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Estimating One-Electron Reduction Potentials Of Quinones, Steven P. Bradbury, Ovanes G. Mekenyan, V. B. Kamenska
Estimating One-Electron Reduction Potentials Of Quinones, Steven P. Bradbury, Ovanes G. Mekenyan, V. B. Kamenska
Steven P. Bradbury
The one-electron reduction potential ∗ E1 7 of benzo-, naphtho-and anthracenequinones is related to their ability to undergo redox cycling and elicit cytotoxicity through oxidative stress. To evaluate a general approach to estimate the E1 7 of benzo-, naphtho-and anthracenequinones, QSAR approaches based on gas phase and solvation based methods were employed. Stereoelectronic descriptors of ground state quinones, respective intermediates of the redox cycle, and the di erences in parameters for the transition between intermediates were evaluated. The variation of E1 7 was correlated with descriptors of the parent quinones and speci c transition parameters. The energy of the highest …
Sar Models For Futile Metabolism: One-Electron Reduction Of Quinones, Phenols And Nitrobenzenes, Steven P. Bradbury, Ovanes Mekenyan, G. D. Veith, N. Zaharieva
Sar Models For Futile Metabolism: One-Electron Reduction Of Quinones, Phenols And Nitrobenzenes, Steven P. Bradbury, Ovanes Mekenyan, G. D. Veith, N. Zaharieva
Steven P. Bradbury
Benzoquinones, naphthoquinones and aziridinylbenzoquinones, can be reduced by flavoproteins to semiquinones that react with molecular oxygen to form superoxide anion with the subsequent regeneration of the parent compounds. This redox cycling, a form of futile metabolism, produces reactive oxygen species and depletes the reducing equivalents of cells without concomitant energy production. The ability of a toxicant to redox cycle is related to its one-electron reduction potential, and this study attempted to estimate reduction potential from structure using semi-empirical quantum chemical models for a diverse set of chemicals. The results of this study suggest that one-electron reduction potentials, within structural classes …