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. Author manuscript; available in PMC: 2016 Jun 5.
Published in final edited form as: Chem Biol Interact. 2015 Jan 29;234:85–95. doi: 10.1016/j.cbi.2014.12.040

Fig. 3.

Fig. 3

Elimination of secondary alcohols. In each sub-figure, the concentration of alcohol is represented by filled circle (●), its corresponding ketone by a filled square (■), and the results when another rat was given 1 mmole/kg of 4-methylpyrazole are represented by the open symbols, alcohol (○) and ketone (□). (A) 2-propanol, 10 mmole/kg; (B) 2-propanol-d7, 15 mmole/kg; (C) 2-butanol (racemic mixture of isomers), 10 mmole/kg; (D) 3-pentanol, 5 mmole/kg; (E) cyclopentanol, 5 mmole/kg; (F) cyclohexanol, 5 mmole.kg. The lines represent the fitted values from simultaneous non-linear least squares fits of data for alcohol and ketone for the uninhibited (or inhibited) state to the differential equations for the first order, sequential reactions.