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. Author manuscript; available in PMC: 2008 Aug 6.
Published in final edited form as: Anesth Analg. 2008 Aug;107(2):525–533. doi: 10.1213/ane.0b013e31817b4469

Table 1.

IC50 and IC90 values for competitive antagonism of human nAChRs by various neuromuscular blocking agents. Macroscopic currents were activated by 300 μM ACh, −50 mV. CE50 values are estimates of the clinical concentrations of the antagonists that decrease muscle tension by 50% based on pharmacokinetic/pharmacodynamic modeling (32,33). They are not corrected for the free fraction of drug after accounting for protein binding which ranges from 0.31 for vecuronium to 0.63 for atracurium (33).

Antagonist IC50 (nM) nH IC90 (nM) CE50 (nM) CE50/IC90
(+)-tubocurarine 24 ± 2 1.03 ± 0.07 286 ± 70 606 − 982 1.3 − 2.1
metocurine 18 ± 2 1.04 ± 0.11 149 ± 32
pancuronium 6.3 ± 0.8 0.95 ± 0.08 94 ± 28 154 1.6
vecuronium 15 ± 2 1.03 ± 0.12 129 ± 38 168 − 190 1.3 − 1.5
cisatracurium 10 ± 1 1.02 ± 0.09 88 ± 18 135 − 169 1.5 − 1.9
rocuronium 17 ± 2 0.67 ± 0.05 472 ± 95 1250−1600 2.6 − 3.4
atracurium 17 ± 2 0.56 ± 0.09 744 ± 120