Anileridine
Clinical data | |
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AHFS/Drugs.com | Monograph |
Routes of administration | Tablets, injection |
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Pharmacokinetic data | |
Protein binding | > 95% |
Metabolism | Hepatic |
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E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C22H28N2O2 |
Molar mass | 352.47 g/mol |
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Melting point | 83 °C (181.4 °F) |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Anileridine (trade name: Leritine) is a synthetic analgesic drug and is a member of the piperidine class of analgesic agents developed by Merck & Co. in the 1950s. It differs from pethidine (meperidine) in that the N-methyl group of meperidine is replaced by an N-aminophenethyl group, which increases 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
- ↑ "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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- Piperidines
- Synthetic opioids
- Mu-opioid agonists
- Analgesics