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. 2025 Aug 22;11(34):eadx2434. doi: 10.1126/sciadv.adx2434

Fig. 3. BAY-3827 and BAY-974 kinetics.

Fig. 3.

(A to C) Inhibition of AMPK complexes in cell-free assays by BAY-3827 in high (200 μM) and low (20 μM) ATP concentrations and by (D) BAY-974 at 200 μM ATP. Data are n = 3 represented as means ± SEM. (E) IC50 values (nM) of BAY-3827 inhibition of AMPK complexes in different ATP conditions. (F and G) HTRF assays in U2OS cells measuring phosphorylation (%) of Ser79-ACC1 following BAY-3827 or BAY-974 treatment and phosphorylation (%) of (H and I) Thr172-AMPKα in the presence or absence of AMPK activator MK-8722 (10 μM). (J) Estimated IC50 and EC50 values (μM) shown, respectively, from (F) to (I). Data are means ± SEM with n = 3 technical replicates from three independent experiments.