Literature DB >> 858946

Phenothiazine phototoxicity: an experimental study on chlorpromazine and its metabolites.

B Ljunggren, H Möller.   

Abstract

Chlorpromazine (CPZ) metabolites were studied for their phototoxic potency with the mouse tail technique. The demethylated metabolites were more phototoxic potency with the mouse tail technique. The demethylated metabolites were more phototoxic than CPZ, while CPZ-sulfoxide, 7-hydroxy-CPZ, and 2-chlorphenothiazine were less phototoxic. The phototoxicity of CPZ and desmethyl-CPZ preexposed to UVA was lost, while that of CPZ-sulfoxide was retained. By thin-layer chromatography, CPZ-sulfoxide and promazine were identified as photoproducts of CPZ; the sulfoxide was fairly stable to radiation.

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Year:  1977        PMID: 858946     DOI: 10.1111/1523-1747.ep12494582

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  4 in total

1.  Photodegradation of 2-chloro substituted phenothiazines in alcohols.

Authors:  Carmelo García; Luis Piñero; Rolando Oyola; Rafael Arce
Journal:  Photochem Photobiol       Date:  2008-07-30       Impact factor: 3.421

2.  Photodynamic potentialities of some phenothiazine derivatives.

Authors:  M Saucin; A Van de Vorst
Journal:  Radiat Environ Biophys       Date:  1980-02       Impact factor: 1.925

3.  Photomutagenesis by chlorinated phenothiazine tranquilizers.

Authors:  J G Jose
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

4.  Solvent dependence of the photophysical properties of 2-chlorothioxanthone, the principal photoproduct of chlorprothixene.

Authors:  Luis E Piñero Santiago; Carmelo García; Virginie Lhiaubet-Vallet; Miguel A Miranda; Rolando Oyola
Journal:  Photochem Photobiol       Date:  2011-03-08       Impact factor: 3.421

  4 in total

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