Lofexidine
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| Image:Lofexidine structure.png | |
| Lofexidine
| |
| Systematic (IUPAC) name | |
| 2-[1-(2,6-dichlorophenoxy)ethyl]-4,5-dihydro-1H-imidazole | |
| Identifiers | |
| CAS number | ? |
| ATC code | N07 |
| PubChem | ? |
| Chemical data | |
| Formula | C11H12Cl2N2O |
| Mol. mass | 259.131 g/mol |
| Pharmacokinetic data | |
| Bioavailability | >90% |
| Protein binding | 80–90% |
| Metabolism | Hepatic glucuronidation |
| Half life | 11 hours |
| Excretion | Renal |
| Therapeutic considerations | |
| Pregnancy cat. |
? |
| Legal status | |
| Routes | Oral |
Lofexidine is an alpha2-adrenergic receptor agonist, can be used as a short acting (short half life) anti-hypertensive, but mostly used to help with relief from symptoms of heroin or opiate withdrawal in opiate dependency. Used primarily in the United Kingdom [1]. See also clonidine.
Drugs used in addictive disorders (N07B) | |
|---|---|
| Nicotine dependence/ (Nicotinic agonist) | Nicotine - Bupropion - Dianicline - Varenicline - Lobeline - Mecamylamine - Clonidine - Surinabant |
| Alcohol dependence | Disulfiram - Calcium carbimide - Acamprosate - Naltrexone - Nalmefene - Topiramate - Clonidine - Buprenorphine - Morphine |
| Opioid dependence | Buprenorphine - Methadone - Levacetylmethadol - Fentanyl - Dihydrocodeine - Dihydroetorphine - Clonidine - Lofexidine - Naltrexone - Ibogaine - 18-Methoxycoronaridine - Extended Release Morphine - Extended Release Hydromorphone |
| Stimulant dependence | Dexamphetamine - Bupropion - Vanoxerine - Nocaine - Vigabatrin |
| Benzodiazepine dependence | Clonidine - Diazepam - Phenytoin - Phenobarbital |
| Cocaine dependence | Bupropion - Vanoxerine - Nocaine - Baclofen - Vigabatrin |
| Sedative-Hypnotic dependence | Phenobarbital - Diazepam - Lorazepam - Clonidine - Chloral Hydrate |

