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. Author manuscript; available in PMC: 2013 Nov 29.
Published in final edited form as: Chem Res Toxicol. 2010 Jun 21;23(6):10.1021/tx900367p. doi: 10.1021/tx900367p

Table 1.

Thalidomide hydroxylation catalyzed by human or monkey liver microsomes, recombinant human or monkey P450s expressed in E. coli membranes, and purified human P450s in reconstituted systems.

product

enzyme source P450 (R)-thalidomide (S)-thalidomide


5-hydroxythalidomide 5’-hydroxythalidomide 5-hydroxythalidomide 5’-hydroxythalidomide
pmol formed min−1 (mg protein)−1
human liver microsomes 0.08 0.59 0.03 < 0.01
monkey liver microsomes 0.21 2.28 0.07 0.18
pmol min−1 (nmol P450)−1
E. coli membranes 3A4 2.0 < 0.1 < 0.1 < 0.1
  human 3A5 2.3 < 0.1 < 0.1 < 0.1
3A7 2.8 < 0.1 < 0.1 < 0.1
  monkey 3A8 12 < 0.1 3.4 < 0.1
3A5 9.2 < 0.1 2.9 < 0.1
reconstituted system 2C19 2.4 1.7 1.1 < 0.1
  human 3A4 2.0 < 0.1 0.9 < 0.1
3A5 2.5 < 0.1 0.7 < 0.1

Thalidomide (1000 µM) was incubated with liver microsomes (1.0 mg protein mL−1) or P450 2C19, 3A4, 3A5, 3A7, and 3A8 (100 nM P450) at 37 °C for 60 min. Results are presented as means of results of duplicate determination.