Anileridine
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Anileridine
Anileridine
Anileridine2DCSD.svg
Clinical data
AHFS/Drugs.comMonograph
Routes of
administration
Tablets, injection
ATC code
Legal status
Legal status
Pharmacokinetic data
Protein binding> 95%
MetabolismHepatic
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC22H28N2O2
Molar mass352.47 g/mol g·mol-1
3D model (JSmol)
Melting point83 °C (181 °F)
 ?N?Y (what is this?)  (verify)

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.[1] 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.[2] Anileridine is in Schedule II of the Controlled Substances Act 1970 of the United States as ACSCN 9020 with a zero aggregate manufacturing quota as of 2014. The free base conversion ratio for salts includes 0.83 for the dihydrochloride and 0.73 for the phosphate [3] It is also under international control per UN treaties.

Administration

As tablets or injection.[4]

Pharmacokinetics

Anileridine usually takes effect within 15 minutes of either oral or intravenous administration, and lasts 2-3 hours.[5] It is mostly metabolized by the liver.

References

  1. ^ U.S. Patent 2,897,204
  2. ^ "Discontinued Prescription Drug Products". Canadian Pharmacists' Association. Archived from the original on 19 September 2008. Retrieved 2008.
  3. ^ http://www.deadiversion.usdoj.gov/fed_regs/quotas/2014/fr0825.htm
  4. ^ "Pharmaceutical Information - LERITINE". RxMed. Retrieved 2010.
  5. ^ "Anileridine Consumer Information". MedicineNet. Retrieved 2008.




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Anileridine
 



 



 
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