Anileridine
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Revision as of 03:40, 28 August 2010 by حسن علي البط (Talk) (Adding category Category:Ethyl esters (using HotCat))
| File:Anileridine.svg | |
| Systematic (IUPAC) name | |
|---|---|
|
ethyl 1-[2-(4-aminophenyl)ethyl]-4-phenylpiperidine-4-carboxylate | |
| Clinical data | |
| Routes of administration | Tablets, injection |
| Legal status | |
| Legal status |
|
| Pharmacokinetic data | |
| Protein binding | > 95% |
| Metabolism | Hepatic |
| Identifiers | |
| CAS Number | 144-14-9 |
| ATC code | N01AH05 (WHO) |
| PubChem | CID 8944 |
| DrugBank | APRD00741 |
| ChemSpider | 8600 |
| Chemical data | |
| Formula | C22H28N2O2 |
| Molar mass | 352.47 g/mol[[Script error: No such module "String".]] |
| Script error: No such module "collapsible list". | |
| Physical data | |
| Melting point | 83 °C (181 °F) |
| (verify) | |
Anileridine (trade name: Leritine) is a new synthetic analgesic drug and is a member of the piperidine class of analgesic agents It differs from meperidine (Demerol) in that the N-methyl group of meperidine is replaced by an N-aminophenethyl group, which increase its analgesic activity.
Anileridine is no longer manufactured in the US or Canada.[1]
Administration
Pharmacokinetics
Anileridine usually takes effect within 15 minutes of either oral or intravenous administration, and lasts 2–3 hours.[3] It is mostly metabolized by the liver.
References
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| 35px | This drug article relating to the nervous system is a stub. You can help ssf by expanding it. |
- ↑ "Discontinued Prescription Drug Products". Canadian Pharmacists' Association. Retrieved 28 July 2008.
- ↑ "Pharmaceutical Information - LERITINE". RxMed. Retrieved 16 June 2010.
- ↑ "Anileridine Consumer Information". MedicineNet. Retrieved 28 July 2008.
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