Skip to main content
. 2019 Dec 27;10(8):1492–1510. doi: 10.1016/j.apsb.2019.12.013

Table 3.

Pharmacokinetic properties of ent-4g in ratsa.

i.v. (rat, 7.5 mg/kg)
p.o. (rat, 15 mg/kg)
CL
(L·kg/h)
t1/2
(h)
AUC0–t
(μg/h·L)
Vss
(L/kg)
Tmax
(h)
Cmax
(μg/L)
AUC0–t
(μg/h·L)
F
1.21 1.85 21,092.4 7.36 4.03 5897.5 12,463.8 29.5%
a

Male SD rats (6–8 weeks old, 3 animals per group) were used for pharmacokinetics study.