Pecar S, Schara M, Müller K, Wiegrebe W
Department of Pharmacy, Faculty of Natural Sciences and Technology, University of Ljubljana, Republic of Slovenia.
Free Radic Biol Med. 1995 Mar;18(3):459-65. doi: 10.1016/0891-5849(94)00162-d.
In DMSO solution, anthralin and its C-10 monosubstituted derivatives reduce nitroxides to the corresponding hydroxylamine derivatives, which are not further transformed. The reaction rate depends on the solvent used, the nitroxide, and the structure of the reducer. It is faster in DMSO than in DMF, piperidine type of nitroxides are reduced faster than the pyrrolidine type, and the substitution on C-10 of anthralin has a significant influence on the reaction rate. Anthralin derivatives without protons at C-10 are not able to reduce nitroxides.
在二甲基亚砜(DMSO)溶液中,蒽林及其C-10单取代衍生物可将氮氧化物还原为相应的羟胺衍生物,且这些羟胺衍生物不会进一步转化。反应速率取决于所用溶剂、氮氧化物以及还原剂的结构。在DMSO中反应速率比在N,N-二甲基甲酰胺(DMF)中更快,哌啶型氮氧化物比吡咯烷型还原得更快,蒽林C-10位的取代对反应速率有显著影响。C-10位没有质子的蒽林衍生物无法还原氮氧化物。