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- W1990214627 abstract "Electrostatic potential maps for benzo[a]pyrene, chrysene, 5-methylchrysene, and 12-methyl-benz[a]anthracene are presented and compared. These maps permit an interpretation of the fact that chrysene, a weak carcinogen, becomes as potent as benzo[a]pyrene upon substitution of a methyl group at position 5. It is speculated that a key factor in hydrocarbon carcinogenicity may be the presence of two regions of significant negative potential on opposite sides of the molecule, suitably located with respect to each other." @default.
- W1990214627 created "2016-06-24" @default.
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- W1990214627 date "2009-06-18" @default.
- W1990214627 modified "2023-09-25" @default.
- W1990214627 title "A comparative analysis of the electrostatic potentials of some polycyclic aromatic hydrocarbons" @default.
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- W1990214627 doi "https://doi.org/10.1002/qua.560120731" @default.
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