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. Author manuscript; available in PMC: 2017 Jul 14.
Published in final edited form as: J Med Chem. 2016 Jul 1;59(13):6531–6546. doi: 10.1021/acs.jmedchem.6b00760

Table 5.

In vivo pharmacokinetic parameters of 32 and 33 in rats following IV administration of 5 mg/kg. Data is shown as mean and range between animals.

AUC (h*μ mol/L) CL (mL/hr/kg) Vss (L/kg) T1/2 (hr)
32 167 (160–175) 77 (73–80) 0.91(0.89–0.93) 9.6 (9.5–9.7)
33 45 (31–59) 310 (216–412) 5.8 (4.1–7.5) 13 (12.6–13.4)