198348-39-9Relevant academic research and scientific papers
2-(3-halogen-4-hydroxyphenyl)-1,4-naphthoquinones from their 2-(3,5-di- tert-butyl-4-hydroxyphenyl) congeners, potent 5-lipoxygenase inhibitors 1,4- Naphthoquinones, XXVII
Wurm,Schwandt
, p. 487 - 490 (2007/10/03)
A new simple and fast method for the synthesis of halogenated hydroxyphenyl naphthoquinones as potential 5-lipoxygenase (LOX) inhibitors is presented. While the aryl naphthoquinone 1, a potent 5-LOX inhibitor, with AlCl3 is debutylated to 2a and 2b, the oxidized cyclohexadienylidene derivative 3 reacts comparably by concomitant halogenation to 4a and with AlBr3 to 4b, respectively. As products of a side reaction of 6 with TiCl4 and BBr3 the tetracyclic benzo[b]naphthol[2,1-d]furan derivatives 8a and 8b are isolated. Selected compounds are investigated for 5-lipoxygenase inhibiting and antioxidative properties. There is a clear-cut correlation of both qualities in those compounds with a 3-OH function and with two, one or without any tert-butyl group at the phenyl moiety. In contrast the quinone 6 (3-Cl) and the dibenzofuran 8 a are powerful 5-LOX inhibitors with only low antioxidative activity.
1,4-Naphthoquinones, XXVI: Phenyl-1,4-naphthoquinone derivatives with the hydroxylation patterns of bioflavonoids
Wurm,Gurka
, p. 739 - 743 (2007/10/03)
Flavonoids with special hydroxylation patterns are inhibitors of cylooxygenase and lipoxygenases of the arachidonic acid cascade. To get metabolically more stable compounds with higher lipophilicity and with a similar molecular topography 2-phenyl-1,4-nap
