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Food Chemistry|February 15, 2024
Traceability and authentication in agri-food production: A multivariate approach to the characterization ofthe Italian food excellence elephant garlic (Allium ampeloprasum L.), a vasoactive nutraceuticalGabriele Carullo, Francesca Borghini, Fabio Fusi, et al.Chemmedchem|January 16, 2018
Development of Potent Inhibitors of the Mycobacterium tuberculosis Virulence Factor Zmp1 and Evaluation of Their Effect on Mycobacterial Survival inside MacrophagesMarco Paolino, Margherita Brindisi, Alessandra Vallone, et al.Journal of Medicinal Chemistry|January 11, 2002
Pyrrolo[1,3]benzothiazepine-based atypical antipsychotic agents. Synthesis, structure-activity relationship, molecular modeling, and biological studiesGiuseppe Campiani, Stefania Butini, Sandra Gemma, et al.European Journal of Medicinal Chemistry|September 14, 2019
Development of novel multipotent compounds modulating endocannabinoid and dopaminergic systemsAlessandro Grillo, Giulia Chemi, Simone Brogi, et al.Archiv Der Pharmazie|January 28, 2025
Synthesis and biological investigation of peptidomimetic SARS-CoV-2 main protease inhibitors bearing quinoline-based heterocycles at P<sub>3</sub>Sara Rossi, Graziano Deidda, Lia Fiaschi, et al.European Journal of Medicinal Chemistry|March 24, 2018
Antimalarial agents against both sexual and asexual parasites stages: structure-activity relationships and biological studies of the Malaria Box compound 1-[5-(4-bromo-2-chlorophenyl)furan-2-yl]-N-[(piperidin-4-yl)methyl]methanamine (MMV019918) and analoguesAlessandra Vallone, Sarah D'Alessandro, Simone Brogi, et al.Journal of Medicinal Chemistry|May 12, 2009
Specific targeting of peripheral serotonin 5-HT(3) receptors. Synthesis, biological investigation, and structure-activity relationshipsElena Morelli, Sandra Gemma, Roberta Budriesi, et al.Journal of Medicinal Chemistry|February 19, 2008
Clotrimazole scaffold as an innovative pharmacophore towards potent antimalarial agents: design, synthesis, and biological and structure-activity relationship studiesSandra Gemma, Giuseppe Campiani, Stefania Butini, et al.Journal of Medicinal Chemistry|February 16, 2011
Non-nucleoside inhibitors of human adenosine kinase: synthesis, molecular modeling, and biological studiesStefania Butini, Sandra Gemma, Margherita Brindisi, et al.ACS Pharmacology & Translational Science|February 20, 2025
Spirotetrahydroisoquinoline-Based Histone Deacetylase Inhibitors as New Antifibrotic Agents: Biological Evaluation in Human Fibroblasts from Bronchoalveolar Lavages of Idiopathic Pulmonary Fibrosis PatientsAnna Fontana, Laura Bergantini, Gabriele Carullo, et al.Pageof 15