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Bioorganic & Medicinal Chemistry Letters|May 23, 2006
5-benzylidene-hydantoins as new EGFR inhibitors with antiproliferative activityCaterina Carmi, Andrea Cavazzoni, Valentina Zuliani, et al.
Drug Design and Discovery|December 17, 2003
Synthesis and three-dimensional quantitative structure-activity relationship analysis of H3 receptor antagonists containing a neutral heterocyclic polar groupSilvia Rivara, Marco Mor, Fabrizio Bordi, et al.
Biological Psychiatry|May 22, 2007
Antidepressant-like activity of the fatty acid amide hydrolase inhibitor URB597 in a rat model of chronic mild stressMarco Bortolato, Regina A Mangieri, Jin Fu, et al.
Oncotarget|October 6, 2017
Antiproliferative and pro-apoptotic activity of melatonin analogues on melanoma and breast cancer cellsGiuliana Gatti, Valeria Lucini, Silvana Dugnani, et al.
Chemmedchem|July 29, 2009
A second generation of carbamate-based fatty acid amide hydrolase inhibitors with improved activity in vivoJason R Clapper, Federica Vacondio, Alvin R King, et al.
Chemmedchem|August 29, 2012
MT1-selective melatonin receptor ligands: synthesis, pharmacological evaluation, and molecular dynamics investigation of N-{[(3-O-substituted)anilino]alkyl}amidesSilvia Rivara, Daniele Pala, Alessio Lodola, et al.
Cancers|September 7, 2019
The Autocrine FGF/FGFR System in both Skin and Uveal Melanoma: FGF Trapping as a Possible Therapeutic ApproachSara Rezzola, Roberto Ronca, Alessandra Loda, et al.
Cancers|September 19, 2018
Repurposing of Drugs Targeting YAP-TEAD FunctionsGian Marco Elisi, Matteo Santucci, Domenico D'Arca, et al.
Bioorganic & Medicinal Chemistry|June 24, 2004
Synthesis, pharmacological evaluation, and structure-activity relationships of benzopyran derivatives with potent SERM activityGabriele Amari, Elisabetta Armani, Silvia Ghirardi, et al.
Annali Di Chimica|November 1, 2007
Identification of a bioactive impurity in a commercial sample of 6-methyl-2-p-tolylaminobenzo[d][1,3]oxazin-4-one (URB754)Giorgio Tarzia, Francesca Antonietti, Andrea Duranti, et al.
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