Cyclopentobarbital: Difference between revisions
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| verifiedrevid = 399738699 |
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| IUPAC_name = 5-(1-cyclopent-2-enyl)-5-prop-2-enyl-1,3-<br>diazinane-2,4,6-trione |
| IUPAC_name = 5-(1-cyclopent-2-enyl)-5-prop-2-enyl-1,3-<br>diazinane-2,4,6-trione |
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| image = Cyclopal.svg |
| image = Cyclopal.svg |
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| PubChem = 6454 |
| PubChem = 6454 |
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Revision as of 18:28, 10 September 2011
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| Clinical data | |
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| Other names | Allylpental, Cyclopental, Dormisan, 5-Allyl-5-Δ2-Cyclopentenyl Barbituric Acid |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.000.891 |
| Chemical and physical data | |
| Formula | C12H14N2O3 |
| Molar mass | 234.251 g/mol g·mol−1 |
| 3D model (JSmol) | |
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Cyclopal (Dormisan) is a barbiturate derivative invented in the 1940s. It has sedative and anticonvulsant properties, and was used primarily as an anaesthetic in veterinary medicine.[1] Cyclopal is considered similar in effects to phenobarbital but lasts almost three times as long, and is considered a long-acting barbiturate with a fairly slow onset of action.
References
- ^ Vander Brook MJ, Cartland GF. A Pharmacologic Study of 5-Allyl-5-Cyclopentenyl Barbituric Acid (Cyclopal). Journal of Pharmacology And Experimental Therapeutics, 1944, 80(2): 119-125
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