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'Pyran enamine Derivatives' in keywords
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1993 (1)
1Author    Koichi Yoneyama, Yoshihiro Nakajima, Masaru Ogasawara, Hitoshi Kuramochi, Makoto Konnai, Hajime Iwamura, Fumihiko Sato, Katsunori Ichinose, Tadao Asami, Nobutaka Takahashi, Shigeo YoshidaRequires cookie*
 Title    Photosystem II Inhibition by Pyran-enamine Derivatives  
 Abstract    Through the studies on structure-activity relationships o f 5-acyl-3-(l-am inoalkylidene)-4-hydroxy-2 H-pyran-2,6(3 H)-dione derivatives in photosystem II (PS II) inhibition, overall lipophilicity o f the m olecule was found to be a major determinant for the activity. In the sub­ stituted N -benzyl derivatives, not only the lipophilicity but also the electronic and steric char­ acters o f the substituents greatly affected the activity. Their mode o f PS II inhibition seemed to be similar to that o f D C M U , whereas pyran-enamine derivatives needed to be highly lipophilic to block the electron transport in thylakoid membranes, which in turn diminished the permea­ bility through biomembranes. 
  Reference    Z. Naturforsch. 48c, 163 (1993); received November 3 1992 
  Published    1993 
  Keywords    Photosystem II, Electron Transport Inhibition, Pyran-enamine Derivatives 
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 TEI-XML for    default:Reihe_C/48/ZNC-1993-48c-0163.pdf 
 Identifier    ZNC-1993-48c-0163 
 Volume    48