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. 2012 Jul;40(7):1328–1335. doi: 10.1124/dmd.111.044263

TABLE 5.

Effect of potential inhibitors on [3H]GlySar uptake in P. pastoris cells expressing different mammalian species of Pept1 gene

Data are expressed as means ± S.E. (n = 3). The results were vector-subtracted and are shown as a percentage of control (buffer).

Inhibitory Compound Yeast Transformant
pPIC3.5K-hPept1 pPIC3.5K-mPept1 pPIC3.5K-rPept1
Control 100 ± 28 100 ± 7 100 ± 10
Glycine 130 ± 17 104 ± 6 91.5 ± 6.4
l-Histidine 122 ± 13 103 ± 6 113 ± 8
GlyPro 3.9 ± 1.7* 1.9 ± 1.0* 0.6 ± 0.3*
Cefadroxil 6.4 ± 13.7* 16.7 ± 1.7* 23.1 ± 1.2*
Cephradine 23.2 ± 5.4* 9.8 ± 0.7* 23.4 ± 1.8*
Cefazolin 81.1 ± 2.6 87.4 ± 0.7 93.7 ± 6.3
Cephalothin 84.8 ± 3.3 85.0 ± 4.6 119 ± 1
Cephapirin 100 ± 14 83.7 ± 6.3 122 ± 5
Acyclovir 114 ± 8 99.8 ± 5.6 109 ± 10
Valacyclovir 3.5 ± 3.3* 4.5 ± 1.1* 5.5 ± 0.5*
SITS 127 ± 12 86.1 ± 3.6 107 ± 10
TEA 113 ± 9 83.7 ± 2.0 94.8 ± 5.4
Elacridar 100 ± 6 89.3 ± 3.6 119 ± 3
*

p ≤ 0.001 compared with control. GlySar was studied at 5.0 μM and the potential inhibitors at 10 mM.