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. Author manuscript; available in PMC: 2011 Feb 1.
Published in final edited form as: Bioorg Med Chem. 2010 Jan 15;18(4):1441–1448. doi: 10.1016/j.bmc.2010.01.019

Table 1.

Rates of mitochondrial biotransformation of ω-(phenoxy)alkanoic acids, 3-(phenoxy)acrylic acids, and ω-(1-methyl-1H-imidazol-2-ylthio)alkanoic acidsa

Compound Rate
1a 2.06 ± 0.50
1b 0.39 ± 0.12
1c 0.07 ± 0.02
1d 0.10 ± 0.06
2a 1.27 ± 0.37
2b 0.39 ± 0.12
2c 0.06 ± 0.01
2d 0.01 ± 0.06
3 1.54 ± 0.17
4a 2.50 ± 0.31
4b 0.97 ± 0.16
5 0.54 ± 0.06
6a 1.55 ± 0.14
6b N.D.
Octanoic acid 40.3 ± 6.7
a

The alkanoic acids (Fig. 2) were incubated with rat liver mitochondria, and product formation was quantified, as described in Section 5. Rates are expressed as nmol min−1 mg protein−1. Data are shown as mean ± SD, n = ≥ 3. Statistical analysis (unpaired t-test): 1a versus 2a, p <.05; 1b versus 2b, NS; 1c versus 2c, NS; 1d versus 2d, p <.05; 1a versus 3, p <.05; 2a versus 3, p >.05; 1c versus 5, p <.05; 1c versus 6a, p <0.05; 2c versus 5, p <.05; 1a versus 6a, p <.05. N.D., not detected.