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1 Medical uses  





2 Adverse effects  





3 Synthesis  





4 References  





5 External links  














Periciazine






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From Wikipedia, the free encyclopedia
 

(Redirected from Pericyazine)

Periciazine
Clinical data
Pregnancy
category
  • AU:C
  • Routes of
    administration
    Oral
    Drug classTypical antipsychotic
    ATC code
    Legal status
    Legal status
    • AU: S4 (Prescription only)
  • BR: Class C1 (Other controlled substances)[1]
  • CA: ℞-only
  • UK: POM (Prescription only)
  • In general: ℞ (Prescription only)
  • Pharmacokinetic data
    MetabolismHepatic (mostly via conjugation)[2]
    Elimination half-life12 h[2]
    ExcretionRenal[2]
    Identifiers
    • 10-[3-(4-hydroxypiperidin-1-yl)propyl]-10H-phenothiazine-2-carbonitrile

    CAS Number
    PubChem CID
    DrugBank
    ChemSpider
    UNII
    KEGG
    ChEBI
    ChEMBL
    CompTox Dashboard (EPA)
    ECHA InfoCard100.018.248 Edit this at Wikidata
    Chemical and physical data
    FormulaC21H23N3OS
    Molar mass365.50 g·mol−1
    3D model (JSmol)
    • C1CN(CCC1O)CCCN2C3=CC=CC=C3SC4=C2C=C(C=C4)C#N

    • InChI=1S/C21H23N3OS/c22-15-16-6-7-21-19(14-16)24(18-4-1-2-5-20(18)26-21)11-3-10-23-12-8-17(25)9-13-23/h1-2,4-7,14,17,25H,3,8-13H2 ☒N

    • Key:LUALIOATIOESLM-UHFFFAOYSA-N ☒N

     ☒NcheckY (what is this?)  (verify)

    Periciazine (INN), also known as pericyazine (BAN) or propericiazine, is a drug that belongs to the phenothiazine class of typical antipsychotics.

    Periciazine is not approved for sale in the United States. It is commonly sold in Canada, Italy and Russia under the tradename Neuleptil and in United Kingdom and Australia under the tradename Neulactil.[3]

    Medical uses[edit]

    The primary uses of periciazine include in the short-term treatment of severe anxiety or tension and in the maintenance treatment of psychotic disorders such as schizophrenia. There is insufficient evidence to determine whether periciazine is more or less effective than other antipsychotics.[2] A 2014 systematic review compared periciazine with typical antipsychotics for schizophrenia:

    Periciazine versus typical antipsychotic for schizophrenia[4]
    Summary
    On the basis of very low quality evidence it is not possible to determine the effects of periciazine in comparison with antipsychotics such as chlorpromazineortrifluoperazine for the treatment of schizophrenia. There is some evidence, however, that periciazine may be associated with a higher incidence of extrapyramidal side effects than other antipsychotics.[4]

    Periciazine has also been studied in the treatment of opioid dependence.[5]

    Adverse effects[edit]

    Periciazine is a rather sedating and anticholinergic antipsychotic, and despite being classed with the typical antipsychotics, its risk of extrapyramidal side effects is comparatively low.[6] It has a relatively high risk of causing hyperprolactinaemia and a moderate risk of causing weight gain and orthostatic hypotension.[6]

    Synthesis[edit]

    Thieme Patent (Ex V):[7]

    The final step in the synthesis involves the alkylation of 3-(2-cyanophenothiazin-10-yl)propyl 4-methylbenzenesulfonate, CID:134990672 (1) with 4-Piperidinol [5382-16-1] (2) giving Periciazine (3).

    References[edit]

    1. ^ Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-16.
  • ^ a b c d "NEULACTIL PRODUCT INFORMATION" (PDF). TGA eBusiness Services. sanofi-aventis australia pty ltd. 13 September 2011. Retrieved 2 November 2013.
  • ^ Pericyazine. The Royal Pharmaceutical Society of Great Britain. 23 September 2011. Retrieved 2 November 2013. {{cite book}}: |work= ignored (help)
  • ^ a b Matar HE, Almerie MQ, Makhoul S, Xia J, Humphreys P (May 2014). "Pericyazine for schizophrenia". The Cochrane Database of Systematic Reviews. 2014 (5): CD007479. doi:10.1002/14651858.CD007479.pub2. PMC 11023599. PMID 24825770.
  • ^ Sivolap IuP, Savchenkov VA (1999). "[The use of neuroleptics in treating opiate dependence]". Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova (in Russian). 99 (6): 29–34. PMID 10441864.
  • ^ a b "Approximate relative frequency (not intensity) of common adverse effects of antipsychotics (Table 8.21) [NB1]". eTherapeutic Guidelines complete. Therapeutic Guidelines Limited. February 2013. Retrieved 2 November 2013.[permanent dead link]
  • ^ FR1212031 idem Robert Jacques Georges, Jacob Robert Michel, U.S. patent 3,075,976 (1963 to Rhone Poulenc Sa).
  • External links[edit]


    Retrieved from "https://en.wikipedia.org/w/index.php?title=Periciazine&oldid=1230317850"

    Categories: 
    Typical antipsychotics
    Phenothiazines
    4-Hydroxypiperidines
    Conjugated nitriles
    Hidden categories: 
    CS1 Brazilian Portuguese-language sources (pt-br)
    CS1 errors: periodical ignored
    CS1 Russian-language sources (ru)
    All articles with dead external links
    Articles with dead external links from March 2018
    Articles with permanently dead external links
    Articles with short description
    Short description is different from Wikidata
    Drugs with non-standard legal status
    Articles with changed DrugBank identifier
    Articles with changed ChemSpider identifier
    Articles with changed EBI identifier
    ECHA InfoCard ID from Wikidata
    Articles with changed InChI identifier
    Drugboxes which contain changes to verified fields
     



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