The preparation of some new spiro-substituted 4-hydroxypyranoquinolinones and their corresponding dihydropyrano cis-diols is described. The free radical scavenging activity of the compounds was determined by means of their interaction with the stable free radical 1,1-diphenyl-2-picrylhydrazyl (DPPH) and the superoxide anions generated by the enzymic xanthine-xanthine oxidase system. The spiroadamatylpyranoquinolinone analogue proved to be the most efficient free radical scavenger. © 2009 Pharmaceutical Society of Japan.
CITATION STYLE
Panteleon, V., Kostakis, I. K., Marakos, P., Pouli, N., & Andreadou, I. (2009). Synthesis of some new spiropyranoquinolines and evaluation of their free radical scavenging activity. Chemical and Pharmaceutical Bulletin, 57(5), 446–452. https://doi.org/10.1248/cpb.57.446
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