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• W2277605229 abstract "The present work reports the synthesis of trans-2-amino-5(6)-fluoro-6(5)-hydroxy-1-phenyl-2,3-dihydro-1H-indenes (4a−f, 5a−f) as a continuation of our studies to better understand the significance of the halo substituent in the trans-1-phenyl-2-aminoindane series and to extend knowledge of the monophenolic ligands of DA receptors. The affinity of the new compounds and related methoxylated precursors (10−15 and 18−23) was estimated in vitro by displacement of [3H]SCH23390 (for D1-like receptors) or [3H]YM-09-151-2 (for D2-like receptors) from homogenates of porcine striatal membranes. The results indicate that unsubstituted amines 4a, 5a, 10, and 11 are poorly effective at DA receptors. The introduction of two n-propyl groups on the nitrogen atom (compounds 14, 15, 4c, and 5c) and N-allyl-N-methyl- or N-methyl-N-propyl- substitution (compounds 20−23, 4e, 4f, 5e, 5f) increased the D2-like affinities and selectivity. The D2-like agonistic activity of selected compounds 15, 20, 21, 4e, 5c, and 5e was proved by evaluating their effects on the cyclic guanosine monophosphate (cGMP) content in rat neostriatal membranes. All tested compounds displayed a potential dopamine D2-like agonist profile decreasing basal levels of cGMP. The selective D2-like agonism of compounds 20 and 5e was proved by their effects on basal striatal adenylyl cyclase activity." @default.
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• W2277605229 date "2005-03-09" @default.
• W2277605229 modified "2023-10-01" @default.
• W2277605229 title "Preparation and Pharmacological Characterization of <i>trans</i>-2-Amino-5(6)-fluoro-6(5)-hydroxy-1-phenyl-2,3-dihydro-1<i>H</i>-indenes as D₂-like Dopamine Receptor Agonists" @default.
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• W2277605229 doi "https://doi.org/10.1021/jm040889k" @default.
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