Alpidem
From Wikipedia, the free encyclopedia
Alpidem
|
|
Systematic (IUPAC) name | |
2-[3-chloro-8-(4-chlorophenyl)-1,7-diazabicyclo[4.3.0] nona-2,4,6,8-tetraen-9-yl]-N,N-dipropyl-acetamide |
|
Identifiers | |
CAS number | |
ATC code | ? |
PubChem | |
Chemical data | |
Formula | C21H23Cl2N3O |
Mol. mass | 404.332 g/mol |
Pharmacokinetic data | |
Bioavailability | ? |
Metabolism | ? |
Half life | ? |
Excretion | Renal |
Therapeutic considerations | |
Pregnancy cat. |
? |
Legal status | |
Routes | Oral |
Alpidem (marketed under the brand name Ananxyl®) is a prescription drug used for the treatment of moderate to severe anxiety. Alpidem, a fairly new drug, is not in wide use. In pure form, it is only available generically, but is an additional substance in a few prescription anxiolytic drugs. Alpidem acts selectively on the omega 1 (BZ1) receptor subtype, a benzodiazepine receptor. However, it is not considered of the benzodiazepine class, but is rather an imidazopyridine. Alpidem is a close relative of zolpidem, but does not possess zolpidem's sedative property.
[edit] Indications
Alpidem is generally prescribed to patients with moderate to severe anxiety. Most of these patients have exhibited either sensitivity or resistance to benzodiazepine therapy, and therefore switched to a non-benzodiazepine medication. Alpidem does not produce significant, if any, sedative or hypnotic action. Alpidem is also used as an anticonvulsant at much higher doses.[citation needed]
[edit] See also
[edit] References and notes
- Zivkovic B, Morel E, Joly D, Perrault G, Sanger DJ, Lloyd KG.. "Pharmacological and behavioral profile of alpidem as an anxiolytic." Synthelabo Recherche, L.E.R.S., Bagneux, France. 1990 May;23 Suppl 3:108-13. PMID 1974069
- Sanger DJ, Zivkovic B.. "Discriminative stimulus effects of alpidem, a new imidazopyridine anxiolytic." Synthelabo Recherche, Bagneux, France. 1994 Jan;113(3-4):395-403. PMID 7862851