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Hexobarbital or hexobarbitone, sold both in acid and sodium salt forms as Citopan, Evipan, and Tobinal, is a barbiturate derivative having hypnotic and sedative effects. It was used in the 1940s and 1950s as an agent for inducing anesthesia for surgery, as well as a rapid-acting, short-lasting hypnotic for general use, and has a relatively fast onset of…
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effects used barbiturates metabolism 3hhb hypnotic sodium cytochrome enantiomer reaction also via 3ohb use man research anesthesia effect chloride p450
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Hexobarbital | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Hexobarbital | ATC code | N01AF02 (WHO) N05CA16 (WHO) | 1.00 | infobox |
| Hexobarbital | Boiling point | 378.73 °C (713.71 °F) | 1.00 | infobox |
| Hexobarbital | CAS Number | 56-29-1 Y 50-09-9 (sodium salt) | 1.00 | infobox |
| Hexobarbital | ChEBI | CHEBI:5706 Y | 1.00 | infobox |
| Hexobarbital | ChEMBL | ChEMBL7728 Y | 1.00 | infobox |
| Hexobarbital | ChemSpider | 3482 Y | 1.00 | infobox |
| Hexobarbital | Chirality | Racemic mixture | 1.00 | infobox |
| Hexobarbital | CompTox Dashboard (EPA) | DTXSID9023122 | 1.00 | infobox |
| Hexobarbital | Density | 1.1623 g/cm3 | 1.00 | infobox |
| Hexobarbital | DrugBank | DB01355 Y | 1.00 | infobox |
| Hexobarbital | ECHA InfoCard | 100.000.241 | 1.00 | infobox |
| Hexobarbital | Formula | C12H16N2O3 | 1.00 | infobox |
| Hexobarbital | KEGG | D01071 Y | 1.00 | infobox |
| Hexobarbital | Legal status | CA: Schedule IV | 1.00 | infobox |
| Hexobarbital | Legal status | US: Schedule III | 1.00 | infobox |
| Hexobarbital | Melting point | 146.5 °C (295.7 °F) | 1.00 | infobox |
| Hexobarbital | Molar mass | 236.271 g·mol−1 | 1.00 | infobox |
| Hexobarbital | Protein binding | 25% | 1.00 | infobox |
| Hexobarbital | PubChem CID | 3608 | 1.00 | infobox |
| Hexobarbital | Solubility in water | 0.435 mg/mL (20 °C) | 1.00 | infobox |
| Hexobarbital | Trade names | Hexobarbital, Hexobarbitone, Methylhexabital, Methexenyl, Evipal | 1.00 | infobox |
| Hexobarbital | UNII | AL8Z8K3P6S | 1.00 | infobox |
| Hexobarbital | causes | the chloride ion channel opening to their longest open state of 9 milli seconds | 0.90 | text |
| Hexobarbital | causes | an CNS-depressant effect on the brain by inhibiting the glutamate release and potentiating the GABA-effect.MetabolismThe hepatic metabolism of hexobarbital | 0.90 | text |
| Hexobarbital | causes | an CNS-depressant effect on the brain by inhibiting the glutamate release and potentiating the GABA-effect | 0.90 | text |
| Hexobarbital | is a | substrate | 0.90 | text |
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