3.6
[]. A B Skorniakova, et al. [Chemical toxicological analysis of haloperidol metabolite 4-(4-chlorophenyl)-4-hydroxypipiridine in urine by high-performance liquid chromatography]. Sud Med Ekspert. 009 Jan-Feb;5():45-8.
[]. Ilse Weuts, et al. Salt formation in solid dispersions consisting of polyacrylic acid as a carrier and three basic model compounds resulting in very high glass transition temperatures and constant dissolution properties upon storage. Eur J Pharm Sci. 005 Jul-Aug;5(4-5):387-93.
[3]. J Fang, et al. Determination of 4-(4-chlorophenyl)-4-hydroxypiperidine, a metabolite of haloperidol, by gas chromatography with electron-capture detection. J Chromatogr B Biomed Appl. 996 Jul ;68():83-8.
[4]. José M Entrena, et al. Antagonism by haloperidol and its metabolites of mechanical hypersensitivity induced by intraplantar capsaicin in mice: role of sigma- receptors. Psychopharmacology (Berl). 009 Jul;05():-33.
[5]. L P Pan, et al. In-vitro characterization of the cytochrome P450 isoenzymes involved in the back oxidation and N-dealkylation of reduced haloperidol. Pharmacogenetics. 998 Oct;8(5):383-9.
H30-H35-H37-H38-H4
P6-P64-P70-P7-P73-P80-P30+P35-P330-P36+P364-P50