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. 2015 Dec 8;5:17778. doi: 10.1038/srep17778

Table 1. Remaining activities (%) of UGTs inhibited by 100 μM TKIs.

  Lapatinib Vandetanib Imatinib Axitinib Pos. Ctrl.
UGT1A1 30.8 ± 11.0 48.9 ± 4.9 34.1 ± 0.5 56.7 ± 3.4 37.0 ± 2.1
UGT1A3 96.5 ± 7.5 104.1 ± 2.1 88.8 ± 5.1 47.8 ± 12.8 39.4 ± 6.8
UGT1A4a 40.7 ± 1.9 62.8 ± 0.0 59.1 ± 3.0 14.9 ± 1.8 20.3 ± 6.6
UGT1A6 88.4 ± 5.9 55.1 ± 1.1 67.9 ± 7.1 85.8 ± 3.5 28.2 ± 10.0
UGT1A7 37.7 ± 9.3 22.7 ± 2.7 8.5 ± 3.1 25.0 ± 2.5 25.6 ± 11.2
UGT1A8 73.5 ± 10.6 56.0 ± 6.3 33.1 ± 9.0 54.6 ± 2.4 40.2 ± 5.3
UGT1A9 51.1 ± 7.9 14.1 ± 4.7 49.2 ± 1.9 44.8 ± 0.2 15.2 ± 1.2
UGT1A10 73.6 ± 4.8 49.0 ± 0.4 15.3 ± 9.5 55.5 ± 2.7 37.8 ± 8.0
UGT2B4 105.1 ± 0.2 80.8 ± 6.6 71.0 ± 3.2 42.1 ± 1.6 NDb
UGT2B7 90.5 ± 1.0 49.8 ± 3.7 29.8 ± 5.6 55.9 ± 9.7 16.4 ± 11.9
UBT2B15 109.5 ± 3.1 79.2 ± 1.4 28.3 ± 3.3 49.3 ± 5.2 21.6 ± 11.9
UBT2B17 94.8 ± 5.7 69.7 ± 3.1 14.7 ± 8.2 55.9 ± 0.3 ND

aTFP was used as a substrate, and for all other UGTs, 4-MU was used as substrate.

bno positive inhibitor available.