Table 2

The in vitro inhibition of specific [3H]KMD-3213 binding in rat prostate by KMD-3213, tamsulosin, prazosin, and terazosin

DrugsnHKi
pM
KMD-32131.14  ± 0.11213  ± 37
Tamsulosin1.01  ± 0.1126.3  ± 5.8
Prazosin0.92  ± 0.08116  ± 3
Terazosin0.87  ± 0.111620  ± 300

The in vitro inhibition by KMD-3213, tamsulosin, prazosin, and terazosin of specific [3H]KMD-3213 (0.15 nM) binding in homogenates of rat prostate was measured and thenH and Ki values were estimated. Each value represents mean ± S.E. of three rats.