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Synthesis and biological evaluation of novel delta (δ) opioid receptor ligands with diazatricyclodecane skeletons

Authors :
Gabriele Murineddu
Gian Luca Casu
Paolo Lazzari
Stefania Ruiu
Giovanni Loriga
Gérard Aimé Pinna
Ilaria Manca
Battistina Asproni
Giorgio Marchese
Christian Dessi
Source :
European journal of medicinal chemistry (Online) 69 (2013): 413–426. doi:10.1016/j.ejmech.2013.09.014, info:cnr-pdr/source/autori:Loriga G.; Lazzari P.; Ruiu S.; Marchese G.; Manca I.; Casu G.L.; Dessi C.; Pinna G.A.; Asproni B.; Murineddu G./titolo:Synthesis and biological evaluation of novel delta (?) opioid receptor ligands with diazatricyclodecane skeletons/doi:10.1016%2Fj.ejmech.2013.09.014/rivista:European journal of medicinal chemistry (Online)/anno:2013/pagina_da:413/pagina_a:426/intervallo_pagine:413–426/volume:69
Publication Year :
2013
Publisher :
Elsevier BV, 2013.

Abstract

Considering the interesting pharmacological profile of the delta (?) selective opioid agonist compound SNC-80, conformationally constrained analogs containing two diazatricyclodecane ring systems in place of dimethylpiperazine core motif were synthesized. The compounds showed subnanomolar or low nanomolar ? opioid receptor binding affinity. Depending upon the substituents on the diazatricyclodecane ring, these compounds displayed varying selectivity for ? opioid receptor over ? and ? receptors. Amongst the novel compounds, 1Aa showed the more interesting biological profile, with higher ? affinity and selectivity compared to SNC-80. The ? receptor agonist profile and antinociceptive activity of 1Aa were confirmed using ex-vivo (isolated mouse vas deferens) and in vivo (tail flick) assays. © 2013 Elsevier Masson SAS. All rights reserved.

Details

ISSN :
02235234
Volume :
69
Database :
OpenAIRE
Journal :
European Journal of Medicinal Chemistry
Accession number :
edsair.doi.dedup.....278714a8f6ae83a8d9b63b81f2af6773
Full Text :
https://doi.org/10.1016/j.ejmech.2013.09.014