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. 2016 Feb 8;173(5):925–936. doi: 10.1111/bph.13411

Table 1.

Screening of allosteric effect of citalopram analogues on [3H]‐S‐CIT dissociation

Cpd (50 μM) t 1/2 for [ 3 H ]S‐CIT dissociation (min) n
Control 85 ± 6.9 10
S‐CIT 790 ± 160 4
2 380 ± 26 4
3 1090 ± 130 4
4 1170 ± 240 4
5 280 ± 70 4
6 260 ± 20 4
7 440 ± 30 4
8 570 ± 70 4
9 120 ± 10 4
10 110 ± 9.1 4
11 150 ± 18 4
12 150 ± 9.4 4
13 89 ± 6.5 4
14 85 ± 3.0 4
15 100 ± 15 4
Talopram 100 ± 3.8 4

Effect on t 1/2 (min) for [3H]‐S‐CIT dissociation by 50 μM of the indicated cpds. The t 1/2 values were calculated by non‐linear regression analysis of prebound [3H]‐S‐CIT dissociation on membrane preparations from COS7 cells transiently expressing SERT. Data are shown as mean ± SEM of n number of individual experiments. Due to the high temperature sensitivity of the assay, a control sample was always performed in parallel to the compounds, hence the high sample size for the control.