Showing results (111-120 of 124) with videos related to
Sort By:
Pageof 13
Cell Metabolism|September 4, 2018
Increased Lactate Secretion by Cancer Cells Sustains Non-cell-autonomous Adaptive Resistance to MET and EGFR Targeted TherapiesMaria Apicella, Elisa Giannoni, Stephany Fiore, et al.Cell Chemical Biology|January 3, 2017
Systems Structural Biology Analysis of Ligand Effects on ERα Predicts Cellular Response to Environmental Estrogens and Anti-hormone TherapiesJerome C Nwachukwu, Sathish Srinivasan, Nelson E Bruno, et al.Journal of Medicinal Chemistry|October 2, 2014
CB2-selective cannabinoid receptor ligands: synthesis, pharmacological evaluation, and molecular modeling investigation of 1,8-Naphthyridin-2(1H)-one-3-carboxamidesValentina Lucchesi, Dow P Hurst, Derek M Shore, et al.European Journal of Medicinal Chemistry|October 12, 2020
Design, synthesis and biological evaluation of second-generation benzoylpiperidine derivatives as reversible monoacylglycerol lipase (MAGL) inhibitorsCarlotta Granchi, Giulia Bononi, Rebecca Ferrisi, et al.Journal of Medicinal Chemistry|January 9, 2018
Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) InhibitorsMojgan Aghazadeh Tabrizi, Pier Giovanni Baraldi, Stefania Baraldi, et al.Journal of Medicinal Chemistry|May 6, 2022
Reversible Monoacylglycerol Lipase Inhibitors: Discovery of a New Class of Benzylpiperidine DerivativesGiulia Bononi, Miriana Di Stefano, Giulio Poli, et al.European Journal of Medicinal Chemistry|August 26, 2018
Discovery of long-chain salicylketoxime derivatives as monoacylglycerol lipase (MAGL) inhibitorsGiulia Bononi, Carlotta Granchi, Margherita Lapillo, et al.Journal of Medicinal Chemistry|February 22, 2011
Discovery of N-hydroxyindole-based inhibitors of human lactate dehydrogenase isoform A (LDH-A) as starvation agents against cancer cellsCarlotta Granchi, Sarabindu Roy, Chiara Giacomelli, et al.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.Bioorganic Chemistry|June 24, 2025
Discovery of reversible monoacylglycerol lipase (MAGL) inhibitors based on ortho-hydroxyanilide scaffoldGiulia Bononi, Francesca Gado, Samuele Masoni, et al.Pageof 13