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International Journal of Molecular Sciences|July 14, 2023
Novel Tetrazole Derivatives Targeting Tubulin Endowed with Antiproliferative Activity against Glioblastoma CellsLaura Gallego-Yerga, Andrea Jazmín Chiliquinga, Rafael Peláez
Medicinal Research Reviews|December 24, 2023
Experimental structure based drug design (SBDD) applications for anti-leishmanial drugs: A paradigm shift?Miguel Marín, Marta López, Laura Gallego-Yerga, et al.
Pharmaceutics|June 26, 2026
Antimitotic Naphthalene Sulfonamides Are Potent Antitumor Agents Acting Differently from ColchicineMiguel Marín, Raúl Fuentes-Martín, Baldomero Sánchez, et al.
International Journal of Molecular Sciences|December 23, 2023
Frentizole, a Nontoxic Immunosuppressive Drug, and Its Analogs Display Antitumor Activity via Tubulin InhibitionSergio Ramos, Alba Vicente-Blázquez, Marta López-Rubio, et al.
Chemical Communications (Cambridge, England)|May 31, 2014
Glycoligand-targeted core-shell nanospheres with tunable drug release profiles from calixarene-cyclodextrin heterodimersLaura Gallego-Yerga, Michela Lomazzi, Francesco Sansone, et al.
European Journal of Medicinal Chemistry|January 21, 2026
2-Naphthyl tetrazoles are potent antiproliferative and apoptotic inducers with different tubulin polymerization dynamics inhibitory activityMiguel Marín, Laura Gallego-Yerga, Dominik Fachet, et al.
Computational and Structural Biotechnology Journal|August 25, 2021
Application of ensemble pharmacophore-based virtual screening to the discovery of novel antimitotic tubulin inhibitorsLaura Gallego-Yerga, Rodrigo Ochoa, Isaías Lans, et al.
European Journal of Medicinal Chemistry|July 3, 2024
Promising anti-proliferative indolic benzenesulfonamides alter mechanisms with sulfonamide nitrogen substituentsRaúl Fuentes-Martín, Pilar Ayuda-Durán, Robert Hanes, et al.
Organic & Biomolecular Chemistry|December 5, 2014
Cyclodextrin- and calixarene-based polycationic amphiphiles as gene delivery systems: a structure-activity relationship studyLaura Gallego-Yerga, Michela Lomazzi, Valentina Franceschi, et al.
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