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1 ing effects of GBR 12909, a highly selective dopamine uptake inhibitor.
2 finities of novel drugs within this class of dopamine uptake inhibitors.
3 ign of molecular probes within this class of dopamine uptake inhibitors.
4 t to provide a CoMFA model for this class of dopamine uptake inhibitors.
5 analogues has been prepared that function as dopamine uptake inhibitors.
6 droxyphenylalanine (L-dopa) or the selective dopamine uptake inhibitor 1-2(bis[4-fluorophenyl] methox
10 y)tropane (benztropine) analogues are potent dopamine uptake inhibitors but exhibit behavioral profil
11 the 3alpha-(diphenylmethoxy)tropane class of dopamine uptake inhibitors can result in ligands with hi
12 (diphenylmethoxy)tropane (benztropine)-based dopamine uptake inhibitors do not demonstrate cocaine-li
13 sted that these two classes of tropane-based dopamine uptake inhibitors have distinct pharmacological
14 ds are generally more potent than cocaine as dopamine uptake inhibitors in vitro, although their acti
15 dopamine peak was confirmed by showing that dopamine uptake inhibitors increased the peak and dopami
17 l]acetamide (modafinil, (+/-)-1) is a unique dopamine uptake inhibitor that binds the dopamine transp
18 nd its analogues are tropane ring-containing dopamine uptake inhibitors that display binding and beha
19 and its analogs are tropane ring-containing dopamine uptake inhibitors that produce behavioral effec
20 ies may influence the reinforcing effects of dopamine uptake inhibitors, we investigated the local an
22 SAR in this series and ultimately to design dopamine uptake inhibitors with favorable lipophilicitie
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