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. Author manuscript; available in PMC: 2019 Oct 11.
Published in final edited form as: J Med Chem. 2019 Mar 27;62(7):3753–3772. doi: 10.1021/acs.jmedchem.9b00351

Figure 3.

Figure 3

Mouse pharmacokinetic profile of compound 40 in the plasma and brain. Compound 40 was injected into the peritoneum at 50 mg/kg, and concentrations were quantitatively assessed at 0.5, 1, 2, and 4 h after administration. Experiments were carried out in biological triplicates. Data points represent the mean concentrations ± SEM.