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. Author manuscript; available in PMC: 2019 Jan 1.
Published in final edited form as: Eur J Med Chem. 2017 Oct 19;143:1448–1456. doi: 10.1016/j.ejmech.2017.10.048

Table 3.

Pre-clinical in vivo PK for compound 27 after 25 mg/kg oral dose was administered to a rat.

Cmax (ng/mL) tmax (h) AUClast ((h)*(ng/mL)) thalf (h) %F

27 6222.1 1.7 83173.60 2.04 42.5
1aa ND ND ND ND 0%
a

Plasma concentrations of 1a were under the lowest detectable limit, so all PK parameters after 25 mg/kg oral dose could not be calculated