FAUC 329

Disturbances of neutrotransmission at the dopamine D3 receptor are related to several neuropsychiatric diseases and in particular to drug addiction. Herein, we report the computer‐assisted prediction of D3 selectivities of new fluoroalkoxy‐substituted receptor ligands by means of 3D‐QSAR analysis. As close analogues of the D3‐selective lead compound FAUC 346 and BP 879, the 19F‐substituted test compounds 4 a–d were synthesized and evaluated. In vitro investigation of their binding characteristics in transfected Chinese Hamster Ovary (CHO) cells led to excellent Ki values between 0.12 and 0.69 nM at the dopamine D3 subtype. The benzothiophene‐substituted carboxamide 4 a (Ki=0.12 nM) displayed 133 and 283‐fold selectivity over the structurally related D2Long and D4 subtypes, respectively. Mitogenesis assays showed the behavior of partial agonists. Based on these data, we synthesized the [18F]fluoroethoxy‐substituted radioligands [18F]4 a–d. The N‐[4‐[4‐(2‐hydroxyphenyl)piperazin‐1‐yl]butyl]‐2‐carboxamides 3 a–d were prepared and labeled with 2‐[18F]fluoroethyltosylate in a two‐step procedure. Optimization of the 18F‐labeling conditions led to radiochemical yields between 24 and 65 %.

Elucidation of the physiological role of the D3 receptor and its distribution in the brain using positron emission tomography (PET) is hampered by the lack of bioavailable subtype selective tracer ligands. To develop appropriate D3 radioligands, we designed an integrative procedure involving the elucidation of structural features determining D3 selectivity over both congeners D2 and D4 by comparative molecular analysis. Thus, we have successfully generated CoMFA and CoMSIA models based on the affinitiy differences of a series of 79 ligands representing a broad range of selectivities. These models yielded highly significant cross-validations (q2cv(D3/D2) = 0.86; q2cv(D3/D4) = 0.92) and excellent predictions of a 16-ligand test set (r2pred = 0.79-0.93). Exploiting this information, synthesis and receptor binding studies directed us to the fluorinated lead compounds 78 and 79, featuring subnanomolar D3 affinities and considerable selectivities over D2 and D4 and, subsequently, to the subtype selective PET tracers [18F]78 and [18F]79.