Ethyl loflazepate
File:Ethyl loflazepate.svg | |
File:EtLoflazepate3d.png | |
Systematic (IUPAC) name | |
---|---|
ethyl- 9-chloro- 6-(2-fluorophenyl)- 3-oxo- 2,5-diazabicyclo [5.4.0]undeca- 5,8,10,12- tetraene- 4-carboxylate | |
Clinical data | |
Pregnancy category |
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Routes of administration | Oral |
Legal status | |
Legal status |
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Pharmacokinetic data | |
Bioavailability | ? |
Metabolism | Hepatic |
Biological half-life | ? |
Excretion | Renal |
Identifiers | |
CAS Number | 28911-01-5 |
ATC code | N05BA18 (WHO) |
PubChem | CID 3299 |
DrugBank | ? |
Chemical data | |
Formula | C18H14ClFN2O3 |
Molar mass | 360.7[[Script error: No such module "String".]] |
Ethyl loflazepate (marketed under the brand names Meilax, Ronlax and Victan)[1][2][3] is a drug which is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties.[4] In animal studies it was found to have low toxicity, although in rats evidence of pulmonary phospholipidosis occurred with pulmonary foam cells developing with long-term use of very high doses.[5] Its elimination half life is 51 hours - 103 hours.[6] It's mechanism of action is similar to other benzodiazepines. Ethyl loflazepate also produces an active metabolite which is stronger than the parent compound.[7] Ethyl loflazepate was designed to be a prodrug for descarboxyloflazepate, it's active metabolite. It is the active metabolite which is responsible for most of the pharmacological effects rather than ethyl loflazepate.[8] The main metabolites of ethyl loflazepate are descarbethoxyloflazepate, loflazepate and 3-hydroxydescarbethoxyloflazepate.[9] Accumulation of the active metabolites of ethyl loflazepate are not affected by those with renal failure or impairment.[10] The symptoms of an overdose of ethyl loflazepate include sleepiness, agitation and ataxia. Hypotonia may also occur in severe cases. These symptoms occur much more frequently and severely in children.[11] Death from therapeutic maintenance doses of ethyl loflazepate taken for 2 – 3 weeks has been reported in 3 elderly patients. The cause of death was asphyxia due to benzodiazepine toxicity.[12] High doses of the antidepressant fluvoxamine may potentiate the adverse effects of ethyl loflazepate.[13]
Ethyl loflazeplate is commercialized in Mexico, although is not very used, under the trade name Victan. It's officially approved for the following conditions:[14][15]
- Anxiety
- Post-trauma anxiety
- Anxiety associated with severe neuropathic pain.
- Generalized anxiety disorder (GAD)
- Anxiety "crisis"
- Delirium tremens
See also
References
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External links
- (Japanese) Meilax Fine Granules
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ Ba, BB; Iliadis, A; Cano, JP (1989). "Pharmacokinetic modeling of ethyl loflazepate (Victan) and its main active metabolites". Annals of biomedical engineering. 17 (6): 633–46. doi:10.1007/BF02367467. ISSN 0090-6964. PMID 2574017.
- ↑ "Benzodiazepine Names". non-benzodiazepines.org.uk. Retrieved 2009-04-05.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ Chambon, JP; Perio, A; Demarne, H; Hallot, A; Dantzer, R; Roncucci, R; Bizière, K (1985). "Ethyl loflazepate: a prodrug from the benzodiazepine series designed to dissociate anxiolytic and sedative activities". Arzneimittel-Forschung. 35 (10): 1573–7. ISSN 0004-4172. PMID 2866771.
- ↑ Davi, H; Guyonnet, J; Sales, Y; Cautreels, W (1985). "Metabolism of ethyl loflazepate in the rat, the dog, the baboon and in man". Arzneimittel-Forschung. 35 (7): 1061–5. ISSN 0004-4172. PMID 2864933.
- ↑ Ba, BB; Iliadis, A; Durand, A; Berger, Y; Necciari, J; Cano, JP (1989). "Effect of renal failure on the pharmacokinetics of ethyl loflazepate (Victan) in man". Fundamental & clinical pharmacology. 3 (1): 11–7. doi:10.1111/j.1472-8206.1989.tb00025.x. ISSN 0767-3981. PMID 2714728.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ "Victan". saludzac.gob.mx/. Retrieved 2009-12-25.
- ↑ "VICTAN". Farmacia Guerra. Retrieved 2009-12-25.
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- Benzodiazepines
- Hypnotics
- Ethyl esters
- Carboxylate esters
- Organochlorides
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