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. 2017 May 19;313(2):H381–H391. doi: 10.1152/ajpheart.00772.2016

Table 1.

Blood and plasma pharmacokinetic parameters in male mice after intravenous and oral administration of GBT1118

10 mg/kg iv GBT1118
100 mg/kg po GBT1118
T½, h AUC(0-∞), μg·h·ml−1 Vss, l/kg CL, ml·min−1·kg−1 Blood-to-plasma ratio Tmax, h Cmax, μg/ml AUC(0-∞), μg·h·ml−1 F, % Blood-to-plasma ratio
Blood 13.9 2,929 0.07 0.06 51.4 2 318 13,428 45.8 34.1
Plasma 11.3 60 2.95 3.21 8 12 224 33.5

Blood samples were collected at maximum concentration in plasma (Cmax) after a single intravenous (10 mg/kg) or oral (100 mg/kg) dose of GBT1118. T1/2, terminal half-life; AUC, area under the curve; Vss, volume of distribution; CL, clearance; Tmax, time to reach Cmax; F, bioavailability.