The 4-pyrone and 4-pyridone series were examined as a new type of photosynthetic inhibitor because of a structural resemblance to the co-enzyme plastoquinone, which lies between photosystem II and cytochrome b. These compounds inhibited a Hill reaction at "the plastoquinone pool." From our study of the structure/activity relationships for 4-pyrones and 4-pyridones, it has become clear that these compounds need no strict structural resemblance to the plastoquinone. It is also demonstrated that the brominated 4-pyridone series has remarkably higher inhibitory activities than those of its non brominated analogues.
References (10)
Related articles (0)
Figures (0)
Content from these authors
Supplementary material (0)
Result List ()
Cited by
This article cannot obtain the latest cited-by information.