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. Author manuscript; available in PMC: 2010 Mar 16.
Published in final edited form as: Chem Biol Interact. 2008 Nov 5;178(1-3):16–23. doi: 10.1016/j.cbi.2008.10.037

Fig. 1.

Fig. 1

Hammett plots of the quantitative structure-activity relationship for oxidation of p-substituted benzyl alcohols by SceADH2. The data are from Table 6, where V1/Et (●) and V1/Kb (■) are plotted against the σ+ values for CH3O-, CH3- CH(CH3)2- H-, Cl-, Br-CF3-, from left to right. The lines were calculated by linear regression, but the slopes were not significantly determined: for log (V1/Et) slope is (0.19 ± 0.25)σ+, and for log (V1/Kb) slope is (0.06 ± 0.36)σ +.