Table 7.

Pharmacokinetics of G1 in rats following intravenous and oral administration (n = 3).

Parameter	G1 (n = 3)	G1 (n = 3)
	iv (10 mg / kg)	po (50 mg / kg)
Tmax(h)	0.03	0.25
Cmax(nM)	3.77	2.92
t1/2(h)	5.72	5.55
CL(L / h / kg)	0.29	1.70
VZ(L / kg)	2.39	13.12
AUC(0–8) (nM∙h)	6.13	6.39
AUC(0−∞) (nM∙h)	11.47	10.15
F (%)		20.85