Table 4.
Inhibition of [3H]TCP Binding at the PCP Binding Site by Substituted N-(2-(Chloro-5-alkylthiophenyl)-N′-(3-(trifluoromethyl)phenyl)-N′-methylguanidines
| ||
|---|---|---|
| ligand | R | inhibition (%)a |
| 36b | Me | 96.1 |
| 41 | Et | 86.4 |
| 42 | Pr | 62.1 |
| 43 | Bu | 82.7 |
| 44 | iPr | 22.6 |
| 45 | sBu | 48.8 |
| 46 | CH2F | 57.5 |
| 47 | CH2CH2F | 82.1 |
| 48 | Bn | 88.6 |
At 1.0 μM (mean from two experiments).
From Table 3; shown for ease of comparison.