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International Journal of Molecular Sciences|July 27, 2024
Three-Dimensional Quantitative Structure-Activity Relationship Study of Transient Receptor Potential Vanilloid 1 Channel Antagonists Reveals Potential for Drug Design PurposesBeatrice Gianibbi, Anna Visibelli, Giacomo Spinsanti, et al.
European Journal of Pharmacology|February 8, 2024
3,3'-O-dimethylquercetin: A bi-functional vasodilator isolated from green propolis of the Caatinga Mimosa tenuifloraNinh The Son, Beatrice Gianibbi, Alice Panti, et al.
Journal of Molecular Biology|December 7, 2025
Structure-based Discovery of a Non-competitive FTO Inhibitor Bound to a Cryptic Site at the Domain InterfaceAayushi Singh, Francesco Pettini, Beatrice Gianibbi, et al.
Bioorganic Chemistry|December 23, 2022
Artificial intelligence-driven identification of morin analogues acting as CaV1.2 channel blockers: Synthesis and biological evaluationGabriele Carullo, Federica Falbo, Amer Ahmed, et al.
Archiv Der Pharmazie|September 6, 2024
Exploring the chemical space around chrysin to develop novel vascular CaV1.2 channel blockers, promising vasorelaxant agentsFederica Falbo, Gabriele Carullo, Alice Panti, et al.
International Journal of Molecular Sciences|August 27, 2021
The Antimalarial Mefloquine Shows Activity against Mycobacterium abscessus, Inhibiting Mycolic Acid MetabolismGiulia Degiacomi, Laurent Roberto Chiarelli, Deborah Recchia, et al.
Antibiotics (Basel, Switzerland)|October 28, 2025
STOP Strategy to Inhibit P. falciparum and S. aureus Growth: Molecular Mechanism Studies on Purposely Designed HybridsBeatrice Gianibbi, Riccardo Corina, Nicoletta Basilico, et al.
European Journal of Medicinal Chemistry|April 29, 2022
Tapping into the antitubercular potential of 2,5-dimethylpyrroles: A structure-activity relationship interrogationDorothy Semenya, Meir Touitou, Domiziana Masci, et al.
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