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Journal of Medicinal Chemistry|July 5, 2013
Synthesis and structure-activity relationship studies of O-biphenyl-3-yl carbamates as peripherally restricted fatty acid amide hydrolase inhibitorsGuillermo Moreno-Sanz, Andrea Duranti, Laurin Melzig, et al.European Journal of Medicinal Chemistry|May 18, 2021
Chemical modification of NSC12 leads to a specific FGF-trap with antitumor activity in multiple myelomaRiccardo Castelli, Sara Taranto, Lucia Furiassi, et al.European Journal of Medicinal Chemistry|August 31, 2021
A sulfonyl fluoride derivative inhibits EGFR<sup>L858R/T790M/C797S</sup> by covalent modification of the catalytic lysineFrancesca Ferlenghi, Laura Scalvini, Federica Vacondio, et al.Proceedings of the National Academy of Sciences of the United States of America|November 21, 2009
Selective N-acylethanolamine-hydrolyzing acid amidase inhibition reveals a key role for endogenous palmitoylethanolamide in inflammationCarlos Solorzano, Chenggang Zhu, Natalia Battista, et al.European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|August 25, 2004
Imidazole H3-antagonists: relationship between structure and ex vivo binding to rat brain H3-receptorsFederica Vacondio, Marco Mor, Claudia Silva, et al.Nature Neuroscience|November 22, 2011
A catalytically silent FAAH-1 variant drives anandamide transport in neuronsJin Fu, Giovanni Bottegoni, Oscar Sasso, et al.Journal of Medicinal Chemistry|September 4, 2015
Highly Potent and Selective MT2 Melatonin Receptor Full Agonists from Conformational Analysis of 1-Benzyl-2-acylaminomethyl-tetrahydroquinolinesGilberto Spadoni, Annalida Bedini, Simone Lucarini, et al.Journal of Medicinal Chemistry|February 16, 2010
Novel irreversible epidermal growth factor receptor inhibitors by chemical modulation of the cysteine-trap portionCaterina Carmi, Andrea Cavazzoni, Stefano Vezzosi, et al.Nature Medicine|December 4, 2002
Modulation of anxiety through blockade of anandamide hydrolysisSatish Kathuria, Silvana Gaetani, Darren Fegley, et al.European Journal of Medicinal Chemistry|November 26, 2018
Balancing reactivity and antitumor activity: heteroarylthioacetamide derivatives as potent and time-dependent inhibitors of EGFRRiccardo Castelli, Nicole Bozza, Andrea Cavazzoni, et al.Pageof 20