The interactions of the antifouling compound TCMS (2,3,5,6-tetrachloro-4-methylsulphonyl pyridine) with rat liver mitochondria have been investigated. The results indicate that the compound inhibits ATP synthesis. Further investigations regarding the ATP syn- thesis mechanism suggest that TCMS inhibits succinic dehydrogenase of the mitochondrial respiratory chain. As the respiratory chain is similar in all living organisms, it can be concluded that the toxic effect of TCMS most likely depend on the different bioavailability of the compound and on the different importance of mitochondria in the ATP production in the animal species
The hepatic conjugation of xenobiotics with sulfate, glucuronic acid, and glutathione is decreased I...
AbstractThe assumption that reversible inhibition of mitochondrial respiration by nitric oxide (NO⋅)...
Trialkyl tin compounds have been shown to be potent inhibitors of oxidative phosphorylation, oligomy...
The interactions of the antifouling compound TCMS (2,3,5,6-tetrachloro-4-methylsulphonyl pyridine) w...
The interactions of the antifouling compound TCMS (2,3,5,6-tetrachloro-4-methylsulphonyl pyridine) w...
The interactions of the antifouling compound Sea-Ninetwith rat liver mitochondria have been studied....
The interactions of Co2+ with mitochondria have been investigated. The results indicate that Co2+ in...
The interactions of the tributyl, triethyl and trimethyllead compounds with energized mitochondria h...
The mechanism of DCCD inhibition of ATP synthetase, and the components of the mitochondrial membrane...
AbstractThis paper describes the problems of measuring the allosteric ATP-inhibition of cytochrome c...
AbstractThe present study reveals that the previously described effect of ATP-synthetase inhibition ...
The interactions of five dibenzofurans with the mitochondria from rat liver have been investigated. ...
We recently reported that mitochondria-targeted derivatives of resveratrol are cytotoxic in vitro, s...
Effect of ATP and substrates on 2,4-dinitrophenol-induced adenosine triphcsphatase (E. C. 3.6. 1. 4....
AbstractWe recently reported that mitochondria-targeted derivatives of resveratrol are cytotoxic in ...
The hepatic conjugation of xenobiotics with sulfate, glucuronic acid, and glutathione is decreased I...
AbstractThe assumption that reversible inhibition of mitochondrial respiration by nitric oxide (NO⋅)...
Trialkyl tin compounds have been shown to be potent inhibitors of oxidative phosphorylation, oligomy...
The interactions of the antifouling compound TCMS (2,3,5,6-tetrachloro-4-methylsulphonyl pyridine) w...
The interactions of the antifouling compound TCMS (2,3,5,6-tetrachloro-4-methylsulphonyl pyridine) w...
The interactions of the antifouling compound Sea-Ninetwith rat liver mitochondria have been studied....
The interactions of Co2+ with mitochondria have been investigated. The results indicate that Co2+ in...
The interactions of the tributyl, triethyl and trimethyllead compounds with energized mitochondria h...
The mechanism of DCCD inhibition of ATP synthetase, and the components of the mitochondrial membrane...
AbstractThis paper describes the problems of measuring the allosteric ATP-inhibition of cytochrome c...
AbstractThe present study reveals that the previously described effect of ATP-synthetase inhibition ...
The interactions of five dibenzofurans with the mitochondria from rat liver have been investigated. ...
We recently reported that mitochondria-targeted derivatives of resveratrol are cytotoxic in vitro, s...
Effect of ATP and substrates on 2,4-dinitrophenol-induced adenosine triphcsphatase (E. C. 3.6. 1. 4....
AbstractWe recently reported that mitochondria-targeted derivatives of resveratrol are cytotoxic in ...
The hepatic conjugation of xenobiotics with sulfate, glucuronic acid, and glutathione is decreased I...
AbstractThe assumption that reversible inhibition of mitochondrial respiration by nitric oxide (NO⋅)...
Trialkyl tin compounds have been shown to be potent inhibitors of oxidative phosphorylation, oligomy...