Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

2,3 -Diaryl-1 -naphthols,from

Oxygenation by SLO-1 is inhibited by various additives. Some of the reasons are (1) the reduction of active iron from the ferric form to the ferrous form, e,g, by N-alkylhydroxylamine [268], phenyldiazene [269], 2-benzyl-1-naphthol [270], diaryl-N-hydroxyurea [271] (2) oxidation of residues, e.g, methionine residues, by hexanal phenylhydrozone [272] (3) coordination to the active site, e.g. catechol [273], cysteine [274], hydroperoxy acids [275], chelating reagents [276], and Pt complex [277] (4) reaction with the active site, e.g. 12-iodo-ci5-9-octadecenoic acid [278]. In addition, it is reported that leukotriene A4, the electrophilic product of 5-lipoxygenases, irreversibly inactivates the enzyme [279]. [Pg.73]


See other pages where 2,3 -Diaryl-1 -naphthols,from is mentioned: [Pg.310]    [Pg.907]    [Pg.793]    [Pg.155]    [Pg.47]    [Pg.36]    [Pg.50]    [Pg.500]    [Pg.122]    [Pg.276]    [Pg.32]    [Pg.220]   


SEARCH



From naphthols

© 2024 chempedia.info