Structure‐activity relationship studies of dibromo phenolic derivatives as photosynthetic electron chain inhibitors
- 1 August 1986
- journal article
- research article
- Published by Wiley in Pesticide Science
- Vol. 17 (4) , 396-402
- https://doi.org/10.1002/ps.2780170410
Abstract
A number of 2,6‐dibromophenols with different substituents in the 4‐position have been synthesised and their effect on the whole electron transport chain and on photosystem II have been determined. A study was made to relate the chemical characteristics of the 4‐substituent group and the inhibition of the uncoupled electron transport of isolated chloroplasts from spinach plants. The chemical nature of the 4‐substituent group varies greatly in the active compounds and it is therefore suggested that this group does not participate in the inhibitor‐receptor interaction. The results indicated that the inhibiting power of these compounds increased with the electron‐attracting capacity of the 4‐substituent group, decreased with increase in its size and that there was no correlation with its hydrophobic nature.This publication has 22 references indexed in Scilit:
- Evidence for two different herbicide-binding proteins at the reducing side of Photosystem IIBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1982
- Photoaffinity labelling of the photosystem II herbicide binding proteinFEBS Letters, 1980
- Charge accumulation at the reducing side of system 2 of photosynthesisBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1974
- The action of indophenols and nitrophenols on the deactivation reactions in the water-splitting system of photosynthesisBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1973
- Requirement of an acidic proton in substances which act as accelerators of the deactivation reactions in the water‐splitting enzyme system of photosynthesisFEBS Letters, 1972
- The action of 2-anilinothiophenes as accelerators of the deactivation reactions in the watersplitting enzyme system of photosynthesisBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1972
- The number of sites sensitive to 3-(3,4-dichlorophenyl)-1,1-dimethylurea, 3-(4-chlorophenyl)-1,1-dimethylurea and 2-chloro-4-(2-propylamino)-6-ethylamino-s-triazine in isolated chloroplastsBiochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis, 1965
- A New Substituent Constant, π, Derived from Partition CoefficientsJournal of the American Chemical Society, 1964
- Preparation of EthylenethioketalsJournal of the American Chemical Society, 1954
- Ueber die NitrosophenoleEuropean Journal of Inorganic Chemistry, 1884