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. Author manuscript; available in PMC: 2015 Nov 4.
Published in final edited form as: Xenobiotica. 2008 Jul;38(0):656–675. doi: 10.1080/00498250802109207

Table IV.

Experimentally determined Ki value {Ki (Exp)} and enantioselectivity determined using the CMAC(hOCT1) column, where the stereoselectivity factor (α) is defined as the ratio of the Ki of the compound with the experimentally determined lowest affinity for the hOCT1 divided by the Ki of the compound with the highest experimentally determined affinity.

Compound Ki (Exp) (µM) α
(R)-verapamil 0.05
(S)-verapamil 3.46 69.2
(S)-atenolol 0.46
(R)-atenolol 0.98 2.13
(S)-propranolol 2.85
(R)-propranolol 0.95 3.04
(1R,2R)-pseudoephedrine 1.12
(1S,2S)-pseudoephedrine 1.71 1.53
Quinidine 6.33
Quinine 10.18 1.61
(S,S)-fenoterol 3.73
(R,R)-fenoterol 12.6 3.38
(S,R)-fenoterol 6.18
(R,S)-fenoterol 13.2 2.14
(S)-isoproterenol 180
(R)-isoproterenol 120 1.5
(R)-disopyramide 15.0
(S)-disopyramide 30.0 2

Note: For experimental details, see Moaddel et al. (2007b).