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Journal of Enzyme Inhibition and Medicinal Chemistry|November 23, 2023
Inhibition of pathogenic bacterial carbonic anhydrases by monothiocarbamatesSimone Giovannuzzi, Anil Kumar Marapaka, Nader S Abutaleb, et al.European Journal of Medicinal Chemistry|July 14, 2020
Discovery of first-in-class multi-target adenosine A2A receptor antagonists-carbonic anhydrase IX and XII inhibitors. 8-Amino-6-aryl-2-phenyl-1,2,4-triazolo [4,3-a]pyrazin-3-one derivatives as new potential antitumor agentsCostanza Ceni, Daniela Catarzi, Flavia Varano, et al.International Journal of Molecular Sciences|July 27, 2022
Squaramide-Tethered Sulfonamides and Coumarins: Synthesis, Inhibition of Tumor-Associated CAs IX and XII and Docking SimulationsGiulia Arrighi, Adrián Puerta, Andrea Petrini, et al.Future Medicinal Chemistry|January 29, 2025
A series of benzensulfonamide derivatives as new potent carbonic anhydrase IX and XII inhibitorsSusanna Nencetti, Doretta Cuffaro, Lidia Ciccone, et al.ACS Medicinal Chemistry Letters|April 19, 2019
N-Nitrosulfonamides as Carbonic Anhydrase Inhibitors: A Promising Chemotype for Targeting Chagas Disease and LeishmaniasisAlessandro Bonardi, Alane Beatriz Vermelho, Veronica da Silva Cardoso, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|June 27, 2022
Structure-activity relationship studies for inhibitors for vancomycin-resistant Enterococcus and human carbonic anhydrasesWeiwei An, Katrina J Holly, Alessio Nocentini, et al.Journal of Medicinal Chemistry|June 15, 2026
Discovery of Subnanomolar and Highly Selective Carbonic Anhydrase II Inhibitors Featuring L-Shaped Scaffolds via Active-Site-Matched Fragment GrowingYitong Wang, Alessio Nocentini, Marta Ferraroni, et al.European Journal of Medicinal Chemistry|December 6, 2021
Natural inspired ligustrazine-based SLC-0111 analogues as novel carbonic anhydrase inhibitorsDiaaeldin M Elimam, Wagdy M Eldehna, Rofaida Salem, et al.European Journal of Medicinal Chemistry|July 6, 2019
Application of hydrazino and hydrazido linkers to connect benzenesulfonamides with hydrophilic/phobic tails for targeting the middle region of human carbonic anhydrases active site: Selective inhibitors of hCA IXHeba Abdelrasheed Allam, Samar H Fahim, Mahmoud F Abo-Ashour, et al.Journal of Medicinal Chemistry|October 8, 2024
Benzoxaborinine, New Chemotype for Carbonic Anhydrase Inhibition: Ex Novo Synthesis, Crystallography, In Silico Studies, and Anti-Melanoma Cell Line ActivitySimone Giovannuzzi, Anna Nikitjuka, Andrea Angeli, et al.Pageof 29