Anileridine
From Self-sufficiency
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".]] |
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Physical data | |
Melting point | 83 °C (181 °F) |
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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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