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European Journal of Medicinal Chemistry|November 17, 2023
Design, synthesis, ADME and biological evaluation of benzylpiperidine and benzylpiperazine derivatives as novel reversible monoacylglycerol lipase (MAGL) inhibitorsMiriana Di Stefano, Samuele Masoni, Giulia Bononi, et al.Journal of Natural Products|July 11, 2017
Constituents of Polygala flavescens ssp. flavescens and Their Activity as Inhibitors of Human Lactate DehydrogenaseMarinella De Leo, Lorenzo Peruzzi, Carlotta Granchi, et al.Bioorganic & Medicinal Chemistry|September 29, 2012
Salicylaldoxime derivatives as new leads for the development of carbonic anhydrase inhibitorsTiziano Tuccinardi, Simone Bertini, Carlotta Granchi, et al.Fitoterapia|September 22, 2018
New diterpenes from Salvia pseudorosmarinus and their activity as inhibitors of monoacylglycerol lipase (MAGL)Marinella De Leo, Conny Guillen Huallpa, Britt Alvarado, et al.Nucleosides, Nucleotides & Nucleic Acids|June 20, 2024
Evaluation of the combination of gemcitabine, carboplatin, and lactate dehydrogenase A inhibitor on malignant mesotheliomaMarika A Frańczak, Federica Borea, Ryszard T Smoleński, et al.Phytochemistry|April 20, 2015
Phenylpropanoids and flavonoids from Phlomis kurdica as inhibitors of human lactate dehydrogenaseAmmar Bader, Tiziano Tuccinardi, Carlotta Granchi, et al.Journal of Biomolecular Structure & Dynamics|May 26, 2020
Discovery of a new ATP-citrate lyase (ACLY) inhibitor identified by a pharmacophore-based virtual screening studyVibhu Jha, Salvatore Galati, Valerio Volpi, et al.Bioorganic & Medicinal Chemistry|May 24, 2014
Identification and characterization of a new reversible MAGL inhibitorTiziano Tuccinardi, Carlotta Granchi, Flavio Rizzolio, et al.Organic & Biomolecular Chemistry|August 30, 2013
Assessing the differential action on cancer cells of LDH-A inhibitors based on the N-hydroxyindole-2-carboxylate (NHI) and malonic (Mal) scaffoldsCarlotta Granchi, Emilia C Calvaresi, Tiziano Tuccinardi, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|September 23, 2017
Development of terphenyl-2-methyloxazol-5(4H)-one derivatives as selective reversible MAGL inhibitorsCarlotta Granchi, Isabella Caligiuri, Eleonora Bertelli, et al.Pageof 12