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. 2019 Sep 16;15:2170–2183. doi: 10.3762/bjoc.15.214

Table 1.

Sirt1–3 inhibition for compounds 2a–h, 4a/4b and 8a.

Compound Sirt1 inhibitiona Sirt2 inhibitiona Sirt3 inhibitiona

2a 27% @ 50 µM 24.6 ± 2.8 µMb 41.7 ± 2.0 µMb
2b 71% @ 10 µM 8.7 ± 0.2 µMb 89% @ 50 µM
2c 51% @ 100 µM 6.6 ± 0.5 µMb 7.5 ± 0.9 µMb
2d 51% @ 10 µM 64% @ 10 µM 90% @ 50 µM
2e 61% @ 50 µM 69% @ 50 µM 60% @ 50 µM
2f 26% @ 10 µM 21% @ 10 µM 79% @ 50 µM
2g 52% @ 50 µM 62% @ 50 µM 87% @ 50 µM
2h n.i. 9% @ 10 µM n.i.
4a n.i. 48% @ 10 µM 38% @ 10 µM
4b n.i. 45% @ 10 µM 38% @ 10 µM
8a n.i. n.i. n.i.

aPercent inhibition relative to controls at the indicated concentration, n.i. = no inhibition detected. bIC50 values (μM) with statistical limits; values are the mean ± SD of duplicate experiments.