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. Author manuscript; available in PMC: 2009 Aug 1.
Published in final edited form as: Chem Res Toxicol. 2008 Jul 26;21(8):1503–1508. doi: 10.1021/tx800133d

Table 1.

Monochlorophenols and dichlorophenols as substrates for hSULT2A1.

Molecule Structure Sulfation at 10 µM (nmol/min/mg) Sulfation at 50 µM (nmol/min/mg) Relative activity (%)a
2-Chlorophenol graphic file with name nihms58763t1.jpg 0 0.2 ± 0.1 0.3
3-Chlorophenol graphic file with name nihms58763t2.jpg 0 1.4 ± 0.7 2.3
4-Chlorophenol graphic file with name nihms58763t3.jpg 0 1.6 ± 0.5 3.8
2,3-Dichlorophenol graphic file with name nihms58763t4.jpg 0.6 ± 0.2 4.2 ± 0.5 9.8
2,4-Dichlorophenol graphic file with name nihms58763t5.jpg 1.1 ± 0.3 2.7 ± 0.3 5.4
2,5-Dichlorophenol graphic file with name nihms58763t6.jpg 1.7 ± 0.1 6.9 ± 0.2 13.3
2,6-Dichlorophenol graphic file with name nihms58763t7.jpg 0.3 ± 0 2.5 ± 0.5 5.8
3,4-Dichlorophenol graphic file with name nihms58763t8.jpg 0.3 ± 0.2 2.9 ± 0.2 6.9
3,5-Dichlorophenol graphic file with name nihms58763t9.jpg 2.3 ± 0.4 7.2 ± 0.2 17.1
a

Relative activity is expressed as a percentage based on the ratio of the rate of sulfation of the chlorinated phenol at 50 µM to the rate of sulfation of 50 µM DHEA under the same assay conditions.