Methohexital
From Wikipedia, the free encyclopedia
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Methohexital
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| Systematic (IUPAC) name | |
| 5-hex-3-yn-2-yl-1- methyl-5-prop-2-enyl-1, 3-diazinane-2,4,6-trione | |
| Identifiers | |
| CAS number | |
| ATC code | N01 N05CA15 |
| PubChem | |
| DrugBank | |
| Chemical data | |
| Formula | C14H18N2O3 |
| Mol. mass | 262.304 |
| Pharmacokinetic data | |
| Bioavailability | I.V. ~100% Rectal ~17% |
| Metabolism | Hepatic |
| Half life | 5.6 ± 2.7 minutes |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
B (USA) |
| Legal status |
? |
| Routes | Intravenous, rectal |
Methohexital (marketed under the brand name Brevital) is a drug which is a barbiturate derivative.[citation needed] It is classified as short-acting, and has a rapid onset of action. It is similar in its effects to sodium thiopental, a drug with which it competed in the market for anaesthetics.
[edit] Pharmacology
Methohexital binds to a distinct site which is associated with Cl− ionophores at GABAA receptors.[citation needed] This increases the length of time which the Cl− ionopores are open, thus causing an inhibitory effect.
Metabolism of methohexital is primarily hepatic (i.e., taking place in the liver) via demethylation and oxidation.[citation needed] Side-chain oxidation is the primary means of metabolism involved in the termination of the drug's biological activity.
Protein binding is approximately 73% for methohexital.[citation needed]
[edit] Indications
Methohexital is primarily used to induce anesthesia, and is generally provided as a sodium salt (i.e. methohexital sodium). It is only used in hospital or ambulatory care (i.e. in an ambulance) settings, under strict supervision.[citation needed] It has been commonly used to induce deep sedation, "twilight sleep" or general anesthesia for oral surgery and dentistry. It is also used to induce anesthesia prior to ECT(electroconvulsive therapy).
[edit] External links
- RxList.com - Methohexital
- Drugs.com - Methohexital Sodium
- DrugLib.com - Brevital (Methohexital Sodium)
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