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Journal of Medicinal Chemistry|November 11, 2005
Specific targeting highly conserved residues in the HIV-1 reverse transcriptase primer grip region. Design, synthesis, and biological evaluation of novel, potent, and broad spectrum NNRTIs with antiviral activityCaterina Fattorusso, Sandra Gemma, Stefania Butini, et al.Journal of Medicinal Chemistry|September 12, 2014
Identification of the first inhibitor of the GBP1:PIM1 interaction. Implications for the development of a new class of anticancer agents against paclitaxel resistant cancer cellsMirko Andreoli, Marco Persico, Ajay Kumar, et al.Journal of Medicinal Chemistry|February 19, 2008
Design, synthesis, and structure-activity relationship studies of 4-quinolinyl- and 9-acrydinylhydrazones as potent antimalarial agentsCaterina Fattorusso, Giuseppe Campiani, Gagan Kukreja, et al.Molecules (Basel, Switzerland)|October 16, 2025
1,2,4-Thiadiazolidin-3,5-Diones as Inhibitors of Cysteine ProteasesMaria Aparecida Juliano, Marco Persico, Beatrice Severino, 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|December 31, 2008
Combining 4-aminoquinoline- and clotrimazole-based pharmacophores toward innovative and potent hybrid antimalarialsSandra Gemma, Giuseppe Campiani, Stefania Butini, et al.Pageof 6