|AHFS/Drugs.com||International Drug Names|
|ATC code||N05AD07 (WHO)|
|Chemical and physical data|
|Molar mass||381.443 g/mol|
|3D model (Jmol)||Interactive image|
|(what is this?)|
Benperidol is a drug which is a highly potent butyrophenone derivative. It is the most potent neuroleptic on the European market, with chlorpromazine equivalency as high as 75 to 100 (about 150 to 200% potency in terms of dose compared to haloperidol). It is an antipsychotic, which can be used for the treatment of schizophrenia, but it is primarily used to control antisocial hypersexual behaviour, and is sometimes prescribed to sex offenders as a condition of their parole, as an alternative to anti-androgen drugs such as cyproterone acetate.
Benperidol was discovered at Janssen Pharmaceutica in 1961.
- Timiperone has the same structure but thiourea instead of normal urea.
- Pimozide & Oxiperomide & Neflumozide are also made from 4-(1-Benzimidazolinone)piperidine prec.
- Droperidol is self-same albeit with a tetrahydropyridine ring.
- Möller; Müller; Bandelow: Neuroleptika, 2001, WVG; ISBN 3-8047-1773-X (in German)
- Bobon J, Collard J, Lecoq R, Benperidol and promazine: a "double blind" comparative study in mental geriatrics, Acta Neurol Belg. 1963 Oct;63:839-43.
- British National Formulary (49th), British Medical Association 2005 p 183
- Murray MA, Bancroft JH, Anderson DC, Tennent TG, Carr PJ., Endocrine changes in male sexual deviants after treatment with anti-androgens, oestrogens or tranquillizers, Journal of Endocrinology. 1975 Nov;67(2):179-88.
- BE 626307 (1963 to Janssen), C.A. 60, 10690c (1964), corresp. to GB 989755 .
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