Crane, F. L. published the artcileStimulation of photosynthesis by carbonyl compounds and chelators, Application In Synthesis of 1139-46-4, the publication is Biochemical and Biophysical Research Communications (1977), 74(4), 1362-8, database is CAplus and MEDLINE.
A number of carbonyl compounds including HCO3-, ethylene carbonate, dimethyl carbonate, propylene carbonate, bis(pentamethylene)urea, and glycidol, and several chelators were tested for their effect on photosynthetic reactions in isolated spinach chloroplasts. Carbonyl compounds inhibited the DCMU-insensitive silicomolybdate reduction by photosystem II but stimulated the O evolution associated with ferricyanide reduction in the presence of DBMIB and the H2O â?methylviologen reaction. Many chelators behaved in the same manner except 1,10-phenanthroline which showed the opposite effect. The carbonyl compounds did not uncouple because they stimulated the proton gradients associated with noncyclic photophosphorylation, whereas some chelators, such as bathocuproine or bathophenanthroline inhibited the proton gradients 100%. Electron transport in the presence of ADP and inorganic phosphate showed a stimulation of rates beyond that obtained in presence of an uncoupler. The data are discussed in terms of inhibition of cyclic electron flow around photosystem II which leads to increased electron transport rates toward photosystem I.
Biochemical and Biophysical Research Communications published new progress about 1139-46-4. 1139-46-4 belongs to alcohols-buliding-blocks, auxiliary class Benzene,Phenol, name is 4-(2,4,4-Trimethylpentan-2-yl)benzene-1,2-diol, and the molecular formula is C14H22O2, Application In Synthesis of 1139-46-4.
Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts