Sabatino Maione

5'-C-Ethyl-tetrazolyl-N(6)-substituted adenosine and 2-chloro-adenosine derivatives as highly potent dual acting A1 adenosine receptor agonists and A3 adenosine receptor antagonists.

Riccardo Petrelli, Ettore Novellino, Antonio Lavecchia, 2015, Journal of medicinal chemistry.

Intravenous neural stem cells abolish nociceptive hypersensitivity and trigger nerve regeneration in experimental neuropathy

A. Vescovi, L. Rodella, P. Sacerdote, 2012, PAIN®.

New resorcinol-anandamide "hybrids" as potent cannabinoid receptor ligands endowed with antinociceptive activity in vivo.

Federico Corelli, Tiziano Tuccinardi, Adriano Martinelli, 2009, Journal of medicinal chemistry.

Forebrain pain mechanisms

Vasco Galhardo, S. Mackey, V. Neugebauer, 2009, Brain Research Reviews.

Design, synthesis, and pharmacological characterization of indol-3-ylacetamides, indol-3-yloxoacetamides, and indol-3-ylcarboxamides: potent and selective CB2 cannabinoid receptor inverse agonists.

Federico Corelli, Simone Brogi, Pier Andrea Borea, 2012, Journal of medicinal chemistry.

Endocannabinoids and neuropathic pain: focus on neuron–glia and endocannabinoid–neurotrophin interactions

Livio Luongo, Vincenzo Di Marzo, V. Di Marzo, 2014, The European journal of neuroscience.