3 |pages=43–50|pmid=3439474 }}</ref> and is still used in for example Poland, but only as compound.<ref>{{Cite web|last= |first= |year= |title=APTECZKA BABUNI - KROPLE ŻOŁĄDKOWE KROPLE 20 G |publisher= |publication-place= |language=Polish |url=http://www.domzdrowia.pl/29439,apteczka-babuni-krople-zoladkowe-krople-20-g.html |archiveurl=https://web.archive.org/web/20071031195035/http://www.domzdrowia.pl/29439,apteczka-babuni-krople-zoladkowe-krople-20-g.html |archivedate=October 31, 2007 |accessdate=March 10, 2013|postscript= <!-- Bot inserted parameter. Either remove it; or change its value to "." for the cite to end in a ".", as necessary. -->&#123;&#123;inconsistent citations&#125;&#125;}}</ref>
|last= |first= |year= |title=APTECZKA BABUNI - KROPLE ŻOŁĄDKOWE KROPLE 20 G |publisher= |publication-place= |language=Polish |url=http://www.domzdrowia.pl/29439,apteczka-babuni-krople-zoladkowe-krople-20-g.html |archiveurl=https://web.archive.org/web/20071031195035/http://www.domzdrowia.pl/29439,apteczka-babuni-krople-zoladkowe-krople-20-g.html |archivedate=October 31, 2007 |accessdate=March 10, 2013}}</ref>


==References==
==References==

Revision as of 02:29, 8 February 2014

Allobarbital
Clinical data
Other names5,5-Diallylbarbituric acid, Allobarbital
ATC code
Legal status
Legal status
Identifiers
  • 5,5-diprop-2-enyl-1,3-diazinane-2,4,6-trione
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.000.129 Edit this at Wikidata
Chemical and physical data
FormulaC10H12N2O3
Molar mass208.214 g/mol g·mol−1
3D model (JSmol)
  • O=C1NC(=O)NC(=O)C1(C\C=C)C\C=C
  • InChI=1S/C10H12N2O3/c1-3-5-10(6-4-2)7(13)11-9(15)12-8(10)14/h3-4H,1-2,5-6H2,(H2,11,12,13,14,15) checkY
  • Key:FDQGNLOWMMVRQL-UHFFFAOYSA-N checkY
  (verify)

Allobarbital, also known as allobarbitone and branded as Cibalgine or Dial-Ciba (in combination with ethyl carbamate), is a barbiturate derivative invented in 1912 by Ernst Preiswerk and Ernst Grether working for CIBA. It was used primarily as an anticonvulsant[1] although it has now largely been replaced by newer drugs with improved safety profiles. Other uses for allobarbital included as an adjutant to boost the activity of analgesic drugs, and use in the treatment of insomnia and anxiety.

Allobarbital was never particularly widely used compared to better known barbiturates such as phenobarbital and secobarbital, although it saw more use in some European countries such as Bulgaria and Slovakia,[2] and is still used in for example Poland, but only as compound.[3]

References

  1. ^ Chocholova L.; Radil-Weiss, T. (1971). "Effect of allobarbital on focal epilepsy in rats". Physiologia Bohemoslovaca. 20 (4): 325–34. PMID 4335127.
  2. ^ Getova, D.; Georgiev, V. (1987). "GABA-ergic mechanisms in the anticonvulsive activity of newly synthesized barbiturates. I. Effects of barbiturates on the convulsive action of GABA-antagonists". Acta Physiologica et Pharmacologica Bulgarica. 13 (3): 43–50. PMID 3439474.
  3. ^ "APTECZKA BABUNI - KROPLE ŻOŁĄDKOWE KROPLE 20 G" (in Polish). Archived from the original on October 31, 2007. Retrieved March 10, 2013{{inconsistent citations}}{{cite web}}: CS1 maint: postscript (link)
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