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Journal of Enzyme Inhibition and Medicinal Chemistry|September 21, 2019
Novel 2-substituted-benzimidazole-6-sulfonamides as carbonic anhydrase inhibitors: synthesis, biological evaluation against isoforms I, II, IX and XII and molecular docking studiesCiro Milite, Giorgio Amendola, Alessio Nocentini, et al.
Biochemical Pharmacology|March 19, 2022
(+)-Catharanthine potentiates the GABAA receptor by binding to a transmembrane site at the β(+)/α(-) interface near the TM2-TM3 loopHugo R Arias, Cecilia M Borghese, Allison L Germann, et al.
Molecules (Basel, Switzerland)|July 27, 2024
Dual Inhibitors of P-gp and Carbonic Anhydrase XII (hCA XII) against Tumor Multidrug Resistance with Piperazine ScaffoldLaura Braconi, Chiara Riganti, Astrid Parenti, et al.
Journal of Medicinal Chemistry|January 26, 2026
First-in-Class Dual PDGFR/Carbonic Anhydrase IX/XII Inhibitors: 6,7-Dimethoxyquinoline-Sulfonamides as Promising Antileukemic AgentsEslam Roshdy, Eva Řezníčková, Mostafa M Elbadawi, et al.
Journal of Medicinal Chemistry|July 28, 2023
1,5-Diaryl-1,2,4-triazole Ureas as New SLC-0111 Analogues Endowed with Dual Carbonic Anhydrase and VEGFR-2 Inhibitory ActivitiesAhmed E Elsawi, Mostafa M Elbadawi, Alessio Nocentini, et al.
Bioorganic Chemistry|March 18, 2019
Synthesis of benzensulfonamides linked to quinazoline scaffolds as novel carbonic anhydrase inhibitorsAdel S El-Azab, Alaa A-M Abdel-Aziz, Sivia Bua, et al.
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