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. 2016 Aug 10;8(8):237. doi: 10.3390/toxins8080237

Table 1.

Stability constants K for the block of binding components channels formed by C2II and Iota b by chloroquine and related aminoquinolinium salts in lipid bilayer membranes a. * The results of similar titration experiments performed with C2IIa channels and chloroquine are given for comparison.

Chloroquine Analog K/103 M−1 KS/µM K/103 M−1 KS/µM
- C2II Iota b
Chloroquine 110 * 9.1 * 7.1 ± 1.7 140
C 23 1.5 ± 0.4 710 0.82 ± 0.21 1200
C 164 18.5 ± 2.5 54 0.39 ± 0.13 2400
C 268 198 ± 15 5.1 2.5 ± 0.4 400
C 280 6200 ± 40 0.16 12.5 ± 2.1 80

a The data represent means ± SD of at least three individual titration experiments. The membranes were formed from diphytanoyl phosphatidylcholine/n-decane. The aqueous phase contained 150 mM KCl, 10 mM MES-KOH, pH 6, and about 10 ng/mL activated C2II or about 20 ng/mL Iota b; T = 20 °C. * The stability constant K for binding of chloroquine to C2IIa channels is given for comparison and was taken from Bachmeyer et al. (2003) [45].