1246754-36-8Relevant academic research and scientific papers
1,3-Dioxolane-based ligands incorporating a lactam or imide moiety: Structure-affinity/activity relationship at α1-adrenoceptor subtypes and at 5-HT1A receptors
Franchini, Silvia,Prandi, Adolfo,Baraldi, Annamaria,Sorbi, Claudia,Tait, Annalisa,Buccioni, Michela,Marucci, Gabriella,Cilia, Antonio,Pirona, Lorenza,Fossa, Paola,Cichero, Elena,Brasili, Livio
, p. 3740 - 3751 (2010)
A series of 1,3-dioxolane-based compounds incorporating a lactam (2-4) or imide (5-7) moiety was synthesized and the pharmacological profile at α1-adrenoceptor subtypes and 5-HT1A receptor was assessed through binding and functional experiments. Starting from the 2,2-diphenyl-1,3-dioxolane derivative 1, previously shown to be a selective α1a(A)/α1d(D)-adrenoceptor subtype antagonist, over α1b(B) subtype and 5-HT1A receptor, and replacing one phenyl ring with lactam or imide moiety a reduction of α1/5-HT1A selectivity is observed, mainly due to the increase in 5-HT1A affinity. In functional experiments lactam derivatives seems to favour 5-HT1A receptor antagonism (pKb = 7.20-7.80) and α1B-adrenoceptor antagonist selectivity (α1B/α1A and α1B/ α1D of about 10-fold). The most interesting of the various imide derivatives is compound 7t, which is a selective α1D- adrenoceptor antagonist (pKb = 8.1 and α1D/α1A and α1D/α1B selectivity ratios of 16 and 11 respectively) whereas at 5-HT1A receptor it is a potent partial agonist (pD2 = 7.98, Emax = 60%).]. Given that cis and trans diastereomer pairs for 2-7 are possible, a computational strategy based on molecular docking studies was used to elucidate the atomic details of the 5HT1A/agonist and 5HT1A/antagonist interaction. The lactam derivatives seems to favour 5-HT1A receptor antagonism and α1B-adrenoceptor antagonist selectivity. The imide derivative 7t is a selective α1D-adrenoceptor antagonist whereas at 5-HT1A receptor it is a potent partial agonist.
