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In the 1,5- isomers, after irradiation of triazole proton there is no enhancement of ethyl proton. On the other hand, after irradiation of triazole proton in the 1,4-isomers, there is clear enhancement of ethyl proton which comes near 4.6 ppm and 2.81 ppm
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In the 1,5- isomers, after irradiation of triazole proton there is no enhancement of ethyl proton. On the other hand, after irradiation of triazole proton in the 1,4-isomers, there is clear enhancement of ethyl proton which comes near 4.6 ppm and 2.81 ppm
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Compounds were evaluated in vitro for dopamine D2 D3, D4 receptors binding affinity by measuring their ability to displace radioligand ([3H]Methylspiperone for D2 and D3, [3H]YM-09151- 2 for D4) from the cloned human dopamine receptors D2Long D3 and D4.2 which were stably expressed in CHO or Sf9 cells, respectively. For serotonin receptors, compounds were biologically evaluated against human recombinant 5-HT1A, 5- HT2A, 5-HT2C, 5-HT6 and 5-HT7 receptors stably expressed by CHO-K1 cell lines through [3H]8-OH-DPAT, [3H]Ketanserin, [3H]Mesulergine and [3H]LSD binding assay, respectively
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Compounds were evaluated in vitro for dopamine D2, D3, D4 receptors binding affinity by measuring their ability to displace radioligand ([3H]Methylspiperone for D2 and D3, [3H]YM-09151- 2 for D4) from the cloned human dopamine receptors D2Long, D3 and D4.2 which were stably expressed in CHO or Sf9 cells, respectively. For serotonin receptors, compounds were biologically evaluated against human recombinant 5-HT1A, 5- HT2A, 5-HT2C, 5-HT6 and 5-HT7 receptors stably expressed by CHO-K1 cell lines through [3H]8-OH-DPAT, [3H]Ketanserin, [3H]Mesulergine and [3H]LSD binding assay, respectively
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