نتایج جستجو برای: quinol oxidation inhibitor

تعداد نتایج: 325143  

Journal: :American journal of physiology. Regulatory, integrative and comparative physiology 1999
Mark I Friedman Ruth B Harris Hong Ji Israel Ramirez Michael G Tordoff

Inhibition of fatty acid oxidation stimulates feeding behavior in rats. To determine whether a decrease in hepatic fatty acid oxidation triggers this behavioral response, we compared the effects of different doses of methyl palmoxirate (MP), an inhibitor of fatty acid oxidation, on food intake with those on in vivo and in vitro liver and muscle metabolism. Administration of 1 mg/kg MP selective...

2012
Amy Capes Stephen Patterson Susan Wyllie Irene Hallyburton Iain T. Collie Andrew J. McCarroll Malcolm F.G. Stevens Julie A. Frearson Paul G. Wyatt Alan H. Fairlamb Ian H. Gilbert

Quinols have been developed as a class of potential anti-cancer compounds. They are thought to act as double Michael acceptors, forming two covalent bonds to their target protein(s). Quinols have also been shown to have activity against the parasite Trypanosoma brucei, the causative organism of human African trypanosomiasis, but they demonstrated little selectivity over mammalian MRC5 cells in ...

Journal: :Biochemistry 2001
G M Soriano W A Cramer

Plastoquinol oxidation and proton transfer by the cytochrome b(6) f complex on the lumen side of the chloroplast thylakoid membrane are mediated by high and low potential electron transport chains. The rate constant for reduction, k(bred), of cytochrome b(6) in the low potential chain at ambient pH 7.5-8 was twice that, k(fred), of cytochrome f in the high potential chain, as previously reporte...

Journal: :Anesthesiology 2000
A L Dawidowicz E Fornal M Mardarowicz A Fijalkowska

BACKGROUND The metabolism of propofol is very rapid, and its transformation takes place mainly in the liver. There are reports indicating extrahepatic metabolism of the drug, and the alimentary canal, kidneys, and lungs are mentioned as the most probable places where the process occurs. The aim of this study was to determine whether the human lungs really take part in the process of propofol bi...

Journal: :Biochemistry 2000
V P Shinkarev N B Ugulava A R Crofts C A Wraight

N,N'-dicyclohexylcarbodiimide (DCCD) has been reported to inhibit proton translocation by cytochrome bc(1) and b(6)f complexes without significantly altering the rate of electron transport, a process referred to as decoupling. To understand the possible role of DCCD in inhibiting the protonogenic reactions of cytochrome bc(1) complex, we investigated the effect of DCCD modification on flash-ind...

2016
Jessica Jones-Carson Maroof Husain Lin Liu David J. Orlicky Andrés Vázquez-Torres

In the course of an infection, Salmonella enterica occupies diverse anatomical sites with various concentrations of oxygen (O2) and nitric oxide (NO). These diatomic gases compete for binding to catalytic metal groups of quinol oxidases. Enterobacteriaceae express two evolutionarily distinct classes of quinol oxidases that differ in affinity for O2 and NO as well as stoichiometry of H+ transloc...

Journal: :British Journal of Pharmacology 2008
M E Callister L Pinhu M C Catley A D Westwell R Newton S K Leaver G J Quinlan T W Evans M J Griffiths A Burke-Gaffney

BACKGROUND AND PURPOSE Subtle changes in the intracellular reduction-oxidation (redox) state can modulate nuclear factor-kappaB (NF-kappaB) activity. Thioredoxin-1 (Trx) is a small, ubiquitous, redox-active thiol (-SH) protein that, with thioredoxin reductase-1 (TrxR), modifies the redox status of NF-kappaB pathway components. PMX464 is a novel thiol-reactive quinol thought to inhibit the Trx/T...

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